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Jobs - Biotech & Science classifieds in los angeles

<![CDATA[We are an independent Food and Environmental Testing laboratory in the City of Commerce that is rapidly growing. We are currently looking to expand our Microbiology Team. Microbiology Laboratory Technician duties include but are not limited to: receiving samples, logging in samples, preparing serial dilutions, preparing enrichments, and initiating analyses. Analytical techniques include: pour plating, spread plating, MPN tubes, petrifilm, pathogen enrichments, pathogen confirmations, running automated-PCR and ELISA assays. A successful candidate must be able to work in a fast paced environment, work well with others, work efficiently with minimal supervision, have flexible availability, and a positive attitude. Knowledge of aseptic technique and good laboratory practices a must. B.A. or B.S. degree in a biology-related field is a must; previous lab experience is a plus. This is a part time position but may become a full time position, it requires to work on weekends and late shifts. 12-14/hr BOE. ]]>

<![CDATA[Manufacturing biotech firm needs doctor, preferably ophthalmologist, as medical director part time. We need deal license to work with pharmaceuticals. ]]>

<![CDATA[F/T Medical Assistant position for a highly qualified candidate. Our office is seeking an excellent Medical Assistant who has a minimum of 2 years of medical office patient experience. Candidate must interacting with patients on a daily basis, taking medical histories, monitor patients, assist with minor surgeries and follow-up with prescription telephone calls as well as working with multiple physicians. Our office is looking for a detailed oriented Medical Assistant who possess a professional attitude, work accurately and efficiently while assist MDs, Physician Assistants, RN and other staff. We offer outstanding salary and benefits for the qualified candidate. PLEASE DO NOT APPLY IF THERE IS ONLY EX-TERN OR INTER-SHIP EXPERIENCE ON THE RESUME. Candidates must possess the following skills: -MA certificate -minimum of 2 yrs of clinical office experience -OSHA and CLIA compliance -excellent written and oral communication skills -ability to record medical histories with accurate detail -work in an efficient and highly professional manner -personable and friendly -ability to assist with minor surgeries -able to learn new software computer programs -ability to work with multiple physicians and staff -professional attitude If the above outline describes your professional skills and objectives, please forward your resume for consideration. Thank you. ]]>

<![CDATA[Are you currently taking a statin such as Zocor, Crestor, or Lipitor? Do you have high triglycerides? Do you have diabetes or a history of heart problems? If so, you may qualify to participate in a research study to test an investigational medication, while still remaining on your current medications. You may be eligible if you: - Are 18 years of age or older, - Are currently taking a statin such as ZocorÒ, CrestorÒ, or LipitorÒ - Have high triglycerides - Have Diabetes, or history of cardiac problems If eligible, you will receive at no cost: - Study-related physical examinations - Study-related laboratory tests - Investigational study medication - Compensation for your time and travel For more information please call (310) 552-5700. ]]>

<![CDATA[Medical Marijuana Collective is seeking a detail-oriented, accurate, honest, and trustworthy individual to join the team. Job description is much similar to that of a Pharmacy Assistant, as you will be responsible for stocking medications, preparing medication vials with the correct amounts, maintain complete and organized records and reports, and audit the inventories. This position is Part-time with a fixed schedule. 24 hours a week. Monday, Wednesday, Friday, and Sunday, 10am to 4pm. Ideal candidates will: -Have some experience in pharmacy assisting -Have reliable transportation -Be accurate and responsible -Be able to work under an extremely controlled atmosphere with strict rules Compensation starts at $11.50/hour (roughly $270 per week) Please send in your resume with your experience, references, and contact information. ***DUE TO THE OVERWHELMING RESPONSE*** Please understand that this position is intended for a responsible professional, it is not a "weed hookup." Those without any relevant experience, this position might not be for you. Due to the nature of the establishment, it might be easy to confuse the position with a receptionist or "budtender," however, the position we are hiring for does not entail any customer service or interaction, thus customer service and "deal-making" are not relevant experience that we are seeking (great skills nonetheless, just not relevant to this particular position). ]]>

<![CDATA[Having a tough time finding the right job? Consider starting your own business…….. $450 Business Plan Includes: - Executive Summary - Sales & Marketing Plan - 3 years - Income Statement - 3 years – Balance Sheet Statement - 3 years – Cash Flow Statement Perfect for investor presentations and bank loans. Principal Experience - 18 years experience writing business plans - Raised in excess of $10M – investors and loans - Entrepreneur, consultant and college instructor The first step is responding to this email......... ]]>

<![CDATA[Sample processing Supervisor UCLA Title: SRA III - Supervisor Job No.: H51688 Work Hours: Monday - Friday 1:30pm - 10:00pm Work Location: UCLA Olympic Lab Job Type: Career Job Duties: A Sample Processing Supervisor at the UCLA Olympic Analytical Laboratory will be responsible for scheduling and day to day operation of receiving samples, storage, aliquoting, extraction and instrumental analysis. In coordination with other supervisors and Scientific Director(s)/Scientific Specialist(s), he/she will be expected to monitor the relevant work flow and quality of results, supervise the personnel in assigned sections and shifts and participate in task executions. He/she will be expected to handle any matters related to sections supervised, with the goal of providing accurate results to clients in a timely fashion and to participate in research and special projects as they arise. Requires rotation in providing afternoon shift, weekend and holiday coverage as needed. Supervision for this position will be limited. Directions will be given by Scientific Director(s), Scientific Specialist(s), and Laboratory Director. Job Qualifications: Supervision will be focused in particular on the areas of Receiving, Assay Chemistry, Instrumentation and LC/IRMS Data Reading. Must be proficient in full evaluation of sample preparation and instrumental analysis. Will provide input for employee performance appraisals. Requires a BS or BA in chemistry, biological sciences or other relevant field, 2 years experience in a laboratory setting or comparable training and previous supervisory experience APPLY VIA FAX to: 310-206-9077 ]]>

<![CDATA[<center><img src="http://www.jobelephant.com/banners/6110.gif"></center> California Institute of Technology Research Technician Assistant - Biology Open Until Filled Job Summary Assisting researchers on molecular neurobiology projects using molecular biology techniques and providing general technical lab support. Job Duties Preparation of solutions, buffers, media, reagents, and bacterial plates Transformation of E.coli with plasmid DNA Preparation of plasmid minipreps and maxipreps Restriction enzyme digestion of DNA and agarose gel electrophoresis analysis PCR analysis of DNA samples Stocking and ordering supplies Other miscellaneous general laboratory technical support duties as assigned. Basic Qualifications B.A. in Biology, Biochemistry, Chemistry or related field. One year or more experience working in a molecular biology lab Must have experience with Excel database, PowerPoint, and Word programs Experience performing histology and molecular biology techniques DNA subcloning and miniprep analysis PCR, and large scale plasmid isolation Preferred Qualifications Experience in preparing DNA for sequencing and maintenance of tissue cultured cells desired. To be considered for this position please visit our web site and apply on line at the following link: <a href="http://apptrkr.com/140457" rel="nofollow">http://apptrkr.com/140457</a> Caltech is an Affirmative Action/Equal Opportunity Employer. Women, Minorities, Veterans and Disabled Persons are encouraged to apply. <img src="http://jobelephant.com/img.php?id=140457&image=logo"> Copyright ©2009 Jobelephant.com Inc. All rights reserved. <a href="http://www.jobelephant.com/" rel="nofollow">Posted by the FREE value-added recruitment advertising agency</a> <div>jeid-fce799a86c0863b11069481e3d0cbb4a</div>]]>

<![CDATA[ A growing environmental laboratory in the Southern Los Angeles/Northern Orange County area has immediate openings for technicians, analysts, and a supervisor in the metals department. Analysts must have at least one year experience with ICP/MS. Supervisors must have at least three years analytical experience which includes: - ICP/MS - One year experience in managing other employees - A.B.S. Degree - Ability to work well with others - Good communication skills - Strong work ethic The company is an equal opportunity employer and offers a competitive compensation package including: - Health Benefits - Vacation/Sick time - Holidays - 401(k) plan Candidates interested in any of these positions should reply by email and include a resume. Immediate openings available. ]]>

<![CDATA[Hamilton Company is a global enterprise headquartered in Reno, Nevada with manufacturing facilities in Reno, Boston and Bonaduz, Switzerland. Branch sales offices are located in France, Germany, and the United Kingdom. We are the worldwide leader in the design and manufacture of manual, semi-automated and robotic products for precision fluid measuring. For over 50 years, Hamilton has been satisfying customer needs by combining quality materials with skilled workmanship, ensuring the highest level of performance of every precision fluid measuring device we manufacture. We are seeking a talented Field Service Specialist in the Los Angeles, CA area. The ideal candidate will work out of their home when not traveling to our clients in Southern California. Responsibilities include: Manage assigned territory, including on site installation and repair of automated laboratory instruments, follow up on service escalations. Must have the ability to program methods using the user software and service software to test automation. Provide e-mail/telephone technical support for assigned territory, member of the Hamilton on call support team on a rotating schedule. Keeps accurate records of service calls, maintain inventory of service parts, tools and test equipment. Maintain a neat professional appearance. Follow laboratory safety practices as defined by the Company and/or the customer’s site safety code. Bachelor of Science or Technical degree 5 years Scientific Instrument Industry or laboratory experience. Ability and willingness to maintain a travel schedule and to travel on short notice including international travel (50 – 70% Travel). Valid drivers license required. Must pass drug test, criminal and professional background check. Hamilton Company offers an excellent benefits package to full-time employees including medical, dental, vision, paid time off, STD, LTD, 401k, tuition reimbursement and much more. Learn more about us at <a href="http://www.hamiltonrobotics.com/" rel="nofollow">http://www.hamiltonrobotics.com/</a> or at www.hamiltoncompany.com . Hamilton Company is an equal opportunity employer (EOE) and strongly supports diversity in the workforce. Must have prior service experience on medical equipment. ]]>

<![CDATA[Territory Coverage: Los Angeles, Riverside, Irvine, Santa Ana, Torrance, and Santa Monica, CA Ideal location: Los Angeles Position Type: Contract position, with base salary plus commission Areas of Expertise: Life science reagent/service sales, business development Description We are seeking a commission-based territory sales representative to cover the defined territory with our products or services. The individual, working together with our internal territory manager and technical support team, will lead the effort of sales/business development activities in the territory. We are an equal opportunity employer, headquartered in the San Francisco bay area. The company was founded in 1994, and specialized in supplying molecular and cell biology products/services to pharmaceutical, biotechnology and academic researchers. Please check out our websites for details of our products and services: www.biochain.com service.biochain.com Duties and Responsibilities: Include but not limited to: * Proactive sales and market-information collection * Expand sales to existing clients while building and maintaining client relationships * Discover and develop new clients aggressively * Prepare sales and call reports on a weekly basis. Qualifications The candidate should be self-motivated, proactive, independent, and result-driven. Minimal education: Bachelor of Science in biology, biotechnology or other related fields. Basic computer literacy required. Preferred experience and skills: * Prior experience in life science research or sales * Strong inter-personal skills * Strong written and oral communication skills. Please Email your resume to hr@biochain.com ]]>

