About this role
QA In Process Engineer at Vantive. Location: Castlebar, Mayo, Ireland. Role: reviewing batches, managing complaints, supporting audits Requirements: Experience in regulated manufacturing (pharma/biotech/medical device), strong QA and GMP knowledge, batch record review, complaint investigation, CAPA, SOP writing, audit support, technical writing, and cross-functional collaboration. Category: Quality Assurance Seniority: Mid Level Commitment: Full Time Workplace: Onsite Languages: English