CSV

Pharma & Sciences - Validation

Provides technical expertise and supports all Validation aspects in the project
Reviews and approves the Qualification and Validation protocols and reports to ensure compliance with the current regulations
Supports Data integrity and risk assessments
Creates and maintains the validation documentation and other relevant GxP documents within the Document Management System
Manages and executes Periodic Reviews

Reference number (48193)

What are we looking for?

Bachelor or Master’s degree in pharmaceutical sciences field (biology, chemistry, chemical,…) or relatable experience.
Proven experience in Computerized System Validation is a MUST
1-5 years’ experience in Quality Assurance, in a regulated environment (pharma, biotech)
Good knowledge of GMP, deviation, CAPA, Changes control, Risk Management and quality systems
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