Description
Responsibilities of the JobTo support compliance activities on site, working within the QA department. The successful candidate will work within the QP team to support batch disposition activities and to support quality systems to ensure the site remains compliant with current GMP requirements. Supplier management and the oversight of the internal audit program are key components to the role.
Work within the QP team to support the batch disposition process, including review of third party batch paperwork.
Responsible for review and maintenance of third party agreements for third party manufacture.
Generate the annual audit plan, using Quality Risk Management principles.
Monitoring the completion of CAPAs identified and closure of the audit report.
Perform QA duties with respect to validation and qualification activities; providing compliance support and reviewing and approving validation documents, as required.
For more information on this role please send an updated CV to Sarah Irvine, or call for more information.
If you're looking for new roles but this opportunity doesn't quite match your requirements please contact us to discuss our latest vacancies with you.