Validation Specialist - Olst, Nederland - Abbott

    Abbott
    Abbott Olst, Nederland

    Gevonden in: Talent NL C2 - 1 week geleden

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    Beschrijving

    Abbott is a global healthcare company devoted to improving life through the development of products and technologies that span the breadth of healthcare. At Abbott, we're committed to helping you live your best possible life through the power of health. For more than 125 years, we've brought new products and technologies to the world -- in nutrition, diagnostics, medical devices and branded generic pharmaceuticals -- that create more possibilities for more people at all stages of life.

    For our site in Olst we are looking for a Validation Specialist

    Who are we looking for?

    Are you an experienced Validation Specialist who wants to work on a wide variety of validation projects and is not afraid to broaden your experience while doing so? Then we are looking for you

    Where will you be working?

    There are fifteen skilled and motivated colleagues within the Validation Support and Packaging department of Abbott in Olst.Our goal is to achieve and maintain the validated state of production equipment and utilities on the site. The site consists of three production facilities where a number of branded generic pharmaceuticals are manufactured, filled and packaged.

    As a Validation Specialist you will be working on different validation projects within the production facilities.

    What will you be doing?

    The projects you will be working on are very diverse. It goes from new equipment that Is installed and initially validated to existing equipment that is upgraded and improved to the latest standards. As a Validation Specialist, you are involved from the start until the project is finished and the equipment is released for production.

    Examples of equipment to be validated are:

  • Filling lines
  • Packaging lines
  • Serialization / aggregation systems
  • Autoclaves
  • Washers
  • Cleaning validation
  • Cleanroom validation
  • Isolators
  • Temperature mapping
  • Etc. etc.

    • Tasks and responsibilities.

  • Writing the validation documentation and getting the documentation approved by all involved stakeholders. Executing or supervising the validation activities (IQ, OQ, PQ).
  • Acting as a validation SME during audits and within project teams.
  • Advising on policy proposals on the implementation of new (external) developments in the field of validation and GMP.
  • Coaching/informing the team and other (external) colleagues in the context of validation (and its importance).

    • What do we offer?

    Abbott provides a varied, challenging, and international position in a dynamic and pleasant working environment. In our organization, you can count on excellent primary and secondary benefits, a positive working atmosphere, a personal growth plan, extensive training opportunities, and a good career perspective. We are in the business of advancement, both in health solutions and in the lives and careers of our employees. Our work across the world and in many areas of healthcare provides a rich environment for our employees to explore career paths, interests, and opportunities.