QA Specialist

Locatie: Deventer

In this position as QA Specialist you play a crucial role in ensuring quality and compliance oversight to marketed global pharmaceutical products. Do you bring QA experience in a pharmaceutical environment and would you like to be part of global project teams? Apply now!

Het is niet meer mogelijk om te solliciteren op deze vacature. Back to overview

What will your job be

As QA Specialist you will provide support of global quality & compliance strategy for commercialized pharmaceutical products with global or multiregional scope. Your responsibilities include:

  • Serve as product quality and compliance contact person during planning and execution of major changes of commercialized global products (e.g. product remediations, alternative supplier qualifications etc.)
  • Provide product quality and compliance leadership to stakeholders 
  • Provide expert knowledge of global regulations and guidances and contribute to the final decision-making process
  • Drive the application of risk management principles for proactively identifying compliance risks and preparing decisions
  • Liaise with regional organizations and ensure proper communication and alignment for divisional driven product quality and compliance initiatives
  • Promote innovation and continuous improvement

What are we looking for

For this position as QA Specialist we are looking for a candidate who recognizes him- or herself in the following profile:

  • BSc or MSc degree in Chemistry, Pharmacy, Biology, Microbiology,or other relevant scientific area
  • Minimum 3+ years QA experience in a Pharmaceutical manufacturing environment
  • Knowledge of international and local quality system and compliance legislations and standards
  • Ability to use Quality Risk Management tools.
  • Troubleshooting and issues resolution skills and project management expertise

What do we offer

  • A contract for 12 months at CheckMark, with the possibility of an extension
  • Salary indication from €4000,- gross per month based on a full-time position
  • Full-time position, where 32 hours a week is negotiable
  • Dayshift

Where will you work

An international pharmaceutical company in Deventer. You will be part of the Operations Quality and Compliance department, which has a global focus.

More information

Ref.nr: 8146
Het is niet meer mogelijk om te solliciteren op deze vacature.