Job Details
Validation Specialist
4922
Posted: 03/09/2024
- €Competitive
- Lostock Gralam, Cheshire West and Chester, United Kingdom
- Permanent
A global, innovative pharmaceutical company are searching for an ambitious Validation Specialist. In this role, you will be responsible for ensuring that the validation of production equipment, processes, and areas meets the highest local and global Quality and Regulatory standards (GMP, GLP).
What will you be doing?
What do you bring to the table?
What will you be doing?
- Coordinate, develop and execute various validation activities (as related to production equipment, production processes, production areas etc.).
- Create IQ, OQ, and PQ protocols, executing them, and providing reports and recommendations on validation frequencies.
- Maintain validation guidelines, draw up procedures and company regulations and evaluate validations and follow-up actions.
- Validation file management.
- Design research proposals.
- Process optimisation and implementation.
What do you bring to the table?
- Demonstrable pharmaceutical industry experience, specifically within validation.
- Strong working knowledge of GMP/GLP regulations.
- Graduate degree in chemistry, pharmacy, technology or related topic.
- Excellent communication and interpersonal skills.
- Fluent English and Dutch.
Robyn O'Toole
Recruitment Consultant