<![CDATA[<img src="http://chrisyu.bol.ucla.edu/DrE%20Logo.jpg"> Summary: Doctor Evidence is in the business of creating customized databases of relevant evidence derived from clinical medical studies. Medical manufacturers, including device companies, medical imaging companies, surgical device companies, diagnostic test companies, biotech and pharmaceutical companies use clinical studies as their primary asset to obtain regulatory and industry approval, as well as to promote their products. Doctor Evidence has created state-of-the-art technologies (and services) that build customized distributive evidence databases for manufacturers. Role and Responsibilities include: • Reading, analyzing, and translating clinical studies to our digital template. • Collecting clinical outcomes and adverse events from studies. Minimum Requirements • Recent graduate from a 4 year educational institution (e.g. UCLA/USC/UCI) with a Bachelor's or Master's in any science/healthcare related field. • Possess a strong disposition to computer technology • Experience using Microsoft Office Suite (e.g. Excel) • Strong attention to detail Ideal Candidate: Pre-medical/pharm/public health student looking to gain additional healthcare/science knowledge from reading and interpolating research articles. General Attributes: • Highly motivated, over achiever, team player, facilitator • Passion for improving healthcare quality and enjoys the scientific method • Excellent analytical skills with ability to back up recommendations with valid research and analysis • Ability to ask and define important questions • Ability to successfully overcome invalid objections • Highest level of integrity/honesty • An "Out of the Box" thinker who is both creative and innovative • Ability to work on a “as needed” basis • Propensity to succeed both personally and professionally • Focused on achieving defined results, and exceeding goals and objectives • Ability to work well with others • Shared interest in ensuring accuracy of data collect while maintaining an adequate level of efficiency This is a full-time position offered with benefits and competitive pay. If you are interested, please visit our website at www.doctorevidence.com to learn more about what we do. Address CVs/Resumes to Chris: cyu@doctorevidence.com ]]>

<![CDATA[<img src="http://www.diceelectronics.com/images/cyan_sm.gif"> Company overview: DICE Electronics, LLC is a private company in business since 2002, specialized in manufacturing, distribution and marketing of various electronics products. Our office is located near the Long Beach Airport; 405 FWY DICE Electronics is proud to be an equal opportunity employer. Position: We are looking for senior & junior embedded software engineers with experience in microcontroller (PIC / ATMEL) programming, software development and hardware development. If you are proficient in embedded C programming, this position will fit you well! If you know how to program a PIC micro controller and built digital & analog circuit boards, this is certainly the right position for you. Skills required: - Bachelors degree or higher in Computer or Electronics Engineering is a plus - Excellent C, C++ skills with recent work experience - Assembly and other languages are a plus but not required - Experience in formal software engineering principles and UML - Experience with embedded microcontrollers; preferably PIC & ATMEL development - Electronics knowledge of analog and digital circuits - Understanding of communication protocols such as UART, I2C, - Hands on circuit schematic, layout, prototyping and troubleshooting experience This is a full time position. Business hours are Monday to Friday, 9am to 6pm Please contact us via Email by submitting your resume to engineeringjob2010@diceelectronics.com *** CANDIDATE MUST BE AVAILABLE FOR ON-SITE INTERVIEW AT OUR SIGNAL HILL, CA OFFICE *** Please copy your resume to the email without attachments. NO HEADHUNTERS, NO ENGINEERING FIRMS, NO OUTSIDE CONSULTANTS & NO TELEPHONE CALLS. Immediate hire]]>

<![CDATA[URGENT NEED for Regional Monitor West Coast. Recent solid (8 yrs plus) regional CRA experience functioning as a home-based monitor and accustomed to being on the road for multiple site visits. No short term assignments in past year looking for longevity and consistency. Prepare and conduct study initiation, closeout and monitoring visits at clinical investigative sites to ensure adherence to procedures, protocols and project plans in accordance with FDA regulations. Maintain site files, trial master files and study documentation. Develop status reports, SOP revisions and document quality control. Review and process regulatory documentation, ensure the execution of clinical trials in a timely and efficient manner. Work within established timelines and budgets. Track clinical trial supplies, patient recruitment activities, and Serious Adverse Events, review Case Report Forms for accuracy and completeness and conduct query resolution. May participate in clinical protocol writing and case report form design. Minimum site visits handled in one study MUST have exp handling 16-20 plus site visits on one study, EDC experience. Must live fairly close to one of these airports: LAX, SanDiego OR Orange County. The CANDIDATE MUST BE AVAILABLE TO TRAIN IN RTP on 3/17 and 3/18. Please call 919 674 3340 or malvin@a10clinical.com. Please put job # in Subject line. Thank you. ]]>

<![CDATA[Neuroscience Program The Saban Research Institute Childrens Hospital Los Angeles Los Angeles, California Research lab technician position is available in the lab of Dr. Makita to study peripheral nervous system development. This position will undertake laboratory management and experiments that will include: Maintaining mouse colonies Histological analysis of developing nervous system and their innervations Ordering and maintaining lab equipment, supplies and consumables Minimum qualifications: BS in Biology, Biochemistry, or equivalent qualifications Experience in mouse colony maintenance PCR genotyping skill Application Instructions: Please send 1) a cover letter, 2) a complete CV, and 3) a list of the names and contact information of three references to makita@usc.edu. ]]>

<![CDATA[AETL is an environmental laboratory, doing analytical testing on soil, water, and air samples. With a diverse staff and a friendly environment, we have been in business in Southern CA for the past 20 years. We currently have one opening for Wet Chemistry and Instrumental Analysis in the Inorganic department of our laboratory. Applicant must be of science major (Chemistry, Biology, or Physics). Experience in environmental laboratory (not Clinical) is preferred. We will provide hands-on training. ]]>

<![CDATA[Contract-based job for geologists or qualified environmental professionals for writing Phase I ESA reports.]]>

<![CDATA[Stetson Engineers Inc. is recruiting a Soil Scientist for full time employment in its office in Albuquerque, NM. The candidate must have at least a Master degree in Soil Science. Professional experience as a practicing soil scientist and certification as a soil scientist through ARCPACS (American Registry of Certified Professionals in Agronomy, Crops, and Soils) is preferred but not required. Stetson Engineers is a multi-disciplined professional water resources firm with headquarters in San Rafael, California and (currently) offices in Covina and Bakersfield CA, Reno NV, Centennial, CO, and Mesa, AZ. This position is to provide journeyman soil science expertise on a variety of projects, under the supervision of a certified soil scientist and/or project engineer. Projects include (1) gathering soil and land information for irrigation project development on various projects in the western US; (2) providing soil science expertise and assistance to established and ongoing irrigation projects, especially in the areas of soil salinity mapping and management, and irrigation drainage; (3) conducting soil surveys in various settings, especially the floodplain areas of the Rio Grande River and Colorado River; and (4) reclamation, remediation, and permitting studies on mined lands and oil/gas extraction sites. The applicant must have excellent writing and oral communication skills. A working knowledge of GPS technology as well as ArcGIS is desired, but not required. Projects are located in various states, and the position will require considerable travel (estimated 30 to 40% of the time). This position offers the potential for advancement and major growth to the right person. The target date for filling this position is on or before April 1, 2010. Resumes and cover letters may be sent to: Stetson Engineers Inc. 2171 E. Francisco Blvd., Ste K San Rafael, CA 94901 FAX (415) 457-1638 ]]>

<![CDATA[Manager, QC Chemistry Grifols has been a leader in the healthcare industry since 1940 by creating innovative products and services based on the values of ethics, quality and responsibility. Grifols’ focus and mission is to fulfill the needs of its patients, as well as healthcare professionals working in therapeutics, pharmacy, diagnostics and blood banking. For more than 60 years, Grifols has developed, manufactured and marketed products designed to improve human health. At our Los Angeles facility, Grifols manufactures plasma derived biopharmaceutical products of proven efficacy, quality and safety. The Grifols family of companies includes Grifols Inc., Grifols USA, Grifols Biologicals, Biomat USA and Plasma Collection Center, Inc. Grifols Biologicals researches, develops and produces therapeutic proteins from human plasma and uses the most cutting-edge technology for protein purification. Our modern facilities are organized according to Good Manufacturing Practices (GMP) and have been certified under the FDA Establishment License. This division of our company has an immediate opening for a Manager of QC Chemistry, offering competitive salary, along with an excellent benefits package, including medical, dental, vision, 401(K) plan, life insurance, educational assistance, and five (5) weeks of paid time off. Job Responsibilities: (This job description is accurate at the date of publication and may change over time. It is not intended as an exhaustive description of the job. Other duties may be assigned and qualifications required may change.) <ul> <li>Oversee the daily activities in the QC Chemistry laboratory to ensure that all cGMP, company specifications, procedures and guidelines are followed.</li> <li>Plan and analyze work flow, delegate and prioritize, to ensure tests and projects are completed in a timely manner. </li> <li>Direct the identification of assay problems and offer explanations and/or solutions where possible.</li> <li>Perform trending and investigations as needed and generate reports. </li> <li>Oversee the maintenance of accurate and complete records and review of test record results for accuracy and completeness. </li> <li>Provide hands-on guidance in the technical area of chemical laboratory operations when needed.</li> <li>Oversee and ensure adequate inventory of lab reagents and supplies. </li> <li>Conduct performance reviews of personnel. </li> <li>Write and revise laboratory standard procedures as needed.</li> <li>Assist in the development of, and performance of method validation studies and production validation studies.</li> <li>Designs and executes laboratory protocols necessary to complete Quality and Production-originated projects. Also, provides scientific advice and counsel regarding projects as needed</li> <li>Maintains current knowledge of regulatory and related scientific enhancements, trends and advancements through independent reading and training.</li> </ul> Skills/Experience, Qualifications, and Educational Requirements: (To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions). <ul> <li>MS or Ph.D. in chemistry, biochemistry or related scientific field. </li> <li>Minimum of 3 years of managerial or supervisory experience in a biologics, biotech, or pharmaceutical laboratory is required.</li> <li>Knowledge of and proficiency in the use of analytical instruments, including troubleshooting skills.</li> <li>Strong knowledge of small molecule analytical technologies (e.g. GC, HPLC, AA, etc.).</li> <li>Strong knowledge of analytical techniques for biologics or protein-based therapeutics.</li> <li>Understanding of immunological based method of analysis desired.</li> <li>Prior experience with blood coagulation products and coagulation-specific analytical techniques desired (APTT clotting assays, RCo and vWF analysis, etc.) </li> <li>Strong knowledge of cGMP regulations and prior experience successfully handling US and international regulatory agency audits and inspections.</li> <li>Ability to follow a wide array of Standard Operating Procedures and ensure laboratory personnel follow all SOPs.</li> <li>Experience with investigating Out of Specification events, and writing thorough reports regarding the investigational findings.</li> <li>Experience in statistical analysis and good computer skills.</li> <li>Excellent oral and written communication, as well as good organizational and decision making skills.</li> <li>Demonstrated leadership skills with ability to guide, train, coach and develop subordinates.</li> <li>Strong technical writing skills.</li> <li>Strong interpersonal and communication skills with ability to interact with all levels of personnel in a professional manner.</li> </ul> APPLY VIA URL: <a href="http://hostedjobs.openhire.com/epostings/submit.cfm?fuseaction=app.dspjob&jobid=216875&company_id=16052&jobboardid=550" rel="nofollow">http://hostedjobs.openhire.com/epostings/submit.cfm?fuseaction=app.dspjob&jobid=216875&company_id=16052&jobboardid=550</a>]]>

