Validation Specialist
Pauwels Consulting
- Wavre, Brabant Wallon
- Contrat
- Temps-plein
- Review and write Validation documentations, plans and reports
- Plan, organize and manage Validation activities
- Review and monitor change control
- Identify and solve problems
- Bachelor or Master's degree with scientific orientation or relatable experience
- 1-5 years of experience in Validation (Process Validation/CSV/Method Validation) within the pharmaceutical industry
- Experience in cleaning validation is a plus
- Good knowledge of GMP regulations
- Autonomous, conscientious, and positive problem-solving mindset.
- Fluent in French and good level of English
- Challenging projects based on your interests and skills
- Personal follow-up and clear, transparent communication both before and after commencement of employment
- Possibility to follow extra training
- Inspiring network events and legendary after work drinks
- Strong network of industry leading clients
- Expertise within IT, Engineering and Life Sciences
- A flying start for every junior, growth opportunities and possibility to share gathered knowledge for more senior employees