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<![CDATA[ABOUT THE COMPANY: EPIS, Inc. is a premier energy-application software development company that is completely independent of large holding companies and totally owned by employees. EPIS is the developer of the AURORAxmp® Electric Market Model, proven software for simulating energy markets that helps energy professionals prepare reliable electric-market price forecasts, resource valuations and market-risk analysis. Grow and expand your career with a company committed to helping the industry meet the energy needs of the economy. AURORA results make a difference by providing an on-going market analysis capability for future resource decisions and trading decisions related power positions. AURORA is now the tool of choice for leading power marketers, resource developers, regulatory agencies, and trusted energy consultants throughout the U.S. and Canada. Offices are located in West Linn, Oregon and Sandpoint, Idaho. ABOUT THE POSITION: In this position you get the opportunity to perform market analyses by analyzing results of forecasted prices, in conjunction with other market information, to help clients develop their own view on economic fundamentals of future markets; and evaluate investment or trading opportunities. You will be able to actively work with the nodal functionality in state of the art market simulation tools to simulate the North American electric power system. The responsibilities include researching, compiling, refining, mapping load flows and energy dispatch data. The successful candidate will be able to work with power system load flows, review and update transmission inputs, run load flow simulations, and compare model behavior to actual market operations to understand contingencies, flows, and LMP components, etc. Provide support to clients on uses of models and data interfaces to enable clients to simulating LMP energy markets. Minimum Qualifications: Experience: The qualified candidate will have a minimum of two years of experience in energy market analysis including transmission planning or LMP (Locational Marginal Pricing) market analysis. Application Software: Experienced in the use of load flow programs, i.e., PowerWorld®, PSS/E®, etc. Have experience or an aptitude for using state of the art models, i.e., AURORA® Electric Market Model and integrated software interfaces. Qualities: Organized, dependable, with a high level of integrity and the ability to work both individually and in a team. Has an aptitude for working with details and meeting deadlines. Skills: Strong analytical and problem solving skills, and a willingness to research and learn new techniques and software applications. Use of SQL and programming skills in Visual Basic would be beneficial. Education: Bachelor of Science degree in electrical engineering, math, economics or similar is required; an advanced degree is beneficial. Legal: Must be eligible to work in the United States in accordance with current immigration laws, and you must be capable of securing Critical Energy Infrastructure Information (CEII) clearance from FERC, and approval to access power load flow information from Independent System Operators. Location: Northwestern United States. COMPENSATION PACKAGE: We take pride in creating an environment where the team members enjoy helping our clients’ succeed and the employees share in the successes. • Competitive salaries. • Incentive bonuses based on corporate performance. • A 401(K) profit sharing plan to which the Company directly contributes a percent of your total annual earnings. • Medical, dental and vision coverage. • Healthcare spending accounts. • Disability insurance. • Life and accident insurance. • Educational assistance program. • Progressive paid time-off benefits. Position Type: Full-time Salary: Competitive pay commensurate with qualifications. Submit cover letter and resume by fax (208) 263-4515 or email employment@epis.com For more information visit <a href="http://www.epis.com/Company/Careers.htm" rel="nofollow">http://www.epis.com/Company/Careers.htm</a>]]>

<![CDATA[Job Title: Building Diagnostics Professional/Engineer Company: SabCo, Inc. (www.sabco.us) Status: Full Time Employee JOB DESCRIPTION: We are a state licensed general contractor located in southeast Florida that specializes in Water Intrusion Evaluations, Indoor Air Quality Testing and Consulting, and Forensic Building Evaluations. We are seeking a Professional with experience in Building Diagnostics, Forensic Building Evaluations, and knowledge of building construction practices, construction technologies, construction materials, building codes, Indoor Air Quality and HVAC systems. Knowledge of low, mid and high rise structures and Green Building practices are preferred. Candidate must have excellent verbal and written communication skills. Must demonstrate excellent report writing and skills to clearly communicate investigative results. Strong interpersonal skills are essential. Regular interfacing with clients and position serves as company representative at state and local professional organizations. REQUIREMENTS: * Must be able to pass a background and driving record check * Must be able to pass a drug test. Our company is a Drug-Free Workplace * Must have reliable transporation * Must be english speaking Qualified Candidates, should email resume for consideration to: RonHuggins@sabatellocompanies.com ]]>

<![CDATA[Research Scientist needed for health project. Home based.]]>

<![CDATA[I am an older student taking basic statistics at BCCC (as a prereq for MBA). I need a statistics pro who will tutor me once a week for the balance of the fall semester. Please contact: bass.player@ymail.com ]]>

<![CDATA[Many healthcare facilities need qualified medical coding and billing specialist to accurately bill patients for treatments. This program prepares you for entry level employment as medical coding and billing specialist in hospitals , clinics, physican practice groups, surgery centers, long term facilities , and home health care agencies. call me to find out more 786.221.6519 ]]>

<![CDATA[MISource Medical & Science, a local recruiting company focusing on careers in the medical, biotech, pharmaceutical and food/beverage industries has SEVERAL openings for QC chemists in the Miami and Ft. Lauderdale areas. Minimum requirements: Bachelor's degree in Chemistry or related life science At Least two years of hands-on QC chemistry experience Experience working in an FDA and GMP/GLP environment Our clients are seeking candidates for permanent hire, contract-to-perm, and contract positions. Compensation, location, and benefits vary by client. If you are interested in learning more about the opportunities we currently have available. Please email your resume to Kayla Klofenstine at kklofenstine@misource.net today! I look forward to working with you to advance your career!]]>

<![CDATA[Hey My name is Joseph I'm a chemist with more then 25 years experience in the chemistry industries. I have a lot of knowledge and i can help with any kind of chemicals projects organic or inorganic products. For more information please contact me at: cell- 305 763 6657 or by E-mail at jobit75@yahoo.com ]]>

<![CDATA[Scheda Ecological Associates, Inc (Scheda) is a Florida-registered corporation committed to providing both private and public sector clients with innovative, cost-effective solutions for a changing environment. Scheda is in search of a Staff Research Scientist STA Everglades Division – Fire Project Research Team. The Staff Research Scientist will be an employee of Scheda Ecological Associates, Inc., but the position will be based at the District’s Gun Club Road facility in West Palm Beach, Florida. Qualifications: • Bachelor’s degree in either biology, botany, or chemistry and more than 5 years of related research experience. • The ability to collaborate as part of an ecosystem research team is an absolute necessity. This position requires working as a member of a multi-disciplinary ecosystem team and provides exposure to a wide range of ecosystem studies. The focus of this position is to provide office and field support for the Fire Project research efforts. It is estimated that this position will be in the office approximately 70 percent of the time and in the field approximately 30 percent of the time. Primary Responsibilities: 1. Research-oriented data organization, quality assurance review, and data entry into appropriate software programs. 2. Preliminary data analysis using Excel functions. 3. Preliminary data graphing using SigmaPlot. 4. Technical writing to document preliminary analyses and results. 5. Assisting with organizing and performing a wide variety of vegetation and water quality field studies to support the overall goals of the Fire Project, and it’s numerous sub-studies. This includes field data collection and sample processing. 6. Assisting with field and greenhouse experiments and other assigned tasks; and 7. Other assigned tasks as needed. Scheda offers an excellent benefits package, including comprehensive medical, dental, vision, life, vacation and personal time and a 401(k) plan. To Apply: Send resume and cover letter to: Scheda Ecological Associates, Inc. 5892 East Fowler Avenue Tampa, FL 33617 Attention: Marie Reynaud Or to request a full job description and/or submit your resume and cover letter via email: mreynaud@scheda.com EOE ]]>

<![CDATA[A cosmetic formulator is needed to run an R&D lab in Palm Beach county . Compensation: Open to disucss - Possible partnership. Thanks ]]>