<![CDATA[Quality Assurance – Project Manager Grifols has been a leader in the healthcare industry since 1940 by creating innovative products and services based on the values of ethics, quality and responsibility. Grifols’ focus and mission is to fulfill the needs of its patients, as well as healthcare professionals working in therapeutics, pharmacy, diagnostics and blood banking. For more than 60 years, Grifols has developed, manufactured and marketed products designed to improve human health. At our Los Angeles facility, Grifols manufactures plasma derived biopharmaceutical products of proven efficacy, quality and safety. The Grifols family of companies includes Grifols Inc., Grifols USA, Grifols Biologicals, Biomat USA and Plasma Collection Center, Inc. Grifols Biologicals researches, develops and produces therapeutic proteins from human plasma and uses the most cutting-edge technology for protein purification. Our modern facilities are organized according to Good Manufacturing Practices (GMP) and have been certified under the FDA Establishment License. This division of our company has an immediate opening for a Quality Assurance – Project Manager, offering competitive salary, along with an excellent benefits package, including medical, dental, vision, 401(K) plan, life insurance, educational assistance, and five (5) weeks of paid time off. Position Summary: <ul> <li>Responsible for managing various facets of quality projects related to submissions to the FDA, review and approval of Validation documents and the management of Methods Validation </li> </ul> Job Responsibilities: (This job description is accurate at the date of publication and may change over time. It is not intended as an exhaustive description of the job. Other duties may be assigned and qualifications required may change.) <ul> <li>Develop quality objectives, manage, and maintain project plans</li> <li>Interface with various groups to ensure that objectives and timelines are met specifically for preparing complex technical submissions related to major facility projects</li> <li>Review and approve validation protocols and final reports</li> <li>Ensure implementation and maintain compliance of Methods Validation</li> <li>Write and revise documents and procedures</li> </ul> Skills/Experience, Qualifications, and Educational Requirements: (To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions). <ul> <li>Bachelor’s Degree in a related scientific or technical discipline.</li> <li>Thorough knowledge of USA FDA, EU and international cGMP’s</li> <li>Five years experience in quality assurance in the pharmaceutical industry</li> <li>At least four years of experience in Regulatory Affairs, Compliance, Quality Engineering, Quality Control or Quality Assurance with a strong emphasis of cGMP and GLP concept.</li> <li>Strong technical writing skills</li> <li>Proficient in Microsoft applications - Excel and Word</li> <li>Strong interpersonal and communication skills with ability to interact with all levels of personnel in a professional manner.</li> <li>Good organizational skills with ability to perform multiple priorities efficiently and effectively.</li> <li>Self-starter with the ability to work independently and use good judgment while performing multiple tasks.</li> <li>Proactive, results oriented, with a strong attention to detail</li> <li>Bilingual in Spanish is a plus</li> </ul> APPLY VIA URL: <a href="http://hostedjobs.openhire.com/epostings/submit.cfm?fuseaction=app.dspjob&jobid=216959&company_id=16052&jobboardid=550" rel="nofollow">http://hostedjobs.openhire.com/epostings/submit.cfm?fuseaction=app.dspjob&jobid=216959&company_id=16052&jobboardid=550</a>]]>

<![CDATA[Principal Scientist - Research  Grifols has been a leader in the healthcare industry since 1940 by creating innovative products and services based on the values of ethics, quality and responsibility. Grifols’ focus and mission is to fulfill the needs of its patients, as well as healthcare professionals working in therapeutics, pharmacy, diagnostics and blood banking. For more than 60 years, Grifols has developed, manufactured and marketed products designed to improve human health. At our Los Angeles facility, Grifols manufactures plasma derived biopharmaceutical products of proven efficacy, quality and safety. The Grifols family of companies includes Grifols Inc., Grifols USA, Grifols Biologicals, Biomat USA and Plasma Collection Center, Inc.  Grifols Biologicals researches, develops and produces therapeutic proteins from human plasma and uses the most cutting-edge technology for protein purification. Our modern facilities are organized according to Good Manufacturing Practices (GMP) and have been certified under the FDA Establishment License. This division of our company has an immediate opening for a Principal Scientist, offering competitive salary, along with an excellent benefits package, including medical, dental, vision, 401(K) plan, life insurance, educational assistance, and five (5) weeks of paid time off.  Job Responsibilities:  (This job description is accurate at the date of publication and may change over time.  It is not intended as an exhaustive description of the job.  Other duties may be assigned and qualifications required may change.) <ul> <li>Identify and isolate new plasma protein therapeutics</li> <li>Manage the development and implementation of processes that will improve manufacturing efficiency of plasma products and enhance product quality.</li> <li>Make recommendations for process changes based on thoughtful analysis of product and process data.</li> <li>Identify and implement new research and production technologies. Assist business development by supplying technical input for the preparation of proposals</li> <li>Write development reports and process procedures.  Assist in the validation of new processes transferred to the production area.</li> <li>Communicate technical activities (both verbally and in writing) to all levels within the company.  When appropriate, write scientific papers for journal publication and make outside meeting presentations</li> <li>Serve as leader for selected projects and/or team leader for interdepartmental teams assigned to critical issues.</li> <li>Use her/his specific training and experience to provide training and supervision to junior staff members in the department.</li> <li>Assist in the design of scientific studies needed to support new and existing regulatory submissions. </li> </ul> Skills/Experience, Qualifications, and Education:  (To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions). <ul> <li>M.S. or Ph.D. (preferred) in Biochemistry, Molecular Biology or a Life Sciences field. </li> <li>Requires at least five years experience working in a laboratory (may include graduate and post-doctoral work).</li> <li>Strong interpersonal, organizational and oral/written communication skills.</li> <li>Requires an understanding of the fundamentals of protein biochemistry, immunochemistry, electrophoresis, spectroscopy, ELISA, molecular biology.</li> <li>Must be able to work both independently and as part of a team.</li> </ul> APPLY VIA URL: <a href="http://hostedjobs.openhire.com/epostings/submit.cfm?fuseaction=app.dspjob&jobid=216880&company_id=16052&jobboardid=550" rel="nofollow">http://hostedjobs.openhire.com/epostings/submit.cfm?fuseaction=app.dspjob&jobid=216880&company_id=16052&jobboardid=550</a>]]>

<![CDATA[Manager of Methods Development and Validation  Grifols has been a leader in the healthcare industry since 1940 by creating innovative products and services based on the values of ethics, quality and responsibility. Grifols’ focus and mission is to fulfill the needs of its patients, as well as healthcare professionals working in therapeutics, pharmacy, diagnostics and blood banking. For more than 60 years, Grifols has developed, manufactured and marketed products designed to improve human health. At our Los Angeles facility, Grifols manufactures plasma derived biopharmaceutical products of proven efficacy, quality and safety. The Grifols family of companies includes Grifols Inc., Grifols USA, Grifols Biologicals, Biomat USA and Plasma Collection Center, Inc.  Grifols Biologicals researches, develops and produces therapeutic proteins from human plasma and uses the most cutting-edge technology for protein purification. Our modern facilities are organized according to Good Manufacturing Practices (GMP) and have been certified under the FDA Establishment License. This division of our company has an immediate opening for a Manger of Methods Development and Validation, offering competitive salary, along with an excellent benefits package, including medical, dental, vision, 401(K) plan, life insurance, educational assistance, and five (5) weeks of paid time off. Position Summary: <ul> <li>Responsible for overall operations of the QC Methods Development and Validation group, ensuring that all required product tests are validated in a timely and GMP-compliant manner.   </li> </ul> Job Responsibilities:  (This job description is accurate at the date of publication and may change over time.  It is not intended as an exhaustive description of the job.  Other duties may be assigned and qualifications required may change.) <ul> <li>Manages group of scientists responsible for ensuring that Grifols Quality Control (QC) analytical methods are developed and validated in a timely manner.</li> <li>Develops new biochemical and microbiological methods for testing Grifols products and process samples.</li> <li>Designs protocols for validating existing and new test methods and supervises execution of these protocols.</li> <li>Assists in the transfer of validated methods to the Grifols QC laboratory.</li> <li>Develops and maintains a schedule for the validation of QC tests for process intermediates and final product.</li> <li>Designs protocols for installation, operation and performance qualifications of new QC analytical instruments and maintains the schedule for completing these qualifications.</li> <li>Identifies all resources, including staff, equipment and supplies, that are required to perform validation of process intermediate and final product tests according to the established goals and timelines..</li> <li>Maintains system for timely purchase and qualification of laboratory equipment and reagents.</li> <li>Reviews and revises standard operating procedures for technical accuracy and compliance with regulatory requirements. </li> <li>Assists the QC department in troubleshooting or investigating instrument and assay problems. </li> <li>Provides information for internal and external audits on the GMP validation status of QC equipment, reagents and tests.  Assist in the resolution of audit observations related to validations and proposes corrective actions.</li> <li>Notifies QC senior management of any potential quality issues related to test validations and provide recommendations for quality improvement.  </li> </ul> Skills/Experience, Qualifications, and Educational Requirements:  (To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions). <ul> <li>Ph.D. in Biochemistry, Chemistry or related Life Sciences field.</li> <li>Minimum of 5 years experience in laboratory management with 3 years spent in a cGMP environment. </li> <li>Must have experience in laboratory method validation and familiarity with ICH and U.S. and European pharmacopeia guidelines for analytical method validation.</li> <li>Demonstrated strong leadership, communication, interpersonal, organizational and decision making skills.</li> <li>Requires an understanding of the fundamentals of statistics and analytical methodology, protein biochemistry, immunochemistry, chromatography, electrophoresis, spectroscopy, ELISA.</li> <li>Exceptional verbal and written communication</li> <li>Strong interpersonal skills with ability to interact with personnel at all levels.</li> </ul> APPLY VIA URL: <a href="http://hostedjobs.openhire.com/epostings/submit.cfm?fuseaction=app.dspjob&jobid=216879&company_id=16052&jobboardid=550" rel="nofollow">http://hostedjobs.openhire.com/epostings/submit.cfm?fuseaction=app.dspjob&jobid=216879&company_id=16052&jobboardid=550</a>]]>

