Role: Quality Assurance Associate (QA Associate)
Location: St. Albans
My client are global leaders in the pharmaceutical industry, they have best in class experience in Neurology and Oncology. They are a people first organisation, putting both employees and patients first.
In this role you will be ensuring that the development quality assurance (DQA) activities comply with current company and industry standards and regulations. Support the review and writing of policies systems and procedures. To ensure the DQAs QMS and other systems and processes support the current business goals and objectives.
Reviewing batch records, documents and approval of intermediate product
Support the approval of master batch records, QC methods, label text, Supply Strategy Study Documentation and other associated documents
Write under supervision SOPs associated with DQA activities
Participate in internal and external audit process and audit schedules.
Support the preparation and hosting of competent authority inspections.
Support the processes associated with the development and review of Quality Agreements.
Raise and support the investigation of deviations and associated CAPAs.
Amongst other relevant responsibilities
Good working experience with Quality Assurance, GMP, Quality systems
Working experience of SOPs and CAPAs
Understanding of manufacture, test and packaging of highly regulated pharmaceutical products
Knowledge and understanding of EU Clinical trial regulation
- Agency: Cpl Life Sciences
- Contact: James Ritson
- Reference: JO-2109-475469
Website: Cpl Life Sciences
- Posted: 1st September 2021
- Expires: 29th September 2021