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Details

Quality Systems Specialist


Reference:RK23300 Location: Tipperary
Qualification:DegreeExperience:3-4 Years
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: Quality Systems Specialist

Quality Systems Specialist
RK23300
Contract – 11 months
Tipperary



We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Tipperary. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.



The role requires the specialist to support the Quality Systems activities in the both the Drug Substance and Drug Product facilities


Duties:

  • Complete sub-system responsibilities per site System Ownership List.
  • Drive Quality performance metrics and continuous improvement within owned systems.
  • Serve as Quality SME for validation across Drug Substance and Drug Product operations.
  • Participate in PVC, WVC, CVG, and EQVC committees.
  • Approve validation documentation and support capital projects.
  • Maintain validated state post-change; develop summary reports and quality plans.
  • Principal Quality contact for all site change requests affecting processing.
  • Conduct full lifecycle reviews for change controls and material strategy assessments.
  • Provide QA oversight for laboratory systems, documentation, and incidents.
  • Approve stability reports and support OOS investigations.
  • Act as the Microbiology QA Point of Contact for water, utilities, environment, and product-related issues.
  • Own and maintain the Site Master File, Validation Master Plan, and key procedures.
  • Oversee Annual Review and Quality Agreement systems.
  • Approve user access reviews and site application controls.
  • Participate in internal audits, customer complaints, and supplier change evaluations.
  • Support site regulatory inspections and license/filing documentation requests.
  • Manage returned goods disposition in line with quality requirements.
  • Lead scheduling, minutes, and follow-ups for monthly Quality Council meetings.
  • Actively promote GMP awareness and continuous improvement site-wide.


Educational and Experience
  • A degree or post-graduate qualification in Science, Pharmacy, or Engineering is required.
  • 3+ years’ experience in a regulated pharmaceutical manufacturing environment preferred.
  • Experience with quality system ownership, validation, and regulatory audit support is highly desirable.
  • Experience in quality management systems such as Veeva, SAP, LIMs, Trackwise


If interested in this posting please feel free to contact Rachel Kent at Life Science Recruitment for further information.