<![CDATA[Lab Technician Duties Tests and analyzes in-process product (bulk), finished products and stability samples according to protocol. Includes water testing. Provides Production support in equipment release. Provides support to raw material testing. Writes reports and fills out QC forms completely. Submits all completed forms to QC Supervisor for final approval and release. Prepares and standardizes test solution and reagents. Maintains supplies necessary for designated area. Maintains cleanliness and good housekeeping in work area including proper disposal of waste products. Audits completeness of Batch Records and samples prior to testing. Maintains filing system for specifications and assay reports. Maintains and organizes: ]]>

<![CDATA[We care for thousands of patients, we care for you! Advanced Medical Reviews (AMR) provides medical review services utilizing innovative technologies and adhering to the highest healthcare standards. We are a fast-growing dynamic company looking for people who want to grow with us. (Check out our website: www.admere.com) AMR provides a friendly, professionally rewarding and innovative environment. Review Coordinator AMR’s Medical Coordinators enjoy an exciting diverse ENTRY-LEVEL position with many growth opportunities: • Review and summarize medical records • Communicate with clients • Communicate with AMR’s network of physicians Full-time entry level hourly position Mon-Fri in West LA: 10780 Santa Monica Blvd, Suite 333 Los Angeles, CA 90025 Please email your resume (*include your pay history AND expectations*) and cover letter by replying to this ad. Position requirements: • Bachelor’s degree from a 4-year college is required • Excellent oral and written communication skills • Prior healthcare experience and knowledge of medical terminology - highly desired but not a requirement • Attention to detail • Ability to manage multiple priorities and deadlines • Strong computer skills with emphasis on Microsoft Office • We will train qualified candidates AMR provides medical benefits, 401k and paid time off. AMR is an equal opportunity employer. All employment decisions (including recruitment, hiring, promotion, compensation, transfer, training, discipline and termination) are made without regard to race, sex, national origin, color, age, religion, sexual orientation or disability. Compensation: Hourly based on experience includes medical, dental, vision, paid time off, and 401K]]>

<![CDATA[-Quality Assurance / Quality Control Technician – Signal Hill, CA.- Custom Spice and Seasoning blending company seeking an individual with a 4 year Food Degree to assist in our expanding QC / QA lab. Experience in the meat industry is a plus. HACCP or Sanitation experience would be beneficial. -Responsibilities may include assisting in new Micro-lab, lab testing, monitoring the batching process, performing quality line checks, organizing retention samples, testing of finished goods, monitoring label information, blending small batches and samples, as well as other duties. Some lifting may be required (up to 50 lbs) when blending. Email: frankp@eversonspice.com ]]>

<![CDATA[ChromoLogic is actively engaged in multiple cutting edge applied research and development programs. We bring a unique, multi-disciplinary approach to compelling scientific challenges and our core capabilities stem from the diverse talents of our staff. We provide a highly creative, collaborative and challenging work environment where each individual can not only attain their full potential, but also grow and learn new technical and life skills. Our open culture of collaborative research extends beyond our facilities to that of our extensive academic and industrial collaborators – providing our staff with unparalleled research and product development perspective. We have immediate openings for 1. PhD scientist with approximately 2-5 years work experience in bioengineering, applied physics or optics from an accredited US institution of higher education. Must have excellent leadership and communication skills coupled with hands-on laboratory skills. The ideal candidate will have a grants/proposal preparation experience, strong instrumentation and/or optics background – preferably applied to biotechnology. 2. Electronics Engineer with 2-5 years industrial experience in analog/digital circuit design (board layout, simulations, parts selection). Must have a BS/MS from an accredited US institution of higher education and excellent communication skills. The ideal candidate should be extremely hands and enthusiastic about novel electronics designs with a hobbiest interest. Applicants should display familiarity with reliable embedded systems and digital electronics, one or more communications protocols, analog systems such as power supplies and laser drivers and data acquisition systems. Experience with circuit schematic capture and simulation, as well as PCB layout, is required. All candidates must be U.S. citizens/permanent residents.]]>

<![CDATA[Can you explain stoichiometry or matrices or the ramifications of the War of 1812 so that it actually makes sense? Every day, we in the tutorial department of The Princeton Review get calls from anxious parents looking for those special tutors who can help their children truly understand complex and often difficult concepts. We needs smart, passionate, fun, and articulate tutors in order to make this happen. Becoming a tutor has many rewards, but one of the greatest is helping students appreciate math, science, and foreign languages. The Princeton Review thrives on helping students succeed on the AP and SAT Subject tests and on their schoolwork in general. We get the most requests for math (especially Calculus), science (Chemistry, Physics, Biology), and history (European, World, and US). We get some requests for foreign language tutoring and computer science. By the way, this is the best and most interesting job you’re going to read about today--or tomorrow for that matter. In just 25 years, The Princeton Review has revolutionized the attitude and approach to making educational transitions in North America. This is your chance to be everything that you probably wished all your educators were: attentive, brilliant, caring, and on-the-ball. If you want to work someplace where your intelligence, your creativity, your drive, and your capacity to keep all the balls in the air will be immediately put to the test and put to work, you aren’t going to find a better opportunity. We train tutors with appropriate subject matter knowledge for the SAT and AP tests in sciences, math, and history. If you have the necessary background and the desire to inspire students, please send resume and cover letter (and make the cover letter interesting!) to: Ms. Jessica Bell, Recruiting Manager of the San Fernando Valley Office, Email: infovalley@review.com. Starting Pay is $20-35/hour based on your previous teaching experience. Tutors are needed in the Ventura County, San Fernando Valley, Santa Clarita Valley, and San Gabriel Valley areas. ]]>

<![CDATA[Everson Spice Company is a custom seasoning company. We are looking for someone with a degree in either food/meat/animal science to help us create new products for the food industry. Technical skills in meat science or experience in the meat / food industry are required. Duties will include product creation, duplication and general R & D. Ability to work well and closely with outside sales staff is a must. Salary plus 401(k), health / dental. Full time.]]>

<![CDATA[Caldera Medical, a growing women's health medical device company, has an immediate need for a temporary on-site person to clean and decontaminate instruments returned to us by customers. The project consists of: 1. Manually cleaning the instruments 2. Using the Cidex method, decontaminate the instruments 3. Work with QA manager to determine viability of instruments 4. Sort and prepare an inventory of the instruments by model and lot number 5. Package instruments in bubble wrap and shipping container. Instructions are available upon request. This position is temporary and expected to last up to 40 hours but may require additional time. All appropriate safety and OSHA standards strictly adhered to. ]]>

<![CDATA[Forensic Analytical Laboratories, Inc., an environmental testing company, is seeking a full-time supervisor for its Los Angeles environmental microbiology laboratory. Duties include: analysis of client samples: fungal air and bulk samples, both viable and non-viable; identification of fungi to species; coliform bacteria analysis; gram-staining bacteria cultures; investigation of new service offerings; refining lab procedures for new and established analyses; reviewing and amending established SOPs; implementation of the quality control program, and the supervision of employees. Experience with ELISA-based allergen and endotoxin analyses is an asset, as is a background in bacteriology. Requirements: Applicants must have a BS in a life science (MS or Ph.D. in microbiology preferred), 2 years of experience including sampling and sampling analysis, and a minimum of 8 semester hours of microbiology coursework. Deadline: April 1, 2010 ]]>

<![CDATA[Director, Brand Development (Pharmaceuticals) Description Our company is a premier international branding agency, has been in business since 1993. As we continue to expand our operations to provide our global clients with industry leading service in strategically positioned areas of the world, we are looking for a qualified individual to serve as Director, Brand Development, for our Los Angeles Office. We provide a variety of services to our pharmaceutical, consumer and B2B clients, including name development, worldwide trademark screening, linguistic analysis and market/safety research. Responsibilities: • Develop and maintain a client base by selling branding, market research and consultancy services • Act as the client's point of contact throughout all phases of the project from the initial meeting to project completion and/or name approval • Travel to client sites and visit with decision makers for capabilities presentations, conduct project meetings and present final results • Strategize with internal colleague to accomplish business goals • Entrepreneurial attitude targeting potential clients Requirements • Branding consultancy, advertising agency or client side branding experience a plus • Experience in a services industry or client management • Business knowledge of the pharmaceutical/medical industry preferred • Business development and project management skills preferred • Bachelor's Degree required, post graduate degree in medical field preferred or a plus (B.Sc Phrm, Pharm. D, MD., Ph.D (Pharmaceutical Sciences, Medical Chemistry, etc.)) • Extensive experience with Microsoft® Office Suite with a emphasis on PowerPoint® • Extensive traveling – 5 days a week, no overnight stay required • Must live in Los Angeles This position pays an attractive base salary plus commission. Competitive benefits package includes health insurance, life insurance, retirement plan, paid vacation and personal days. Total package is commensurate on qualifications and experience. Please send your cover letter, salary requirements and resume, your background and qualifications to careers@brandinstitute.com. No phone calls please. Due to the high volume of responses, we will contact those candidates who fit the job description specified above. ]]>

<![CDATA[Our alternative fuels technology start-up in Pasadena, near CalTech, is looking for a laboratory technician. This is a full-time, hourly position with full benefits. Infrequent overtime may be required. We need someone sharp and organized. Regular duties include: • Synthesize raw materials for production. • Operate USI coating sprayer. • Fabricate and assemble components for testing. • Maintain and clean laboratory supplies and equipment as directed by the Lab Manager. • Participate in pertinent company meetings, especially with respect to improvements in laboratory equipment, layout, and procedures. • Maintain knowledge of technological advancements of the company. • Perform laboratory testing that involves complex, non-standardized and innovative procedures. • Prepare and maintain required documentation of test results; record and analyze data according to established laboratory procedures, or as directed by the Laboratory Manager. • Perform related duties as assigned. Some lifting, bending, and carrying of materials and components up to 50 lbs. is required. Respond with resume and cover letter.]]>

<![CDATA[<big>Lab Manager/Technician Position</big><hr> Overview: Senior Lab manager required for day-to-day operations in a world-class, multicultural stem cell biology laboratory at the Keck School of Medicine at the University of Southern California. Expectations: <blockquote>-Successful candidate will serve in the capacity as the primary liaison between the P.I. and the laboratory staff and students. -Successful candidate will be responsible for training all incoming graduate students in the basics of tissue culture, molecular biology techniques, and laboratory etiquette. -Successful candidate will be expected to perform directed, original research with the ultimate goal of peer-reviewed publication -Successful candidate will aid in fiscal oversight of lab, fielding and filling orders, and facilitating communication between lab members. -Successful candidate will facilitate compliance with all national and university policies.</blockquote> Skills Required: Excellent communication skills, both written and oral, are mandatory. Bachelor of Science required, masters of science or 5 years experience preferred, but not required. Candidate should be able to demonstrate managerial or supervisory experience. All degrees should be earned in a life science field, preferably biology. Stem cell biology experience, mouse and/or rat embryo manipulation training a plus, but not required. If interested, please email relevant CV to “Lab Search Committee” at the above address]]>

