Plan and prioritize the Pre-Production aspects of the packaging of clinical trial supplies, including:
Creation of accurate Pack Designs that reflect the needs of the client and meet GMP requirements.
Ensure appropriate QIF’s are raised in the event that final Pack Designs differ from the original contract.
Procurement with approved vendors to purchase required packaging components, label stock and equipment in a timely manner to hit Production timelines.
Working closely with the Project Management team to ensure good understanding of the projects and that all client required documentation is received and approved in a timely manner e.g. Label Approvals.
Working with the Centre of Excellence for Label Printing (Catalent SCH) to organize the set-up of new labels within the lab...
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