QA Documentation Specialist 2

Are you a quality-focused professional looking to safeguard the integrity of high-impact life sciences manufacturing? Join our team in Visp as a Quality Batch Record Reviewer, where your attention to detail ensures every medicine meets the highest compliance and safety standards before release.

This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.

What you will get:

• An agile career and dynamic working culture.

• An inclusive and ethical workplace.

• Competitive hourly rate / compensation package.

Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge.

What you will do:

• Perform meticulous paper-based review of executed batch records within defined timeframes to support timely batch release.

• Serve as a critical compliance line of defense, ensuring production strictly follows standard operating procedures (SOPs) and Good Manufacturing Practice (GMP) regulations.

• Track, report, and monitor batch record review metrics to maintain on-time release milestones.

• Partner closely with the Operations team on site, raising and resolving observations and discrepancies in a timely and collaborative manner.

• Identify continuous improvement opportunities within documentation and review workflows.

• Contribute directly to the overall quality culture and operational excellence of the Visp site.

What we are looking for:

• Minimum 2 years of professional experience within a GMP production or quality assurance environment.

• Prior experience in paper-based batch record review is highly preferred.

• Educational background in Pharmaceutical Technology, Biotechnology, Chemistry, Pharmacy, or equivalent scientific discipline.

• Business fluent German language skills are mandatory; proficiency in English is preferred.

• Exceptional attention to detail and strong capability to work independently.

• Great communication skills to effectively collaborate with Operations and cross-functional teams.

About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment.

As Lonza’s talent acquisition partner, please note, Randstad is responsible for the engagement and contracting of this contingent role.

Ready to play your part in shaping the future of life sciences? Apply now.