<![CDATA[Club Leader Job Description OVERALL RESPONSIBILITIES: •Plan and implement fun and enriching activities for members of their club. •Recruit and maintain club participants. •Develop positive relationships with youth in their program, parents, and school staff. •Youth Counselors are accountable to the Site Coordinator and Program Manager for assigned duties. RESPONSIBILITIES: •Develop and implement program activities according to program goals and monthly themes. •Supervise and participate in children's activities. •Maintain and turn in attendance daily. •Write and turn in lesson plans of program activities for each session in advance. •Maintain professionalism at all times, consistent attendance, on time and prepared. •Develop and maintain positive relationships with school staff, parents, and youth. •Make weekly calls to students in their group who do not attend. •Maintain maximum membership levels at all times. •Implement weekly, monthly or quarterly fund-raisers as assigned. •Develop and implement "end of session" performances or displays. •Other related duties as assigned. QUALIFICATIONS AND EXPERIENCE: •AA Degree in Child Development or a related field is preferred or minimum of one year of experience as a group leader working with children and 6 units in child development. •Expertise in a specialty area such as fine and performing arts, science, community service, conflict resolution, physical education, etc. •Work well with young children and/or youth. •Good oral and written communication. Computer literacy or willingness to learn ***Must submit resume in order to be considered for the position, please note this is a part time job and hours vary from 2.50 to 3.50 depending on daily activities*** Positions available: Basketball coach, Hip-hop Instructor, General Dance Instructor, Karate Instructor Science, Fine Arts, Cooking, Drama, Drawing, Crocheting, Table Tennis, Leadership, Photography, Animation, Computers, Guitar, Drums, Keyboards, Recreation and choir. ]]>

<![CDATA[Drug Delivery medical device firm looking bring on part-time consultant with a strong knowledge base for large molecule protein drugs. Ultimately, we'll be conducting drug experiments on longevity testing for antibody and antibody fragments, and I'd like this person to: --write Standard Operating Procedure for handling large and small molecules --understand data for protein and small molecule analysis (Ion Exchange Chromatography, etc) --review current publications on the subject matter --interpret/extrapolate the results for our firm. Part time consultant: pay will depend on experience. This is a 1099 position.]]>

<![CDATA[We are looking for a full-time (Monday through Friday) entry-level QA/QC Technician to oversee the Quality Control system for our Chemistry Department. Responsibilities include performing quality control tests, documentation control, calibrations, daily interaction with technicians, reviewing control data, and assisting and reporting to the Quality Manager. No previous QA/QC experience is required. Applicants must have some college education in the Chemical sciences, and chemistry and/or food chemistry courses are a plus. A successful candidate must be able to work in a fast paced environment, work well with others, work efficiently with minimal supervision, be eager to learn all aspects of the quality system, and have a positive attitude. ]]>

<![CDATA[Responsible to set up Calibration and PM system, including purchasing standard and monitoring equipment and instruments in accordance to FDA and ISO regulations. Able to validate equipment, including IQ/OQ/PQ in accordance to FDA/ISO regulations. Experience in developing SOP desired. Do not apply unless you have at least a college degree and 5 years experience in manufacturing for biotech companies (medical devices preferred, but pharmaceuticals/drugs/biologics acceptable). Position is temporary and Part time: 100 hours of work over the next two months. Starts immediately. Salary based on experience. This is a 1099 position. Keywords: calibration, quality, manufacturing, installation, operations, preventative maintenance, medical devices, drugs, qualifications, standard operating procedures.]]>

<![CDATA[For over 30 years, Quantimetrix has been manufacturing innovative clinical laboratory quality control products. We are currently recruiting for a full-time Sales Representative. SUMMARY: Support distributor accounts with an emphasis on increasing sales. Develop new direct customer accounts. Increase sales of existing customer accounts. Develop new OEM and PTM accounts. Maintain knowledge of industry trends and competition. MAJOR DUTIES AND RESPONSIBILITIES: • Domestic distributor account management with an emphasis on increasing sales to meet annual forecast • Develop new direct customer accounts • Increase sales of existing customer accounts • Develop new OEM and PTM accounts • Maintain daily CRM records • Fulfill literature and sample requests • Make presentations of sales activities to executive management • Travel to trade shows and key accounts • Maintain knowledge of industry trends and competition • Contribute to a positive work environment with an emphasis on teamwork QUALIFICATIONS: • Bachelor’s degree in science or medical technology background preferred • 5 years of sales or cold calling experience preferably within the healthcare/pharmaceutical or biotech industries • Excellent phone personality, verbal and written communication skills • Strong analytical and organizational skills • Knowledge of Microsoft Office, CRM, and internet applications We offer a competitive compensation and benefits package that includes medical, vision, dental, life insurance, matching 401(k) plan, PTO and other great benefits. For more information about us, please visit our website: <a href="http://www.4qc.com" rel="nofollow">http://www.4qc.com</a>. Then send your resume with salary history to hr@4qc.com. Equal Employment Opportunity Employer ]]>

<![CDATA[Top research lab needs a motivated and organized post-doctoral fellow to conduct independent research projects. The lab research focus is on understanding the pathogenesis of multiple sclerosis using the animal model experimental autoimmune encephalomyelitis (EAE). Lab expertise includes neuroimmunology, neuroendocrinology, and neuroscience. MUST BE A U.S. CITIZEN. Can have completed anywhere from 0-3 years of prior post-doctoral training. Must have background in either immunology, neuroscience, or genetics. Must be available to start by April 1st. ]]>

<![CDATA[About the Job We are seeking an experienced biotech sales representative to sell DNA sequencing and genotyping services. Must be southern California resident with experience selling biotech products in southern California, although the sale territory is not limited to California. Requirements: - B.S. in Life Science. - 2 or more years of proven successful sale experiences in the life science market. - Experience selling to the Universities, Research Institutes, Biotech, Biopharma or other life sciences organizations in California - Strong communication, interpersonal and organizational skills - Knowledgeable in molecular biology techniques such as sequencing, PCR, DNA prep, cloning etc Keywords: Account manager, sale representative, biotech services, DNA sequencing, genotyping, PCR, DNA, genomics, biotech. ]]>

<![CDATA[ Are you a closet meteorologist? Are you fanatical about science? We have the job for you. The Weather Channel is currently casting for several new series. See our requirements below and file your submission if you think you have what it takes. Please send a link showing off your on-camera skills as well as your headshot and resume. We are looking for a host, not an actor, so please don't send an acting reel. Requirements: A rugged and adventuresome person who is not afraid of getting his/her hands dirty Passionate and knowledgeable about weather; scientific background a plus A big / fiery personality who is entertaining and clever Loves the outdoors On-air experience necessary; no professional actors, please Please send your submissions to weather.gig@gmail.com. No Phone Calls!]]>

<![CDATA[Licensed Bioanalyst ( californian license ) needed For more information email or call Jamie @ 310-699-7907 Vizzit Home Health Care, Inc Re-CLIA Labs. 3820 Del Amo Blvd ste 223 Torrance TX 90503 310-699-7907 ]]>

<![CDATA[Biophase Solutions specializes in placing the top talented professionals in the leading Biotechnology companies in Southern California. We are currently recruiting for numerous lab technician openings for a Biotechnology company near Long Beach, CA. Responsibilities include working in the clinical trials department performing rapid infectious disease testings. Techniques include: Multi-Channel Pipetting, Serial Dilutions, Aseptic Techniques and other related methods. We are looking for candidates with Academic or at least 1 year of industry experience, but must have a BS/BA Degree in Biology or Molecular Biology. Chemistry degrees will not be reviewed for this position. This is a 24 week temp assignment paying $14-$15/hr. Also, please visit www.biophaseinc.com to view additional opportunities throughout Southern California! ]]>

<![CDATA[<center><img src="http://www.jobelephant.com/banners/6110.gif"></center> California Institute of Technology Research Technician - Biology Open Until Filled Job Summary Full-time position assisting researchers on molecular neurobiology projects as well as providing other general technical lab support. Job Duties Preparation of solutions, buffers, media, reagents, and bacterial plates Transformation of E. coli with plasmid DNA Preparation of plasmid minipreps Restriction enzyme digestion of DNA and agarose gel electrophoresis analysis PCR analysis of DNA samples Cloning DNA fragments into plasmids Assistance with brain stereotaxic injection experiments Assistance with brain histology and immunohistochemistry Assistance with mouse behavioral experiments Basic Qualifications B.A. in Biology, Biochemistry, Chemistry or related field At least one year working in a molecular biology laboratory or neuroscience laboratory Must have experience performing histology including tissue cryosectioning, staining, and immunohistochemistry. Must have experience in molecular biology techniques including DNA subcloning, mini-prep analysis and PCR Preferred Qualifications Experience in mouse behavioral experiments helpful but not essential To be considered for this position please visit our web site and apply on line at the following link: <a href="http://apptrkr.com/139311" rel="nofollow">http://apptrkr.com/139311</a> Caltech is an Affirmative Action/Equal Opportunity Employer. Women, Minorities, Veterans and Disabled Persons are encouraged to apply. <img src="http://jobelephant.com/img.php?id=139311&image=logo"> Copyright ©2009 Jobelephant.com Inc. All rights reserved. <a href="http://www.jobelephant.com/" rel="nofollow">Posted by the FREE value-added recruitment advertising agency</a> ]]>

<![CDATA[The Weckerle Group is a successful, family owned cosmetics company with a global presence. We are headquarted outside of Munich, Germany with facilities in France, Switzerland, Brazil and Carson, CA. Our facility in Carson, CA is currently seeking a Quality Control Chemist . This position will report to the Department Manager . The Quality Control Chemist is responsible for all incoming raw materials / and or components in addition to approving formulated bulk. This includes analytical analysis in accordance to specification, filing of C of A’s, retains, documentation and all the results including but not limited to: Responsibilities: • In charge of QC testing of raw materials and compounded batches. • Verify that batch sample are in accordance with customer standards in terms of: Color, Odor, Texture, Appearance. • Follow all SOPs when approving batches. • Make recommended adjustments to bulk if not up to standard (color matching). • Analyze volatile content in moisture apparatus. • Analyze water content using Karl Fischer apparatus. • Test of softening and melting point of all liners as control. • Submit internal approved compounded lipstick bulk sample for final approval before production process. • Coordinate all outside testing with external lab. • Enter QC test results in the QC cards for finished products. • File certificates of analysis of raw materials with their respective Qc cards • Will troubleshoot, maintain and calibrate various analytical instruments and will report and document any unusual occurrences. • Will determine if analytical results conform within all appropriate written specifications for identification, purity and quality. • Update MSDS files Requirements: EDUCATION: • Bachelor's degree (B. A.) from four-year College or university; and requires at least 5 years of experience in the field or in a related area. EXPERIENCE: • Minimum 5 years experience in QC Environment in similar position, clerical experience. • Working knowledge of MS Office, Word and Excel. • Strong written and verbal communication skills, needed to effectively communicate with, Management, guests, customers, vendors, suppliers, etc. To Apply: We are an equal opportunity employer. All interested and qualified applicants should send their resume to jobsus@weckerle.com ]]>

