Senior Scientist QC

Lonza Group Ltd.; Oberwallis; Vor Ort; Vertraulich; Vollzeit

Zusammenfassung

Lonza Group Ltd. in Visp, Switzerland is seeking a Quality Compliance professional to ensure GMP-compliant QC processes and robust regulatory readiness. You will translate regulatory requirements into practical laboratory guidance, lead deviation investigations, CAPAs, and drive cross-functional improvements.

The role emphasizes strong technical writing, data integrity, and collaboration with QC, QA, Manufacturing, and Technical Operations, with English as a must and German as a plus.

Qualifikationen

• Master’s or doctoral degree in life sciences, chemistry, pharmacy, biotechnology, or a related field; or a bachelor’s degree with extensive relevant experience.
• At least two to three years of experience in a GMP-regulated pharmaceutical or biotechnology environment.
• Practical knowledge of Swissmedic, FDA, EU GMP requirements, EMA expectations, ICH guidelines, and the US and European Pharmacopoeias.
• Experience working with regulatory authorities and supporting inspections.
• Extensive experience writing and leading deviation investigations, identifying root causes, and developing CAPAs.
• Experience identifying compliance gaps, applying quality risk management, and leading improvement projects across teams.
• Clear technical writing, analytical, and communication skills, with the ability to build agreement and independently complete initiatives.
• Clear communication skills in English with a collaborative working style; German is an advantage.

Aufgaben

• Assess QC processes against Good Manufacturing Practice (GMP) requirements, identify compliance risks, and implement lasting improvements.
• Translate regulatory requirements into practical guidance on laboratory processes, data integrity, and documentation.
• Support inspection readiness and regulatory inspections, advising QC teams on compliance questions.
• Lead and write deviation investigations, identify root causes, and develop effective corrective and preventive actions (CAPAs).
• Review and approve compliance documentation and quality records to ensure they meet regulatory expectations.
• Lead improvement projects with QC, Quality Assurance, Manufacturing, and Technical Operations, using quality metrics and trends to address recurring issues.
• Coach colleagues on GMP, quality risk management, and inspection readiness, encouraging shared responsibility for quality.

Kenntnisse

Technical writing

Analytical thinking

Communication

Team collaboration

English proficiency

Ausbildung

Master's or PhD in life sciences / chemistry / pharmacy / biotechnology

Jobbeschreibung

Location

This position is based in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families.

What you will get

• Opportunities to develop your career and lead meaningful quality improvements.
• An inclusive and ethical workplace where your ideas are valued.
• A competitive salary and compensation programs that recognize high performance.
• A range of lifestyle, family, and leisure benefits.
• Explore our benefits in Visp.

What you will do

• Assess QC processes against Good Manufacturing Practice (GMP) requirements, identify compliance risks, and implement lasting improvements.
• Translate regulatory requirements into practical guidance on laboratory processes, data integrity, and documentation.
• Support inspection readiness and regulatory inspections, advising QC teams on compliance questions.
• Lead and write deviation investigations, identify root causes, and develop effective corrective and preventive actions (CAPAs).
• Review and approve compliance documentation and quality records to ensure they meet regulatory expectations.
• Lead improvement projects with QC, Quality Assurance, Manufacturing, and Technical Operations, using quality metrics and trends to address recurring issues.
• Coach colleagues on GMP, quality risk management, and inspection readiness, encouraging shared responsibility for quality.

What we are looking for

• A master’s or doctoral degree in life sciences, chemistry, pharmacy, biotechnology, or a related field; or a bachelor’s degree with extensive relevant experience.
• At least two to three years of experience in a GMP-regulated pharmaceutical or biotechnology environment.
• Practical knowledge of Swissmedic, FDA, and EU GMP requirements, EMA expectations, ICH guidelines, and the US and European Pharmacopoeias.
• Experience working with regulatory authorities and supporting inspections.
• Extensive experience writing and leading deviation investigations, identifying root causes, and developing CAPAs.
• Experience identifying compliance gaps, applying quality risk management, and leading improvement projects across teams.
• Clear technical writing, analytical, and communication skills, with the ability to build agreement, constructively question processes, and independently complete initiatives.
• Clear communication skills in English with a collaborative working style.
• German language is an advantage.

About Lonza

At Lonza, our people are our greatest strength. Our teams work together to manufacture the medicines of tomorrow. Collaboration, Accountability, Excellence, Passion, and Integrity guide how we work, and everyone’s ideas can help improve lives. We value diverse backgrounds and perspectives and are committed to creating an inclusive environment for all employees.

Ready to shape the future of life sciences?