Medicines and Healthcare products Regulatory Agency in South Mimms, Hertfordshire, is seeking a Quality Lead for a permanent full-time role within the Health & Safety and Quality Assurance function of the Science and Research group.
The successful candidate will advise and train Scientists on Quality Management Systems to support Control Testing and Batch Release testing of biological medicines, with emphasis on ISO 17025, WHO and EDQM requirements.
#J-18808-LjbffrQuality Lead — ISO 17025 & QA Training (Biotech) employer: Medicines and Healthcare Products Regulatory Agency
The Medicines and Healthcare products Regulatory Agency (MHRA) is an exceptional employer, offering a dynamic work environment in the heart of Canary Wharf, London. With a strong commitment to employee growth, the agency provides opportunities for professional development and collaboration with leading experts in healthcare and research. The hybrid working model promotes a healthy work-life balance, while the agency's focus on innovation and public health ensures that employees contribute to meaningful projects that enhance the well-being of millions.
Contact Details:
Medicines and Healthcare Products Regulatory Agency Recruitment Team