<![CDATA[Use your insight and vision. Explore and create the next generation of Medical Devices. We want candidates to use their imagination and move towards excellence. We have exciting positions to discuss with you in the Medical Device sector. The position is extraordinary. We are seeking exceptional candidates to drive the next generation of medical devices. You will direct ideas from the beginning and execute the products throughout its development. We would prefer cutting-edge candidates with remarkable knowledge of the medical device sector. Research & Development Leader Core Team Leader Advanced Concepts Development Leader Must have MS in Mechanical Engineering and Science/ PharmD/ MD, with strong business acumen; Medical Device & Technical experience vital. Advanced Degree, PhD/MD/PharmD/MS, with top tier MBA; Top tier MBA with deep domain expertise in marketing, finance and clinical; EXPERIENCE: 5 plus years of experience in medical device or pharmaceuticals or health care practitioner. Please send an in-depth cover letter and CV/Resume for consideration ASAP. ]]>

<![CDATA[South Florida Water Engineering firm is seeking a field technician for its North Palm Beach office. The part-time position is for up to 20 hrs per week. Job duties will include stream gauging and other engineering-related field work. The candidate should be familiar with the use of an outboard boat motor, driving a 4-WD vehicle with a trailer. Specific field training procedures will be provided. The following qualifications are expected: Having enthusiasm and dedication to field work Must be able to work Thursdays (12-hour day) and 1 more work day if necessary (additional work day flexible) Being able to master streamgauging (water flow measuring) procedures after one month of in-house training Valid Florida Drivers License and Clean Driving Record Required. Interested candidates please reply with resume. Equal Opportunity Employer / Drug-Free Workplace / E-VERIFY ]]>

<![CDATA[South Florida Water Engineering firm is seeking an Entry Level Engineer for its North Palm Beach office. The position is opened immediately. Job duties will include stream gauging, water quality monitoring, data analysis, and technical report writing/editing. The candidate should have a B.A. or B.S. with an emphasis in water resources or an environmental related field. Applicable degrees include Water Resources Engineering, Environmental Engineering, and Civil Engineering. The following qualifications are expected: Minimum cumulative GPA of 3.0 Having enthusiasm and dedication to field work Having strong oral communication and good writing ability Being able to work under minimal supervision Being able to master stream gauging (water flow measuring) after one month of in-house training Proficiency with MS-Office software Valid Florida Drivers License Interested candidates please reply with resume. Equal Opportunity Employer/Drug-Free Workplace/E-Verify ]]>

<![CDATA[Ultrasound instructor needed to teach one-on-one for the ARDMS Ultrasound Registry. Must have knowledge of Ultrasound Physics and Ultrasound Abdomen. Please email resume to mjoy6274@aol.com or call 954-415-3315 if you have questions. Thanks, Mar ]]>

<![CDATA[Collection of Exotic Animals and Birds. Ranch Job duties include but not limited to food preperation , feeding, watering, cleaning, and observing animals under your total care. This job involves all day Outdoor work in South Fla. Heat and Humidity. Long -Term Employment. Career Oriented. Excellent Job Security in todays tough economic times. Free Cell Phone with full-time employment. Will Train however outdoor work experience prefered. Full- time or part-time. For Full-time position-Optional On-Site housing for single individual available with employment. Some weekends and some holidays. Must be able to work a full day outdoors. Part-time mornings or full-time possible. No visible tatoos or piercings. Smoke free, Drug free, and Alcohol free applicants only to be considered. Backround checks and testing performed on all applicants prior to hiring. Looking for a person that wants a long-term career oriented stable job with economic growth potential. Need own car. MUST E-mail Resume with Full Work Experience History and MUST E-mail WORKPLACE Phone Number and supervisor/owners name to be considered for this position! ]]>

<![CDATA[The Scripps Research Institute is seeking a Safety Technician II for Waste and Chemical Compliance for its newly formed Environmental Health and Safety Department in Florida. Primary responsibilities will include the removal and transport of chemical, mixed chemical, biological, and radioactive waste from laboratories for processing, packaging, and manifesting for appropriate offsite disposal and/or treatment. This individual will also conduct surveys and will process incoming packages of radioactive and biological materials and chemical substances. Duties will also include manual and electronic recordkeeping such as entering and updating chemical inventory and hazard classification information into a database. Work will be conducted in accordance with Federal and State of Florida environmental, health, and safety regulations and permit requirements. This position will also perform a wide range of other environmental, health, and safety duties as assigned. Requires: High school diploma or equivalent, and a minimum of two (2) years of related experience in Environmental Health and Safety. Must be able to lift 50 pounds unassisted and pass a respirator physical. Must possess a clean driving record and be able to pass a background check. This position must be available to be on call 24/7 for facility emergencies. Florida and Palm Beach County residents preferred. Associate's or Bachelor's degree in a Physical Science or related field is strongly preferred. Demonstrable knowledge of OSHA and EPA regulations for hazardous chemicals is strongly preferred. Experience with Chemistry coursework and certification in 40-hour OSHA HAZWOPPER training is desirable. For more information and to apply online visit <a href="http://careers.scripps.edu." rel="nofollow">http://careers.scripps.edu.</a> TSRI embraces diversity and recognizes it as being a key to our success. EOE/M/F/V/D ]]>

<![CDATA[Prestigious laboratory in Miami, FL (near University of Miami) with an established worldwide clientele base is looking for a part-time marketing assistant to help promote its laboratory services to the archaeology, geology and energy/plastics (related to global warming issues) community. Position is ideally suited for someone looking for flexible hours (15 to 30 hours per week). Ideal candidate will be someone who is meticulous and autonomous. A background in science is not necessary. Please send your CV to info@betalabservices.com or tel: 786-268-8363. ]]>

<![CDATA[Busy, well established animal hospital seeks an experienced technician or technician assistant. Must be able to draw blood, administer IV and medications, have good customer service abilities, and be able to multi-task. FUN work environment, great learning opportunities, competative salaries and benefits package!]]>

<![CDATA[We are looking for a consultant or part time regulatory advisor.]]>

<![CDATA[Relocation Paid by Client Position Responsibilities 1- Prepare and Operate purification equipment to SOP’s, including Chromatography Columns, Bioprocessor, Stirred Cells and Tangential Flow Filtration (TFF). 2- Organize and prepare sterile buffers. 3- Complete all cGMP documentation diligently and report any deviations to management. 4- Participate in the writing and execution of validations. 5- Participate in the writing of new batch records, specifications and SOP’s. 6- Any other task deemed necessary for manufacturing. 7- Must be able to multi task projects. 8- Person will constantly interact with QA, QC, Process Development and Materials Management. Position Requirements 1- BSC, Associates, in a relevant field. 2- Experience in a cGMP environment preferably in Upstream or Downstream manufacturing 3- Must be able to follow detailed instructions and record information clearly and accurately. 4- This is an entry level position that welcomes candidates that are self motivated, enthusiastic and would enjoy the challenges of a busy Manufacturing environment.]]>

<![CDATA[Responsibilities will include; Diving, care and maintenance of marine fish exhibits and life support systems, quarantine of animals, ordering supples and management of support staff. This is a full-time position of approximately 45 hrs. Send resume to Rodger White by E-mail or call 407.827.8500 Ext. 108 ]]>

<![CDATA[Our client, a leading beverage manufacturing facility, has an immediate need for a QA Technician. The QA Technician will be running tests on beverage samples. Requirements include a BS in Biological Sciences and previous work experience testing beverage/dairy/food samples. Candidates must be willing to work any shift and be a hard charging, motivated employee. To be considered please reply with resume. Thank you!]]>

