Validation QA Supervisor
Location: BelgiumSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science 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!
THE COMPANY
Our client is a professional Pharmaceutical organization, based in Brussel Belgium.
It is a big international company leading in the pharmaceutical and healthcare industries. The client is committed in improving the quality of human life.
ROLE DESCRIPTION
The QA Validation is part of the QA team. You ensure the QA oversight of the continuous validation activities for one production units.You will take part in the establishment, the implementation, the follow-up and the maintenance of the continuous validation plan and define validation strategy.
RESPONSIBILITIES
- Challenge, review and approve qualification and validation documentation and ensure they are written in accordance,
- Write some validation documentation,
- Ensure both adequate oversight and follow-up on the validation deviations in terms of content,
- Support from a compliance point of view other processes and departments as Production and QA Operations for validation topics.
- Build a strong partnership with these key stakeholders.
- Support the validation approach and decision during internal and external inspection and prepare the strategy of defense
- Ensure implementation of validation related commitments towards internal and external authorities and organize the follow-up.
REQUIREMENTS
- University degree (Pharmacist, Engineer or equivalent)
- At least 2 years + professional experience in pharmaceutical environment
- Good interpersonal relationship skills to be a good team player
- Good oral and written communication skills in French & English
- Problem solving and achievement oriented, proposals and negotiating ability and belief
- Knowledge of GMP Regulated environment related to validation activities
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Laura Hoekstra.
