(Senior) QA Expert Compliance 80-100% — Lonza
- Location
- CH
- Contract
- full-time
- Posted
- 35 days ago
Role overview
The actual location of this job is in Stein, AG, Switzerland.
Relocation assistance is available for eligible candidates and their families, if needed.
Join Lonza AG as a (Senior) QA Expert Compliance, partnering with senior stakeholders to ensure robust Quality Management Systems, GMP compliance, and training oversight across various systems and document management platforms.
- The actual location of this job is in Stein, AG, Switzerland.
- Relocation assistance is available for eligible candidates and their families, if needed.
- This highly dynamic, transformation-driven role includes change review board responsibilities and cross-functional interface management, ideal for a resilient, curious professional who thrives on shifting priorities, works independently, and drives quality excellence in a fast-growing sterile manufacturing environment.
- Check out Your Career in Drug Product Services at Lonza!
Main responsibilities
- This highly dynamic, transformation-driven role includes change review board responsibilities and cross-functional interface management, ideal for a resilient, curious professional who thrives on shifting priorities, works independently, and drives quality excellence in a fast-growing sterile manufacturing environment.
- Check out Your Career in Drug Product Services at Lonza!
- 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 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 What you will do:
- Lead and participate in the development, implementation, and maintenance of the Quality Management System (QMS) in accordance with cGMP, ISO, and other applicable regulatory requirements.
Application process
- now.
- Lonza is a global leader in pharma and biotech manufacturing.
- The company operates major production facilities in Visp (Valais), Basel, and Stein (Aargau), Switzerland.
Additional details
- Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
- The full list of our global benefits can be found here: https://www.lonza.com/careers/benefits
- Stay abreast of evolving global regulations and industry trends related to quality and compliance, proactively assessing their impact on Lonza's operations What we are looking for:
- Systems know-how: Hands-on experience with document management and quality systems (e.g., TrackWise, MasterControl, DMS, Cornerstone); Experience with Veeva is highly beneficial
- Mindset & skills: Analytical, decisive, and resilient professional who communicates complex topics clearly, works independently, and thrives in fast-paced, changing environments
Notes and original content
- What you will get:
- What you will do:
- Stay abreast of evolving global regulations and industry trends related to quality and compliance, proactively assessing their impact on Lonza's operations
- What we are looking for:
- Systems know-how: Hands-on experience with document management and quality systems (e.g., TrackWise, MasterControl, DMS, Cornerstone);
- Experience with Veeva is highly beneficial
- About Lonza
Questions about this listing
What salary does Lonza offer for this role?
Lonza lists CHF 85'500 - 129'500 gross per year for this position in CH. This is the salary published in the original listing (or, when the employer omits a figure, a realistic estimate for the role and sector) — the calculator on this site converts it to 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.
