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

A leading Pharma/biotechnology company who's mission is to discover and innovate medicines for patients with serious illnesses. Our client is rapidly growing the quality team.

Role Description

From a QA perspective you are responsible for Equipment, Automation and IS Validation.

Responsibilities

Perform review and approval of equipment and automation validation documentation, ensuring that Corporate, Site and Regulatory requirements are met.
- Keeps quality oversight on validation strategy and deliverables for specific projects.
- Maintain a close contact and familiarity with Quality systems.
- Provide guidance and direction to Quality, Production, Warehouse/Distribution and Supply Chain staff in regards to compliance with quality policies, standards and procedures.

Requirements

- Degree in Life Sciences
- Relevant experience in GMP environment
- Experience in QA and manufacturing/packaging environment
- English Language skills

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Cees Roffelsen.