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Freelance QA Officer

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The company

Our client is a professional Pharmaceutical organization, based in Noord-Brabant Netherlands. They a world leader in healthcare. A company that delivers their part in a healthier world. In over 140 counties they help people and animals with medicals, vaccines etcetera in an innovative way. If you like to be challenged in your work, this is the company to work for.

Role description

You will be responsible to ensure cGMP compliance for the quality systems. On the site you will make sure you get insight in the quality and compliance. It is your responsibility to develop, improve and maintain the Quality Systems including the QMS strategy. The end date of this project is not yet known, expected 6-8 months.

Responsibilities

As an interim QA officer you will focus on coordinating and improving the quality policy. You have the ability to optimize the current work methods and take a leading role in this part.
- Lead internal and external audits
- Coordinate Health Authority inspections
- Promoting Lean behaviors and manage your team
- Coordinate, describe, document, research the processes

Requirements

- BSc. or MSc.
- At least 5 years of QA experience within the pharmaceutical industry
- Experience within regulated environment
- Project management skills
- Fluent in English and Dutch



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SIRE Life Sciences®

Ref. number: 34019
Listed by: SIRE Life Sciences®
Listed on: 20-07-2017
Country: The Netherlands
Region: Noord-Brabant
Employment: Freelance
Expertise: 6 - 10 years
Location Type: On location
Language: English
Sector: Pharmaceutical
Specialisation: Quality

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SIRE Life Sciences B.V.

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6211 AS Maastricht


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