GMP/ISO 13485 Validation Lead (IQ-OQ-PQ)

A specialized recruitment agency is seeking a Validation Specialist for a 6-month contract in Bracknell. The successful candidate will ensure that systems and processes meet regulatory compliance and operational excellence standards. Key responsibilities include executing validation protocols and documenting results, developing validation documentation per ISO standards, and ensuring audit readiness. Applicants should have a strong background in validation engineering within a GMP or ISO 13485 environment, demonstrating attention to detail and effective communication skills.