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 Dublin, together we are looking for a Quality Specialist to join their team on a 12-month contract.
Ideal applicants will have a minimum 3 years' experience in a similar role within the Pharmaceutical Industry.
Tasks & Responsibilities:
- You will be responsible for supporting all C&Q activities and ensuring that the appropriate levels of validation are executed for both new and existing systems in line with regulatory requirements.
- You will be responsible for reviewing and supporting the execution of validation activities.
- Approving all commissioning and qualification documentation (e.g. risk assessment, URSs protocols & reports)
- Activities include risk assessments, data analysis and report generation.
- Processing all C&Q documents in line with SOP's/FDA/EMA requirements.
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.