<![CDATA[Microbiologists A -TEK, a leading Government Contractor, has exciting career opportunity for a results-oriented laboratory professional in Boston, Massachusetts. We are currently seeking experienced Microbiologist (Junior Level) to perform a variety of molecular (particularly PCR) and biological tests to identify the presence of pathogenic microorganisms/agents. EMPLOYEE BENEFITS: The individual hired for this position would be eligible to participate in our rich benefits package which includes approximately 90% employer-paid premiums for all employee coverage. The company also supplements the premium payment for spouse and/or dependents coverage under each of the health-care insurance plans only. Most benefits are effective on the first of the month following the date of hire. The following outlines the benefits provided to full-time employees: • Medical Insurance and Prescription Benefits – 3 Plan Options available under Anthem BC.BS PPO • Dental Insurance – 2 Plan Options under SunLife • Vision Insurance (Vision Service Plan) • Life Insurance (1x annual salary up to $100k max) • Accidental Death & Dismemberment Insurance (1x annual salary up to $100k max) • Long-Term Disability • Short-Term Disability • Professional Development/Tuition Assistance/Professional Associations ($10,500 per year) • 401(k) Plan • Premium Only Plan • Paid Leave beginning at 15 days per year • Paid Holidays at 10 days per year • Direct Deposit in up to 3 different accounts POSITION DESCRIPTION: Microbiologist This individual will be responsible for: • Performing a variety of non-research biological science work utilizing microbiological and molecular techniques, including DNA extraction and real-time polymerase chain reaction (PCR) including handling, receipt, and processing of samples, containing potentially high hazard biological threat agents. • Assuring that incoming specimens are recorded, processed, and triaged appropriately while maintaining "chain-of custody". • Reporting test results to appropriate individuals using established procedures. • Applying knowledge of these advanced molecular techniques and microbiological procedures to appropriately interpret and report the findings of the assays. • Performing quality control and quality assurance procedures including, but not limited to routine equipment maintenance and calibration, and documentation of quality control and quality assurance activities as needed. Ensuring that reagents, supplies and equipment are adequately maintained. • Maintaining documentation collection on findings and protocols. • Providing laboratory support for field responses and investigations as directed. • Reporting test results to appropriate individuals using established communication protocols with Local, State and Federal agencies. Individuals must be available for rotating schedule that provides coverage for a “24 hours/7 days a week” laboratory operation. This position routinely works 2 or more weekends per month as directed. REQUIRED QUALIFICATIONS: • Knowledge of established scientific methods and techniques of microbiology to perform recurring assignment of moderate difficulty (i.e. the methods and techniques are well established, apply to most situations encountered and do not require significant deviation from established methods) or discrete portions of the complex projects. • Minimum one year "laboratory bench" experience performing research or diagnostic PCR testing (includes nucleic acid extraction methodology, set up and analyses of real time PCR assays, detection and determination of DNA contamination events). • Basic knowledge of bioterrorism agents. • Knowledge of biohazard regulations in the proper and safe handling and transport of materials containing virulent and pathogenic disease agents and toxicants. • Knowledge of chain-of-custody regulations and procedures. • Basic knowledge of computer systems methods and applications, including word processing, and statistical data management software packages. • Experience in the use of laboratory instrumentation related to cellular and molecular biology. • Experience maintaining Quality Assurance and Quality Control Documentation and organizational records to ensure adequate reagents and material for 24/7/365 operation. EDUCATION: Microbiologist: A Bachelor’s degree from an accredited University in Microbiology, Molecular Biology or related course work in Biological Sciences and at least one year of laboratory bench experience, utilizing polymerase chain reaction (PCR) technology, aseptic techniques and biological assays. Alternatively, equivalent biological laboratory bench experience for at least four years is acceptable. BACKGROUND INVESTIGATION: • Requires passing a law enforcement background check. • May require specific state certifications to work in Public Health facilities, registration with the CDC Select Agent Program, and passing of a Department of Justice background check. • Individual selected will be subject to a background investigation and must meet eligibility requirements for access to sensitive information. The position may require a SECRET clearance. • U.S. Citizenship required. RESUME SUBMISSION REQUIREMENTS: 1. Submission MUST include your Salary requirement (either as specific amount or acceptable range). 2. Include a reference to job # BTCOMB-1900 3. EMAIL your Resume to LabJobs@a-tek.net or FAX to 703-669-1109. A-TEK, Inc. is not a recruiting agency and will not disclose any of your personal information to any outside party. ]]>

<![CDATA[A Statistics expert is needed to help in running the needed statistical tests for a research study. A complete knowledge of MANOVA and Repeated Tests ANOVA is required. The statistics tests can be performed using SPSS or Minitab. Fees are negotiable. (This is not a full-time or part-time job) ]]>

<![CDATA[Primary function is to help maintain the day-to-day operation of the laboratory according to GMP guidelines. The laboratory technician also assists the QC Manager and Formulation Pharmacist in QC and R&D activities as directed. Duties include: 1. Routine analysis of raw materials and finished products for QC approval. Techniques include testing pH, specific gravity, and viscosity. 2. Preparation of samples for microbiological analysis. 3. Maintenance of retention samples of all product batches and finished goods. 4. Calibration and upkeep of all laboratory instruments. 5. Monitoring the purified water system for microbiological and particulate contamination. 6. Maintenance of neat and accurate laboratory notebooks and data logs. 7. Data entry in computer programs such as Excel, Quickbooks, and Fishbowl. 8. Ordering and receiving samples and raw materials for new product development and manufacturing. 9. Ensuring necessary lab supplies are kept stocked and organized. 10. Performing necessary housekeeping functions to ensure the lab is clean and orderly. 11. Occasionally assisting in formulating and packaging products under the direction of the Formulation Pharmacist. ]]>

<![CDATA[Wanted: Creative, Realiable R&D Chemist with experience in the packaging Industry. This position requires a reliable, detail-oriented person that is a self-starter. The person must be able to multitask and have the ability to work in a fast-paced environment. A Chemistry degree or science related degree is required. Recent college graduates will be considered. Candidates MUST be Bilingual(English-Spanish). All interested party's email resumes ]]>

<![CDATA[A highly motivated individual with solid training in cell biology, molecular biology or animal models of human diseases is sought to study the molecular mechanisms of skin and hair disorders. Please apply online at the Careers website for University of Miami Miller School of Medicine (www.med.miami.edu/) (click on "Careers", then search for position #035394, Department of Dermatology & Cutaneous Surgery). Candidates must have a Ph.D. (in any area of biomedical sciences) or M.D., with hands-on experience in basic molecular biology and cell biology techniques such as subcloning, nucleic acid extraction, PCR, RT-PCR, Western blot analysis and immunostaining. Must show proof of eligibility to work in the U.S. Must be able to work independently and as a team player. Good communication skills in English are essential. ]]>

<![CDATA[DOCTOR'S TOY STORE IS LOOKING FOR A CERTIFIED BIOMED TECH. MUST HAVE EXPERIENCE IN ALL TYPES OF MEDICAL EQUIPMENT. FOR MORE INFO CALL ROB AT (954) 849-4671]]>

<![CDATA[Use your insight and vision. Explore and create the next generation of Medical Devices. We want candidates to use their imagination and move towards excellence. We have exciting positions to discuss with you in the Medical Device sector. The position is extraordinary. We are seeking exceptional candidates to drive the next generation of medical devices. You will direct ideas from the beginning and execute the products throughout its development. We would prefer cutting-edge candidates with remarkable knowledge of the medical device sector. Research & Development Leader Core Team Leader Advanced Concepts Development Leader Must have MS in Mechanical Engineering and Science/ PharmD/ MD, with strong business acumen; Medical Device & Technical experience a must Advanced Degree, PhD/MD/PharmD/MS, with top tier MBA; Top tier MBA with deep domain expertise in marketing, finance and clinical; EXPERIENCE: 5 plus years of experience in medical device or pharmaceuticals or health care practitioner. Please send an in-depth cover letter and CV/Resume for consideration ASAP. ]]>

<![CDATA[The Scripps Research Institute is currently seeking a Senior Buyer – IT Sourcing for its Florida facility. This individual will be responsible for purchasing high-risk/high-cost materials, capital equipment, computer hardware/software, and services for research labs. Responsibilities include developing RFP’s, facilitating evaluation teams, contract preparation, and leading negotiations through to contract execution. Duties also include managing or assisting with special projects of medium to high technical complexity, protection of property, liability, and intellectual property. Performs other related duties as assigned. Requires: a Bachelor's degree in business administration or an equivalent combination of education, training and/or experience. A minimum of five (5) years of direct or related industry buying experience. Subject matter expert of market drivers, trend analysis, cost drivers, and industry best practices. Position requires contract negotiating experience, strong written/verbal communication skills, and demonstrated analytical ability. Must be proficient in Microsoft Office Suite i.e. Word, Excel, Project, PowerPoint, and Outlook. Certification in Procurement such as a C.P.M. is strongly preferred. Experience with ERP systems such as SciQuest, Ariba Sourcing & Contracts, Bi-Tech and/or Procuri is strongly preferred. Florida and Palm Beach County residents preferred. For more information and to apply online visit <a href="http://careers.scripps.edu." rel="nofollow">http://careers.scripps.edu.</a> TSRI embraces diversity and recognizes it as being a key to our success. EOE/M/F/V/D ]]>

