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<![CDATA[We have an outstanding career opportunity for a Sales Representative with Wastewater Treatment Product sales experience to join BioLogix a leading Manufacturer Bio-Augmentation Products. We are searching for a Sales Representative with Wastewater Treatment product sales experience to join our sales team. Requirements: Experience in selling products to Industrial Waste Water Treatment plants Experience selling products to Municipal Waste Water Treatment plants Working knowledge of Waster Water Treatment process The applicant must have good, to exceptional skills in, Telephone communication, E-mail, and Letter Writing. Experience with in MS Office helpful. We offer an excellent compensation and benefits package: Comprehensive Compensation Package: Salary plus Commissions Proven Prospecting System Major Medical Insurance plan Opportunity to advance to Management Product training Ongoing technical and marketing support For Consideration, e-mail resume and cover sheet ]]>

<![CDATA[An established downtown St. Louis pharmaceutical testing lab is seeking a qualified chemist for its 2nd Shift contract lab operations. The qualified candidate will have: * A background in pharmaceutical analysis, preferably in a QC environment * Specific experience using HPLC, Dissolution & UV Vis * A degree in chemistry * Trouble-shooting experience with standard lab equipment (preferred) We have successfully been in business for more than 40 years, and have an excellent track record among both customers and regulatory agencies. Average employee tenure exceeds 15 years. The work is both interesting and varied as testing is done on a multitude of products. This permanent, full-time position on our second shift runs from 3:30 to midnight, Sunday through Thursday. Excellent benefits are offered. Reply in confidence. ]]>

<![CDATA[An established downtown St. Louis pharmaceutical testing lab is seeking a qualified chemist for its 1st Shift contract lab operations. The qualified candidate will have: * A background in pharmaceutical analysis, preferably in a QC environment * Specific experience using HPLC, Dissolution & UV Vis * A degree in chemistry * Trouble-shooting experience with standard lab equipment (preferred) We have successfully been in business for more than 40 years, and have an excellent track record among both customers and regulatory agencies. Average employee tenure exceeds 15 years. The work is both interesting and varied as testing is done on a multitude of products. This is a permanent, full-time position. Excellent benefits. Reply in confidence. ]]>

<![CDATA[Manages all Cleaning Validation, Process Validation, Computer Validation, Facility Qualification and Utility Qualification for entire site valued at >$400MM cost of goods. Validation activities support continuous operations, new products and process improvements. Validation activities span over 200 Finished Products, 30 production lines in 17 buildings, >4000 pieces of equipment and >30,000 production instruments as well as all utilities. Provide strategic and technical input into standard and best practices for validation in order to maintain and advance the state of the art in validation technology --- included in this function is the use of validation technology and principles to improve quality while reducing the overall cost and risk of business Develop and provide proper training to maintain knowledgeable professional staff. Ensure that equipment, ancillary systems, and processes meet all pertinent regulations and guidance documents. Provide interpretation and guidance of cGMP and other regulatory documents with regard to validation. Provide support and guidance to the Quality organization and site leadership regarding enhancement of cGMP compliance and quality performance improvements. Provide on-site direction and consultation to other sites on the various aspects of validation, as needed. Ensure consistency of validation processes Review and approve site validation policies and ensure their implementation Participate in compliance audits and respond to audit observations Provide direction and tools to ensure a secure and safe work conditions Provide resources to other functional groups for information and decisions relating to process, cleaning validations, water and utility issues Stay abreast with cGMP and validation requirements by attending conferences, seminars, and training courses Hold group accountable for compliance with site HSES policies Participate in site HSE, OpEx, Lean, QIP, and related initiatives designed to improve site operations to meet key business objectives. Requirements Education and Experience: 1. Minimum BS in Chemistry, Chemical Engineering, Pharmaceutical Science, or related science (advanced degree is preferred) 2. Minimum 10 years in FDA-regulated industries with 5 years experience in validation 3. Proven project management and personnel management history 4. Complete knowledge of validation regulations, concepts and principles 5. Expert knowledge of cGMPs for both API and dosage pharmaceutical products ]]>

