Posted: 18 June
The role
Excellent opportunity for a QA Supervisor to join a Biopharma in Galway on a 12 month contract. The QA Supervisor will manage Quality during the evening shift. Working hours: 15.00 – 23.30 Monday to Thursday and Friday 13.00 to 21.00.
Overview of your responsibilities (full job description available on request)
Lead and support Quality Management System activities, including investigations, CAPAs, risk assessments, complaints, supplier non-conformances, and quality metrics.
Review and maintain GMP documentation and SOPs to ensure compliance with site and global quality requirements.
Act as Quality SME for incoming inspection, packaging, and QA operations.
Oversee QA processes including line clearance, batch documentation review, artwork approval, and incoming inspection.
Develop and deliver quality training to site personnel.
Prepare quality reports and performance metrics for senior management and key stakeholders.
Partner with cross-functional teams to implement quality initiatives and drive compliance improvements.
Support internal audits, regulatory inspections, and external audits.
Provide technical quality guidance across pharmaceutical and medical device operations.
Lead or support quality activities for new projects, product introductions, and technology transfers.
Mentor junior team members and provide leadership support when required.
Act as Quality Manager delegate and support broader quality objectives as needed.
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