Description
Optimus Life Sciences are an industry leading Recruitment Consultancy currently working with some of the world's most renown companies across the whole of Europe.My client is a Global Pharmaceutical company based in West Dublin, together we are looking for a QA Validation Specialist join their team on a 12-month contract.
Ideal applicants will have a minimum 3 years' experience in a similar role within the Industry.
Tasks & Responsibilities:
- Generating validation protocols and reports.
- Conduct qualification / validation activities.
- Review of technical documents like SMF, DMF, Validations, and Regulatory Approvals received from vendorsas per respective SOP.
- Ensure new equipment is assessed and qualified as required by the Site Validation Master Plan (SVMP).
- Experience in Equipment and Process Validation
- Experience in the Installation of New Systems
- Deviations, CAPAs and change controls
My client would like to interview candidates for this role immediately. If you are interested in finding out more about this role, then please send your CV over to , and we can arrange a time to talk in more detail.