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(n) Project Lead ASAT (f/m/d)

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

Job responsibilities

• Primary QC contact for external clients and partners;
• Representative of the QC department in the different project teams and responsible for making the link between the client and department. In this function, you have direct contact with the applicable people within the QC department to ensure that all project activities are performed based on the project needs;
• Execution of multiple client projects from preparation till completion;
• Ensures all QC project deliverables are within pre-defined timelines;
• Writing of method validation documentation (protocols/reports) with no practical lab work involved (100% office position).

Qualifications required

• University degree (preferred) in biotechnology, biochemistry, (analytical) chemistry, microbiology or medical biology with minimal 3 years of work experience in biotechnology or pharmaceutical environment in a QC department. HBO/HLO with relevant/extensive experience will also be considered;
• Extensive knowledge on, and experience with method validation, method qualification and method verification (a must);
• Well established oral and written communication capabilities in English;
• Capable of maintaining overview on diverse activities in multiple projects;
• Residing and 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: 29180