Catalent ยท 12 hours ago
Distribution Project Coordinator
Catalent, Inc. is a leading global contract development and manufacturing organization dedicated to improving health outcomes. The Distribution Project Coordinator role involves managing the distribution of clinical supplies for trials, maintaining client relationships, and ensuring compliance with protocols.
BiotechnologyHealth CareManufacturingPharmaceutical
Responsibilities
Coordinate and dispatch shipments of clinical trial material to sites, ensuring compliance with SOPs and the approved study-specific protocol
Collaborate with Project Management to define distribution needs, align with project timelines, and ensure execution meets customer expectations/scope of services
Act as the primary customer point of contact for distribution, leading internal and client meetings to facilitate project completion and issue resolution
Manage the customer order pipeline and backlog, guiding S&OP teams and Distribution on scheduling and upcoming orders
Generate, maintain, and review the Distribution Summary Protocol/Checklist for all shipments, ensuring conformance to Catalent Standards
Anticipate, rectify, and report distribution problems to Project Management and the client; lead investigations and service complaint resolution
Coordinate with the Distribution Department to schedule and manage international and large-volume shipments
Support material management systems by reviewing distribution-specific material setup in ERP/IVRS and other client portals, including inventory monitoring
Ensure financial and quality system accuracy by verifying billing codes, reviewing MRAPs, and documenting upstream quality issues
Support quality assurance and team development by assisting with quality issue resolution, leading new hire training, and participating in customer audits and meetings
Manages project initiation including kick-off meetings and protocol development
Processes specialized purchase orders and coordinates new item number requests for distribution-only products
Ensures timely and compliant shipment readiness, specifically handling dangerous goods documentation and daily operational escalations
Acts as a subject matter expert for pharmaceutical import/export regulations and supports continuous process improvement projects
All other duties as assigned
Qualification
Required
Associate degree is required
Demonstrate strong analytical skills and problem-solving skills
Physical Requirements: Individual may be required to sit, stand, walk regularly and occasionally lift up to 25 pounds
Preferred
Bachelor's degree is preferred
ERP system experience; JD Edwards preferred
At least 2 years of Customer Service experience in a cGMP regulated environment is preferred
Benefits
Defined career path and annual performance review and feedback process
Diverse, inclusive culture
Positive working environment focusing on continually improving processes to remain innovative
Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
152 hours of PTO + 8 paid holidays
Several Employee Resource Groups focusing on D&I
Dynamic, fast-paced work environment
Community engagement and green initiatives
Generous 401K match
Medical, dental and vision benefits effective day one of employment
Tuition Reimbursement - Let us help you finish your degree or start a new degree!
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Company
Catalent
Catalent - Blow-Fill-Seal Sterile CDMO Business is focusing on complex clinical to commercial stage formulation and manufacturing. It is a sub-organization of Catalent Pharma Solutions.
Funding
Current Stage
Late StageTotal Funding
unknown2021-01-06Acquired
Leadership Team
Recent News
Maryland Daily Record
2025-11-23
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