Senior QA Qualification Specialist (Manager) 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.
- Location: the actual location of this job is in Visp, Switzerland.
- Relocation assistance is available for eligible candidates and their families, if needed.
- In this role you will own all quality related responsibilities for the daily qualification activities of facilities/equipment/systems related to the cGMP manufacture of pharmaceutical drug products (DP). What you will get:
- An agile career and a dynamic work culture.
- in Visp: https://bit.ly/3wjkoFi What you will do:
- Compile, review and release Qualification Documents (URS, Qualification Plan & Report, DQ/IQ/OQ/PQ Reports, etc.)
Main responsibilities
- In this role you will own all quality related responsibilities for the daily qualification activities of facilities/equipment/systems related to the cGMP manufacture of pharmaceutical drug products (DP). 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.
- Our full list of tailored local benefits can be found below.
What the company offers
- in Visp: https://bit.ly/3wjkoFi What you will do:
- Compile, review and release Qualification Documents (URS, Qualification Plan & Report, DQ/IQ/OQ/PQ Reports, etc.)
- Perform assessments and approvals of technical change requests and their relevance to the qualified state of equipment, utilities and systems
- Support and approve quality risk analysis (e.g. FMEA)
- Ensure relevant deviations are appropriately investigated and recorded in Deviation Reports
- Responsible to drive CAPA and Effectiveness Checks items to completion and timely closing
- Confirm the qualified state of facilities, equipment and systems during their life cycles by ensuring periodic reviews or periodic re-qualifications
- Ensure that documents are correct and adhere to SOPs and customer’s requirement
- Represent specific areas as Subject Matter Expert (SME) and provide guidance’s and recommendations in these areas to internal customers
- Lead or support specific projects in his area of SME to develop further the quality standards
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
- In this role you will own all quality related responsibilities for the daily qualification activities of facilities/equipment/systems related to the cGMP manufacture of pharmaceutical drug products (DP).
- Benefits in Visp: https://bit.ly/3wjkoFi
- Support and approve quality risk analysis (e.g.
- Train and mentor junior employees to better accomplish and perform in their duties as quality professionals What we are looking for:
- Strong individual contributor and decision maker
Notes and original content
- What you will get:
- What you will do:
- Train and mentor junior employees to better accomplish and perform in their duties as quality professionals
- What we are looking for:
- About Lonza
Questions about this listing
What salary does Lonza offer for this role?
Lonza lists CHF 83'500 - 126'500 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.