<![CDATA[Fortune 500 Company is in search of a Researcher for a 3-6 month project beginning in January. Duties will include planning, planting, inoculating, and harvesting of plants in a greenhouse setting. Responsibilities will also include managing and maintaining of seed inventories and seed handling. Qualified candidates will have a Bachelor's degree in Biology or a related field. Research and/or greenhouse experience is preferred. ]]>

<![CDATA[Responsible for coordinating all functions related to the Application, Testing and Analytical department. Prioritize, direct and coordinate all requests of panel preparation, proper coating application and curing to ensure complete, accurate and on-time delivery as scheduled and agreed upon by the sales organization or customer. Direct and manage internal and external performance evaluations, testing, failure analysis and report documentation, in accordance with industry recognized testing standards or internally developed proprietary methodology. Provide specific analytical characterization, competitive product reverse engineering, raw material analysis and characterization, in support of the Development Laboratories product development and maintenance project activities. EDUCATION REQUIREMENTS: 4 year BS Degree in Chemistry, or Advanced Degree. 5-7 years Chemist or coating formulation experience in a related performance coatings or raw material field. 3 - 5 years supervisory or management experience is a strong benefit. Must be proficient in the use of advanced analytical testing equipment such as DSC, FTIR, GCMS, Photomicroscopy, as relevant to coating failure analysis and the identification of coating composition, characterization and raw materials. PHYSICAL REQUIREMENTS: Lifting up to 75 pounds; exposure to chemicals including but not limited to: Amines, Polyamides, Isocyanates, Epoxies, Alkyds, Acrylics, and certain inorganic compounds. Personal protective equipment would be utilized. Must pass annual respirator medical evaluation and pulmonary function test as required by OSHA. Respirator to be worn up to 75% of the time. DUTIES: ¿ Responsible for accepting all panel orders, requests for testing or analytical services, and for managing the process to ensure on-time completion of the projects. ¿ Order all materials and supplies as necessary to perform the duties related to panel preparation, coating, testing and specified ]]>

<![CDATA[SUMMARY: Apply and interpret standard scientific or engineering theories, concepts, and techniques in a scientific or engineering specialty requiring a working knowledge of related disciplines. Work on a wide range of problems where causal relationships are progressively difficult to establish and the use of creative thinking is required. Extends the responsibilities of Development Chemist. Report to Lab Manager, or more senior lab personnel. EDUCATION REQUIREMENTS: 1) 4 year Chemistry or related science degree with 3-5 years chemistry experience, or 2) more advanced chemistry or related science degree with no required experience. PHYSICAL REQUIREMENTS: Lifting up to 50 pounds; exposure to chemicals including but not limited to: Amines, Polyamides, Isocyanates, Epoxies, Alkyds, Acrylics, and certain inorganic compounds. Personal protective equipment would be utilized. Must pass annual respirator medical evaluation and pulmonary function test as required by OSHA. DUTIES: ¿ Prepare project requests or research proposals on assigned projects. Create ideas for new products or approaches and conduct individual investigations. Apply creative approach to problem solving and formulation. ¿ Execute laboratory projects and continuously assess effectiveness. Develop research findings, draw conclusions, and make recommendations. Prepare and present written or oral reports. ¿ Contribute to research programs of others through communications and participation in technical work groups and design teams. ¿ Responsible for meeting project goals within time, quality and budget constraints. Utilize initiative to keep projects on track. ¿ Coordinate work of others, anticipate, and resolve priority conflicts. ¿ Supervise efforts of technicians. ¿ Acquire and maintain technical expertise in coatings industry and its technologies. ¿ Understand and follow safety, technical, and quality procedures ]]>

