Validation Supervisor - Quality Systems
The Company
Our client is a Belgian Biopharmaceutical company, specialized in the production of intermediates and finished products out of blood plasm. They are currently expanding their business and therefore we are looking for a Validation Supervisor - Quality Systems
Role Description
The Validation Supervisor will be responsible for everything regarding Validation within the plant. He/she will conduct Method Validation, Process Validation, Equipment Validation and CSV. Furthermore, the Validation Supervisor will coordinate a team of consultants on site.
Responsibilities
- Conduct validations within production and QC labs
- Writing and review of qualification/validation documents
- Participate in improvement projects regarding validation
- Maintain the GMP standards
- Handling of CAPA's, risk assesments, change controls and deviations
- Give training to other personnel regarding validation
- Coordinate consultants on site during projects
Requirements
- BSc. / MSc. Pharmacy in Life Sciences / Engineering
- 3+ years of experience in validation
- Extensive knowledge of GxP
- Fluent in Dutch/English or French/English
- Strong communication skills
- Experience with Trackwise is seen as an asset
Other information
My client is offering an undetermined contract with a good basic salary, topped up with attractive extra benefits (42 Holidays, Pension Plan, possibility for Company Car, Health Insurance, ...)