MSAT - Process Engineer

Job Title:

MSAT - Process Engineer

Job Location (Short):
Amsterdam, NLD, 1105 BJ

Posting

Start Date:

6/19/26

We are WACKER – Reliable. Determined. Ambitious. As one of the world's most research‑intensive chemical companies, we have been producing countless products that are an integral part of everyday life 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. We are the largest dedicated microbial Contract Development & Manufacturing Organization (CDMO) in the world. Our four dedicated and fast‑growing production sites are based in Germany (Halle and Jena), The Netherlands ( Amsterdam ) and the United States (San Diego, CA). At our Amsterdam‑based centre Wacker Biotech B.V. focuses on the GMP‑compliant 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 a  MSAT – Process Engineer .

Responsibilities

Ensuring technology transfer from and to production by being the production representative in the relevant project core‑team(s) and ensuring that the execution of the production (associated) work within the company is scientifically and technologically correct, efficient, and cost‑competitive (within the boundaries of SHE and cGMP requirements, as well as client’s expectations).

Ensuring life‑cycle management of a process from transfer, via process validation to continuous process verification.

Providing, if needed, process‑related support to shop‑floor for production activities.

Qualifications

Academic or HLO level with expertise in the bioprocess field.

Working for 5 years or more in a (Bio‑)-pharmaceutical environment or a relevant (bioprocess) research field.

Extensive knowledge of (bio) pharmaceutical processes with experience in downstream processing, specifically protein/polysaccharide purification.

Document writing skills in English.

Comfortable in project teams, interacting with clients, training colleagues, and working in matrix structures.

Application knowledge of GMP standards (writing batch documentation and SOPs).

Familiarity with process validation, trending, and data analysis.

Capability to coordinate and perform technology transfer and process validation activities within the manufacturing organization.

Capability to prepare accurate documentation (batch documentation, validation documentation, scientific reports).

Capability to resolve problems.

Capability to summarise and present complex information in an audience‑appropriate format (operators, clients, management, etc.).

Residing in and eligible to work in The Netherlands (valid work permit).

What 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, and a subsidised pension plan.

Work‑life balance:
Flexible working hours (where possible) and 30 days of vacation.

Versatile development opportunities:
Support for professional development.

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: 31128

#J-18808-Ljbffr