Description
Optimus Search are an industry leading Recruitment Consultancy currently working with some of the world's most renown companies.My client is a leading Pharmaceutical company based in Dublin Ireland, together we are looking for a CQV Engineer to join their team on a 12-month contract.
Tasks & Requirements;
- Assisting in development of Validation Plans and development of Installation Verification, Functional Testing and Performance Qualifications (PQs) for equipment.
- Working with the Quality team to ensure all aspects of activity within the commissioning and Validation of equipment adhere to required policies and procedures, including safety and training
- Ensuring that the Site meets the quality requirements of its customers and applicable regulations FDA, EU & International Standards
- Preparing and executing validation protocols and can complete risk assessments from a quality system perspective
- Assisting with Engineering and external vendors regarding equipment User Requirement Specifications (URS's), DQ
- Assisting in the implementation of any existing Validation program to ensure continued compliance to the necessary regulations
- Assisting in deviation and exception resolution and root cause analysis
- Equipment and Systems Qualification Experience up to and including PQ
- Previous CQV experience within GMP pharma environment packaging some, or all of the following: Medical Devices, Vials, Syringes, Ampules or Tableting.
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.