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8 Jobs in Westport, IRL

  • Quality Lab Manager

    AbbVie - Westport, Ireland
    ... WWQA standards and FDA, HPRA and other MOH regulatory requirements. This schedule compliance will be ... LinkedIn. Job Description We are now hiring a Manager Quality Laboratory on our ...
  • Manufacturing Shift Manager - Biologics

    AbbVie - Westport, Ireland
    ... , curious team We are currently sourcing an experienced Manufacturing Shift Manager to join our ... facility in line with all safety, regulatory and operational requirements. This is a shift ...
  • Pharmaceutical Technology Specialist III

    AbbVie - Westport, Ireland
    ... project documentation in compliance with corporate and regulatory standards. Ensure timely ... Laboratory Equipment Review Process as per the current rotas. Regulatory Compliance ...
  • Unit Dose Shift Manager

    AbbVie - Westport, Ireland
    ... supportive space for you to thrive—at AbbVie and beyond We are now recruiting Unit Dose Shift Manager ... manufacturing, filling & tampoprinting in the Unit Dose Department in line with all safety, regulatory and ...
  • Technical Shift Lead

    AbbVie - Westport, Ireland
    ... all regulatory requirements, achieve desired financial performance, including cost reductions, and ... Promote and develop a culture of contamination control and compliance with aseptic best practices ...
  • Biologics (Manufacturing) Technical Shift Lead

    AbbVie - Westport, Ireland
    ... with all regulatory requirements, achieve desired financial performance, including cost reductions, and ... compliance with aseptic best practices Communicate departmental goals to provide cost-effective ...
  • Pharmaceutical Technology Scientist

    AbbVie - Westport, Ireland
    ... during project. Responsible for compliance with all applicable Corporate and Divisional policies ... Knowledge and experience with GMP regulatory inspections Excellent report / procedure writing skill ...
  • Biologics Manufacturing Technician

    AbbVie - Westport, Ireland
    ... compliance with site and GMP procedures, and that scheduling and manufacturing meets global request timelines ... Strong knowledge of GMP regulatory guidelines, quality systems, drug product manufacturing and validation ...