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Das Unternehmen

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.

Rollenbeschreibung

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.

Verantwortlichkeiten

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

Voraussetzungen

- 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®

Ref. Nummer: 33957
Veröffentlicht von: SIRE Life Sciences®
Veröffentlicht am: 20-07-2017
Land: The Netherlands
Region: Limburg
Beschäftigung: Freiberufler / Selbstständig
Sachverstand: 3 - 5 Jahre
Standorttyp: Auf locatie
Sprache: Englisch
Sektor: Pharmazie
Spezialisierung: Qualität

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