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Hello, My name is George Rogers and I represent The Fountain Group. We are a national staffing firm and are currently seeking a Quality Engineer II position for a prominent client of ours. This position is located in Los Angeles, CA. Details for this position: • Professional experience in Quality Assurance, specific to working within a GMP facility. • In depth experience working with complaints and other quality related investigations. • Must be able to coordinate complaint investigation ...

Job Description IntegraGen, Inc. is seeking a Regional Account Manager to grow the company’s revenue in the Western part of the United States. This field sales position will be based in California and be responsible for the growth of IntegraGen’s ARISk® Autism Risk Assessment Test (www.arisktest.com) within the assigned geography through selling and promotional activities to targeted clinicians.    Applicants MUST currently reside in either the Los Angeles or San Francisco Bay area. No relocation ...

Local Healthcare facility in Tehachapi is currently hiring Clinical Lab Scientists! For more info, Contact JayKay Staffing, we will be glad to help. Mon-Fri 6a.m - 2p.m shift! **Must have at least 1yr experience! Megan Donnelly 800-442-5441 ext 107 OR Fax your resume to 800-809-0158 (Attn: Megan) OR E-mail your resume to megand @ jaykaystaffing.com

Regional CRA position! 2+ years on-site monitoring experience.  MUST have CNS experience.  MUST have good tenure with current/past companies. MUST be open to some travel.  

Position title:    Associate Scientist II (JP#22044) Location:          Thousand Oaks, CA Duration:          Contract, 13 months   Our client is the world leading human therapeutics company in the biotechnology industry. We are seeking an Associate Scientist II to provide scientific support for development, qualification, transfer and oversight of clinical flow cytometry based biomarker assays. Job Details: To perform experiments, organize data and analyze results under minimal supervision. With ...

Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis. Title: Data Analyst II Job ID: 21926 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Duration: 6 Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate) Job Summary Run validation reports to ensure data integrity, manage wholesaler data to ensure data ...

Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis. Title: Quality Assurance (QA) Senior Associate Job ID: 21742 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Duration: 18 Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate) Provide swing shift (1:30-10:30 PM or later) Quality Assurance oversight for ...

 Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis. Title: Associate Scientist II Job ID: 22044 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Duration: 12 Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate) Seeking a qualified individual to provide scientific support for development, qualification, ...

At Praedicat, we’re using technology to change the way the world manages emerging risk. Our team is blazing trails in forward-looking, science-based risk analytics, web technologies, and emerging risk signal processing. Praedicat faces not only many of the same exciting challenges as other companies experiencing rapid growth, but also a number of unique challenges, including tackling big data. The large data requirements of science-based engineering require us to continually push boundaries to ...

At Praedicat, we’re using technology to change the way the world manages emerging risk.  Our team is blazing trails in forward-looking, science-based risk analytics, web technologies, and human guided knowledge engineering.  Praedicat faces not only many of the same exciting challenges as other companies experiencing rapid growth, but also a number of unique challenges, including tackling big data.  The large data requirements of science-based engineering require us to continually push boundaries to ...

$5000 Hiring Incentive for Qualified Candidates! Covance is seeking Clinical Research Associates / CRA / Monitors with cardiovascular / coronary artery disease therapeutic experience for a special hypercholesterolaemia project.   Positions are home-based and urgently needed in the following locations:  Raleigh, Dallas, Boston, Chicago, Minneapolis, NYC, Florida, and California.   Our Clinical Research Associates /CRAs / Monitors manage all aspects of site monitoring responsibilities for ...

Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis. Title: Project Manager III Job ID: 21911 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Duration: 12 Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate) Responsibilities:   Resource allocation and all phases of development life cycle (i.e. ...

Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis. Title: Senior Engineer Job ID: 21982 & 21983 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Duration: 12 Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate) Responsibilities:   Work cross-functionally with individuals and project teams in ...

