Senior Quality Investigator – QC & Data Integrity (80-100%)

Ophtapharm AG; Hettlingen; On-site; CHF 110,000 - 140,000; Full time

Benefits offered by this job

Pension benefits

Free parking

Public transport access

Job summary

Ophtapharm AG in Switzerland seeks a Senior Quality Investigator to lead QC OOS, OOT and Data Integrity investigations in a GMP environment. You will review lab data, audit trails and analyst practices, while driving QE and Veeva governance and providing training to investigators.

The role emphasizes analytical rigor and governance orientation, with collaboration across QA, Manufacturing and Regulatory Affairs.

Qualifications

• Degree in Analytical Chemistry, Pharmacy, Microbiology or related field.
• At least 5 years GMP experience in a pharmaceutical laboratory or QA environment.
• Experience in OOS/OOT and Data Integrity investigations.
• Strong knowledge of electronic quality systems (Veeva) and ALCOA+ principles.

Responsibilities

• Lead and drive complex QC OOS, OOT and Data Integrity investigations.
• Review laboratory data, audit trails and analyst practices to ensure scientifically sound conclusions.
• Own QE and Veeva portfolio governance and ensure timely execution and escalation.
• Review and approve investigations and coach investigators on quality and consistency.
• Monitor investigation trends and provide meaningful reporting to support quality improvements.

Skills

Analytical mindset

Governance

Education

Analytical Chemistry degree

Pharmacy degree

Microbiology degree

Tools

Veeva

Excel

Power BI

Job description

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.

Senior Quality Investigator – QC & Data Integrity (80-100%)

The Quality Investigations team plays a key role in ensuring product quality and compliance in a sterile GMP environment. Working closely with QA, Manufacturing and Regulatory Affairs, the team drives investigations, identifies root causes and supports sustainable quality improvements.

To support the ongoing development of our Quality Investigations team, we are looking for an analyticaland governance-oriented professional to join us as Senior Quality Investigator – QC & Data Integrity (80–100%), starting immediately or by mutual agreement.

Your Role

• Lead and drive complex QC OOS, OOT and Data Integrity investigations.
• Review laboratory data, audit trails and analyst practices to ensure scientifically sound conclusions.
• Own QE and Veeva portfolio governance and ensure timely execution and escalation.
• Review and approve investigations and coach investigators on quality and consistency.
• Monitor investigation trends and provide meaningful reporting to support quality improvements.

Your Profile

• Degree in Analytical Chemistry, Pharmacy, Microbiology or a related scientific discipline.
• At least 5 years of GMP experience in a pharmaceutical laboratory or QA environment, including OOS/OOT and Data Integrity investigations.
• Experience in aseptic manufacturing or sterile GMP operations.
• Strong knowledge of analytical methods, audit trails, ALCOA+ principles and electronic quality systems (e.g. Veeva).
• Fluent in English; German and data analysis skills (Excel, Power BI) are an advantage.

What you can expect

• A central role improving the scientific quality and operational control of Ophtapharm’s investigation portfolio.
• Ownership of complex laboratory and Data Integrity investigations, with visible responsibility for QE/Veeva governance.
• The opportunity to build reliable portfolio reporting and strengthen investigator capability across functions.
• Close collaboration with QA, QC, Manufacturing, IT, Regulatory Affairs and senior quality leadership.
• Attractive employment conditions, including pension benefits, free parking and convenient public transport access.

Do you have any questions?

Our HR team is happy to assist you. Tel: [phone].