<![CDATA[I am reaching out today regarding an exciting opportunity. My client is the “best of the best” in food safety companies. They cater to the agriculture industry and offer a range of food safety services. This is an opportunity to work in a fast-paced, deadline driven environment as part of a dynamic team of microbiologists and chemists. This company is focused on state of the art technology and continuing education for their staff. The role that is currently available is a microbiology supervisor. This is an opportunity to be the right hand to upper management, to be a problem solver, a leader and an integral part of the organization. This position will offer future growth into upper management positions. If you possess a degree in Microbiology, Biology or another related degree and have at least 3 years of experience (bench work) in a micro lab working with food and are interested in this exciting opportunity, please don't hesitate to contact me! Nick Executive Recruiter]]>

<![CDATA[A new start-up biomedical company in the L.A. area is looking for an experienced lab technician or research associate with BS or MS or PhD degree. More important than the degree is the relevant laboratory/research experience of the applicant, as detailed below. The position is available immediately and might involve, at least partially, work on the Health Sciences Campus (HSC) of the University of Southern California (USC) in Los Angeles. The ongoing research project deals with antitumor drug development and involves the testing of novel pharmacologic agents in mammalian cell culture systems in vitro, as well as in mouse tumor models in vivo. The ideal applicant has extensive hands-on experience in a variety of techniques of modern biomedical research, such as tumor cell culture, transfection of mammalian cells with cDNA vectors or siRNA, MTT assays, colony-formation assays, Western and Northern blot analysis, PCR, immuno-histochemistry, and work with mouse tumor models. In addition, experience with data archiving, presentation, and evaluation is desirable. Interested applicants should send their curriculum vitae (as a PDF), which should include a detailed description of their education and their hands-on research experience, especially with regards to the above-listed techniques. Short-listed applicants will be asked to provide letters of reference and a photo (headshot). American citzenship or permanent residency (green card) is required for this position. ]]>

<![CDATA[Fast growing clinical laboratory in Van Nuys is seeking a full time experienced biller. The candidate must have at least two years of billing experience. Experience with CPT codes, ICD9, and Medicare-Medical-Insurance companies, appeal process is necessary. the candidate must have good communication skills to be able to speak to the insurance companies for following up with the claims. salary will be based on the experience of the individula. We pay higher than all our competition. email you resume to busheris@yahoo.com]]>

<![CDATA[ Join an International Leader in Pediatrics. Childrens Hospital Los Angeles is a special place where children have been cared for and cured for more than 100 years. Our hospital has become one of the world’s top pediatric facilities, acknowledged throughout the United States and around the world for our leadership in pediatric and adolescent health. With its “Magnet Recognition” for Nursing Excellence, the American Nursing Credentialing Center has made “official" what so many of our patient families, and those within the profession, have come to know - that this hospital is very, very special place, and its nurses are, too. The Sr. Research Lab Manager manages a large and complex laboratory, consisting of research assistants, graduate students, research postdoctoral fellows, and other rotating students and trainees. Designs, conducts, and documents research projects. Oversees research project budgets and all fiscal matters for the laboratory. Under the guidance of the P.I., leads the day-to-day operations for the laboratory, insuring optimal laboratory functioning and compliance with all institutional policies and procedures. Qualifications: Bachelors degree in a scientific field. 5-8 years progressively more complex laboratory experience, including supervisory and laboratory management experience. Knowledge, Skills and Abilities Required: Research skills in molecular biology, manipulation of mouse embryos, phenotypic analysis of mouse mutants, and tissue culture. Ability to conduct, analyze and document laboratory research at multiple locations. Ability to communicate effectively, verbally and in writing. Confidentiality for all human resources and financial matters. Childrens Hospital Los Angeles (CHLA) is a special place where children have been cared for and cured for more than 100 years. Our hospital has become one of the world's top pediatric facilities, acknowledged throughout the United States and around the world for our leadership in pediatric and adolescent health. EOE/AA If you are interested in working with the very best physicians, surgeons and nurses, in a place where kids come first please visit our website www.childrenshospitalla.org To Apply for this position, please <a href="http://chla.contacthr.com/15306120" rel="nofollow">CLICK HERE</a> ]]>

<![CDATA[Do you have asthma, do not smoke and have used or are using some kind of asthma medication? If you are eligible you can participate in a Research study and be compensated from $900 up to $1300 for your time and participation. If you are interested please fill out the signup sheet at <a href="http://www.calallergy.com/trials_signupform_la.html" rel="nofollow">http://www.calallergy.com/trials_signupform_la.html</a> or call (310) 966 9050 extn # 1 ]]>

<![CDATA[ An FDA registered independent laboratory is looking for an analytical chemist to join the chemistry department. Looking for an individual that is very knowledgeable with Chemstation software and use of HPLC (agilent 1100) . Individual need to be able to understand USP,AOAC, or customer supplied methods to run assays. They are expected to have familiarity with other instruments such as spectroscopy and GC. The person should be able to run assays such as Vitamin A, Vitamin E, and other Nutritional and OTC actives. Searching for a bright individual that will be able to work independently as well as work with the Senior Chemist. Knowledge of method development and validation is a plus. Minimum 3-4 years experience and a Science degree in Chemistry. ]]>

<![CDATA[ ICF International (NASDAQ: ICFI) partners with government and commercial clients to deliver consulting services and technology solutions in the energy, climate change, environment, transportation, social programs, health, defense, and emergency management markets. The firm combines passion for its work with industry expertise and innovative analytics to produce compelling results throughout the entire program life cycle, from analysis and design through implementation and improvement. Since 1969, ICF has been serving government at all levels, major corporations, and multilateral institutions. More than 3,000 employees serve these clients worldwide. ICF's Web site is www.icfi.com ICF International has joined forces with Jones & Stokes, one of the premier multidisciplinary environmental consulting firms in the western United States. For nearly 40 years, Jones & Stokes has supported a broad mix of federal, state, and local government and private-sector clients on infrastructure improvement projects, restoration and planning projects, and compliance with mandated government programs. ICF Jones & Stokes provides an array of integrated services in environmental planning and natural resource management, especially in the transportation, water, energy, and natural resources sectors. ICF Jones & Stokes’ Web site is www.jonesandstokes.com This on-call position can be assigned to any of our southern California offices - Los Angeles, Irvine, Redlands, Temecula, or San Diego. Field work will be conducted in the general southern California region. Duties will include survey, testing, evaluation, data recovery, and construction monitoring, as well as other tasks as assigned. This individual will assist senior archaeologists in monitoring of archaeological resources, fieldwork, laboratory analysis and preparation of technical reports and environmental documents. The position requires a B.A. or an M.A. in anthropology (emphasis in archaeology) and at least 2-4 years of experience. Candidates must be able to demonstrate at least one year of field experience in archaeological survey and reconnaissance. Knowledge of computers and GPS equipment is critical. Background in prehistoric archaeology required; additional experience in historic archaeology is a plus, as is prior experience in California, Nevada, Utah, Washington, Oregon, Idaho, and/or Wyoming. Ability to conduct fieldwork and travel is required. Position requires artifact analyses, keeping of field notes and records, and writing key sections of reports (methods, analyses, results). Excellent verbal and written communication skills required, as is a firm understanding of Section 106, and CEQA and NEPA as it pertains to cultural resources. ICF offers an excellent benefits package, an award winning talent development program, and fosters a highly skilled, energized and empowered workforce. ICF International is an Equal Opportunity and Affirmative Action Employer – M/F/D/V For a listing of other career opportunities at ICF, please visit our Career Center at <a href="http://jobs.icfi.com" rel="nofollow">http://jobs.icfi.com</a> To Apply for this position, please <a href="http://icfinternational.contacthr.com/15292053" rel="nofollow">CLICK HERE</a> ]]>

<![CDATA[Biophase Solutions specializes in placing the top talented professionals in the leading Biotechnology and Pharmaceutical companies in Southern California. We are currently seeking a Sr. Analytical Chemist to work for a small lab in Long Beach, CA on medical plants. Duties: Analytical testing for pathogens, molds and pesticides on plants. Ideal candidate has worked for a Nutriceutical Company experienced in analyzing plant matter and roots. Running extractions and isolation's on medicinal oils Must be an expert in GC & GC/MS testings Familiar running a lab and ordering supplies is a major plus. BS/MS in Chemistry, Botany etc. Salary is up to 75K 3+ years of industry experience Please submit your resume to Chris@biophaseinc.com for immediate consideration.]]>

<![CDATA[Position Title: Clinical Trial Assistant Reports to: Director, Clinical Operations City: Los Angeles, CA Experience Level: Entry to junior level. 1-2 years of clinical research experience. Qualifications: • Bachelors degree in a scientific discipline • Knowledge of FDA regulations and ICH guidelines • Understanding of the overall development process for Phase I through Phase IV clinical trials • Proficiency of computer operations in Windows environment and ability to utilize available software for creating documents, spreadsheets and electronic mail • Awareness of issues regarding regulatory strategy, potential areas of concern and new governmental/regulatory developments • Familiarity with and understanding of clinical protocols • Ability to utilize current applications/systems to compile information for presentation or distribution • Demonstrated success managing multiple projects simultaneously • Strong attention to detail • Must be able to work independently as well as in a team environment • Excellent communication skills (oral and written) and interpersonal abilities required Position Responsibilities: • Generation of document packages for regulatory submissions, annual renewals to the FDA, IRB and pharmaceutical sponsor • Ensuring adherence to FDA regulations and guidelines • Preparation and review documents for regulatory submission • Instructing study sites on proper collection of regulatory documents • Research, edit and submit various regulatory documents including items such as new and revised protocols, informed consent forms, investigator documentation, safety reports and recruitment materials • Project point-of-contact, timeline development and timeline management • Collect and report adverse events, in a timely fashion, to the IRB, FDA, and pharmaceutical sponsor • Assist with the development of study documents such as monitoring plan, case report forms, data management plan, source document worksheets, study site budgets, central laboratory specifications, etc • Organize and prioritize work according to study timelines and proactively address potential problems • Maintain current Regulatory Affairs files to ensure compliance with regulatory requirements • Monitor project history file for completeness and accuracy • Work with other departments (such as data management) to address site issues • Support company goals, objectives, policies and procedures • Maintain a professional and credible image with consultants, vendors, customers and clients and co-workers • Assist in preparing and submitting Confidentiality Agreements to potential principal investigators • Generate monthly study progress reports for study sponsor • Generate and maintain tracking tools for all submissions • Generate and maintain tracking tools for study enrollment and regulatory documents for each site This position is located in Los Angeles, CA and does not offer relocation. Interested candidates should email Cheryl Cross at cac@cacrosscom.com with a current resume. ]]>

