Freelance Compliance Manager
Tilburg, Netherlands
5 dagen geleden

SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation.

We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies.

By using highly advanced algorithms, we enable our team of Resource & Data Strategists to maintain the most advanced, detailed and complete Life Sciences network in Europe.

This big data enables us to work Reverse Recruitment : we first analyze the market in-depth before we go out to the market.

Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment , making sure we, or better yet, you find the right career!Our client is a professional Pharmaceutical organisation, based in Noord-Brabant Netherlands.

The Company

They are an international organization who focus especially on services in pharmaceutical development and manufacturing. A company that has the top clients of the world in pharmaceutical and biotech.

Role Description

Currently we are looking for a freelance compliance manager. You will be responsible for implement and maintain the quality systems.

You are well known with international quality requirements as determined by EMEA, FDA etc. This has to be in compliance with manufacturing biopharmaceutical products.

For every product the compliance need to be audited. The end date of this project is not yet known, expected 6-8 months.


Your responsibility is to check and manage all the activities of the QA and final disposition of the products. You will add improvements in the processes.

  • Lead audits
  • Lead QA projects
  • Manage QA systems in a cost effective c GMP policy
  • Knowledge of regulations and guidelines such as EMEA, ICH and FDA)
  • Work together with quality specialists
  • Work with GMP system
  • Requirements

  • MSc. in a related area such as Biotechnology or Pharmacology
  • 5 years or more of experience in related area
  • Experience with pharmaceutical cGMP systems and international cGMP
  • Experience with project management
  • Fluent in English and Dutch
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