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Freelance QA Officer

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The company

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.

Role description

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.

Responsibilities

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

Requirements

- 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. number: 33957
Listed by: SIRE Life Sciences®
Listed on: 20-07-2017
Country: The Netherlands
Region: Limburg
Employment: Freelance
Expertise: 3 - 5 years
Location Type: On location
Language: English
Sector: Pharmaceutical
Specialisation: Quality

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Contact

SIRE Life Sciences B.V.

Mondriaan Tower
Amstelplein 52, 25th floor
1096 BC Amsterdam
+31 (0) 20 658 9800

SIRE Life Sciences Belgium BVBA

Science 14 Atrium
14b, Rue de la Science
1040 Bruxelles
+32 (0) 2 588 1277

SIRE Life Sciences Deutschland GmbH

Fünf Höfe
Theatinerstraße 11
80333 München
+49 (0) 89 3803 8966

SIRE Life Sciences Maastricht

ROOOMS Maastricht
Boschstraat 21
6211 AS Maastricht


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+31 (0) 85 044 4650

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