The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

The site in Visp, Switzerland is growing and for our Bioconjugates organization, we are currently looking for MSAT Process Validation Specialist (80-100%). In this role, you will be responsible for manufacturing process validation in the biopharmaceutical plants, including process characterization, validation activities at scale and Product Quality Reviews (PQRs). Are you ready to join this outstanding team? Apply now!

What you’ll get:

• An agile career and dynamic working culture

• A highly collaborative environment that fosters teamwork and inclusion

• A range of professional development programs to grow your skills and career

• An ethical workplace where tasks are carried out in accordance to the relevant procedures

• Compensation programs that recognize high performance

What you'll do:

• Prepare validation documents (study design / writing protocols and reports) according to Lonza procedure and in compliance with regulatory guidance.

• Own the process validation including communication with customers.

• Review and approving of process characterization documents.

• Responsible for the validation assessment on changes and deviations (approval of deviation and changes).

• Prepare and maintain a documented continued process verification plan.

• Authoring, a ssessing and approving of PQRs

What we're looking for:

• Master or Ph.D in Chemistry, Biotechnology, Life Sciences or related field, or equivalent experience

• Experience in project management, preferable in MSAT, Operation, Quality and Compliance.

• Experience in interaction with different teams within an organization and with regulatory agencies (Swissmedic, FDA etc.) would be an advantage.

• Ability to work on different tasks simultaneously and in a timely manner.

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.