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  1. IT Coordinator at StatRad LLC

    IT, computer science:. Ensure all policy compliance controls are adhered to. The IT Coordinator’s primary role is to support internal and external end users of...

  2. Associate Scientist, Structural & Chemical Biology at Celgene

    Pharmaceutical industry or Biotech work experience, preferred. With a presence in more than 70 countries - and growing we look for talented people to grow our...

  3. Materials Coordinator Team Leader at Bachem

    A Bachelor’s Degree in Science or related discipline, certification from a biotech program or equivalent industry experience....

  4. Diesel Mechanic at Clairemont Equipment Co

    Fuel systems, complete diagnostics, Injectors, R & R Fuel Injection Pumps, set timing on re installation of injection pumps....

  5. IT Support Specialist at StatRad LLC

    Ensure all policy compliance controls are adhered to. Document management systems and help desk software a plus....

    Ads
    1. QA Documentation Control Specialist

      Responsibilities:· Responsible for supporting the execution of the Document Control and Engineering Change systems activities in accordance with ISO9001 and company quality standards, including expeditious processing of changes to SOP's and other content, tracking and initiating change orders associated with documentation and SAP objects, and securing completed documentation.· This position ...

    1. Scientist II, Biochemistry - Protein Homeostasis at Celgene

      Align science and functional area goals with business strategies. Ideally, someone with at least one year of Pharmaceutical Industry or Biotech experience....

    1. Sr. Cleaning Validation Engineer

      Azzur Group CA is seeking a Sr. Cleaning Validation Engineer for a pharmaceutical manufacturing site in Oceanside, CA. In this role, you will be responsible for drafting policy level cleaning validation documents and for project planning and strategy around cleaning validation for a new product introduction at the site. Prior cleaning validation experience in a cGMP facility is required. ...

    1. Principal Scientist, Computational Biology at Celgene

      Strong interest in the inter-disciplinary application of computational analysis methods to life sciences data is imperative, as is rich background and...

    1. Materials Coordinator- 6507

      MATERIALS COORDINATOR – TEAM LEADER - Simply Biotech (6507)OVERVIEWImmediate opening for a Materials Coordinator – Team Leader in Vista, CA who possesses:Scientific Degree or related discipline or equivalent experience in biotech industry  2+ years of industry level experience biotech or lab environment with knowledge of FDA, cGMPStrong understanding of Chemistry and raw ingredients ...

    1. Senior Scientist, Epigenetics Biochemistry at Celgene

      In Biochemistry with at least 6 years of relevant work experience, biotech or pharmaceutical experience, preferred....

    1. QA Inspector, Manufacturing- 6501

      QA Inspector, Manufacturing- Simply Biotech (6501)OVERVIEWImmediate opening for a QA Inspector, Manufacturing in San Diego, CA who possesses:High School Diploma Required. BA/BS degree in physical science or Quality Experience preferred.Strong communication skills and ability to follow written and verbal instructionsAbility to document information completely and accuratelyAbility to multitask ...

    1. Principal Scientist, Protein Homeostasis & Structural Informatics at Celgene

      Keen interest in inter-disciplinary application of computational methods to life sciences data is imperative....

    1. Quality Assurance Software Engineer

      PSC Biotech is one of the world's largest compliance consulting firms specializing in compliance consulting in the life sciences industry. Presently we are recruiting for experienced and knowledgeable Senior Quality Software Engineer for our client in San Diego.ResponsibilitiesResponsible for providing Quality Assurance leadership, for software development teams. Subject matter expertise and ...

    1. QA Document & Control Specialist at Company Confidential- North County San Diego

      QA DOCUMENT & CONTROL SPECIALIST*. Five years minimum experience in document control. Responsible for the system and the accuracy of all required GMP documents...

