QA Validation Manager / Randstad / Permanent / Life Science Sector / Salary € 4500 - € 5500 per mont
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 Zuid-Holland Netherlands.
- Oversee the functional teams to ensure compliance with all documented validation policies and procedures;
- Increase the level of compliance in accordance with policies from IQ, OQ, PQ and PPQ;
- Monitor cGMP compliance of projects through a thorough impact assessment and ensure that critical aspects are acnhored in qualification and validation plans and protocols;
- Advice and support colleagues/managers during visits and audits.
- Expertise and experience with validations in accordance with the latest industry/cGMP standards;
- People management skills;
- Experience with FDA regulated industries.
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.
The Company
They are one of the world's leading manufacturers and marketers of cosmetics, with over half a billion customers a year.Role Description
You support the site in the development, implementation and improvement of the validation processes in accordance with cGMP norms. Your main responsibility will be to set up, execute and coordinate various validation activities. You are also the main source of expertise on the site when it comes to validation and cGMP, and the validation SME for site audits.Responsibilities
- Work closely with the Sr. Compliance Manager to develop and implement validation processes across the site;- Oversee the functional teams to ensure compliance with all documented validation policies and procedures;
- Increase the level of compliance in accordance with policies from IQ, OQ, PQ and PPQ;
- Monitor cGMP compliance of projects through a thorough impact assessment and ensure that critical aspects are acnhored in qualification and validation plans and protocols;
- Advice and support colleagues/managers during visits and audits.
Requirements
- Msc in Life Sciences;- Expertise and experience with validations in accordance with the latest industry/cGMP standards;
- People management skills;
- Experience with FDA regulated industries.
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.
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