Production Quality Specialist

☞ Randstad

View: 142

Update day: 24-04-2024

Location: Visp Valais VS

Category: Pharmaceutical / Chemical / Biotech

Industry: Ressources humaines et recrutement

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Job content

Jobdescription

We are looking for a Production Quality Specialist (m/f/d) for Lonza AG (100%). This is a temporary position for 6 months with an opportunity to extend.

Today, Lonza is a global leader in life sciences operating across three continents. While Lonza works in science, there’s no magic formula to how they do it. Their greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, they let their people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work Lonza wants to be part of.

Key responsibilities

Is accountable to manage and conduct the review 1 and/or 2 of the executed Batch Record (EBRs) based on the criteria listed in the SOP CHVI-413406 Attachment A.

Ensures that all control parameters for intermediates and biological drug substances are checked for compliance with defined specifications before a batch is dispatched.

Ensure that all open issues within EBRs explained and closed

Is responsible to identify GMP events requiring a Deviation

Open EBR review related Deviations and support CAPAs

Functie-eisen

Degree in the area of Chemistry, Chemical Engineering, Biotechnology, Bioengineering or related disciplines

Work experience as QC technician or manufacturing operator (e.g. production biotechnologist, manufacturing specialist)

Knowledge of English and German
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Deadline: 08-06-2024

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