A QA Validation Specialist is required for a 12 month contract, working onsite at LSC’s major biopharma client based in west Dublin. This is a key role providing site wide QA activities to support the implementation of an MES system, and must ensure effective interaction with other departments and locations regarding GMP Document review and finished product releases.
As QA Validation Specialist you will:
-QA support for implementation of MES computer system validation deliverables.
-Review and approval of engineering functional area documentation
-Authoring, review and approval of QA-related procedures.
-Oversee documentation and tracking of quality management system activities
-Review and approve Validation protocols.
-Support the vendor quality management programme.
-BSc. in science/engineering with a minimum of 5 years QA experience in a pharmaceutical -manufacture/biopharmaceutical environment.
-Strong process knowledge to include upstream and/or downstream processing.
-Bulk Drug Substance experience is essential.
Call or email Kathy on 021 4777329 / email@example.com for futher info on this and other QA and Validation roles.