<![CDATA[Y: Apply and interpret standard scientific or engineering theories, concepts, and techniques in a scientific or engineering specialty requiring a working knowledge of related disciplines. Work on a wide range of problems where causal relationships are progressively difficult to establish and the use of creative thinking is required. Extends the responsibilities of Development Chemist. Report to Lab Manager, or more senior lab personnel. EDUCATION REQUIREMENTS: 1) 4 year Chemistry or related science degree with 3-5 years chemistry experience, or 2) more advanced chemistry or related science degree with no required experience. PHYSICAL REQUIREMENTS: Lifting up to 50 pounds; exposure to chemicals including but not limited to: Amines, Polyamides, Isocyanates, Epoxies, Alkyds, Acrylics, and certain inorganic compounds. Personal protective equipment would be utilized. Must pass annual respirator medical evaluation and pulmonary function test as required by OSHA. DUTIES: ¿ Prepare project requests or research proposals on assigned projects. Create ideas for new products or approaches and conduct individual investigations. Apply creative approach to problem solving and formulation. ¿ Execute laboratory projects and continuously assess effectiveness. Develop research findings, draw conclusions, and make recommendations. Prepare and present written or oral reports. ¿ Contribute to research programs of others through communications and participation in technical work groups and design teams. ¿ Responsible for meeting project goals within time, quality and budget constraints. Utilize initiative to keep projects on track. ¿ Coordinate work of others, anticipate, and resolve priority conflicts. ¿ Supervise efforts of technicians. ¿ Acquire and maintain technical expertise in coatings industry and its technologies. ¿ Understand and follow safety, technical, and quality procedures ]]>

<![CDATA[Ingenuity is a group of creative, energetic and motivated people helping life science researchers understand core biological mechanisms. We deliver systems biology expertise to biologists and bioinformaticists through pathways analysis software, genome-scale computable network datasets, and knowledge management services and infrastructure, resulting in increased R&D productivity and faster drugs to market. We are passionate about our products, and dedicated to providing researchers with the knowledge required to make Better Decisions Faster™. As a Consulting Ontologist you will contribute to building Ingenuity’s Knowledge Base. Key Responsibilities: · Represent and connect biological concepts in Ingenuity’s Ontology · May be involved in quality control of modeled biological concepts or pathways knowledge Education, Skills & Experience Required · MS in a biological discipline (Molecular Biology, immunology, genetics, biochemistry or other related field) · Detail-oriented · Strong logic skills · Internet savvy · Familiar with Microsoft Office tools · Available for minimal on-site learning; position is off-site · Must maintain minimum level of productivity (currently corresponds to about 10 hrs/week) · Must be legally able to accept consulting work in the US Education, Skills & Experience Desired · PhD candidacy or PhD degree is desirable · Research experience is a plus Position location Remote To apply click on the link below <a href="http://tbe.taleo.net/NA6/ats/careers/requisition.jsp?org=INGENUITYSYSTEMS&cws=1&rid=59" rel="nofollow">http://tbe.taleo.net/NA6/ats/careers/requisition.jsp?org=INGENUITYSYSTEMS&cws=1&rid=59</a>]]>

<![CDATA[Ingenuity is a group of creative, energetic and motivated people helping life science researchers understand core biological mechanisms. We deliver systems biology expertise to biologists and bioinformaticists through pathways analysis software, genome-scale computable network datasets, and knowledge management services and infrastructure, resulting in increased R&D productivity and faster drugs to market. We are passionate about our products, and dedicated to providing researchers with the knowledge required to make Better Decisions Faster™. As a Consulting Ontologist you will contribute to building Ingenuity’s Knowledge Base. Key Responsibilities: · Represent and connect biological concepts in Ingenuity’s Ontology · May be involved in quality control of modeled biological concepts or pathways knowledge Education, Skills & Experience Required · BA/BS in a biological discipline (Molecular Biology, immunology, genetics, biochemistry or other related field) · Detail-oriented · Strong logic skills · Internet savvy · Familiar with Microsoft Office tools · Available for minimal on-site learning; position is off-site · Must maintain minimum level of productivity (currently corresponds to about 10 hrs/week) · Must be legally able to accept consulting work in the US Education, Skills & Experience Desired · Completion of graduate level coursework is a plus · MS degree, PhD candidacy or PhD degree is desirable · Research experience is a plus REMOTE POSITION To apply: click on the link below <a href="http://tbe.taleo.net/NA6/ats/careers/requisition.jsp?org=INGENUITYSYSTEMS&cws=1&rid=59" rel="nofollow">http://tbe.taleo.net/NA6/ats/careers/requisition.jsp?org=INGENUITYSYSTEMS&cws=1&rid=59</a> ]]>