<![CDATA[Groundwater & Environmental Services (GES) is a leader in providing innovative, high quality environmental services, specializing in soil and groundwater contaminant assessment and remediation since 1985. Our employees are committed to providing responsive environmental services to a diverse, progressive client base that includes the petroleum industry, government agencies, and industrial markets. We have over 680 employees coast to coast, and are still growing. GES seeks a Fort Lauderdale based Corporate Health & Safety Officer to support our southern offices and International Programs by training employees on GES’ HSSE and behavior based safety programs. Our successful candidate will also be involved with reviewing current programs and assisting in developing new programs and guidance. This position requires at least 25-50% travel to local offices and to countries in Central America and the Caribbean. Responsibilities and Duties: Provide Loss Prevention System (LPS) training to office staff and subcontractors Schedule & provide required training sessions, in conjunction with GES Corporate Director and local HSSE Officers, such as: 8 Hour Refresher, OSHA Supervisory Training, CPR, First Aid and Defensive Driving training modules. Assist local HSSE Officers in follow-up/investigation of accidents/injuries. Assist local HSSE Officers in scheduling new employees for medical surveillance, training, etc. Develop and/or assist offices in the development of Site Specific Health & Safety plans. Provide or assist local HSSE Officers in New Employee HSSE program Orientation. Conduct or assist local HSSE Officers in completing field, office and warehouse inspections. Provide project-specific HSSE program and LPS support as needed, field or administrative Requirements: A Bachelor's or Master's Degree in Safety, Environmental Health, or a related science degree and 4-7+ years of safety management, preferably in the environmental consulting field Experience in HSSE programs is preferred. Hands-on field experience a plus Working knowledge of LPS and/or LPS trainer certification is a plus Must possess excellent communication, organizational, facilitation, time management, and computer skills Alcohol/Drug screening and a Background Check are required Application Instructions: Click the following link to apply online: <a href="https://www.hirebridge.com/application/appchoice.asp?jid=65301" rel="nofollow">https://www.hirebridge.com/application/appchoice.asp?jid=65301</a> Our comprehensive benefits include: medical, dental, vision, 401k, FSA, LTD, STD, New Parent Leave, 529 CollegeBound Fund, Tuition Assistance, Bonus Plan, and more. GES is an equal opportunity/affirmative action employer that strongly values diversity. EOE/AA/M/F/V/D]]>

<![CDATA[Utility Arborists act as a liaison between the utility company, their clients, contractors and customers. Responsibilities for this position include: inspection and assessment of customer requests for pruning or removals, securing clear rights-of-way for new line and pole construction, handling customer complaints related to scheduled pruning or completed pruning, auditing the tree contractor's work for compliance with the utility's specifications, assisting in storm and emergency situations, and other miscellaneous line clearance projects. Assist in investigating and recommending future R-O-W maintenance requirements. Operate system forestry computer programs and record systems. The position requires daily contact with the client, contractors, and the public. Perform duties in a manner that will promote and maintain good public relations. Assume other duties and responsibilities as assigned. Qualified individuals have solid tree identification skills, strong problem solving abilities, an attention to detail, and exceptional public relations/interpersonal skills best meet the challenges of a Utility Arborist position. We prefer candidates with a two or four-year degree in Forestry or a related field. Certification as an ISA Arborist is a plus. All candidates must possess a valid driver's license and a good driving record. Bi-Lingual (Spanish) is a plus. ECI is an EEO /AA employer. Email, Fax or Call. 800-871-1308 - Fax 800-394-1324 - Phone ]]>

<![CDATA[Hey My name is Joseph I'm a chemist with more then 25 years experience in the chemistry industries. I have a lot of knowledge and i can help with any kind of chemicals projects organic or inorganic products. For more information please contact me at: cell- 305 763 6657 or by E-mail at jobit75@yahoo.com ]]>

<![CDATA[Examkrackers, Inc. is a test preparation company with a passion for excellence. We are currently looking for instructors to teach our Medical College Admissions Test (MCAT) preparation classes. The position is part time in the evenings from 4 to 16 hours per week. Talented, first-time teachers can earn up to $40/hr. The science knowledge required is at the first year undergraduate level; however, the test questions use a holistic approach and require a deep understanding of the subject matter. The students are highly motivated premeds making the instructor's job both challenging and rewarding. We strive to make any association with our organization a pleasurable and rewarding experience whether you're an instructor or a student. Requirements: Applicants must be passionate about teaching and about the subject matter. Applicants must have taken the MCAT in the past 5 years. Applicants must have a thorough understanding of any or all of the following: 1st year undergraduate biology including some physiology; 1st year undergraduate organic chemistry; 1st year undergraduate inorganic chemistry; 1st year undergraduate physics. Applicants must be reliable, punctual, organized, and enthusiastic. Interested applicants should send a resume and MCAT scores to jobs@examkrackers.com Please write 'Instructor FL" in the subject heading. Remember: Applicants must have taken the MCAT in the past 5 years. *Example of an e-mail to a med student or med school dean of students: ]]>

<![CDATA[The Scripps Research Institute is currently seeking an Administrative Assistant II for its Florida facility. This individual will provide administrative support to a growing biomedical resources services department. Duties will include answering telephones, sorting and distributing mail, maintaining databases and calendars, and ordering supplies, coordinating meetings, preparing annual report materials, performing data entry, preparing correspondence, and making travel arrangements,. Duties also include data management relating to income and cost accounting, and performing budget reconciliations. Other duties as assigned. Requires: High School diploma or equivalent and a minimum of two (2) years of related experience or equivalent training and experience. Must possess excellent organizational skills, be detail-oriented and flexible, and have the ability to work independently. Must also have excellent written and verbal skills and the ability to prioritize multiple tasks and function well within a team environment. Experience with Word, Excel, PowerPoint, and the ability to learn other software programs specific to the department. Professional level typing and editing skills. Prior experience working with accounting/budgets is strongly preferred. Florida and Palm Beach County residents preferred. For more information and to apply online visit <a href="http://careers.scripps.edu." rel="nofollow">http://careers.scripps.edu.</a> TSRI embraces diversity and recognizes it as being a key to our success. EOE/M/F/V/D ]]>

<![CDATA[Imagery Analyst /Remote Sensing Technician - Gain Great Experience - Build your Resume Are you looking for the opportunity to expand your skills in Satellite imaging? Are you a team player? Would you be interested in working with some of the government’s top scientists? We are looking for an individual who can work in a team environment and is willing to learn remote sensing techniques. The position requires someone with strong communication skills and experience working in imaging. Knowledge and experience with any of the following software is helpful: - Image Processing/GIS Software: ArcGIS, ENVI or Imagine - Microsoft Office, specifically Excel and Word - Any Satellite Data (I.E. Landsat, SPOT, Quickbird, IKONOS, MODIS) The successful candidate will gain real-world experience in remote sensing and geospatial analysis. Specifically, the technician will assist in the collection of ground-based meteorological and remote sensing data from established sampling sites in the Everglades National Park/South Florida. The technician will also evaluate the performance of commercial off-the-shelf and project developed georeferencing, calibration, and information extraction software. Academic Requirements include: - Course work or equivalent experience in remote sensing & GIS software; and - At least 2 years course work in Geography, Geology, Computer Sciences or related fields. For the right candidate, we will consider a part time schedule. Salary will commensurate with experience. TO APPLY, you can <a href="mailto:careers@etipros.com?subject=Craigs_List-5075_Remote_Sensing_FL" rel="nofollow">Email Us Your Resume</a> ETI Professionals provides technical support services and project support personnel to our Government and industry partners. Our highly skilled experts support and supplement the mission, expertise, and skill sets of our clients. Utilizing our customer-intimate approach, we partner with our clients to provide strategic solutions that maximize the use of human and financial resources to ensure that mission-critical projects are completed on time and within budget. Our website can be found at <a href="http://www.etiprofessionals.com" target="_blank" rel="nofollow">ETI PROS</a> , where you will learn more about our company as well as an updated list of positions available nationwide. ETI is proud to be an Equal Opportunity and Affirmative Action employer. ]]>

