Supervisor Qc Protein Analytics
2 weken geleden
Do you want to take responsibility and make a difference with your work? With your expertise, we can achieve great goals together. 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) **Supervisor QC Protein Analytics**
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.
**Job responsibilities**:
- Supervision of QC analysts including appraisals and individual performance mentoring;
- Execution of preparative activities and preparation of detailed testing schedules;
- Managing execution within a timely manner and align shift tasks with supervisor team;
- Responsible for appropriate training status, GMP compliance and safety compliance;
- Support during (customer) audits;
- You are a Subject Matter Expert (SME) with respect to the equipment and involved in maintenance, validation and calibration.
**Qualifications required**:
- At least an HBO level of education with experience in a pharmaceutical/GMP environment > 8 years experience;
- Leadership skills on supervisor level > 5 years experience;
- Analytical, accurate, structured, flexible and quality and safety-conscious;
- Team player with a high degree of autonomy;
- Good Dutch and English written and oral communicative skills;
- 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.
**Reference Code**:28241
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