QA Validation
Contracting – Wavre
Our partner is looking for a QA Validation to join its teams. This international company is well known for its pharmaceutical products.
Your responsibilities?
- Ensure QA oversight in validation activities (IQOQ / PQ / PV…)
- Review/Approve the validation documentation regarding the GMP requirements and the Vaccines procedures
- Ensure that production practices are aligned with validation conclusion
- Attend all project meetings as QA validation representative
- Ensure timely escalation to Management of critical issues during validation
- Contribute to the deviation process providing QA oversight and approving deviation for deviations related to validation activities and/or impact of manufacturing deviations to validation activities
- Pro-actively identify potential quality and compliance risks and manage these risks through the risk register and quality plan process
- Work in autonomy with supervision/coaching
- To define the validation strategies through the change control process
- To write and implement some validation documentation (Validation Plan, Validation Summary Report, Risk Assessment, Gap Analysis , Periodic review ….)
Let's talk about you !
- You hold a Master’s Biotechnology, Agronomy, Chemistry or Pharmacy
- You have experience with SAP
- You have knowledge of GMP’s standards
- You have good communication skills to be the only point of contact between other stakeholders
- You are Fluent in French and able to speak and understand 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.
You’re interested in this job? We kindly invite you to apply.
You’re interested in this job? We kindly invite you to apply.
Do you have any questions? You can contact Aurélie Montes Suarez: [email protected] or +32472/44.83.18
