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AbbVie is seeking a QC Compliance Specialist for our Cork manufacturing site on a 12-month fixed-term contract. This role ensures quality assurance processes and safety protocols are consistently followed within the laboratory environment, maintaining the highest standards of quality and safety.
You will monitor and ensure compliance with laboratory quality control procedures and safety guidelines. The role includes leading Laboratory Compliance and Safety Walkdown programmes, writing laboratory investigations, and implementing effective CAPA. You will generate QC department PQR reports on a biannual basis, support audit readiness for internal and external inspections, and collaborate with management to improve lab processes. Additional responsibilities include preparing compliance reports and SOPs, participating in risk assessments, and leading the QC safety team to drive improvements.
The ideal candidate holds a primary degree in analytical science or equivalent subject. You should demonstrate strong attention to detail, understanding of GMP requirements, and ability to drive continuous improvement initiatives. Experience with compliance systems and laboratory operations is highly valued.
Join a global healthcare leader where your work ensures the quality and safety of medicines reaching patients worldwide. This contract role offers valuable experience in pharmaceutical quality systems and opportunities to contribute to site excellence initiatives.