<![CDATA[We are an independent Food and Environmental Testing laboratory in City of Commerce that is rapidly growing. We have a wide range of internal laboratories, including Microbiology, Chemistry, Instrumentation, Entomology, Environmental, and Proximate. Our company is making a major commitment to expanding its professional team. We are looking for a qualified chemist/technician to perform analyses on food and food-related samples. Completion of college level chemistry courses with a Bachelors Degree in Chemistry or a related science is preferred. Experience in a food-science laboratory or related field is ideal but not required. This is a full-time position and requires flexibility and willingness to work in more than one department. Specifically the Dairy and Metals departments. Experience in these areas is a plus but not required. ]]>

<![CDATA[We are a Food and Environmental Testing Laboratory in the City of Commerce. We are looking for a Microbiology Sample Prep Technician. A successful candidate must be able to work in a fast paced environment, work well with others, work efficiently with minimal supervision, have flexible availability, and a positive attitude. Duties include receiving samples, logging in samples, preparing serial dilutions, preparing enrichments and initiating analyses. Other responsibilities are routine laboratory maintenance, occasional media preparation and emergency sample pick-up. Knowledge of aseptic technique and good laboratory practices are a plus, however NO SCIENCE OR LABORATORY EXPERIENCE IS REQUIRED. All training is done on site at the laboratory. This is a full-time position, MUST be able to work both Saturday and Sunday. Shift: 12-8pm or as needed. ]]>

<![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for Los Angeles and Orange County's scientific community. We are currently looking for an HPLC/Research Chemist to work for an North Los Angeles biotechnology company. HPLC/Research Chemist Position Candidate will assay active ingredients using official methods and to develop and validate non-official methods. Assist in the management of the Analytical Laboratory by coordinating activities of the HPLC/GC testing. Schedule the assays for the instruments based on priority, perform HPLC/GC assays, comply with GLP (Good Laboratory Practices), and prepare batches and formulations. Requires thorough knowledge of dyes, materials, supplies and makes daily R&D batches according to assigned schedule. Must have at least 2 years experience. Please submit resume today for immediate consideration! Also, visit www.biophaseinc.com to view additional opportunities in Southern California! ]]>

<![CDATA[In business 23 years, small, cutting edge environmental consulting firm in Los Angeles is seeking an experienced air quality engineer. We specialize in projects that process Municipal Solid Waste (MSW) such as: recycling, composting, anaerobic digestion, gasification, and other advanced technologies. Key areas of work involve: • Preparation of applications for Permits to Construct and Operate from local APCDs and AQMDs throughout CA; particularly the SCAQMD and the SJVAPCD • Coordination and liaison with local air districts • Evaluation of current and new legislation in Sacramento related to GHG reductions, AB32, the Low Carbon Fuel Standard, and other air topics that affect our projects • Evaluation of emissions data from emerging technologies for converting MSW into electricity or fuels • Preparation of CEQA support documents • Input on planning and feasibility studies • Participate in power point presentations and interviews for Company and clients Looking for five or more years of experience in the field, and particularly the areas outlined above. Must be able to take on a variety of projects and produce on time and budget. Work tends to be fast-paced and results oriented. Must also be comfortable working with small family businesses in the waste and recycling industry. Self-motivation and “can do” attitude required. Strong writing and communication skills essential. Also extensive computer skills and research capability a plus (Word, Excel, Power Point, Adobe). Majority of work is in the private sector, with the occasional governmental project with local counties, or cities serviced by Company clients. Work is focused in California. Compensation commensurate with experience and capability. Full medical coverage, standard paid holidays and vacation. Resumes only. ]]>

<![CDATA[Paragon Laboratories, a leading manufacturer of Dietary Supplements, located in Torrance, CA has an immediate opening for an Analytical Chemist/ Product Formulator of Dietary Supplements and Herbal Products. Responsibilities: • Testing by HPLC, FTIR, AA, UV VIS. • Formulation of Dietary Supplements, including tablets, two-piece capsules and powdered dosage forms. • Research of ingredients to develop new products. • Review of existing formulations to see if there are opportunities for improvement. • Perform Microbiological testing Requirements: • Should be able to interpret various test requirements and specifications. • Experience in Microbiology or Chemistry Lab required. • Should have excellent written and verbal communication skills. Education: • BS or equivalent degree in Biology or Chemistry. Please forward resumes to hr@paragonlabsusa.com. ]]>

<![CDATA[ Kotura, Inc., a worldwide leader in silicon photonics, has an immediate opening for Test Technician (can be entry level). This position involves responsibility for the testing of silicon chips/devices and analyzing/interpreting the test data. Duties of Position: • Operate tools for the testing of silicon chips/devices through various test systems and equipment. • Maintain charts for tracking test performance; take diagnostic actions when the process is out of control. • Help engineers in the development of new processes and the calculation of data. Requirements/Qualifications: • AA degree or equivalent is required. • Good written and oral communication skills • Good analytical skills For more info, visit www.kotura.com Send resume to hr@kotura.com Fax resume to 626-236-4513]]>

<![CDATA[Biophase Solutions specializes in placing the top talented professionals in the leading biotechnology and pharmaceutical companies in Southern California. We currently have a Microbiologist and HPLC Chemist opening. Microbiologist - $18/hr 3-4 WEEK TEMP ONLY Test in-process, finished products and stability samples using official microbiology test methods. Analyze raw materials, in-process products (bulk), finished products and stability samples according to protocol. APC YM Gram + and Gram- Preservative Challenge Testing Water and Environment Testing Validation Studies (Cleaning, Methods, Process, Equipment) Growth Promotion All pertaining USP and in-house micro testing protocols Develops, validates and writes test methods. Writes reports and fills out forms completely. Submit all completed forms to QC Supervisor for final approval and release as required. BS Micro + 1-2 years experience HPLC Chemist - $18/hr Contract to Hire Schedule the assays for the instruments based on priority. Communicate with the QC Manager: -What needs to be done -When the tests will be completed -Specials Projects -Stability Projects -Water Sample Testing -Instrument Maintenance/Instrument Services Verify and sign analyst and standard logbooks for the HPLC/GC laboratory. Perform HPLC/GC assays. BS Chemistry + 1-2 years of experience Please send your resume to Chris@biophaseinc.com for immediate consideration. ]]>

<![CDATA[Medical Laboratory Specialist. Established Biomedical company in the Los Angeles South Bay area. Military lab training preferred. License not required. Excellent work environment and career opportunity. E-mail resume or fax to (310) 637-3927]]>

<![CDATA[Are you currently taking a statin such as ZocorÒ, CrestorÒ, or LipitorÒ? Do you have high triglycerides? Do you have diabetes or a history of heart problems? If so, you may qualify to participate in a research study to test an investigational medication, while still remaining on your current medications. You may be eligible if you: - Are 18 years of age or older, - Are currently taking a statin such as ZocorÒ, CrestorÒ, or LipitorÒ - Have high triglycerides - Have Diabetes, or history of cardiac problems If eligible, you will receive at no cost: - Study-related physical examinations - Study-related laboratory tests - Investigational study medication - Compensation for your time and travel For more information please call (310) 552-5700. . ]]>

<![CDATA[Biophase Solutions specializes in recruiting the top talented professionals for the leading Biotech and Medical Device companies in Southern California. We have multiple packaging positions available. Clean room experience preferred! Job Summary: Performs a variety of manufacturing activities of medical devices within a clean room/controlled environment. Reports to Operations Manager and receives work orders through Production Team Lead. Essential Functions: • Under minimal supervision, perform manufacturing activities to include blending of materials, molding of implants, packaging, documenting completed tasks and shipping of finished goods. • Ensure that manufactured products will meet or exceed the requirements of internal and external customers, never losing sight of the patient as the ultimate end customer. • Will be expected to contribute to the continued development of continuous flow manufacturing lines. • Ensure proper clean room procedures are followed in accordance with ISO standards. • Maintain World Class work spaces by ensuring production lines are neat and clean. Education/Experience Requirements: • Ability to read, write and speak English • Basic knowledge of computer applications (Microsoft suite, ERP/MRP) • Manufacturing experience preferred • Must be able to lift 50lbs. 3-6 month temp - M-F 8am-4pm $10/hr Please send your resume to Chris@biophaseinc.com with the subject (Packaging). ]]>

<![CDATA[ Join an International Leader in Pediatrics. Childrens Hospital Los Angeles is a special place where children have been cared for and cured for more than 100 years. Our hospital has become one of the world’s top pediatric facilities, acknowledged throughout the United States and around the world for our leadership in pediatric and adolescent health. With its “Magnet Recognition” for Nursing Excellence, the American Nursing Credentialing Center has made “official" what so many of our patient families, and those within the profession, have come to know - that this hospital is very, very special place, and its nurses are, too. The Diagnostic Medical Sonographer's primary function for this position is to perform Diagnostic Medical Ultrasound procedures in accordance with established standards of the Radiology Department, and under the supervision of the attending Radiologist or his / her designee. Must be able to distinguish normal vs abnormal anatomical findings, and demonstrate the ability to record the most appropriate images in order to render the correct interpretation. Secondary Purpose: Perform CT Scans. Individual must have a dual license and the competencies necessary to operate the CT Scanners. Qualifications: Must be a graduate of an accredited school of Radiology Technology as well as a formal and accredited school of Ultrasound. One year Ultrasound experience. Pediatric experience of at least 2 years is required. License, Registration or Certification Required: RDMS and ARRT; CRT Skills: Required Ability to perform diagnostic Medical Sonographic examinations, and a wide range of CT procedures Childrens Hospital Los Angeles (CHLA) is a special place where children have been cared for and cured for more than 100 years. Our hospital has become one of the world's top pediatric facilities, acknowledged throughout the United States and around the world for our leadership in pediatric and adolescent health. EOE/AA If you are interested in working with the very best physicians, surgeons and nurses, in a place where kids come first please visit our website www.childrenshospitalla.org To Apply for this position, please <a href="http://chla.contacthr.com/15250762" rel="nofollow">CLICK HERE</a> ]]>

<![CDATA[Currently we are enrolling for the following studies: Diabetic Neuropathy: You must have Type I or II diabetes and have pain in your feet. Lower Back pain Study Epilepsy: partial seizures. Adolescence : Age 14 to 17 having ADHD All of these studies include free exams and compensation per visit (about $50.00 per visit) If interested please e-mail the following information to ilerner.pimr@verizon.net or call (310)208-7144 Study interested: Medication Currently Taken: ]]>

<![CDATA[Company Description Rapidly growing global leader in the production and distribution of advanced materials. Products include nanotechnology, rare elements, high purity materials used in high technology, fuel cells, solar energy, green technology, pharmaceuticals, defense, space and energy. With its corporate and administrative offices in Los Angeles (Westwood) and Cheshire (UK), the company maintains production and research operations in several U.S. locations and distributes worldwide. Job Description 1. Initially the candidate will devote substantial time learning the area of Advanced Materials and the company’s capabilities and systems. 2. Thereafter he/she will perform duties in all aspects of sales, including direct and online product sales assuming customer contact and additional management responsibilities as skill development warrants. 3. Candidate to develop into an integral long term member of our corporate team who will successfully rise in responsibility to a management role in the sales group. Job Qualifications 1. B.A. or B.S degree (materials science, chemistry, engineering or related field desirable). 2. 1-2 years experience in Sales and/or Marketing (science-related business desirable) 3. Well-versed in Excel and the operation of a functional data base. 4. An extremely high caliber, productive individual who enjoys setting and achieving aggressive goals. 5. Once trained, can successfully function as a member of our sales group functioning in a rapidly changing and very competitive high tech environment.]]>

