Process Validation Specialist 60-100%

• Preparing, executing, and documenting validation protocols and reports.

• Supporting Continued Process Verification (CPV) and Product Quality Reviews (PQR) throughout the product lifecycle.

• Assessing the validation impact of deviations, investigations, and change requests.

• Acting as the Process Validation representative in customer meetings and cross-functional projects.

• Serving as the subject matter expert during customer audits and regulatory inspections.

• Ensuring compliance with internal procedures, cGMP requirements, and relevant regulatory guidelines (ICH, FDA, EMA, PIC/S).

Key requirements:

• PhD or Master's degree in Chemistry, Chemical Engineering, or a related scientific discipline.

• Experience in pharmaceutical or chemical manufacturing; GMP experience is highly preferred.

• Strong analytical and problem-solving skills.

• Ability to work effectively in multidisciplinary teams.

• Strong communication and stakeholder management skills.

• Ability to manage multiple priorities in a fast-paced project environment.

• Fluent English language skills, both written and spoken. German is a plus.

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.