This job at Baxter International is not available

We're sorry, the job you are looking for at Baxter International on EuroPharmaJobs has expired.

Click here to see more jobs at Baxter International .

We still have many live jobs. Click below for similar jobs in:

or go to our job search page.

Similar jobs selected for you

  • Senior Quality Manager

    Galderma
    London, United Kingdom

    Lead and perform Quality and compliance specific tasks including but not limited to processing product complaints, review of information about secondary packaging/redressing, ensure proper labelling of products at the distributor, and product recall

    Medical Devices Quality Assurance
    Posted 2 days ago   
  • Quality Control Manager

    Zoetis
    Rathdrum, Ireland

    Responsible to supervise and lead the Laboratory release function including Raw Materials, Intermediates, DPI and API’s (including the stability program) and In Process Control and provide core technical support in areas of chromatography,

    Manufacturing and Logistics Quality Assurance
    Posted 3 days ago   
  • R&D Senior Laboratory Specialist

    Reckitt
    Nowy Dwór Mazowiecki, Poland

    Laboratory testing of household chemical products and raw materials, in a regulated environment where GMP/GLP standards apply. Formulation of laboratory samples for stability and consumer testing. Participation in industrial trials, supervising compliance

    Biotechnology and Genetics Manufacturing and Logistics Pre-clinical Research and Development Quality Assurance
    Posted 4 days ago   
  • Senior Manager, Bio-Tox Analytical QA

    AbbVie
    Westport, Ireland

    Responsible for developing and overseeing a robust Quality Assurance strategy focused on the transfer of New Product Introduction (NPI) QC methods to manufacturing sites and Third-Party Laboratories. This role supports the Test Method Gate Review process,

    Manufacturing and Logistics Quality Assurance
    Posted 5 days ago   
  • Develop, implement, and maintain the quality management system applicable to R&D activities (SOPs, work instructions, standards, etc.). Ensure compliance of R&D projects assigned to CMO Office with relevant regulations (e.g., GCP, GVP, GMP, GLP, ISO, ICH,

    Clinical Research Manufacturing and Logistics Pre-clinical Research and Development Quality Assurance
    Posted 6 days ago   

EuroPharmaJobs Logo

© EuroJobsites 2025