Senior QA Specialist, QA Analytics 80-100% (f/m/d) — Lonza
- Location
- Visp
- Contract
- full-time
- Posted
- Yesterday
Role overview
Location: The actual location of this job is in Visp, Switzerland.
Relocation assistance is available for eligible candidates and their families, if needed.
As a Senior Quality Assurance (QA) Specialist (f/m/d) for Analytics, you will ensure the Quality oversight on GMP-relevant activities carried out by the Quality Control and Analytical Development (AD) departments, also for externally formulated drugs (external DP final samples).
- Location: The actual location of this job is in Visp, Switzerland.
- Relocation assistance is available for eligible candidates and their families, if needed.
- in Visp: https://bit.ly/3wjkoFi What you will do:
- Represent the QA concerns to the Quality Control (QC) and Analytical Development (AD) departments and ensures that GMP requirements are met and SOPs are followed
What the company offers
- in Visp: https://bit.ly/3wjkoFi What you will do:
- Represent the QA concerns to the Quality Control (QC) and Analytical Development (AD) departments and ensures that GMP requirements are met and SOPs are followed
- Control and release of GMP-relevant documents of the QC / AD
- Review and approval of SOPs, analytical test methods, method transfer protocols/reports, method validation protocols/reports, and OOX gLIMS investigations issued be the QC/AD departments
- QA supervision of OOX events during investigation in QC/AD departments: Review and approve Out –of-Specifications/-Expectations/-Trend results
- Write or revise SOPs in your area of expertise and be the owner of these documents
- Ensure compliance with GMP in the areas of stability testing and reference standards
- Cooperation, review and approval of deviations (DRs), Investigations (INVs), changes (CRs), and CAPAs within analytics (QC) Support inspection/audit
- Ensure compliance of Lonza QC test methods with Pharmacopoeias where applicable. What we are looking for:
- Academic degree in Chemistry/Biotechnology/Life Sciences or related field
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
- Moreover, as a Quality and Compliance representative, you are a key member of cross-functional project teams.
- An agile career and dynamic working culture An inclusive and ethical workplace
- Compensation programs that recognize high performance A variety of benefits dependant on role and location
- Benefits in Visp: https://bit.ly/3wjkoFi
- Cooperation, review and approval of deviations (DRs), Investigations (INVs), changes (CRs), and CAPAs within analytics (QC) Support inspection/audit
- Ensure compliance of Lonza QC test methods with Pharmacopoeias where applicable. What we are looking for:
- Strong background in cGMP regulations; incl. USP, European- and Japanese Pharmacopoeia
- German language knowledge is advantageous.
Notes and original content
- What you will get:
- An agile career and dynamic working culture
- An inclusive and ethical workplace
- Compensation programs that recognize high performance
- A variety of benefits dependant on role and location
- What you will do:
- Cooperation, review and approval of deviations (DRs), Investigations (INVs), changes (CRs), and CAPAs within analytics (QC)
- Support inspection/audit
- Ensure compliance of Lonza QC test methods with Pharmacopoeias where applicable.
- What we are looking for:
Questions about this listing
What salary does Lonza offer for this role?
Lonza lists CHF 124'500 - 207'000 gross per year for this position in Visp. 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 Valais?
EU/EFTA residents living in the border zone of the country adjoining Canton Valais 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 Valais'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.
