QA Specialist

at  Lonza

Title: QA Specialist
Location: Visp
Hybrid working pattern
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.

KEY REQUIREMENTS:

• Degree in Biology, Chemistry, Biotechnology, Life Science or other related field or experience in the field of pharmaceutical industry
• Previous experience in GMP regulated pharmaceutical industry is an advantage
• English fluency and German good command is an advantage
• Ability to prioritize and manage work to critical project timelines in a fast-paced environment.
• Excellent verbal, written and interpersonal communications skills
  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

THE ROLE:

Currently we are looking for a QA Specialist to join multinational QA Operations team in the Bioconjugates Business Unit at the Visp site. You will work closely with various quality and operational functions to ensure GMP-compliant manufacturing and documentation. You will also get exciting insights into our IBEX environment and can develop into QA project management role in perspective.

KEY RESPONSIBILITIES:

• Review executed electronic and/or manufacturing protocol for compliance to GMP. Support implementation/ revision of manufacturing protocols for GMP manufacturing
• Ensure that internal/ external GMP standards and regulatory requirements related to process validations are adhered to in projects.
• Participate in cross-functional investigations to determine impact to product quality and the definition of associated corrective measures
• Support deviations and change management in the context of GMP manufacturing
• Prepare disposition package according to internal and customer requirements
• Participate and support regulatory inspections and customer audits. Represent the Quality Unit in cross-functional teams