Are you an experienced QA officer with previous experience in Pharmaceutical laboratory?
This is a 12 month contract opportunity paying up to £34,000 per annum
Search Scientific are a recruitment partner to a global pharmaceutical manufacturer based in Liverpool. They are looking to recruit a quality associate to join their expanding team. .
QA review and approval of procedures, master batch records, and any other relevant cGMP documentation. They will also work as a member of cross-functional teams as defined by the Quality Assurance Manager.
Review and approve procedures, master batch records, and any other technical or cGMP documentation in accordance with SOP, cGMP and license requirements.
Provide support for deviation investigations, ensuring effective root cause analysis
Investigations are performed and product quality implications accurately assessed. Identify repeat deviations and ensure appropriate corrective actions are taken.
Ensure that deviations, CAPAs, protocols/reports and other applicable documents are approved within the designated timelines.
A BSc or equivalent in a relevant discipline, or able to demonstrate capabilities to this level.
Previous cGMP experience
Experience of QA and QA Validation
Previous experience in Batch record review and batch records
If your skills match the above and you are interested in this position , then please apply online or contact Pabudu on 0161 835 8359 or Email to Pabudu.email@example.com
Search is an equal opportunities recruiter and we welcome applications from all suitably skilled or qualified applicants, regardless of their race, sex, disability, religion/beliefs, sexual orientation or age