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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 Packaging Engineer Job ID: 22023 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Duration: 11 Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate) The position requires organizational, project management, technical problem solving and ...

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 ...

  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 ...

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 ...

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 ...

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 ...

Regulatory Affairs Specialist Reporting to the General Counsel, the Regulatory Affairs Specialist ensures regulatory compliance on branding packaging, marketing materials and other corporate documents and affairs pertaining to labeling, legal items as well as compliance items regarding product development. • Provide support in the dietary supplement categories by reviewing product descriptions, marketing material, labels and claims to determine compliance with the rules and regulations of federal ...

GENERAL DESCRIPTION   This position is responsible for the coordination, design, execution and oversight of analytical method transfer and validation requirements to support the chemical laboratory.     Must have working knowledge in a pharmaceutical and nutraceutical quality control or development laboratory environment. Ability to perform and operate laboratories test methods and instruments, including HPLC, GC, ICP, FTIR, UV/VIS Spectrometer. Ability to design & validation ...