Intern - QA Specialist Batch Record Review — Lonza
- Location
- CH
- Contract
- full-time
- Posted
- 61 days ago
Role overview
The Batch Record Review Intern supports the Quality Assurance team (QA OPS) by assisting in the review, verification, and organization of electronic GMP manufacturing documentation. This role provides hands‑on exposure to regulated industry practices, including data integrity, documentation control, and compliance with internal procedures and regulatory standards. The intern will work closely with QA specialists and cross‑functional teams to ensure timely and accurate batch record processing.
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.
- An agile career and a dynamic work culture.
- Compensation programs that recognize high performance.
- Review of the Executed Batch Records (e.g. cleaning logs, production documentation review, temperature reports, test procedures, raw data, logbooks)
- Review comments added to the Executed Batch Records, clarify with the operations team and evaluate with the responsible QA Manager
- Support the initiation of deviations and investigations for Batch Record review related observations
- Bachelor degree or relevant work/ internship experience in Biology, Chemistry, Biotechnology, Life Science or other related field
- Previous experience in GMP regulated pharmaceutical / API industry is an advantage
- Ability to identify non-compliance and gaps from 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.
Company and context
- The Batch Record Review Intern supports the Quality Assurance team (QA OPS) by assisting in the review, verification, and organization of electronic GMP manufacturing documentation.
- This role provides hands‑on exposure to regulated industry practices, including data integrity, documentation control, and compliance with internal procedures and regulatory standards.
- The intern will work closely with QA specialists and cross‑functional teams to ensure timely and accurate batch record processing.
- 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. What you will do:
- Review of the Executed Batch Records (e.g. cleaning logs, production documentation review, temperature reports, test procedures, raw data, logbooks)
- Review comments added to the Executed Batch Records, clarify with the operations team and evaluate with the responsible QA Manager
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.
- Compensation programs that recognize high performance.
- Support the initiation of deviations and investigations for Batch Record review related observations What we are looking for:
- German: Good to have.
Notes and original content
- What you will get:
- What you will do:
- Support the initiation of deviations and investigations for Batch Record review related observations
- What we are looking for:
- About Lonza
Questions about this listing
What salary does Lonza offer for this role?
Lonza lists CHF 49'500 - 66'500 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 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.
