Senior QA Specialist Validation
Location: NetherlandsSIRE® 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.
- 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.
- 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 Daniel Woudenberg.
The Company
Our client is a professional Pharmaceutical and Biotechnology organisation, based in Noord-Brabant Netherlands. 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 Daniel Woudenberg.
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