We are seeking an experienced Quality Compliance Lead to oversee and maintain GMP compliance for on-site and contractor activities within a pharmaceutical environment based in This role would be a great opportunity for a Quality Professional within Pharmaceuticals who is looking to move into a broad QMS and people management position.
This is a permanent opportunity offering hybrid working.
Key Responsibilities: Manage the day-to-day operations of the Quality Management System (QMS), including: Document Control Change Control Deviations and CAPA Complaints and vendor qualification activities Internal and external audits Lead and mentor a team of quality compliance professionals.
Maintain and report on quality metrics.
Support regulatory inspections and ensure compliance with HPRA, EU/US regulations.
Provide quality oversight for product launches in new markets.
Drive continuous improvement initiatives across procedures, processes, and systems.
Requirements: Bachelors degree (or equivalent) in a scientific discipline.
Minimum 5 years experience in a similar role within pharmaceutical manufacturing.
Previous experience leading teams is highly desirable Broad knowledge of QMS compliance and EU/US pharmaceutical regulations (HPRA, USP, ICH, EU GMPs, FDA etc.)
Strong organizational and interpersonal skills, with the ability to manage multiple responsibilities.
For a confidential discussion about this opportunity please contact Ranait Coughlan Skills: QMS Compliance HPRA USP ICH EU GMPs FDA