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regulatory affairs in Central Valley

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  1. Reporter, Los Angeles at Law360

    Experience in news reporting (AP Style), covering legal, regulatory affairs, or business news. Law360, a LexisNexis company, is an online newswire for business...

  2. Product Development Analyst at Sterling Hoffman Life Sciences

    Collaborate with a team of laboratory scientists, bioinformaticians, regulatory affairs and quality assurance specialists to build clinical assays meeting CLIA...

  3. Global Director, Regulatory Affairs at Sterling Hoffman Life Sciences

    Preference will be given to people with recent experience in regulatory affairs. Our client, a leading medical device company, is currently seeking an...

  4. Director of Regulatory Affairs at Sterling Hoffman Life Sciences

    Represent the Regulatory Affairs Department in interdepartmental meetings. Our client is looking for a Director of Regulatory Affairs with solid electronic...

  5. Medical Writer at Sterling Hoffman Life Sciences

    Experience of 4 years in Regulatory Affairs in a Biotech or Pharmaceutical company (preferred in Oncology)....

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    1. Commercial Banking Relationship Manager

        POSITION SUMMARY The Relationship Manager develops and manages relationships with commercial clients in assigned business segments and/or geographic areas. Presents a variety of product solutions to meet client needs. Provides responsive, quality service. Approves transactions within delegated authority. Manages overall relationship profitability and portfolio risk.   MAJOR ...

    1. Toxicologist at Fairway Consulting Group

      Provides toxicology support for planned US and international regulatory submissions, including authoring the nonclinical components of regulatory dossiers and...

    1. Associate Director / Director Medical Affairs at Fairway Consulting Group

      Understanding of regulatory compliance framework within which Medical Affairs operates. Represent Medical Affairs on the Medical Affairs Review Committee and...

    1. Regulatory/QA Expert at PSC Biotech

      An experienced QA person with regulatory skills and knowledge of CFR 820 to support one of our clients in Southern CA....

    1. Field Medical Educator (Immuno-Oncology) - West at The Medical Affairs Company

      Identifies, collects, and communicates clinical insights and intelligence to address medical information, in addition to insights on trends and changes,...

    1. Field Medical Educator at The Medical Affairs Company

      Identifies, collects, and communicates clinical insights and intelligence to address medical information, in addition to insights on trends and changes,...

    1. Regulatory Affairs Specialist at Sterling Hoffman Life Sciences

      Preference will be given to people with recent experience in regulatory affairs. Provide regulatory reviews of customer complaints and define regulatory report...

    1. Medical Science Liaison - Hospital CV /CC (West/S. CA, NM, AZ) at The Medical Affairs Company

      Working knowledge of regulatory and compliance requirements. Medical Science Liaison - Hospital CV/CC....

    1. Medical Science Liaison-Institutional/Pain (WEST) at The Medical Affairs Company

      Awareness of pharmaceutical regulatory agencies (FDA), OIG, and PhRMA code. Track record of success in opinion leader development and/or in Medical Affairs...

    1. Quality Assurance and Regulatory Affairs Specialist at TeraRecon, Inc.

      We are seeking for a Quality Assurance and Regulatory Affairs Specialist who will assist in regulatory compliance, submissions and maintenance of the TeraRecon...

    1. Quality Engineer at Sterling Hoffman Life Sciences

      Minimum 3+ years of experience in working in a regulated industry (medical devices) in quality, regulatory affairs, manufacturing or new product development....

      1. Senior Regulatory Affairs Specialist at Sterling Hoffman Life Sciences

        Preference will be given to people who have recent experience in regulatory affairs. Represent regulatory affairs on various design and development teams by...

      2. Animal Originated Tissue Expert at Tuv America

        Perform evaluations of regulatory submissions including:. Perform regulatory audits of clients per European Medical Device Directives (AIMD, MDD, IVDD),...

      3. Prin Medical Writer at Medtronic

        Collaborate with regulatory teams on all phases of regulatory submissions and approvals, including clinical document preparation and review, regulatory document...

      4. Clinical Study Design Specialist II at IDEXX Laboratories

        Familiarity with regulatory processes, clinical research processes and standards. Works with medical affairs and others to establish/refine study scope...

      5. Instruments Sr Sales Rep APM at Thermo Fisher Scientific

        Initiate and develop productive client relationships in multiple functions (e.g QA/QC, R&D, production, procurement, finance, regulatory affairs, etc) with...