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Salary
≈ $94k – $234k per year (Estimated)
Location
In office (Visp)
Employment
Part-Time

Confirmed on the employer's own hiring board on Oct 14, 2026. First seen by Alion on Oct 6, 2026.

Overview
Company
Impact
Profile match
Lonza is a Swiss contract development and manufacturing organization that produces small molecules, biologics, cell and gene therapies and capsules for pharmaceutical, biotechnology and nutrition companies. Founded in 1897 and listed on the SIX Swiss Exchange, it runs manufacturing sites in Europe, the United States and Asia, including Visp in Switzerland, Portsmouth in New Hampshire and Bend in Oregon. The company is headquartered in Basel, Switzerland.

Process Validation Specialist, 60-100%

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 position as Process Validation Specialist is ideal for a scientist or engineer who enjoys combining technical expertise, GMP compliance, cross-functional collaboration, and customer interaction. The role offers significant ownership and visibility across a diverse portfolio of commercial manufacturing projects.

Key responsibilities:

  • Developing process validation strategies for commercial manufacturing processes.
  • 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.

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