<![CDATA[The Scripps Research Institute is currently seeking a Research Assistant II for the Cancer Biology Department, within its Florida facility. The chosen candidate will participate in experimental design, data collection and data analysis for publication. This will include designing and performing experiments utilizing mammalian tissue culture, expression, purification and crystallization of target proteins. Will also develop and troubleshoot new protocols to perform these experiments with automated equipment and will train and supervise students and other employees. Will assist with lab management including ordering supplies and equipment set-up and maintenance as well as communicate experimental procedures and results to lab personnel and at scientific meetings. Requires: Bachelor's Degree and a minimum of 4 years experience or Master's Degree and minimum of 2 years of relevant scientific experience in a laboratory setting, or an equivalent combination of experience. Specifically, experience must include working with mammalian tissue culture as well as experience designing experimental procedures for HTS automation and equipment for protein expression, purification and crystallization. Strong organizational and computer skills are required, must be able to work independently and supervise and organize projects as assigned. Florida and Palm Beach County residents preferred. For more information and to apply online visit <a href="http://careers.scripps.edu." rel="nofollow">http://careers.scripps.edu.</a> TSRI embraces diversity and recognizes it as being a key to our success. EOE/M/F/V/D ]]>

<![CDATA[Use your insight and vision. Explore and create the next generation of Medical Devices. We want candidates to use their imagination and move towards excellence. We have exciting positions to discuss with you in the Medical Device sector. The position is extraordinary. We are seeking exceptional candidates to drive the next generation of medical devices. You will direct ideas from the beginning and execute the products throughout its development. We would prefer cutting-edge candidates with remarkable knowledge of the medical device sector. Research & Development Leader Core Team Leader Advanced Concepts Development Leader MS in Mechanical Engineering and Science/ PharmD/ MD, with strong business acumen; Advanced Degree, PhD/MD/PharmD/MS, with top tier MBA; Top tier MBA with deep domain expertise in marketing, finance and clinical; EXPERIENCE: 5 plus years of experience in medical device or pharmaceuticals or health care practitioner Please send CV/Resume and an in-depth cover letter ASAP for consideration. ]]>

<![CDATA[Local Clinical Trials Recruitment Company is looking for a Patient Recruitment Associate. Responsibilities include but are not limited to conducting telephone interviews of potential research participants, assisting with marketing, advertising and research projects and networking with local physicians and health-related organizations. Candidates Must: •Have excellent communication skills (written and verbal) •Be fully bilingual in English and Spanish •Be detail orientated, highly organized and a team player •Be driven and willing to go the extra mile – clock watchers need not apply! •Computer skills are essential. •Medical background is necessary – Medical Assistant, etc •Prior clinical trial experience a plus •Possess reliable transportation Looking for someone to start ASAP. Please email resume to garnetconsulting@gmail.com and reference Patient Recruitment Associate. ]]>

<![CDATA[Advertisement: Associate Scientist, Cellular Analysis – Miami/San Francisco The Immune Tolerance Institute, Inc., (www.iti-immune.org) is a non-profit start-up biotechnology corporation founded in partnership with the University of California, San Francisco to fill critical unmet needs for the translation of fundamental scientific discoveries into new therapies for the prevention and treatment of the broad range of diseases related to the human immune system. Unique in its design and mission, ITI joins cutting-edge academic research with comprehensive bio-pharmaceutical industry expertise to establish the leading center of excellence in translational immunology in order to advance promising new medicines from lab bench discoveries to bedside benefit. This assistant/associate scientist will be responsible for sample processing for cellular assays for immune system monitoring in a Good Clinical Laboratory Practice environment. Implementation will include the use of state-of-the-art capabilities in flow cytometry and laboratory automation. The platforms will be implemented to execute a range of mechanistic assays to interrogate immune system function in therapeutic settings. ITI has established a Cellular Analysis Laboratory at Beckman Coulter in Miami Florida, where most of the initial work will occur. The successful candidate will have a BA in Cell Biology, Immunology or related field and prior laboratory experience. Direct experience with cellular assays, including cytometry on human samples preferred. This person should be very “hands on,” comfortable working within a small to medium size laboratory environment and have success following and developing both standard operating procedures and new experimental protocols. Level will be commensurate with experience. Please send cover letter and formatted (Word, pdf, etc) CV to: careers@iti-immune.org ]]>

<![CDATA[CRB Geological and Environmental Services, Inc is looking for a qualified technician to sample monitoring wells, and conduct and oversee other types of environmental field activities. In addition, we are also looking for a qualified person to complete Phase I due diligence reports, contamination assessments and other types of environmental reporting requirements. Experience is a plus.]]>

<![CDATA[ In-home private tutoring position for expert in either Physics- Bio- chemistry science.]]>

<![CDATA[The Scripps Research Institute (TSRI) is seeking an Animal Technician I/II for its Florida facility. Job duties include the daily care of the vivarium by providing food and water, maintaining a clean environment, and monitoring overall health. Duties also include preparing, sterilizing and washing laboratory caging and equipment; performing minor housekeeping within the facility; maintaining cage wash machinery; waste disposal; receiving supplies of feed, bedding, and equipment; and compiling inventories. Requires: High school diploma or equivalent and a minimum of one (1) year of experience with animal husbandry. Must be able to lift 50 pounds unassisted and perform repetitive motions with arms, wrists, and hands. Must be available for weekend and holiday rotation. Florida and Palm Beach County residents strongly preferred. AALAS certification or AS in Veterinary Technology is preferred. For more information and to apply online visit <a href="http://careers.scripps.edu." rel="nofollow">http://careers.scripps.edu.</a> TSRI embraces diversity and recognizes it as being a key to our success. EOE/M/F/V/D ]]>

