GMP Compliance Specialist for Pharmaceutical Companies
2 weeks ago
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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