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Freelance QA Officer

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L'entreprise

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

Description du rôle

You will be responsible for the daily quality documentation by planning and execution. The activities will mainly focus around leading quality assurance projects executed by project teams. You will ensure the compliance of GMP guidelines and safety standards. The end date of this project is not yet known, expected 6-8 months.

Responsabilités

You will be organizing of and participating in Quality Assurance projects. You will make sure that everything is compliant with GMP.
- Validation of protocols and reports
- Administration of Quality Key Performance Indicators in a setting of QRB
- Performing quality assurance audits and inspections

Exigences

- BSc. in life science- Biotech related field
- 3-5 experience in a GMP related industry
- Fluent in English and Dutch
- Flexible, accurate and a team player



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SIRE Life Sciences®

Réf. nombre: 33957
Placé par: SIRE Life Sciences®
Posté le: 20-07-2017
Pays: The Netherlands
Région: Limburg
Emploi: Free-lance
Compétence: 3 - 5 années
Type de lieu: Sure place
Langue: Anglais
Secteur: Pharmaceutique
Spécialisation: Qualité

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