**Relocation Options Available - US Based Candidates Only** Job Description:  Responsible for the accuracy and completeness of the clinical data collected during a clinical trial. At the trial level coordinate and perform the following activities:   - Development of the data specifications and eCRF design, including leading the review meeting - User Acceptance Testing of eCRF and other tools - Development of the Data Management Plan, including leading the review meeting - Data review, query ...

Responsible for the accuracy and completeness of the clinical data collected during a clinical trial. At the trial level coordinate and perform the following activities: - Development of the data specifications and eCRF design, including leading the review meeting - User Acceptance Testing of eCRF and other tools - Development of the Data Management Plan, including leading the review meeting - Data review, query generation, data coding, electronic data reconciliation - Identification of ...

Contract opportunity through 5/30/2014 Request Notes: Biomedical Engineering degree preferred, Engineering degree required, 1 year of experience required, 1-3 years technical experience preferred, Medical device experience preferred. Creates and maintains systems to monitor project status, budgets and timetables through the use of specialized software applications. Ensures documentation requirements are met. Applies extensive knowledge of and experience in company operations to assist in the ...

our client in northridge, CA is looking for a senior chemist. This is a long term consulting position. If interested, please apply to this ad Job Description: Applies a board range of analytical techniques (e.g., HPLC, GC, IC, spectroscopic techniques, ICP-AES, ICP-MS, GC/MS, LC/MS, Karl Fisher, etc.) and sample preparation/extraction/separation techniques to characterize key product attributes and resolve technical issues. Techniques include but not limited to surface analysis (SEM and EDS) and ...

The Senior Product Manager will direct market analysis and implementation of marketing plans for key asset in the companies ophthalmics franchise. This complex ($1.0b) business segment needs a strong marketer to grow share/develop offensive marketing strategies and position the brand for future success. With autonomy and managing a direct report this role is critical to success of current brand and a projected launch in Q4 2013! The ideal candidate will also have strong market research and ...

SCIENCE/BIOTECH POSITIONS - CLS'S, MOLECULAR, FISH, CYTO, HISTO, ETC. (Chula Vista) Description: HUNDREDS OF SCIENCE/BIOTECH POSITIONS - CLS'S, MOLECULAR, FISH, CYTO HUNDREDS OF BIOTECH POSITIONS AVAILABLE NATIONWIDE MOLECULAR; CYTOGENETICS; FISH; HISTO'S, PATHOLOGIST'S, CLS'S-NATIONWIDE, ETC..... Description: WE SPECIALIZE IN RECRUITING FOR ALL POSITIONS AND JOB LEVELS WITHIN THE BIOTECH/PHARMA INDUSTRY NATIONWIDE! WE REPRESENT SEVERAL HUNDRED CLIENTS THAT HAVE THE FOLLOWING ...

  This position is responsible for performing any/all of the following tasks and responsibilities, as well as any other tasks deemed appropriate by the Supervisor:   ·        Monitor activities at assigned clinical study sites to assure adherence to ICH GCPs, local regulatory requirements, TRIO Standard Operating Procedures (SOPs), Standard Guidelines (SGs), Instruction Manuals (IMs), study protocols and study-specific SGs/IMs, for multiple projects ·        Conduct Pre-Study Site Visits (or calls), ...

::Contact Devin for more details at 815-756-1221. Attach resume when responding to this posting:: The Plant Manager will be responsible for operations of all site activities, maintenance of the EH&S compliance, budgetary issues, act as change agent, direct all aspects of plant operations. Qualifications: - BS Chemistry, Chemical Engineering or related - 8+ years of batch chemical plant experience - 5+ years in a management or supervisory role - Preferred experience in polymer resin or emulsion ...

Below is a template Description. Each position at each client is a little different. Requirements: License/Certification/Education: Normally a B.A./B.S. in Biology and meet all licensing requirements w/1-3 years of experience. NY State Licensure required. Job Description: Performs laboratory tests and analyses according to established procedures in designated technical department. Evaluates procedures and methods under direct supervision of more senior technologist, department supervisor, or ...