<![CDATA[Quality Assurance Engineer Description (QA-Systems): PLEASE SEND A MS WORD VERSION RESUME that highlights your exp with the requirement below and also in email explain why you are a good fit for the position, availability, salary expectations and contact info. We are working directly with the hiring manager. Primary site contact for one or more of the following areas: Stability Testing, Change Control/Regulatory, Supplier Relations, Internal Auditing, Investigations, Corrective Action Program, Complaints, Document Control, or Annual Product Reviews. Provide backup support in one or more of the following areas: Stability Testing, Change Control/Regulatory, Supplier Relations, Internal Auditing, Investigations, Corrective Action Program, Complaints, Document Control, or Annual Product Reviews. Provide support for FDA or other regulatory agencies for on-site audits. Provide support in the rapid resolution of product complaints, deviations, corrective actions, and/or safety issues. Review Change Control/Management Documents involving product or process changes. Provide quality engineering support in the development and maintenance of facility’s quality systems and procedures. Assemble, analyze and report QA system data to ensure regulatory compliance, identify trends and to identify areas of improvement Conduct quality audits and develop and assess subsequent corrective action recommendation. Additional areas of responsibility may include developing specifications/test methods/sampling plans/standard operating procedures, providing quality system training, or assisting Corporate Product Monitoring in preparation of regulatory submissions. Requirements Qualifications: BS/BA in Engineering or Living Sciences required. Minimum 3-5 years Quality Assurance/Quality Control experience in a finished pharmaceutical environment. Experience investigating deviations and other variances preferred. Working knowledge of cGMP guidelines and their application in an aseptic environment. Ability to adapt quickly in a fast paced dynamic environment. Good analytical and problem-solving skills. Ability to communicate with and positively influence broad and diverse populations within and outside the organization. ]]>

<![CDATA[Soldering under a microscope: Candidates must be able to: • Read schematic drawings and possess a minimum of 1-2 years of precision soldering experience with delicate components under microscopic magnification. • Take a pre-employment test that includes starting with a blank circuit board, reading a schematic drawing, assembling, and soldering parts. Candidates must have strong attention to detail as our customer takes great pride in their ISO Certification and looks forward to providing their customers with continued quality work. The shop is air-conditioned, restrooms are plentiful, and a lunch room complete with vending machines, refrigerator, and microwave is available. Schedule is Monday-Friday, 7:00am-3:30pm. Spartan Staffing 11646 Dorsett Road Maryland Heights, MO 63043 Telephone (314) 291-7070 Fax (314) 291-7077 <a href="http://www.spartanstaffing.com" rel="nofollow">http://www.spartanstaffing.com</a> 7234-br@spartanstaffing.com "Bringing People & Work Together" ]]>

<![CDATA[Chemical Operations Specialist 375th Chemical Company is in need of Chemical, Biological, Radiological, Nuclear Specialists. These specialists are responsible for the defense against terrorist threats stateside and overseas. Training will be provided at Fort Leonard Wood MO. Terms of service include 2, 3, 4, 5, 6 year contracts. We also have part time positions with the Army Reserve in St Louis. Detailed warning, control and evacuation plans must be developed in order to prepare for emergencies and natural disasters. Emergency management specialists, such as the Chemical Operations Specialist, prepare emergency plans and procedures for all types of disasters, including floods, earthquakes, hurricanes, biological warfare or enemy attacks. Chemical Operations Specialists are primarily responsible for operating, maintaining or supervising the use of nuclear, biological and chemical (NBC) detection and decontamination equipment. Some of your duties as a Chemical Operations Specialist may include: Assisting in the establishment and application of NBC defense measures Providing training advice and supervision regarding the proper use and maintenance procedures for chemical equipment and chemical operations Operating and performing operator maintenance on smoke generating equipment, NBC identification/detection and decontamination equipment Assisting in preparing and maintaining disaster operations plans Training military and civilian personnel on what to do in an emergency Operating and maintaining nuclear, biological and chemical detection and decontamination equipment Conducting surveys to determine needs in the event of an emergency Monitoring disaster preparedness activities and training operations Helpful attributes include: An ability to communicate effectively An interest in algebra, chemistry, physics, geometry and trigonometry An ability to plan and organize An ability to work calmly under stress Advanced level Chemical Operations Specialists supervise and train other Soldiers within their discipline. As an advanced level Chemical Operations Specialist, you may be involved in: Leading smoke generating or fuel supply squads Supervising reconnaissance/decontamination operations Serving as company NBC Specialist The skills you learn as a Chemical Operations Specialist will help prepare you for a civilian career with federal, state and local governments, including law enforcement and civil defense agencies. 30 days paid vacation Medical and Dental Benefits up to $40,000.00 Cash Enlistment Bonus up to $72,000.00 for College up to $65,000.00 Student Loan Repayment Program Minimum requirements: US Citizen or have a valid 551 card HS Diploma or GED 18-39 years of age must meet height and weight standards must meet physical standards must meet moral standards SFC Jay Tiegs (636) 346-3567 ]]>

