Technician Qc Protein Analytics

2 weken geleden


Amsterdam, Nederland Wacker Chemie AG Voltijd

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) **Technician QC Protein Analytics (f/m/d)**

Performs routine laboratory testing, in accordance with detailed SOPs and international pharmaceutical and legal regulations. Is involved in noticing work situations and systems to be improved.

**Job responsibilities**:

- Testing of intermediates, Drug Substance and Drug Product using a variety of techniques (e.g. HPLC, spectrophotometry, SDS-PAGE, ELISA);
- Testing of utility samples (on weekly basis) using TOC, nitrates and conductivity;
- Testing of raw materials, when applicable, using FTIR, GC and other pharmacopoeia methods;
- Participation in validation studies for product specific methods;
- Participation in Stability studies, i.e. testing;
- General laboratory control (e.g. equipment maintenance and calibration, review of test data, quality documentation).

**Qualifications required**:

- At least finalized MLO education;
- Preferably experience in a pharmaceutical/GMP environment;
- All-round analyst who is analytical, accurate and flexible;
- Good oral and written communication capabilities in Dutch and English;
- You reside in and are eligible to work in The Netherlands (valid-work permit).

Contact Person: Ines Ilic

**Reference Code**:27095



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