Senior QA Expert, Manufacturing 80-100% — Lonza
- Location
- Stein
- Contract
- Full-time
- Posted
- 50 days ago
Full description
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. Check out Your Career in Drug Product Services at Lonza!
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. Ready to shape the future of life sciences? Apply now.
Questions about this listing
What salary does Lonza offer for this role?
The original listing does not state a salary. Our estimate for this role and sector in Stein is CHF 123'000 - 165'500 gross per year — an estimate, not a figure communicated by Lonza. The calculator on this site converts a gross salary into your actual net take-home once cross-border tax and social contributions are applied.
Is this a full-time role, and what type of contract does Lonza offer?
This listing is a full-time position. The contract type shown here comes directly from the employer's original posting; always confirm exact hours, notice period and probation length with Lonza during the application process, since these details can vary by role even within the same contract category.
Do I need a cross-border work permit for a role in Aargau?
EU/EFTA residents living in the border zone of the country adjoining Canton Aargau can apply for a G permit; the Swiss employer files it with that canton's migration office after the contract is signed. Border-zone rules and processing times vary by neighbouring country and canton, so confirm the specifics with Aargau's cantonal migration office or with HR during the application.
How do I apply for this position at Lonza?
Use the "Apply now" button on this page — it links directly to Lonza's original listing at lonza.wd3.myworkdayjobs.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
