Material Coordinator for Clinical Trial Manufacturing
**Job Summary:**
* Coordinate the execution of manufacturing runs for each molecule, ensuring timely and accurate delivery.
* Work closely with the NDP Mfg. Plant Planner to understand schedule and priorities.
**Key Responsibilities:
1. Participate in demand planning conversations and account for MRP actions from purchase order creation to successful incoming receipt and batch disposition.
2. Coordinate activities and communicate timing on incoming and outgoing shipment schedules.
3. Monitor component inventory levels at the Contract Partner (CP) and create deliveries to replenish as needed.
**Requirements:
* Bachelor's degree in Pharmacy, Pharmaceutical Sciences, Chemical/Biochemical Engineering or related field preferred.
* Minimum 1 year of experience in a GMP environment.
**Preferred Skills:
* Experience with oral and/or parenteral product manufacturing.
* Inventory management or complex supply chain management experience.
* Clinical trial manufacturing operations knowledge.
**Benefits:
Lilly offers a premium workspace, flexible hybrid working options, healthcare, pension and life assurance benefits, subsidized canteen, onsite gym, travel subsidies and on-site parking.
The CT Manufacturing organization is responsible for the on-time delivery of drug product for supporting clinical trials (Phase 1 through 4) as well as the associated technical information deliverables.
This is a 12-month Fixed-Term Contract.
We give our best effort to our work, and we put people first.
Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.