GMP Compliance Specialist for Pharmaceutical Companies

2 weeks ago


Dublin, Dublin City, Ireland i-Pharm Consulting Full time

i-Pharm Consulting is seeking a qualified GMP Compliance Specialist for Pharmaceutical Companies to join their team. As a key member of the site's Quality team, you will be responsible for ensuring compliance with cGMP regulations and maintaining high-quality standards.

The successful candidate will have 8-10 years' experience in Quality Assurance, Quality Control, or Technical Operations within the pharmaceutical or biopharmaceutical industry, and strong expertise in QRM, investigations, problem-solving, and GMP compliance.

Your Key Responsibilities:

  • Lead and support compliance initiatives, investigations, and risk assessments.
  • Provide QA oversight for validation, technical transfers, and regulatory approvals.
  • Review and approve Change Controls, Deviations, CAPAs, and GMP documentation.
  • Support product disposition, including material release and detailed eBR review.
  • Train and mentor teams on Quality policies, SOPs, and regulatory requirements.
  • Drive continuous improvement and contribute to internal audit activities.

What We Offer:

  • A dynamic and collaborative environment with cross-functional teams.
  • Competitive salary, career growth opportunities, and professional development support.
  • The chance to work in a world-class biopharmaceutical environment and shape the future of quality assurance.


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