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Pharmaceutical Quality Associate

vor 1 Woche


Solothurn, Solothurn, Schweiz TN Switzerland Vollzeit

TN Switzerland is seeking an experienced Pharmaceutical Quality Associate to join our Integrated Downstream Quality Operations team. As a QA Associate III, you will be responsible for ensuring product safety, efficacy, and purity through comprehensive quality assurance practices.

The successful candidate will have a Bachelor's or Master's degree in Chemical Engineering, Bioengineering, Biotechnology, Bioprocessing, Pharmaceutical Sciences, or related fields. A minimum of experience in pharmaceutical or biotech manufacturing environments is required.

Your key responsibilities will include:

  • Executing QA activities related to downstream operations and GMP manufacturing
  • Reviewing and approving GMP Engineering and Manufacturing documents, including procedures, work instructions, CAPAs, deviations, and change control
  • Collaborating with cross-functional teams during deviation management and investigations

We are looking for a highly skilled individual with strong presentation, organizational, and writing skills, as well as ability to work autonomously and collaboratively with cross-functional teams.