<![CDATA[Quality Resources, Inc. is a service organization providing outsourced services to a Fortune 500 pharmaceutical R&D firm in the Chesterfield area. The following assignment will be full time. The successful candidate will need to be proficient in the following areas: •Ability to demonstrate metrology knowledge and skills used to support pharmaceutical industry. •Write, edit and modify calibration procedures. •Perform calibrations on a wide variety of equipment and perform measurements on a wide array of SIs. Some equipment may be very unique and calling for strong metrology skills. •Work in and update database used to track, schedule and perform calibrations. •Ability to understand customer requirements and develop procedures to perform calibrations to those requirements. •Fully understand all aspects of cGxP regulations. •Ability to articulate processes and procedures. •Audit performance a must. •Ability to work with vendors to complete calibrations, review data produced to ensure it meets needs and articulates the needs of the program to the vendor. •Ability to locate vendors to provide services that can not be performed by the candidate. •Must be able to work in a diverse workspace on a team as well as an individual contributor to deliver services with little supervision. A degree is preferred but not required IF you can demonstrate the related experience. Superior customer service is an absolute necessity. If you believe you have extensive experience in the above areas, please email your resume and salary requirements. ]]>

<![CDATA[New location for an established Contract Food Testing lab will be opening soon. We are now accepting resumes for Microbiology Lab Technicians. Duties will include, but not limited to: sample set up and preparation, weighing out, pipepetting, and streaking. Good Aseptic Technique required. Some Data entry will also be required. This position is full time. Schedule will include weekend hours – Saturday or Sunday. Bachelor’s Degree preferred in related field. Applicants must live within 50 miles of St. Louis, MO. There are no Relocation packages available. Email cover letter and resume with salary requirements through Craig’s List. Compensation is based on qualifications and experience. ]]>

<![CDATA[World-class biotech company with a location in the general area is currently seeking a skilled professional to fill a regular, full-time position. The position offers excellent benefits and an opportunity for advancement. A background in biotechnology, biology, chemistry, pharmaceuticals, etc. is generally required. Previous experience with one or more of the following is required: Biological Scientist, Clinical Lab Technologist, Research Scientist / Associate, Medical Scientist, Lab Technician / Associate, Biotech Sales / Marketing / Administration, etc. <a href="http://ebiotechcareers.com/job.opening.htm" rel="nofollow"> Biotech Lab Assistant Position - Details / Apply</a> Relevant experience is a requisite, along with any essential skills, training, education, etc. The ideal candidate will have the ability to take initiative, work independently and in a team setting, and multi-task effectively. Key Attributes - Characteristics and Personal Attributes: Dependable, honest, proactive, results focused, passionate, dedicated to self improvement and education, positive attitude, resourceful, upbeat, organized, and a high degree of integrity. A strong belief that you are there to make the business, yourself, and the people around you more successful. Equal Opportunity Employer - EEO/AA M/F/V/D St. Louis, MO]]>

