Csv
il y a 1 semaine
**Job description**:
- 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
**Benefits**:
- 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
**Have you got what it takes?**:
- 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
Reference number: 48193
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