    1. Production Associate II- 6484

      PRODUCTION ASSOCIATE II - CONTROLS - Simply Biotech (6484)OVERVIEWImmediate opening for a Production Associate II - Controls in San Diego, CA who possesses:Must have 2+ years' experience working in GMP environment(prefer and ISO certified environment)Must have experience with DNA/RNA Extraction(manual) and Cell Culture Experience  Asceptic Experience and prior experience working with HAZMAT ...

    1. JC1604: Research Scientist at ProSci Incorporated

      We have a Research Scientist position open immediately for a highly motivated, detail oriented and experienced Research Scientist to support the research team...

    1. Medical Writer- 6481

      Medical Writer- Simply Biotech (6481)OVERVIEWImmediate opening for a Medical Writer in San Diego, CA who possesses:Bachelor’s degree requiredAdvanced life sciences degree preferred, e.g., RN, MS, RPhAt least 3 years of medical communications writing experience with development of scientific manuscripts and pharmaceutical regulatory documents.Knowledge of science or an aptitude for ...

    1. West Coast Account Manager at Proteintech Group Inc.

      Must have a Life Sciences qualification (minimum B.Sc). As a rapidly expanding biotech company, you will participate in our worldwide growth and be responsible...

    1. Director, Quality Assurance- 6446

      DIRECTOR, QUALITY ASSURANCE- Simply Biotech (6446)OVERVIEWImmediate opening for a Director, Quality Assurance in Vista, CA who possesses:Degree in Scientific Discipline and 8+ years of Progressive Quality Assurance Experience5+ years of Supervisory or Management experience in Pharmaceutical industry in a Quality RoleDiverse experience with CAPA, Change Control, Vendor Selection, Audits ...

    1. Vice President of Translational Medicine (#79049) at California Institute for Biomedical Research

      Pharma, Biotech, and Clinical Research:. Basic Science and/or clinical research experience in a medical specialty with a proven record of quality publications....

    1. Clinical Laboratory Scientist- 6448

      Clinical Laboratory Scientist- Simply Biotech (6448)OVERVIEWImmediate opening for a Clinical Laboratory Scientist in San Diego, CA who possesses:Degree with an ASCP CLS license (generalist required)MUST have experience within a CLIA/CAP environment3+ years of assay validation experienceEmail resumes to [email removed] or call 858.683.8559.Basic Function and Scope of the Position:The Clinical ...

    1. Field Applications / Controls Engineer at Hardy Process Solutions, a Roper Technologies company

      Provide and document effective solutions for customer use / application issues. BASIC PURPOSE AND OBJECTIVE OF THE POSITION:....

    1. Regulatory Compliance Specialist I

      3E Company is leading the future in the supply chain and environmental, health and safety management industry. At 3E, we pride ourselves as being the guardians of environmental compliance. We are seeking individuals who believe in our mission and will contribute to our team vision. If you like to be challenged and are looking to advance your career in a fast-paced work environment, then 3E ...

    1. Program Support at University of Delaware

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    1. Quality Assurance Associate I

      Summary This position supports the different activities within the Quality Assurance Department. Primary responsibilities include overall facility compliance to standards, writing, executing, follow-through and maintenance of documentation for the quality system, generating and issuing labels, providing line clearance, reviewing log books, reviewing & revising quality documents (SOPs, ...

    2. Quality Assurance Associate II

      SummaryThis position supports the different activities within the Quality Assurance Department. Primary responsibilities include reviewing batch records, generating and issuing labels, providing line clearance, reviewing log books, reviewing & revising quality documents (SOPs, Deviations, MBRs, Work Instructions, etc). Also participates in projects within the QA/RA departments.Essential ...

    3. Quality Assurance Associate – Batch Record Review 6425

      QUALITY ASSURANCE ASSOCIATE – BATCH RECORD REVIEW- Simply BiotechOVERVIEWImmediate opening for a Quality Assurance Associate – Batch Record Review in San Diego, CA who possesses:Candidate will have a BS/BA science degree (Chemistry or Biochemistry preferred).Candidate will have 2-3 years of work experience in a GXP manufacturing environment or similarCandidate must also be highly detail ...