<![CDATA[ Primary site contact for one or more of the following areas: Stability Testing, Change Control/Regulatory, Supplier Relations, Internal Auditing, Investigations, Corrective Action Program, Complaints, Document Control, or Annual Product Reviews. Provide backup support in one or more of the following areas: Stability Testing, Change Control/Regulatory, Supplier Relations, Internal Auditing, Investigations, Corrective Action Program, Complaints, Document Control, or Annual Product Reviews. Provide support for FDA or other regulatory agencies for on-site audits. Provide support in the rapid resolution of product complaints, deviations, corrective actions, and/or safety issues. Review Change Control/Management Documents involving product or process changes. Provide quality engineering support in the development and maintenance of facility’s quality systems and procedures. Assemble, analyze and report QA system data to ensure regulatory compliance, identify trends and to identify areas of improvement Conduct quality audits and develop and assess subsequent corrective action recommendation. Additional areas of responsibility may include developing specifications/test methods/sampling plans/standard operating procedures, providing quality system training, or assisting Corporate Product Monitoring in preparation of regulatory submissions. Requirements Qualifications: BS/BA in Engineering or Living Sciences required. Minimum 3-5 years Quality Assurance/Quality Control experience in a finished pharmaceutical environment. Experience investigating deviations and other variances preferred. Working knowledge of cGMP guidelines and their application in an aseptic environment. Ability to adapt quickly in a fast paced dynamic environment. Good analytical and problem-solving skills. Ability to communicate with and positively influence broad and diverse populations within and outside the organization. ]]>

<![CDATA[For over twenty five years USA Scientific has been a leading supplier of laboratory products for molecular and cell biology. Our focus is on the laboratory essentials used in R&D and we are well known throughout the United States. Do you enjoy talking to people? Do you want to be able to give yourself a raise? Do you want to spend your time with a large variety of customers instead of in a cubicle? We have an opening for an outside sales representative to cover our St. Louis based territory. The successful candidate will call on major universities, pharmaceutical and biotech companies throughout Missouri, Southern Illinois and Eastern Kansas. Although this territory is geographically large, the majority of your time will be spent in a handful of major cities and approximately ½ of your time will be spent in the St. Louis area. Overnight travel for a few days is required about once per month. Our ideal candidate has a degree in life science, at least one year of sales experience and lives within an hour of St. Louis. We will also consider candidates that are currently working in a laboratory but have a strong desire to be in outside sales. If you have the ability to make things happen and would enjoy seeing new people every day, this is the position for you. Our sales reps typically visit 20 - 30 laboratories each day. Although we have an extensive established customer base in this territory, cold calling at existing accounts is an essential part of this position. There is a reason our reps grow their income year after year – we hire self-motivated professionals and give them the tools they need to succeed. Critical to success in this territory is spending time in front of customers so overnight travel Kansas is essential. Compensation includes salary, commission and auto reimbursement. Please send your resume (MS Word or PDF) to jobs@usascientific.com and indicate ter26 and your last name in the subject line of your e-mail. Skills/Qualifications: Bachelors degree – preferably in the life sciences, lab experience is a plus Customer Service Attitude - desire to go the extra mile for the customer Self-motivated - strong desire to succeed is essential People oriented Self-confident 25% overnight travel ]]>

<![CDATA[Quality Resources, Inc. is a service organization providing outsourced services to a Fortune 500 pharmaceutical R&D firm in the Chesterfield area. The following assignment will be part time (approximately 20 hours per week) but could become full time in the future, depending on client needs. The successful candidate will need to be proficient in the following areas: 1. Manage GxP scientific equipment maintenance record retention center. 2. File all records for maintenance completed. 3. Archive all records in accordance with the corporate policy. 4. Serve as document audit “runner”. 5. Support on-line Power 2 Learn training role as needed A degree is preferred but not required if you can demonstrate the related experience. Superior customer service is an absolute necessity. If you believe you have extensive experience in the above areas, please email your resume and salary requirements. ]]>

<![CDATA[Quality Resources, Inc. is a service organization providing outsourced services to a Fortune 500 pharmaceutical R&D firm in the Chesterfield area. The following assignment will be part time (approximately 20 hours per week) but could become full time in the future, depending on client needs. The successful candidate will need to be proficient in the following areas: 1. Manages documents through the Global Document Management System (GDMS), GxP compliance DMS, and be an expert in GDMS numbering, routing, retires, etc. 2. Establishes procedures to meet compliance within GDMS. 3. Creates Standard Operating Procedures (SOP's) utilizing Subject Matter Experts (SME). 4. Writes procedures in conjunction with SME's in the correct format to manage in the Document Management System. 5. Requires working expertise with Global Document Management System. 6. Assist other sites in migration of documents into the correct format or correct database. A degree is preferred but not required if you can demonstrate the related experience. Superior customer service is an absolete necessity. If you believe you have extensive experience in the above areas, please email your resume and salary requirements.]]>

