QA Manager — Lonza
- Location
- Visp
- Contract
- full-time
- Posted
- 3 days ago
Role overview
The actual location of this job is in Stein, Switzerland.
Relocation assistance is available for eligible candidates and their families, if needed.
In order to support our business growth in Stein (Switzerland), we are looking for a Quality Assurance Manager with expertise in Drug Product systems qualification, QC analytical equipment qualification and CSV & Automation.
- The actual location of this job is in Stein, Switzerland.
- Relocation assistance is available for eligible candidates and their families, if needed.
- The main responsibilities are listed below, but not limited to and might be adapted depending on project priorities What you’ll get: An agile career and a dynamic work culture An inclusive and ethical workplace
- Compensation programs that recognize high performance What you will do:
Main responsibilities
- The main responsibilities are listed below, but not limited to and might be adapted depending on project priorities What you’ll get: An agile career and a dynamic work culture An inclusive and ethical workplace
- Compensation programs that recognize high performance What you will do:
- Responsible for Equipment, QC, Computerized System Validation (CSV) and Automation deliverables for new aseptic facilities, equipment and utilities related to the GMP manufacturing of drug products
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.
Company and context
- Representing Quality in the CAPEX project organization in regards to Equipment, QC, Computerized System Validation (CSV) and Automation and Automation
- Reviewing and releasing quality related to Equipment, QC, Computerized System Validation (CSV) and Automation project deliverables
- Ensuring Equipment, QC, Computerized System Validation (CSV) and Automation deliverables meet Global procedures, regulatory requirements and policies
- Being a Subject Matter Expert (SME) and providing guidance and recommendations to internal and external project stakeholders What we are looking for:
- Bachelor or Master degree in computer science, engineering, life science or related field
- Significant experience in the GMP regulated pharmaceutical industry project; preferable in a role within a Quality Unit
- Knowledgeable in commissioning and qualification of aseptic manufacturing systems and QC analytical systems, Annex 1 requirements
- Knowledgeable in CSV, Data Integrity, Automation systems and related Guidelines (21 CFR Part 11, EU GMP Annex 11, GAMP5 and the underlying principles of each)
- Experience in interaction with all kind of interfaces within the organization and with regulatory agencies (Swissmedic, FDA etc.) Sound knowledge of MES and DCS is required
- Fluency in English, German would be an advantage
Additional details
- The main responsibilities are listed below, but not limited to and might be adapted depending on project priorities An agile career and a dynamic work culture An inclusive and ethical workplace
- Compensation programs that recognize high performance
- Being a Subject Matter Expert (SME) and providing guidance and recommendations to internal and external project stakeholders What we are looking for:
- Experience in interaction with all kind of interfaces within the organization and with regulatory agencies (Swissmedic, FDA etc.) Sound knowledge of MES and DCS is required
Notes and original content
- The main responsibilities are listed below, but not limited to and might be adapted depending on project priorities
- What you’ll get:
- An agile career and a dynamic work culture
- An inclusive and ethical workplace
- What you will do:
- Being a Subject Matter Expert (SME) and providing guidance and recommendations to internal and external project stakeholders
- What we are looking for:
- Experience in interaction with all kind of interfaces within the organization and with regulatory agencies (Swissmedic, FDA etc.)
- Sound knowledge of MES and DCS is required
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 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.