    4. Instrument Tech-Electricians-Temporary Travel $48-65/hr

      Huffmaster Companies is recruiting experienced Instrument Tech-Electricians to work during a possible labor dispute at a drug manufacturing facility located in Pennsylvania. The labor dispute is expected to occur early May .$48/hour for the positions requiring no aeseptic Gowning$60/hour for the positions requiring less aeseptic Gowning$65/hour for the departments requiring the most stringent ...

    5. QA Manager- 6404

      QUALITY ASSURANCE MANAGER- Simply BiotechOVERVIEWImmediate opening for a Quality Assurance Manager in San Diego, CA who possesses:Degree and 5+ years of maintaining and monitoring Quality Systems(Quality System setup highly preferred)2+ years of working in a Clinical Lab(CAP or CLIA) in a Quality role Experience working with third party audit groups (CAP, CLIA, FDA  and similar)Email resume ...

    6. Medical Director - Clinical Development - Rheumatology - San Diego, CA

      Seeking experienced Medical Director with background in Clinical Development leadership looking to join a leading pharmaceutical company developing and leading Clinical Trials for new drugs treating autoimmune conditions causing painful inflammation of the skin and joints. Activities: *** Create, revise, and submit clinical development plans. *** Select proof of concept indications for ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    7. Inventory Control Specialist- 6246

      Inventory Control Specialist- Simply BiotechOVERVIEWSimply Biotech specializes in recruiting exclusively for the biotech community. We are currently seeking an Inventory Control Specialist for a leading and growing biotech firm. This position is based in San Diego, California. The Inventory Control Specialist (“ICS”) is responsible for ensuring material flow in and out of the company’s ...

    8. Quality Assurance Associate I- Simply Biotech

      Quality Assurance Associate I- Simply BiotechOVERVIEWImmediate opening for a Quality Assurance Associate I in San Diego, CA who possesses:Candidate will have a BS/BA science degree (Chemistry or Biochemistry preferred).Candidate will have 1 to 2 years of analytical chemistry/HPLC experience (candidates without this experience WILL NOT BE CONSIDERED).Candidate must also be highly detail ...

    9. Clinical Project Manager

      GENERAL PURPOSE The Clinical Project Manager for global clinical trial management is responsible for developing project plans and tracking of clinical projects. Additional responsibilities include generating project milestones and timelines as reflected in the Gantt chart, identifying and monitoring critical path, tracking budgets, expenses, and timelines for the trial both within the Company ...

    10. Quality Tech II- 6332

      QUALITY TECH II- Simply BiotechOVERVIEWImmediate opening for a Quality Tech II in San Diego, CA who possesses:Scientific Degree and 2+ years of experience in Quality Control or similar roleExperience with manual pipetting in a GMP lab environmentExperience with PCR, qPCR or similar molecular knowledge  Email resume to [email removed] or call 858.8070FULL DESCRIPTION:Simply Biotech specializes ...

      1. Computer System Validation Specialist at Bachem

        BS degree in Computer Science or Life Science. Development and maintenance of life cycle documents necessary to address the validation lifecycle (Risk...

      2. Senior Statistical Programmer at Agility Clinical, Inc

        Document the quality control review process. Perform quality control for SAS programs and other study documents (e.g., presentations and reports)....

      3. Facilities Manager at NantKwest

        Experience working in a pharmaceutical or biotech or highly matrixed organizational structure. NantKwest is seeking a Facilities Manager to manage the physical...

      4. Post Doc, Computational Chemistry at Celgene

        With a presence in more than 70 countries - and growing we look for talented people to grow our business, advance our science and contribute to our unique...

      5. Post Doc, Protein Homeostasis CoE at Celgene

        § Document, interpret and troubleshoot results. With a presence in more than 70 countries - and growing we look for talented people to grow our business,...