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Production Coordinator
2 months ago
Job Summary:
CK Group- Science, Clinical and Technical is seeking a highly organized and detail-oriented Supplies Administrator to join their team. As a key member of the supply chain team, you will be responsible for generating clinical trial packaging documentation, maintaining high quality standards, and supporting the Supply Chain Manager.
Key Responsibilities:
- Generate clinical trial packaging documentation to meet Company, Client, Study, and Regulatory requirements.
- Complete documentation in accordance with relevant SOPs and to comply with GMP.
- Maintain high quality standards, ensuring all deviations are documented as required.
- Primarily support the Supply Chain Manager.
- Support the Supply Chain and Operations to enable that all assets, processes, and procedures meet GMP/GDP requirements.
Requirements:
- A life science degree is desirable but not essential, depending on candidate and relevant experience.
- Proficient skills in Microsoft Office applications (Word, Excel, PowerPoint, SAP).
- Pharma experience or education highly advantageous.
- Experience in GMP or GDP highly advantageous.
About the Company:
Our client is the global leader in enabling pharma, biotech, and consumer health partners to optimize product development, launch, and full life-cycle supply for patients around the world. They have the goal of putting patients first and to help people around the world live better and healthier lives.