<![CDATA[The Judge Group is seeking an experienced QA Engineer for a direct hire opportunity in the St. Louis area. We’re representing a direct client in the pharmaceutical industry heavily engaged in the development, manufacture and sale of healthcare products for use in clinical and home settings. This position represents an excellent opportunity for long term growth and offers a competitive salary and benefit package. * Primary site contact for one or more of the following areas: Stability Testing, Change Control/Regulatory, Supplier Relations, Internal Auditing, Investigations, Corrective Action Program, Complaints, Document Control, or Annual Product Reviews. * Provide backup support in one or more of the following areas: Stability Testing, Change Control/Regulatory, Supplier Relations, Internal Auditing, Investigations, Corrective Action Program, Complaints, Document Control, or Annual Product Reviews. * Provide support for FDA or other regulatory agencies for on-site audits. * Provide support in the rapid resolution of product complaints, deviations, corrective actions, and/or safety issues. * Review Change Control/Management Documents involving product or process changes. * Provide quality engineering support in the development and maintenance of facility’s quality systems and procedures. * Assemble, analyze and report QA system data to ensure regulatory compliance, identify trends and to identify areas of improvement * Conduct quality audits and develop and assess subsequent corrective action recommendation. * Additional areas of responsibility may include developing specifications/test methods/sampling plans/standard operating procedures, providing quality system training, or assisting Corporate Product Monitoring in preparation of regulatory submissions Job Requirements * BS/BA in Engineering or Living Sciences required * Minimum 3-5 years Quality Assurance/Quality Control experience in a finished pharmaceutical environment. * Experience investigating deviations and other variances preferred. * Working knowledge of cGMP guidelines and their application in an aseptic environment. * Ability to adapt quickly in a fast paced dynamic environment. Good analytical and problem-solving skills. * Ability to communicate with and positively influence broad and diverse populations within and outside the organization. ]]>

<![CDATA[We have multiple openings for Biology Software Analysts! New grads entering the work force with your BS in Biology, today's your lucky day! Are you computer literate? Have you worked with databases? Have you worked in your college computerlab? If you have answered yes to 2 out 3 of these questions, I want to talk to you. Please submit your resume and salary expectations in Word format for immediate consideration.]]>

<![CDATA[The responsibility of a CRA is to oversee the conduct of a clinical trial to ensure the quality and integrity of data and safety and efficacy of the drug. In coordination with the team leader, exercise responsibility for project activities related to monitoring function. Interface with clinical investigators and other site personnel in order to carry out this responsibility. Education: RN, relevant clinical experience or 4 year Life Science degree. Minimum Work Requirements: 24 months of clinical drug trial field monitoring experience with brain cancer or non-small cell lung cancer studies within a pharmaceutical, CRO, or device company. Skills: Ability to communicate with professional medical personnel. Understanding of the drug development process. Ability to complete tasks in an accurate and timely manner. Physical Requirements: Ability to travel. ]]>

<![CDATA[Global company needs Lab Chemist with the heart to willing to learn more, explore more. We are associated with Global application field including NAFTA, Asian Market, EU. Job Description Participation in establishing a new Epoxy, Polyester and Urethane Formulation Laboratory in conjunction with Chinese facility. Learn the fundamentals of Commercial Resin Formulation, Synthesis and Applications. Requirements B.S Degree on Chemistry, Or material engineering. Knowledge of Basic Chemistry and Bench Work Protocol Mandarin and English – spoken and written Interface with colleagues in China Interface with users of products within NAFTA Please visit our website for more information about company www.clearskytechnology.asia ]]>

<![CDATA[Are you ready to join a team of dedicated professionals who are among the best in their field? Then take the time to check out SCI Engineering. SCI is always looking for great people! They may have the perfect job opportunity for you. SCI is a multi-disciplined consulting company seeking an outgoing individual to perform Phase I and II environmental assessments, MRBCA/TACO activities, asbestos, and mold surveys. A BS degree in engineering, geology or related fieldis required. Certifications in asbestos, 40 hr OSHA training a plus. SCI has a mandatory drug testing program. Must be hard working, versatile, have good communication skills and reliable transportation. Our unique combination of size and diversity provides many benefits which include: A great working environment. A rock solid benefits package. Competitive salary. A consistent backlog of a wide variety of work. The ability to work with a wide variety of resources. A small, personable, team oriented environment. E-mail resume and cover letter to: careers@sciengineering.com; FAX to 636-757-1099, or mail to: Human Resources SCI Engineering, Inc. 650 Pierce Blvd O'Fallon IL 62269 ]]>

