Blackfield Associates is supporting the recruitment of a Quality Validation Associate to join a leading pharmaceutical manufacturing organisation within their Quality Operations team.
The Role
This position supports electronic Quality Systems and QC laboratory systems, ensuring compliance with GMP, GAMP, CSV, and data integrity requirements. You will help maintain systems in a validated state, support upgrades and improvements, contribute to qualification and validation documentation, and assist with change control, system administration, and continuous improvement initiatives.
We are seeking candidates with:
- Experience in electronic QMS and/or QC laboratory systems
- Working knowledge of CSV, GAMP, and GMP requirements
- Strong understanding of data integrity principles
- Experience supporting qualification and validation activities
- Excellent communication and problem-solving skills