Job Title: QA Reviewer
Job Location (Short): Amsterdam, NLD, 1105 BJ

Posting Start Date: 6/12/26

Do you want to take responsibility and make a difference with your work? With your expertise, we can achieve great goals togehter. We are WACKER - Reliable. Determined. Ambitious. As one of the world's most research-intensive chemical companies, we've been making countless products that are an integral part of your everyday life possible for over 100 years. From vegan food to resource-efficient buildings to solar cells, we develop sustainable solutions that change the future.

Wacker Biotech, as part of WACKER, is a leading global biotechnology organization specializing in the production of biopharmaceuticals. The company has outstanding technologies for the rapid, efficient and thus cost-effective production of therapeutic proteins for clinical and commercial supply. Currently it is the biggest dedicated microbial Contract Development & Manufacturing Organization (CDMO) in the world. lts four dedicated and fast-growing production sites are currently based in Germany (Halle and Jena), The Netherlands (Amsterdam) and The United States (San Diego, CA). At our Amsterdam-based center Wacker Biotech B.V. focuses on the GMPcompliant microbial based production of recombinant proteins, vaccines and live microbials as drug substance and drug product.

To strengthen our team in Amsterdam,
we are looking for you as a QA Reviewer

For more detailed information please feel free to contact Mrs. Peggy Engels, tel. 0031 (0)20 7503 675.
Please note: Agency acquisition to this vacancy is not appreciated.

The QA Reviewer is the spider in the web, responsible for all the documentation to and from the Quality Assurance Department. You will also be involved in monitoring the progress and will act as the point of contact for all the operational tasks around all the concerning departments.

Job responsbilities:
Review and approval of batch manufacturing;
Review and approval of QC testing records;
Prepare the lot package for batch disposition;
Support the back office during client audits.

Qualifications required:
HBO or BSc degree in Life Sciences Chemistry, (Micro)Biology or Pharmaceutical Sciences;
At least one year working experience in a GMP environment;
Computer fluency in MS Office, e.g. Word, Excel, PowerPoint. Knowledge of TrackWise is a plus;
Profound knowledge of Dutch and English language, verbal and written;
Excellent verbal and written communication skills;
Organizationally and planning skills;
Accurate and eye for detail;
Ability to work with tight deadlines and handle multiple tasks;
Hands-on, quality orientated, problem solving, proactive behaviour, flexibility;
You reside in and are eligible to work in The Netherlands (valid work permit).

What do we offer?

Employment: A challenging and international position in a professional and informal working environment
Compensation: Attractive salary, holiday allowance, home-office travel allowance, participation in the company's success, subsidized pension plan
Work-life balance: Flexible working hours (where possible), 30 days of vacation
Versatile development opportunities: Support for professional development, access to online learning platform GoodHabitz

As an international company, we welcome the diversity of people. We consciously promote equal opportunities and a diverse, inclusive culture in our teams - this is what makes us successful.

We look forward to receiving your application!

Reference Code: 31167

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