Are you looking for a challenging role in quality assurance?
This position involves maintaining the quality and regulatory compliance of biopharmaceutical products within a next-generation manufacturing facility.
The Role
* Develop and maintain quality assurance procedures, policies, and systems
* Conduct routine self-inspections and monitoring assessments to ensure compliance with cGMP and other relevant regulations
* Collaborate with automation, IT, and production teams to ensure quality throughout the manufacturing process
* Investigate and address deviations, non-conformities, and CAPA to maintain quality
The Person
* BSc, Hons BSc, MSc, or PhD in Science, Engineering, Quality, or related discipline
* Minimum of 3 years of experience in quality assurance within a biotechnology, pharmaceutical, or medical device manufacturing environment
* Strong knowledge of cGMP, FDA, Data Integrity, Quality Risk Management, and other biopharmaceutical regulatory requirements
For further details please contact; for further information on this opportunity.