<![CDATA[Biophase Solutions specializes in placing the top talented professionals in the leading Biotechnology and Pharmaceutical companies here in Southern California. We currently have 2 openings for a Materials Chemist. Description: Chemist I Perform standard organic and organometallic chemical syntheses, including use of olefin metathesis catalyst technology. Perform chemical purifications including distillation, TLC, flash and/or column chromatography; Conduct chemical and/or mechanical analysis, collect data and interpret it with knowledge of GC, NMR, HPLC, and GC/MS techniques. The Chemist I will work with bench scale equipment and larger glassware from 5L to 72L size. Will also run syntheses using 50 gallon and 200 gallon reactors. Only accepting BS/MS in Chemistry or Biochemistry Contract to Hire $17-$21/hr Please submit your Microsoft Word resume to Cory@biophaseinc.com for immediate consideration.]]>

<![CDATA[Seeking Business Equity Partner/Vice President A fast-growing company in medical research and life-science industry seeks a highly successful and experienced business partner/vice president. We have established successful producing and marketing model with much lower costs than our rivals. Our customers are located in the areas from the Western to East Coasts including top Harvard, Stanford, Washington Universities, UCSF, UC-Berkley, UCSB, UC-San Diego, National Institute of Health, California Institute of Technology, etc. The ideal partner/vice president with the successful marketing and team management experiences is needed to continue to expand our successful sales and pursue venture capital or angel funding. Responsibilities: *Generate new business *Develop partner channel *Pursue venture capital or angel funding Preferred: *Medical research & life-science experience *Non-profit organization sales experience *Marketing experience *Enterprise & sales experience Please email your resume and questions to info@labbestbuy.com Locations: California and Kansas • Compensation: Based on the experiences. • Business partner needed and benefits are negotiable • Please, no phone calls about the jobs. • Please do not contact job poster about other services, products or commercial interests. Serious inquiries only, and no recruiters please. ]]>

<![CDATA[Top research lab in the field needs a motivated and organized individual to manage the lab and conduct independent research projects. Lab research focuses on the etiology of multiple sclerosis and lupus, treatment of disease, and sex differences in disease. Some of the skills listed below may be acquired after joining the lab. JOB DESCRIPTION A. Perform a variety of animal experimentations, including: 1. Breed mice, tail cut, DNA isolation and genotyping and karyotyping of progeny. 2. Immunize mice, harvest lymph nodes and spleen, attain blood by cardiac puncture and retro-orbital eye bleed. 3. In vitro culture of immune cells. 4. Assess antibody and cytokine responses by ELISA, CBA and Flow Cytometry. 5. Treat mice via subcutaneous pellet implant, i.p. and s.c. injection. 6. Clinical scoring of mice with disease and care for EAE health related issues. 7. Survival mouse surgeries, including ovariectomies and castrations. 8. Perfusion of prenatal and adult mice by cardiac puncture and dissect brain, kidneys, liver, spleen, lymphnodes and spinal cord. 9. Embed and perform cryostat sectioning on CNS tissues. 10. Measure mice proteinurea, blood urea nitrogen levels by retro-orbital eye bleed. 11. Perform immunocytochemistry on floating CNS tissue sections and analyze by confocal microscopy. 12. Assist principal investigator in writing and amending animal research protocols. B. Data management 1. Collect, tabulate, analyze, and perform statistics all required data using Mac or PC with Excel and Photoshop, Adobe Illustrator and Graphpad Prism. 2. Perform library searches as needed to review, analyze and relate to current research practices. 3. Maintain detailed and accurate records of mouse colony. 3. Assist in the writing up of results for publication in peer-reviewed journals. C. Laboratory management 1. Maintain animal inventory by analyzing current and future requirements. 2. Order and monitor laboratory animals. Conform to Federal and University regulations as regards animal use. 3. Order laboratory supplies and equipment as needed following established University and Departmental regulations, including necessary administrative support of the ordering process. 4. Assist Departmental and University staff in the tracking and inventorying of laboratory equipment and expenses as needed. 5. Insure proper operation and maintenance of laboratory equipment. 6. Insure proper use and disposal of hazardous and radioactive material according to the guidelines of EH&S and Radiation Safety Departments. 7. Train new laboratory staff and students on animal experiments, data management, and general lab procedures. D. Supervision 1. Supervise 1 Laboratory Assistant I and 1 Laboratory Helper. 2. Train, assign tasks, and review work. 3. Participate in selection process. 4. Make recommendations for corrective action as necessary. E. Special activities and projects 1. Assist principal investigator to meet necessary grant, conference, presentation meeting deadlines by, for example, preparing slides or other materials. 2. Keep up to date on laboratory techniques and research protocols by attending classes, seminars, meetings, and conferences as requested by the principal investigator.]]>

<![CDATA[Biological Permitting Specialist Sequence is seeking an experienced Biological Permitting Specialist to work on a few of California's most dynamic projects. The ideal individual would have at least 5 years experience permitting land development, energy, transportation and other renewable resource projects throughout the western United States, specifically California. Candidate should posses the skills and abilities with regulatory permitting (state and federal) for endangered species, wetlands and biological resources for CEQA and NEPA documentation projects. This will include working along side personnel from the Fish & Wildlife Services, Corp of Engineers, and other regulatory agencies for application preparation and consulting periods. Must have strong section 404, 401 knowledge. This is a project management level opportunity in which candidates will direct a portfolio of permitting projects and personnel throughout the state. Requires a degree in Biology, Environmental Planning or related disciplines. Master degree preferred. Excellent written and verbal communication abilities required. For consideration, please forward resume or contact directly: Sequence Systems Attention: Michael DeSafey 2008 Opportunity Dr. Suite 150 Roseville, CA 95678 Phone: 916-782-6900 ext. 202 Fax: 916-782-6307 Email: jobs@sequencestaffing.com www.sequencestaffing.com If your background does not exactly meet the above job qualifications, please feel free to forward your resume as we have many opportunities available that are not advertised throughout California. Please visit our website www.sequencestaffing.com. Keywords: permitting, CEQA, NEPA, energy, endangered species, wetlands, planning, environmental, biology, regulatory compliance, delineation, EIR, EIS, biologist, environment, land use, development, entitlement, engineering, engineer, water, utilities, renewable, Fish and Wildlife, San Francisco, San Jose, Northern California, Southern California, California, San Diego ]]>

<![CDATA[Individual needed for part time work conducting spectroscopy experiments. Will be obtaining spectra for various pharmaceuticals and then helping design study using data. Must be senior/grad student level, fluent w. spectroscopy, in this case UV, excel knowledgeable. $15/hr, located 1 block off campus, hrs flexible. Prob 6 hrs/wk to start and will last?# of weeks depending on where the research leads. Pls reply/resume by email.]]>

<![CDATA[CTI is a company that develops new modular electrocoagulation process technology for water treatment. We are looking for an experienced water treatment specialist. Candidate must have knowledge in process design, chemicals used, and experience in marketing of same. ]]>

<![CDATA[We are an herbal supplement company seeking a MD to endorse our men's prostate supplement. We would like to feature you on our website along with a positive quote about our well made and popular prostate pill. The pill in all natural and consists of such ingredients as Saw Palmetto, Pygeum, Beta Sitosterol, zinc and many more. All inquires will be handled discreetly. If you are interested please contact John by email at: stigwood310@hotmail.com Thank you ]]>

<![CDATA[Biophase Solutions specializes in placing the top talented professionals in the leading Biotechnology and Pharmaceutical companies in Southern California. We are currently seeking a Sr. Analytical Chemist to work for a small lab in Long Beach, CA on medical plants. Duties: Analytical testing for pathogens, molds and pesticides on plants. Ideal candidate has worked for a Nutriceutical Company experienced in analyzing plant matter and roots. Running extractions and isolation's on medicinal oils Must be an expert in GC & GC/MS testings Familiar running a lab and ordering supplies is a major plus. BS/MS in Chemistry, Botany etc. Salary is up to 75K 3+ years of industry experience in a nutraceutial Please submit your resume to Chris@biophaseinc.com for immediate consideration.]]>

<![CDATA[NanoPacific Holdings, Inc. (NPH) Biomedical/Drug Development Scientist NPH is a materials science company based in Westwood, California with strong ties to UCLA. The Company is focused on translating novel technology platforms into breakthrough commercial products in healthcare and industrial applications. NPH is searching for a full time biomedical/drug development scientist to lead pre-clinical and clinical development of one or more of our novel product candidates for skin infections and wound-healing. Job Description: To provide project management, as well as scientific and analytical support for Company projects in infectious diseases and wound healing. Candidate will be a key leader for scientific grant writing on his/her own projects. Preferred background would include immunology, microbiology, or immunopathology. This is a full time position. Qualifications of the successful candidate: 1. Advanced degree, PhD, MD or equivalent (with post-doctoral experience preferred) in Microbiology, Immunology or Immunopathology; 2. Strong scientific background and analytical skills; 3. Minimum of three years work experience within research/drug development organizations is preferred; 4. Ability to summarize research in verbal, written and powerpoint presentations; 5. Strong writing skills preferred. Please contact Scott Hayashi, Human Resources at e-mail scott@nanopacific.us if you are interested. ]]>

<![CDATA[Cangene Corporation, a Canadian biopharmaceutical company, is headquartered in Winnipeg, Manitoba and has approximately 800 employees in eight locations across North America. This includes the operation of four specialty plasma collection facilities located in Florida, Maryland, California and Manitoba. Plasma collected from these facilities is used to create life saving medications which are sold worldwide. Visit www.Cangene.com for more information. Cangene Plasma Resources, is a specialty plasma donation facility that collects human blood plasma which is used to create life saving medications. We have an exciting opportunity in our Van Nuys Plasma Center for a Program Manager. POSITION SUMMARY: The program manager is responsible to manage specialty plasma programs and is responsible to assist the center manager in the overall activities, as designated by the center manager, required to meet corporate short and long term operational objectives. Compliance with Regulatory and Corporate policies and procedures is essential to ensure and maintain donor, employee and product safety. 1) Manage Specialty plasma programs 2) Ensure and maintain Regulatory and Corporate compliance 3) Possess working knowledge of all functions and operations of the plasmapheresis center 4) Maintain a high quality medical facility QUALIFICATIONS: The candidate should have lab experience and some blood bank experience is preferred. Current California license as a Clinical Laboratory Scientist, or Medical Lab Technician is preferred but not required. ]]>