Teva Pharmaceutical Industries is looking for a Quality Control Analyst II to join our team. In this role, you will execute our stability program and manage sample staging in stability chambers while ensuring GxP compliance. At Teva, our mission is to make good health more affordable and accessible, and we are bonded across nearly 60 countries by a diverse and rich variety of nationalities and backgrounds.
What You'll Do
- Execute stability program and sample staging in stability chambers.
- Train and mentor new Quality Control Analysts.
- Perform analyses, inspection, and tests of products, raw materials, in-process materials, release test samples, stability samples, packaging materials, and finished products.
- Check and control record documentation.
- Support investigations and implement improvement projects.
- Conduct non-conformance tests of manufactured, packaged, or tested product.
- Prepare and monitor quality statistics and reports.
What We're Looking For
- Bachelor's degree in chemistry, pharmaceutical science, or biology.
- 3+ years of quality experience in pharmaceutical or biotech.
- GxP certification (Internal, based on site and job-specific training system).
- Completion of quality and work procedures trainings.
- Ability to train others and work independently with discretion and judgment.
- Knowledge and experience in own discipline, building knowledge of the organization, processes, and customers.
- Ability to solve a range of straightforward problems and analyze possible solutions using standard procedures.
Nice to Have
- Master's Degree.
Teva Pharmaceuticals is committed to equal opportunity in employment without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status.
