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Quality Assurance Specialist

2 months ago

Stevenage, Hertfordshire, United Kingdom Blackfield Associates Full time

Blackfield Associates is seeking a skilled Quality Assurance Specialist to support a leading clinical-stage biopharmaceutical company in Stevenage. As a key member of the Quality Assurance Operations team, you will play a crucial role in ensuring Good Manufacturing Practice (GMP) compliance and managing various quality-related activities. Your responsibilities will include ensuring cGMP compliance in batch release activities, reviewing Batch Manufacturing Records and Quality Control records, and escalating quality issues. Additionally, you will be responsible for managing record forms in production and QC to maintain batch or test article identity traceability, audit trails, and archiving. The ideal candidate will have 1 to 2 years of experience in a quality assurance role within a pharmaceutical or similar quality management system, with a BSc in pharmaceutical sciences, immunology, biology, or a related discipline. The working hours for this role are Wednesday to Saturday or Sunday to Wednesday, 8 am to 5 pm.