<![CDATA[The Scripps Research Institute is currently seeking a Supplier Diversity Coordinator/Sr. Buyer for its Florida facility. The selected candidate will develop, implement, execute and administer Scripps Florida's corporate-wide Supplier Diversity Program in a manner which supports its multi-cultural supplier initiatives and ensures fair and reasonable procurement opportunities at Scripps Florida for State of Florida certified MWBE's, consistent with the requirements of Scripps Florida's State and County Grants as well as strategically source procurement-related commodity areas, including scientific instruments and equipment, furniture, and/or services. Specific responsibilities may include: establishing a streamlined process for identifying certified, diverse, multi-cultural suppliers for new procurement and sourcing opportunities; developing benchmark reporting mechanisms which track TSRI Florida's progress against previously agreed goals, as well as meet governmental requirements; assisting with goal measurements and process implementation strategy; facilitating training, communication and education program initiatives including the creation of communication and education programs that develop awareness, participation and growth in SBE programs; representing the Institute at Supplier Diversity outreach events; developing and maintaining constructive relationships with diversity and trade groups and/or government groups supporting their participation; interfacing regularly with State, County and local representatives about the Scripps Florida Supplier Diversity Program to assist and develop areas having the potential to increase procurement activity with diverse, multi-cultural suppliers; procuring materials, capital equipment and services, including the preparation of complex and/or high-value contractual agreements for large equipment purchases and/or services; developing, maintaining and implementing sourcing strategies; managing supplier relationships and performance; drafting, negotiating and amending contracts; creating, collecting and summarizing information and documentation necessary for the preparation of competitive bids or quotes, including equipment specifications, facilities requirements and other related procurement issues; evaluating and selecting vendors; negotiating pricing, product availability, payment schedules, installation, training and maintenance agreements, insurance requirements and other purchasing considerations within predetermined scope; identifying and engaging appropriate level of stakeholder, building alliances and partnerships to garner support, including team building; negotiating, executing and amending signed purchase orders and contracts; assisting in the development, modification or implementation of new data collection and purchasing automation procedures, processes and systems; providing departments/labs guidance on purchasing procedures and knowledgeable and/or technical advice in determining specifications for items/services procured; providing specialized training or assistance to other procurement employees; performing other related duties, tasks and responsibilities as required, assigned and directed. Requires: Normally requires a Bachelor's degree, preferably in business administration, accounting or finance or an equivalent combination of education, training and/or experience from which comparable knowledge, skill and abilities have been attained. Normally requires a minimum of 3 years experience in a strong organizational supplier diversity program and a minimum of 5 years direct or related industry senior-level buying experience. Must have a thorough understanding of FARS, State of Florida and local municipality requirements for Small, Woman, Minority, Disadvantaged, Hub-Zoned, Vet-Owned and Service-Disabled Vet-Owned business entities, as well as a familiarity with organizations such as NMSDC, SBA, and WBENC. Requires expertise in data mining and the ability to acquire market intelligence. Requires a solid understanding of procurement systems and related software applications. Must have a thorough understanding of the procure-to-pay process, including the relationships and integration points. Must have demonstrated knowledge and understanding of cost drivers, market influences, and negotiation strategy development, as well as the ability to evaluate short-term options and plan against benefits and risks to longer term functional or business group priorities. Requires the ability to gauge the feasibility and impact of proposed innovations to ensure successful implementation. Must possess advanced analytical and verbal/written communication and formal presentation skills, as well as self-confidence when working cross-functionally (legal) and engaging supplier's high level management. Must have demonstrated ability to manage several projects simultaneously while serving as a resource person for all contacts and providing a high level of customer service. Requires the ability to work independently, within tight timeframes, as well as excel in a collaborative environment. Must have effective computer skills to include MS Office (full suite), ERP systems and other specialized software applications, web searching, downloading, and reporting, database manipulation, and spreadsheets. C.P.M. certification preferred. Florida and Palm Beach County residents preferred. For more information and to apply online visit <a href="http://careers.scripps.edu." rel="nofollow">http://careers.scripps.edu.</a> TSRI embraces diversity and recognizes it as being a key to our success. EOE/M/F/V/D ]]>

<![CDATA[Job Position: Laboratory Technician I Summary: Operates production equipment; responsible for manufacturing and assembly of clinical and commercial products. Follow blueprints, guidelines and/or diagrams to ensure product specifications and tolerance levels are met. Requires a high school diploma and or its equivalent and 0-3 years of related experience. Has knowledge of commonly used concepts, practices, and procedures within a particular field. Relies on instructions and pre-established guidelines to perform the functions of the job. Works under immediate supervision. Typically reports to a supervisor. Description Of Duties General 1.1 Responsible for informing and or advising management matters directly related to Manufacturing and/or the assembly of pharmaceutical and medical devices. 1.2 Responsible for being knowledgeable and understanding Good Manufacturing Practices. (must be familiar with cGMP) 1.3 Responsible for following all Good Manufacturing Practices guidelines. 1.4 Responsible for being knowledgeable and understanding Standard Operating Procedures and Standard Test Methods. 1.5 Responsible for following all Standard Operating Procedures and Standard Test Methods. Production 2.1 Responsible for assisting in manufacturing product from start to finish under GMP conditions. 2.2 Responsible for helping to prepare Master Batch Records. 2.3 Responsible for following procedures and performing sterilization of materials to be utilized for manufacturing of drug-product. 2.4 Responsible for maintaining status reports of each and every Lot manufactured. 2.5 Responsible for performing calculations and obtaining quality control approval prior to Lot production. 2.6 Responsible for performing in-process control testing for product manufactured. 2.7 Responsible for following procedures and documentation related to the release and reject. 2.8 Responsible for following procedures and performing sterilization of final drug product. 2.9 Responsible for sterilization assurance information and data. 2.10 Responsible for quarantine and documentation of rejected doses. 2.11 Responsible for transferring, labeling and packaging operation of manufactured products. 2.12 Responsible for manufacturing, separating, sterilizing, storing and holding samples of final drug product and raw materials. Responsible for the transfer of samples to quality control area for testing. Inventory 3.1 Responsible for following and documenting raw materials control. 3.2 Responsible for performing and documenting materials inventory control. 3.3 Responsible for following procedures and documenting receipt of material for production i.e. containers, closures etc. Sanitation Procedures & Policy 4.1 Responsible for keeping clean, neat and organized manufacturing areas and documentation. 4.2 Responsible for sanitization of environmental controlled workspaces (clean room, gowning area, processing area and packaging/labeling area) as well as equipment. ]]>

<![CDATA[Seeking an experienced Clinical Research Coordinator (Full-time) Mon-Fri. No weekends. Must have experience coordinating a research study with pharmaceutical research subject contact, not laboratory experience. Must be a well-organized, self-starter, team player. We have a great team! Please send resume to aasfvb@yahoo.com ]]>

<![CDATA[Local startup company seeking a talented micro-biologist for full time employment. Credentials might include: Agricultural degree Experience as a soil scientist Having lab research experience Work as an agronomist Interested in formulations Work in Pompano Beach, FL. Job will involve travel and technical sales support. Please email your resume to bdanzansky@gmail.com or call 561-212-7563 ]]>

<![CDATA[JOB SUMMARY Responsible for ensuring compliant and efficient operations of wastewater and water treatment plants in the Florida region. This includes, but is not limited to: reviewing reports/logs on all necessary aspects of equipment, operations, water treatment and testing. Conducting analysis of wastewater and water to ensure compliance with state regulations, reviewing proposals obtained for equipment maintenance or operational modifications, performing water treatment plant and wastewater plant audits. This position requires 100% travel and has to report to the home office in Tampa, FL twice a month. ESSENTIAL JOB DUTIES ·Monitor water and wastewater treatment plants within the ELS community network ·Diagnose operating problems and recommend corrective action(s) ·Reviews logs and records for operations and preventative maintenance ·Performs routine test and analysis to spot check the operational conditions of the plant ·Assists in auditing the condition of the water treatment and wastewater treatment plants and completes auditing reports OTHER JOB FUNCTIONS ·Maintains system reports and records by preparing and logging daily reports in computer system ·Reviews proposals obtained for equipment maintenance or plant modifications and makes recommendations ·Monitors the status of Operator’s sampling, testing, analysis and reporting as required by regulations ·Assists in the start-up of new operations ·Performs special projects as assigned by the Environmental Engineer MUST MEET THESE REQUIRMENTS (Please dont waste mine or yours time. NO resume will be considered if you dont meet these requirments) SKILLS, EDUCATION AND EXPERIENCE ·High School equivalent, or above. ·3 – 5 years of directly related wastewater treatment plant experience ·Experience writing reports and auditing plant operations ·Must posses a ‘Grade C’ FDEP license or above ·Demonstrate ability to use computer ·Must posses a valid driver’s license This position requires driving long distances, working at elevated heights and walking around large open top tanks. ]]>

<![CDATA[REPORTS TO: Quality Control Manager SUMMARY: Analyzes Products and Materials and the composition of their ingredients. ESSENTIAL DUTIES AND RESPONSIBILITIES: Chemist is responsible for the following: Provide technical expertise and instruction to the QC and Stability Laboratories in the proper implementation of new instrumentation and analytical techniques. Engage in method development, transfer, and optimization in support of analytical chemistry functions relating to regulatory requirements. Perform analytical investigation studies aimed at increasing the operating efficiency of the laboratories under the guidance of the Manager. Requirements for this Position: BS Chemistry or related area with 1 to 2 years experience in a pharmaceutical analysis environment with special emphasis on automated processes. Thorough knowledge of compendia requirements and cGMP. Effective written and oral communication skills. Please email your resume to: mbaig@primeenterprises.com. ]]>

