I’m currently working with a leading global pharmaceutical company that is growing its QA function at a high-performing manufacturing site in Tipperary. This is an excellent opportunity for an experienced Quality Assurance Specialist to step into a senior-level position with a strong focus on GMP compliance and quality oversight.

The Opportunity:

• Join a globally recognised pharma organisation known for operational excellence and innovation
• Contribute to the release of both drug substance and drug product, with involvement in QP support
• Work cross-functionally to drive compliance, resolve quality issues, and enhance systems
• Be part of a collaborative QA team where your experience will have real impact on product quality and patient safety

Key Responsibilities:

• Review and approve production and analytical documentation to support QP certification
• Investigate deviations, complaints, change controls, and CAPAs in a timely, thorough manner
• Support internal audits, quality improvement initiatives, and product recall processes
• Maintain and create SOPs and compile data for reporting and presentations
• Build strong relationships across departments to ensure compliance and continuous improvement
• Stay current on global GMP regulations and represent QA in cross-functional teams

Candidate Profile:

• Degree qualified in a Science or Engineering discipline (or equivalent industrial experience)
• Demonstrated experience in a regulated GMP manufacturing environment, preferably pharma or biopharma
• Strong knowledge of quality systems, regulatory compliance, and technical documentation
• Proven ability to work independently and collaboratively in a fast-paced setting

The Next Step for You

Should this position be of interest, please apply through LinkedIn with an up-to-date CV to Jessica from Next Generation Recruitment or call us on the main line at 016629120.

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