QA Validation
Walloon Brabant – contracting
You have experience in quality assurance and validation in the pharma sector? You have an eye for details and for work well done? Keep reading your future job description.
Our partner is looking for a QA Validation to join its team. This international company is well-known for its pharmaceuticals and vaccines.
Your responsibilities?
As QA Validation, you will Provide QA support and oversight to validation activities according to validation procedures.
- To take part in the establishment, the implementation, the follow-up and the maintenance of the continuous validation plan (CVP)
- To define the validation strategies through the change control process
- To write and implement some validation documentation (VP, VSR)
- To review and approve specific qualification and validation documentation (IQ, OQ, PQ, Risk Assessment, Periodic validation)
- To ensure the correct application of the validation quality systems on the field and to define improvement plan as required
- To support the production & technical services teams in the implementation of the validation activities
- To ensure an efficient and compliant CVP implementation
- To provide a compliance and business expertise for some specific technical subjects
- Challenge, review and approve qualification and validation (IQ,OQ, PQ, equivalence certificate, requalification protocol/report) documentation and ensure they are written in accordance with the internal standards and procedures
- Write some validation (VP, PQ, VSR)
- Review Periodic Validation Review documentation according to the company standards and procedures
- Ensure timely escalation to Management of critical issues during validation and/or project
- Pro-actively identify potential quality and compliance risks and be pro-active in escalation.
- Attend all project meetings as QA expert from a compliance point of view the Manufacturing Unit Product & Process, Production and QA Operations for validation topics.
Your profile?
- Engineering or scientific background (or equivalent acquired through professional experience)
- Experience QA and Equipment’s Validation in a GMP Pharma environment
- Understand quickly the characteristics and the mechanism of a broad range of production equipment and process including their potential impact on product and patient safety
- Use a risk-based approach for problem solving and prioritization of tasks
- Blow a quality and compliance mindset through the validation activities
- Good communicator, autonomous and rigorous
- Team player
- Critical mind and quality oriented
- French & English.
Our offer ?
Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way.