<![CDATA[Research Dynamics is a boutique Clinical Research Organization that assists pharmaceutical, medical device and biotech companies in getting their products to market faster. Research Dynamics is looking for a Clinical Research Associate/Field Monitor to monitor the conduct of trials at investigator sites, under the direction of the Project Manager, in the Southeast US. Duties include but are not limited to: The preparation and conduct of study qualification, initiation, monitoring and close-out Visits at the sites to ensure adherence to GCP requirements, and protocols. Monitor will review and verify clinical data to ensure accurate and complete trial data. The successful candidate will have the following qualifications: Bachelor’s degree in science, health, nursing or other related degree 3 yrs healthcare or research-related experience 5+ years monitoring experience in a pharmaceutical, biotech or CRO environment; Excellent written and verbal communication skills/ interpersonal skills Strong organizational skills Ability to independently plan and prioritize own work schedule Expert computer proficiency; EDC experience a plus. Up to 70% travel required. ]]>

<![CDATA[Research Dynamics is a boutique Clinical Research Organization that assists pharmaceutical, medical device and biotech companies in getting their products to market faster. Research Dynamics is looking for Clinical Research Associate/Field Monitor to monitor the conduct of trials at investigator sites, under the direction of the Project Manager in the Southeast US. Duties include but are not limited to: The preparation and conduct of study qualification, initiation, monitoring and close-out Visits at the sites to ensure adherence to GCP requirements, and protocols. Monitor will review and verify clinical data to ensure accurate and complete trial data. The successful candidate will have the following qualifications: Bachelor’s degree in science, health, nursing or other related degree 3 yrs healthcare or research-related experience 5+ years monitoring experience in a pharmaceutical, biotech or CRO environment; Excellent written and verbal communication skills/ interpersonal skills Strong organizational skills Ability to independently plan and prioritize own work schedule Expert computer proficiency; EDC experience a plus. Up to 70% travel required. ]]>

<![CDATA[Position Description: Overview Responsible for production tasks related to long-term wind modeling, power curve testing, turbine selection, investment approval processing, site suitability testing, financing support, and special projects. The primary goal is to provide independent assessment services in support of new development activity. The Analyst utilizes, develops and promotes statistical functions, model scripts, and related data for increased used and acceptance. The Analyst reports to the Project Director ¿ Wind Resource Assessment. A high degree of collaboration is essential, notably with staff in Wind Farm Design and the science or production teams at WindLogics. Primary Duties / Responsibilities 1. Early Project Support ¿ Respond to requests for service directly from customers or customer support. Provide guidance to support staff including work scope proposals, project scheduling, and priorities. Provide practical and creative technical solutions as needed, especially when time constraints are binding. Participate in ¿Operations Acceptance Meetings¿ with WindLogics before model runs to ensure downstream errors, corrections, or warranty work are strictly limited. 2. Backlog Processing ¿ Prepare input data from site data collection and other sources. Run long-term wind and operational assessment models to produce joint distributions of wind speed and wind direction, and estimates of gross versus net energy output for development support, supply chain decisions, and investment approval. Develop expert knowledge for the feasibility analysis of projects and quantitative assessment of economic benefits in wind development. Communicate results to customer support and management. Test and implement models that improve wind assessment and data visualization. Support wind resource analysts, remote teams and vendors as needed. Monitor work product schedules for accuracy and consistency with development priorities, communicating schedule changes as needed. 3. Operations Completion ¿ Prepare reports on management request. Participate actively in quality assurance, reviewing group work products. Participate in ¿Model Reconciliation Meetings¿ between our clients staff. Determine if integrated work product deliverables are suitable for delivery to customers, or require additional change and warranty work. Assume accountability for customer deliverables. As needed, explain work results and implications, and respond to requests for follow-up. Secondary Duties / responsibilities 1. Project Management Support ¿ Work with customer support, technical teams and information management to improve process efficiencies. Proactively and creatively suggest solutions to de-bottleneck customer services. Support cohesive planning, implementation of comprehensive code control. Collaborate with peer analysts on data management, code development, and data visualization projects. 2. Product Development ¿ Maintain in-depth knowledge of the customer to whom any wind assessment activity or products are directed. Apply expert knowledge in support of customer service and new product development. Work with customer support and technical teams to utilize a broad range of knowledge to improve customer satisfaction, and the transparency of project economics and performance. 3. Training and Demonstrations ¿ Assist internal customers to understand work product deliverables. Communicate core methods, economic benefits and other performance benchmarks associated with primary deliverables. Actively support group documentation of code, group methods, and primary processes.@Position Requires: @Work Schedule: @Comments: our client is the nation¿s leader in wind energy generation. The company has advantages that few others in the wind industry have, including financial strength; a proven ability to deliver; world-class expertise in developing, constructing and operating wind facilities; and a strong community focus. Wind development activities at our clients are characterized by a new drive to scale, creating opportunities supporting wind assessment, wind farm design, and asset management.@Qualifications: Liability/Risk Analysis - Advanced;JavaScript - Advanced;Bachelor's - Acct / Finance;Effective Verbal Communications - Competent;Effective Written Communications - Competent;Lotus Notes - Competent;Experience Required: ¿ PhD/MS in Climatology, Statistics, Mathematics, Engineering, or Operations Research. ¿ Proven leadership and project management skills with a demonstrated track record in large scale data management and code development. Past experience in wind resource assessment and climatological modelling highly desired. ¿ Proficiency in MS Office applications. Practical skills involving Unix/Linux, FORTRAN, C++, or S-Plus are desired, but not required. ¿ Ability to be highly successful in a matrix management organization ¿ Must have excellent communication skills, including strong written and oral abilities and integrity in personal relations. ]]>

<![CDATA[We are a Massachusetts-based manufacturer of premium skincare selling worldwide seeking a contract chemist to help us further our knowledge and product offerings in the natural/organic and paraben-free range. Candidate must have strong background in Chemistry or related field, as well as significant bench experience developing natural/organic/paraben-free skin care products. The ideal candidate will • Possess knowledge of base formulations to draw from and jump-start the development process, • Have experience "reverse engineering" other skincare products (not so much by quantitative measurements, but rather, by qualitative properties--viscosity, color, texture, shininess, drying time, etc.) • Have access to formulations lab to perform required formulation development and stability testing, and • Also have experience with anti-aging ingredients and formulations. Please respond with resume and qualifications. Note: This is on a contract basis. ]]>

<![CDATA[Sterile Engineer - for Outstanding Medical Copmany Location - Southern Florida - Confidential SEARCH (Company Paid Relocation) $50K – 65K plus bonus - DOE Full Health, Medical & Dental paid 100% Manage and maintain this International Medical companies Manufacturing sterilization projects in accordance with Quality Systems Requirements. Essential Duties and Responsibilities: • Responsible for monitoring and training regarding the sterility and bioburden in a clean room environment. • Perform activities related to regulatory compliance and product evaluation • Manage and maintain customer sterilization cycles including performing audits of the contract facility • Maintain company files demonstrating vendor compliance and performance • Perform testing and maintain documentation to support the user facility sterilization of single use and reusable instrumentation • Assist in the evaluation, qualification, and validation of sterile products • Ensures that production goals and backlog is kept to a minimum • Tracks and trends non conformances for management review meetings • Encourages a continuous process improvement environment • Recognizes and addresses process problems regularly • Assures proper maintenance of laboratory equipment • Monitors employee performance through goal setting and promptly tackle morale problems • Maintains attendance records and implements company policies • Reviews, counsels, evaluates, disciplines, hires and discharges employees with assistance of HR. • Recommends proper staffing levels based on production needs Bachelors degree or equivalent experience. (3) Three years experience in Sterilization Experience in a medical product setting is strongly preferred. Sterilization Experience of a Medical Product is a must. Proficiency in the use of PC and programs, particularly Excel, Word (or equivalents if changed by the Company), QAD. Please send a MS Word.doc version of your resume to John Marino at: JohnM@er-inc.com John R. Marino Executive Recruiting Consultant Energy Recruiters, Inc. (ERI) 9240 Bonita Beach Road Suite 3314 Bonita Springs, FL 34135 (239) 444-5285 Direct (800) 435-0685 x 235 (239) 949-3386 Fax <a href="http://www.er-inc.com" rel="nofollow">http://www.er-inc.com</a> ]]>

