Ophtapharm AG is an FDA/EU-GMP certified manufacturer in the pharmaceutical sector (ophthalmic products). At our production site in Hettlingen near Winterthur, high-quality products such as eye drops, ointments, and gels are aseptically produced, filled, and packaged for international markets.
You play a central role in ensuring quality and compliance for sterile ophthalmic products in a highly regulated GMP environment. Acting as a key interface across QA, Manufacturing, and Regulatory Affairs, you drive investigations and ensure sustainable solutions.
We are looking for an analytical and solution-oriented professional to join our team as Quality Investigations Lead (80–100%) near Winterthur.
Quality Investigations Lead (Sterile Products) – 80-100%
Your Role
- Lead and coordinate deviation and complaint investigations in a sterile GMP environment
- Identify root causes and drive effective, sustainable CAPAs
- Ensure timely, compliant documentation of all investigations
- Collaborate cross-functionally with QA, Manufacturing, and Regulatory Affairs
- Monitor trends and improve investigation processes and quality standards
Your Profile
- Degree in Life Sciences, Pharmacy, Chemistry, or a related field
- 5+ years’ experience in quality investigations within sterile GMP manufacturing
- Strong knowledge of GMP and FDA requirements for sterile products
- Proven expertise in root cause analysis and CAPA management
- Fluent in English and German
What you can expect
- Real ownership and the opportunity to shape how investigations are run and improved
- A company on a journey where change is real and your impact is visible
- Direct access to decision-makers and cross-functional influence
- A committed team that takes responsibility and works through challenges together
- Flexible working conditions and a solid, dependable employment package
For recruitment agencies:Thank you for your interest. We are not engaging external support for this role.
Arbeitsort
Ophtapharm AG
Riethofstrasse 1
8442
Hettlingen CH