<![CDATA[Direct full time opportunity with a global pharmaceutical company with operations in St. Louis!!!! The Instrument Mechanic is someone with INDUSTRIAL experience as an Instrument mechanic. We strongly prefer someone with a 2 year degree or equivalent (such as a labor union apprenticeship) in Instrumentation Controls, Electrical Engineering, or similar. The successful candidate should be knowledgeable of various types of instruments used in the measurement and control of system pressures, weight, temperatures, conductivity, pH, levels, flow, and density. He/she should be knowledgeable of electrical theory and its practical applications. He/she should be able to inspect, calibrate, measure, and test equipment at prescribed intervals using established procedures with equipment traceable to a nationally recognized standard or document equivalent. He/she should be able to use multi-meters, Hart communicators, frequency calibrators, weights, pressure calibrators, flow meters, digital pressure indicators, RTD calibrators, digital manometers, digital tachometers, etc. to conduct single point and loop calibrations of the above listed instrumentation. The successful candidate should have working knowledge of Lock-out/Tag-out methods and related OSHA safety practices. Practical experience with FDA regulations and CGMP guidelines is a plus. __________________________________________________________________________________ We DO NOT want to see people with experience calibrating instruments in a lab. The industrial equipment that this position calibrates is different, that someone from a lab environment would not have the proper experience to function in the role. Prefer chemical or pharma experience but they will accept someone from a different industrial background. There are a variety of instruments that they calibrate, that are involved with temperature, pressure, and flow of material. ]]>

<![CDATA[ We are seeking full time well qualified Clinical Research Coordinators to conduct industry sponsored trials involving multi-therapeutic areas. Responsibilities include coordination of study start-up requirements, recruitment of eligible subjects according to protocol requirements, data entry of case report forms and maintaining regulatory documents. This person will act as the liaison between the investigators, IRB's, and sponsors. Must have excellent written and oral communication skills, excellent organizational skills and a demonstrated ability to work independently and collaboratively. Competitive salary with bonus structure. Flexible hours possible. Requirements: Bachelor's degree not required; 4 or more years experience as a clinical research coordinator desired. Detail oriented and proven ability to multi-task. If interested please email: <a href="mailto:allen.lang@realcareers.info" rel="nofollow">allen.lang@realcareers.info</a>                                                                 industry has come under criticism of groups such as Adbusters via culture jamming which criticizes throughout the campus and include a workout room with weights and rowing machines, locker rooms, wa code found on the sponsor's product packaging along with a mail entry). The reason why contests are In many countries - namely New Zealand, South Africa, Canada, and many European countries - the adve gnizing the social impact of advertising, Mediawatch-uk, a British special interest group, works to s complicated by uncertainty and tight timescales. Use of classical marketing techniques, in these c Shared vision — The vision of where we want to be in the future is discussed and communicated to all ion to it (throughout the year) must be questioned; and the lessons learned, to be incorporated in t market place. In particular, it aims at generating a competitive advantage relative to its competito Screenshot of the Yahoo main page on April 26, 2007 te television became increasingly prevalent, specialty channels emerged, including channels entirely rkansas and Maine considering bills to implement such a taxation. Florida enacted such a tax in 1987 Alexander Dill are reclaiming the commons and providing definitions that embrace new phenomena like On August 13, 2004, Newmark announced on his blog that auction giant eBay had purchased a 25% stake ousehold, advertisers and agencies recognised the value of women's insight during the creative proce the 19th century, in France, arcades were invented, which were a street of several different shops, words; a googolplex being 1 followed by a googol of zeros, and the HQ being a complex of buildings ( he default Internet Explorer start page, as all of the previous "Microsoft Internet Start" web site Cohesion and identity — the ability to build a community with personality, vision, and purpose Sweepers frequently send out SASE (self addressed, stamped envelopes) to receive free game pieces, o The marketing warfare literature also examined leadership and motivation, intelligence gathering, ty ]]>