<![CDATA[Needed Part Time an experienced cosmetic chemist familiar with high end anti aging creams, hair care products and skin care products. References needed]]>

<![CDATA[Microbiology Sterile Engineer Location - Southern Florida - Confidential SEARCH (Company Paid Relocation) $50K – 65K plus bonus - DOE Full Health, Medical & Dental paid 100% Manage and maintain this International Medical companies Manufacturing sterilization projects in accordance with Quality Systems Requirements. Essential Duties and Responsibilities: IMPORTANT JOB REQUIREMENTS!!!! *****Specialized training in microbiology and sterilization is a must. *** • Responsible for monitoring and training regarding the sterility and bioburden in a clean room environment. • Perform activities related to regulatory compliance and product evaluation • Manage and maintain customer sterilization cycles including performing audits of the contract facility • Maintain company files demonstrating vendor compliance and performance • Perform testing and maintain documentation to support the user facility sterilization of single use and reusable instrumentation • Assist in the evaluation, qualification, and validation of sterile products • Ensures that production goals and backlog is kept to a minimum • Tracks and trends non conformances for management review meetings • Encourages a continuous process improvement environment • Recognizes and addresses process problems regularly • Assures proper maintenance of laboratory equipment • Monitors employee performance through goal setting and promptly tackle morale problems • Maintains attendance records and implements company policies • Reviews, counsels, evaluates, disciplines, hires and discharges employees with assistance of HR. • Recommends proper staffing levels based on production needs Bachelors degree or equivalent experience. (3) Three years experience in Sterilization Experience in a medical product setting is Required!!! Specialized training in microbiology and sterilization is a must!!! Proficiency in the use of PC and programs, particularly Excel, Word (or equivalents if changed by the Company), QAD. Please send a MS Word.doc version of your resume to John Marino at: JohnM@er-inc.com John R. Marino Executive Recruiting Consultant Energy Recruiters, Inc. (ERI) 9240 Bonita Beach Road Suite 3314 Bonita Springs, FL 34135 (239) 444-5285 Direct (800) 435-0685 x 235 ]]>

<![CDATA[I am working with a large Device manufacturer outside of Boston. Due to changes to the complaint procedures, and guidelines on how MDRs and complaints are handled, we will need to give this Complaint group an "injection" of contract help, providing a number of contractors to prepare for the expected volume, and increased complexity/scrutiny of the complaints. Our team will be "embedded" within the Client''s complaint group, working within their Complaint Processing System by processing complaint events through MDR decision trees, and documenting the results in the system along with filing Med Watch forms. Job Purpose: · Assist the Complaint Management Center (CMC) functional management in the day-to-day operations of medical device complaint processing · Ensure complaint handling tasks are completed as required by company policies and procedures, as well as compliant with applicable industry regulations (e.g. FDA 21 CFR Part 820.198, FDA 21 CFR Part 803, ISO 13485-2003, etc.) · Manage product complaint volumes and/or complexities commensurate for a Senior-level Specialist · Identify & implement CMC workstream improvements to increase the effectiveness, integrity, and/or timely management of complaint files · Provide subject matter expertise and mentoring to junior personnel involved in the complaint handling processes and workstreams Job Requirements: · MDR assessments for all assigned products · Accountable for owning and managing, thorough and accurate complaint records, as well as timely closure of complaint files · Ensure complaint records, MedWatch reports (FDA Form 3500A), and applicable complaint handling documents are compliant with Good Documentation Practices (GDP) · Complete mandatory training by established due dates · Maintain accurate and current training records at all times · Partner with Complaint Investigation Sites (CIS) to ensure thorough and timely investigation reports for returned product. · Professional contact with customers to gain insight into each complaint event · Prepare and submit FDA MedWatch and Baseline reports within the mandated timelines · Periodic review (audit) of closed complaint files for thoroughness and accuracy · Complete projects, as assigned · Provide CMC leadership, as required ]]>

<![CDATA[Desired applicant will ideally have a scientific backround (AAS/BS in science) or a minimum of two years experiance in a science related industry. Applicant should be self motivated and eager to work for a company that is dedicated to provide better indoor enviroments to our customers. Eco friendly car and gas provided. AirMD is a indoor air quality, services and product company providing wellness information products and services to Palm Beach, Broward and Dade County, the rest of the country will follow.]]>

<![CDATA[Position Responsibilities: · Demonstrates expertise and knowledge of products, patient treatment trends, clinical trials, and scientific activities within the Disease Area and continuously updates this expertise and knowledge based on training direction and approved resources provided. · Serves as a medical resource for the sales representatives and accurately answers any medical question they may have to help them utilize their approved materials and to help them understand therapeutic issues for their background use. · Supports the field matrix team to ensure that the primary products receive sound field based medical support consistent with the brand medical strategy · Presents approved scientific data of a basic level to Healthcare providers in both group and one-on-one settings in accordance with Company Policies, and applicable laws, regulations and ethical standards. · Demonstrates listening skills by allowing Healthcare providers to express their opinions. · Demonstrates appropriate response and documents the provision of accurate, approved scientific data in response to unsolicited scientific questions or requests posed by Healthcare providers for approved Products and or Brands and for products in development in accordance with Company Policies, and applicable laws, regulations and ethical standards. · In accordance with company strategy, develops and maintains contacts with external experts to further understand and gain insight into treatment patterns, scientific activities taking place within the Disease Area, needs and interests of Healthcare providers, and medical needs of patients. · Identifies and prepares speakers for co’s promotional programs and speaker training meetings. Position Requirements: · MD, PharmD, or PhD in a clinically related field of study · 3 – 5 years experience as a Medical Science Liaison in the pharmaceutical industry, translating scientific or clinical data into high quality medical information. · Prior experience as a MSL strongly preferred. · Prior experience in diabetes or cardiovascular therapeutic area. · Knowledge of clinical trial design and process. · Knowledge of the US Healthcare System the pharmaceutical industry, and relevant compliance standards · Strong communication and presentation skills essential · Functional knowledge of MS Office (Word, PowerPoint, and Excel) program. ]]>

<![CDATA[I am an FAU student majoring in Chemistry and Biology with only 1 semester left to graduate with my Bachelor's in this double major. I plan to attend pharmacy school next fall, and I really need a pharmacy technician job ASAP. I need the experience, and will not let you down because getting and keeping this job is my top priority. My phone number is 954-260-9748 and email is shivanne1086@yahoo.com. I cannot recieve voicemails, but please do not hesitate to call. ]]>

<![CDATA[Climatologist - Wind Resource Assessment Req: PHD/MS in Climatology, Engineering, Statistics, Mathematics Scope: The Quantitative Analyst – Wind Resource Assessment is responsible for production tasks related to long-term wind modeling, power curve testing, turbine selection, investment approval processing, site suitability testing, financing support, and special projects. The primary goal is to provide independent assessment services in support of new development activity. The Analyst utilizes, develops and promotes statistical functions, model scripts, and related data for increased used and acceptance. The Analyst reports to the Project Director – Wind Resource Assessment. A high degree of collaboration is essential, notably with staff in Wind Farm Design and the science or production teams at WindLogics. Climatologist - Wind Operations Assessment Req: Same as above Scope: The Quantitative Analyst – Operations Assessment is responsible for production tasks related to long-term wind modeling, Wind Index reporting, budget support, portfolio analysis, and performance monitoring. The primary goal is to utilize statistical tools to provide independent wind assessment in support of operating projects and budget management. The Analyst utilizes, develops and promotes coded functions, model scripts, and data visualization tools consistent with the needs of Business Management to improve operating results. Value added is a function of realizing documented income increases in Business Management and creating feedback loops that reinforce new investment approvals. The Analyst reports to the Sr Quantitative Analyst – Operations Assessment. The analyst works closely with staff in Wind Farm Design, as well as scientific and operations staff at WindLogics. ]]>