  The Surgical Regulatory Affairs Manager handles all regulatory development aspects for surgical devices as assigned. These include IOLs, Inserters and Solutions. The incumbent participates on the product development team to provide regulatory guidance for surgical devices assigned. They also manage relevant regulatory strategy components and interactions with Regulatory Authorities for their assigned surgical products and may perform due diligence efforts on new product opportunities.   ...

  Specific Job Duties: Provide process engineering and product development support to injector projects Develop methods/processes to improve product performance Lead various engineering and validation studies Interface with various functions, gather requirements, author and execute protocols and write technical reports Participate in project team meetings and provide written and verbal updates Generate design control documentation in support of new product development ...

Colorist/Compounder Leader in paints, films, and coatings applications is seeking a colorist/compounder The ideal candidate will have at least 1 year of color matching experience. Must have a strong visual acuity with color and prior experience with color matching, tinting, and compounding. Duties and Responsibilities • Responsible for pigment milling for the development of color standards • Have the ability to color match • Maintain general knowledge of all Q.S.P.’s and S.O.P.’s that apply to ...

Translational Development Medical Director leads the oncology team to drive translational medicine and early development efforts into Phase I clinical trials. Looking For: *** Successful track record of taking projects from preclinical science into clinical development including the design of first in human trials *** Demonstrated ability to lead multidisciplinary project teams and to influence scientists, clinicians and senior management stakeholders *** Strong network of KOL's throughout ...

Lab Support is looking for a QA Associate in the Ventura county area! Duties: Responsible for assisting Manager with daily operations of quality programs and oversight Data entry and review of documentation as needed Manage sample submission process Prepare documentation as needed Manage CoAs and associated paperwork Provide supervision as requested for the QC Technicians Requirements: BS degree in science, food science, or related field highly desired. Non-degreed candidates may be ...

We are currently looking to hire Permanent Senior Regional CRA's   The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOP and regulations. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required), performing qualification, initiation, ...

If you are a CRA or a Senior CRA we’d like to speak with you!   We currently have a number of different clients looking for CRAs and SCRAs. They each have different perks, options and ways of doing business that make them very appealing. These are all permanent positions, however, if you have a contract background and are looking to make a switch,  that will not disqualify you from any of these roles. Salaries are based on experience, current compensation and market conditions and range from $75K- ...

  Title: Clinical Project Manager Company: Medical Device Company Location: Orange County, CA Status: Permanent Placement, 40 hours/week Role: • Clinical Project Manager manages U.S. field activities for the conduct of clinical research studies in compliance with applicable regulatory standards, IRB/EC policies and procedures and company policies and procedures. This position works with minimal supervision in consort with study management. This ...

The Principal Scientist will be the PKDM Development Project Team Representative on the Early and/or Global Development Teams in the area of Oncology. He/she will support small and large molecule drug development, registration, and post-marketing activities. He/she will be responsible for program-level strategic and resource planning, communication, scientific/technical deliverables, issue resolution, and functional representation for internal governance reviews, face-to-face interactions with global ...

Leading pharmaceutical company seeks Sr. Manager Regulatory Writing to join its growing team.  This is a lead submission writer position and does not manage direct reports. The position can be remote (work from home) for candidates based in the US. Or the company will offer relocation assistance to Thousand Oaks California or South San Francisco California.  The company offers an excellent salary, bonus, and benefits that include 10% 401K match, stock, and 3 weeks of vacation plus ...

The Surgical Sales Representative would be responsible for selling surgical products in accordance with budgeted objectives and to obtain maximum profitability and volume in relation to pre-set standards Responsibilities include: - Educate and inform doctors, nurses, and appropriate staff personnel as to the proper use and maintenance of company products - May direct product evaluations in OR and office settings - May assist in the preparation and operation of trade shows, conventions, and/or ...

