Quality Assurance Associate
Our client a leading Medical Device facility in Tipperary currently have a requirement for an experienced Quality Assurance Associate to join their team on an intial 4 month contract with a view to possible extension.
Roles / Responsibilities:
Collate & receive inspection of all required documentation against applicable specs for external manufactureres products.
Completion of inspection report and dispositioning of lot within JD Edwards system
Reviewing lots for holds/non conformances prior ro final release within JD Edwards
Read interpret & understand written procedures
Perform manual and or system quality related transactions, calculate and confirm the expiration dating, recomcilation, yield calculations
Performs batch record audiets to verify compliance to applicable regulations, standards and to company policies and procedures
Perform all MRP transactions as required to support product release
Determines priority of release requests and how such inquiries should be answered. Possesses the ability to recognize orgent inquiries
Authorizes the release of product for distribution
Maintains GMP compliance
Skills / Experience:
Applicants must be qualified to Certificate / Diploma level in life science or a related discipline and have 2 or more years within a similar role.
Have knowledge of GMP/ISO/FDA requirements.
The ability to handle multiple tasks accurately and prioritize effectively.
Respond to customer needs effectively and on time.
To apply in confidence for this role in confidence please send your cv to Maeve Lawlor in Brunel - jobs@brunel.ie or for further information please call me on 056 7720388