Senior QA Expert, Manufacturing 80-100%

Lonza Group Ltd.; Stein (AR); Hybrid; Vertraulich; Vollzeit

Benefits dieser Stelle

Competitive salary

Lifestyle benefits

Global benefits

Zusammenfassung

Lonza Group Ltd. in Stein (AR), Switzerland, is seeking an experienced QA professional to provide shopfloor oversight for GMP-compliant manufacturing within a dynamic growth project.

You will review GMP documentation, support start-up activities, and partner with manufacturing teams to drive aseptic readiness. The role requires hands-on shopfloor collaboration, strong GMP knowledge, and fluency in German and English.

Qualifikationen

• Proven experience in the pharmaceutical industry within a GMP-regulated environment.
• Experience in quality oversight, management of deviations, CAPAs, and investigations.
• Fluent German and fluent English communication skills.
• Willingness to spend significant time on the manufacturing shopfloor, including full aseptic gowning.
• Bachelor's, Master's or PhD in Life Sciences, Pharmacy, Chemistry, Biology, Biotechnology, or related field.

Aufgaben

• Provide QA oversight for shopfloor manufacturing activities within an exciting growth project, ensuring GMP compliance and operational readiness.
• Review and approve SOPs, work instructions, and GMP documentation to support start-up and sustainable operations.
• Partner with Manufacturing teams to drive aseptic process readiness and training support for APS and media fill activities.
• Lead and coordinate quality events by reviewing deviations, CAPAs, investigations, and related quality records.
• Act as the Quality representative during project discussions, audits, and inspections, communicating the quality oversight strategy.

Kenntnisse

QA oversight

GMP

Deviations & CAPAs

SOP review

Aseptic process

German language

English language

Shopfloor familiarity

Ausbildung

Bachelor's/Master's/PhD in Life Sciences or related

Tools

Documentation systems

Jobbeschreibung

The actual location of this job is in Stein, AG, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. Be part of an exciting project-phase team driving operational readiness from a Quality perspective, ensuring robust documentation, SOP compliance, aseptic process preparedness, and effective deviation and CAPA oversight. This role offers the chance to influence how future manufacturing operations are established, making it an ideal step for professionals looking to transition from production into Quality Assurance. This role is primarily based on site. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. We offer flexibility to work remotely for no more than 20% of your time. Requests are considered on a case-by-case basis, in line with business needs.

What you will get:

• An agile career and a dynamic work culture.
• An inclusive and ethical workplace.
• Compensation programs that recognize high performance.
• In addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits.
• The full list of our global benefits can be found here: https://www.lonza.com/careers/benefits
• Our local benefits: 3cf206339e0e4e41a77e8c806138c2b5

What you will do:

• Provide QA oversight for shopfloor manufacturing activities within an exciting growth project, ensuring compliance with GMP requirements and operational readiness.
• Review and approve SOPs, work instructions, and other GMP documentation to support successful start-up and sustainable manufacturing operations.
• Partner with Manufacturing teams to drive aseptic process readiness, including preparation, training support, and execution readiness for APS and future media fill activities.
• Lead and coordinate quality events by reviewing and approving deviations, CAPAs, investigations, and related quality records, ensuring timely and effective resolution.
• Act as the Quality representative during project discussions, audits, and inspections, clearly communicating the quality oversight strategy and supporting inspection readiness.

What we are looking for:

• Proven experience in the pharmaceutical industry within a GMP-regulated environment, with expertise in sterile and/or drug product manufacturing is a must
• Experience in quality oversight, management of deviations, CAPAs, and investigations.
• Fluent German and fluent English communication skills are essential, enabling effective collaboration with shopfloor operators, cross-functional teams, customers, and regulatory authorities.
• Willingness to spend significant time on the manufacturing shopfloor, including working in full aseptic gowning, and a hands-on approach to supporting operations and driving quality excellence is a must
• Bachelor's, Master's, or PhD degree in Life Sciences, Pharmacy, Chemistry, Biology, Biotechnology, or a related field, combined with a pragmatic, solution-oriented mindset, strong stakeholder management skills, and the agility to thrive in a dynamic greenfield project environment.
• Experience supporting regulatory and customer audits and inspections is an advantage.

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 for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.