Contact Devin for details: 815-756-1221 or attach your resume and respond to this posting. The Analytical Chemist will be responsible for providing lab support to R&D projects. Results needed for projects will be expected to be generated by use of analytical techniques. Must conduct studies under GLP guidelines. Qualifications: - PhD Analytical Chemist - 5+ years of relevant experience - Familiar with GXP regulated working environment - Experience with method developments - Troubleshooting, ...

Personal Care and Cosmetic Company is seeking a Cosmetic Chemist to join their team. Qualified candidates should apply to Lab Support for consideration. Summary: Formulate new and improved personal care and cosmetic products and assist with QC analysis of pilot batches, raw materials, in-process and finished products List of Responsibilities: Prepare batches with new raw materials and conduct testing Interact with suppliers to collect information needed to analyze raw materials Prepare prototype ...

Lab Support is seeking a QA Associate to work at a Food and Supplement Company in the San Fernando Valley. Exciting business and great working enviroment. Qualified candidates will have a B.S. in Microbiology, Biology or related and industry experience with QA and Documentation roles such as data entry and revision to SOPs. Essential Functions: Coordinate compliance testing Create schedule, work with QA to obtain samples, and assure that samples are sent out on time Update formula files and ...

•Reviews manufacturing routers for completeness and accuracy. •Performs quality review of documentation prior to shipment for acceptance. •Evaluates quality records for accuracy. Keeps quality records filed and up to date. •Creates test reports and certifications for the company. •Creates Test Plans in accordance with customer requirements and department procedures. •Ability to create forms for tests requests •Knowledge and interpretation of aerospace specifications •Checks raw material ...

Contact Devin if you meet the job requirements: 815-756-1221 The Compliance Manager will be responsible for implementing a product compliance strategy to ensure compliance with all international, federal, state, and local regulations. Will be in charge of design and implementation of programs and policies. Will consolidate and standardize processes. Qualifications: - BS Chemistry - 5+ years of compliance experience in consumer products - Warning label and regulatory compliance working knowledge - ...

PLEASE READ ENTIRE POSTING. THIS IS TO START IMMEDIATELY, FOR LA RESIDENTS ONLY. Hiring a research intern who has strong interest and knowledge about Space, Space travel, INTERNATIONAL SPACE STATION with 16 countries involved, Aerospace, Aviation industry and Virgin Galactic. Must be strong in research skills, imaginative and have enthusiasm for Aerospace & Aviation projects. The applicant will be apart of a creative team for a boutique label to assist an artist who supports Aerospace & Aviation ...

Seeking at least 5 years experience designing, developing, and validating molecular diagnostic assays for CLIA approved tests. Required: *** Assay process development, documentation, and scale up experience. *** Developed DNA array based molecular assays for diagnostics. *** MS or PhD degree. Starting salary up to $110,000 plus comprehensive benefit packages and the opportunity to collaborate with top scientific personnel on a daily basis. If you are ready to make a difference, do not ...

Contact Jeff at 815-756-1221 Qualifications: - PhD with 12+ years of pet food design and formulation experience - BS/MS with 15+ years considered - Broad depth of experience in pet food development - Experience in other related food industries Duties: - Manage highly technical projects that will facilitate development of new products - Achieve desired research results within the product image and time guidelines - Develop projects and apply technologies as it relates to business objectives - ...

Shall ensure regulatory and ISO 13485 comliance and obtain regulatory approval for medical devices, as well as, manage content, assembly, pre-final review, and filing of medical device applications including IDE's, 510k's and PMA's. Would you like to join a company that has been voted top place to work several years in a row? Commensurate with experience top salary plus bonuses, 401(k), tuition, stock options, full medical, and 3 to 4 weeks paid flexible vacation time. For complete details ...

Position/Program Information 1. Performs a wide range of highly complex forensic human-DNA testing and analyses required in scientific criminal investigations. 2. Positions allocable to this class typically report to a Supervising Criminalist and independently perform forensic human-DNA testing and analyses of evidentiary samples encountered in the course of criminal investigations for forensic or criminalistics purposes not primarily related to patient care. 3. Incumbents in these positions must ...