Contamination Control and Cleaning, Senior QA Specialist 80-100% (f/m/d)

About Us

Today, we are proud to be a global leader in life sciences, operating across three continents. While our work involves science, we believe there is no magic formula to how we do it. Our most valuable asset is our talented team, who collaborate to develop innovative ideas that empower businesses to enhance lives. We encourage our employees to take ownership of their careers, with every idea—big and small—contributing to a better world. This is the kind of impactful work we strive to be a part of.

Our Growth in Visp

As our site in Visp, Switzerland continues to expand, we are seeking a dedicated Senior QA Specialist for our Biologics Quality organization. This role is integral to our QA Operations, focusing on Large Scale Mammalian manufacturing within our unique Ibex® Solutions framework. The successful candidate will collaborate directly with key stakeholders in the Contamination Prevention and Control group, MSAT, Operations, and Hygiene.

What Awaits You

• An agile career path within a dynamic working culture.
• An inclusive and ethical workplace environment.
• Compensation programs that acknowledge high performance.
• A variety of benefits tailored to your role and location.

Your Responsibilities

• Review and approve routine cleaning-related documents, including cleaning plans and reports.
• Investigate and document all cleaning-related deviations and customer product complaints.
• Collaborate closely with the Contamination Prevention and Control group, MSAT, and Operations.
• Approve local procedures to ensure compliance with the site’s Contamination Control Strategy.
• Provide Quality oversight on various CCS topics limited to the facility.
• Review and finalize records such as Standard Operating Procedures (SOPs), Master Manufacturing Batch Records, and Testing Protocols.

Your Profile

• Bachelor's or Master's degree in Microbiology, Chemistry, Biotechnology, or a related field.
• Significant experience in contamination control within the GMP-regulated pharmaceutical industry, particularly in a QA role in a Large Scale stainless steel facility.
• General knowledge of manufacturing processes, cleaning procedures, and analytical methods.
• Preferred experience with GMP management systems like TrackWise, SAP, Syncade, and Microsoft Office.
• Desirable experience interacting with Health Authorities such as Swissmedic and FDA.
• Business fluency in English is required; knowledge of German is a plus.

Our Commitment

Every day, our products and services positively impact millions of lives. We recognize that this great privilege carries an equally great responsibility. Our approach to achieving business results is as vital as the results themselves. We prioritize the respect and protection of our people and our environment, with a firm belief that success is only meaningful when attained ethically.

Join Us

Individuals are drawn to our mission for the challenge and creativity of tackling complex problems and pioneering new ideas in life sciences. In return, we offer the profound satisfaction that accompanies making a significant difference in the lives of people around the world.