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Quality control officer

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Het bedrijf

Our client is a professional organisation, based in Zeeland Netherlands. They are active in the area of clinical trials manufacturing and cell therapy products for the European market. They are a young company with motivated professionals that operates as a Contract Manufacturing Organization.

Functie omschrijving

You will be performing QC procedures like writing and reporting. It is important that you are accurate and precise in this performances and that you have the willingness to work flexible hours when this is necessary.
- Make documentation compliant to cGMP
- Testing, handling and release incoming materials

Verantwoordelijkheden

• het zelfstandig uitvoeren van projecten;
• het verrichten van validatiewerkzaamheden;
• het onderhoud van apparatuur;
• het meewerken aan problem solving;
• de naleving van het kwaliteits- en milieusysteem;
• de veiligheid betreffende de werkzaamheden;
• het opleiden van niet gekwalificeerde medewerkers;
• de algemene werkwijze van het laboratorium.

Vereisten

- BSc. in life science related field
- 0-2 experience in an industrial QC laboratory
- Experience with international GMP/GLP regulations
- Knowledge of LC-MS
- Good knowledge of MS-Office
- Fluent in English and Dutch

Overige informatie



Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Valentijn de Krom.

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SIRE Life Sciences®

Ref. number: 33980
Listed by: SIRE Life Sciences®
Listed on: 12-02-2019
Country: The Netherlands
Region: Zeeland
Employment: Permanent
Expertise: 0 - 2 years
Location Type: On location
Education: Bachelor
Language: Dutch
Sector: Pharmaceutical
Specialisation: Laboratory

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