Regulatory Compliance Specialist
18 hours ago
We are seeking an experienced Clinical Trial Supply Chain Project Manager to join our team in Ridgefield, Connecticut. The successful candidate will have a strong background in project management, regulatory compliance, and supply chain operations.
About the RoleThe Clinical Trial Supply Chain Project Manager will be responsible for representing the Pharmaceutical Development Department in audits and inspections by global regulatory authorities. They will also establish suitable systems and training for IMP Delivery employees and team leaders.
Key Responsibilities- Represent the Pharmaceutical Development Department in audits and inspections by global regulatory authorities
- Establish suitable systems and training for IMP Delivery employees and team leaders
- Introduce new processes and systems in IMP Delivery and other areas
- Masters degree in natural sciences or engineering
- Minimum of five years experience in a similar environment
- Advanced knowledge of project management, GMP, GCP, and HSE guidelines
- A competitive salary and benefits package
- The opportunity to work with a leading global staffing company
- A dynamic and supportive work environment
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