Senior Compliance Specialist
R&D Partners View all jobs
- Cashel, Co Tipperary
- Permanent
- Full-time
- Manage vendor notifications, complaints, and quality defect reporting systems.
- Lead investigations, identify root causes, and implement corrective actions.
- Oversee supplier and contract manufacturer documentation and compliance.
- Support the preparation and review of documents for batch release.
- Coordinate local regulatory activities, including maintaining site master files and manufacturing authorizations.
- Manage the supplier quality system, including quality agreements and periodic reviews.
- Prepare for regulatory audits and corporate visits, ensuring readiness and compliance.
- Conduct self-inspections and internal audits, addressing findings with corrective actions.
- Assist in drafting, reviewing, and approving compliance-related documents such as SOPs, change controls, and reports.
- Provide training to new and existing staff on compliance-related topics.
- Participate in or lead compliance projects as needed.
- A degree in a science or quality-related field, with a Qualified Person (QP) certification.
- Strong knowledge of EU GMP, US FDA, and other relevant regulations, particularly for oral solid, sterile, and combination products.
- Excellent problem-solving skills and attention to detail.
- Strong written and verbal communication skills, with proficiency in English.
- Ability to work independently and collaboratively in a fast-paced environment.
- Familiarity with data integrity and good documentation practices.
- Must be eligible to work in Ireland.
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