Associate - Incoming Materials Disposition - FDE
Job in
Concord, Cabarrus County, North Carolina, 28027, USA
Listed on 2026-02-08
Listing for:
Scorpion Therapeutics
Full Time
position Listed on 2026-02-08
Job specializations:
-
Quality Assurance - QA/QC
Quality Technician/ Inspector, Quality Control / Manager, QA Specialist / Manager -
Manufacturing / Production
QA Specialist / Manager
Job Description & How to Apply Below
Role Summary
Associate - Incoming Materials Disposition at Lilly supports the release of incoming materials using SAP and Lab systems, ensuring materials meet specifications and are released in a timely manner to avoid production delays. This QA role reports to the QA Materials Incoming/Disposition Manager and involves investigating material issues, quarantining nonconforming items, and coordinating with suppliers as needed. The position focuses on cGMP compliance, data integrity, and collaboration with cross-functional teams.
This is a fixed-term position through 2026 with a Sunday–Thursday schedule and potential for overtime or after-hours support.
- Practices safety behaviors with proper PPE and lifting techniques. Supports all HSE Corporate and Site Goals.
- Documenting inspections in accordance with procedures and specifications.
- Ensuring materials not meeting specifications are quarantined, per local procedures.
- Ensure materials are released in a timely manner, as to not delay production.
- Evaluating damaged materials found on inbound shipments or within the warehouse and determine acceptability.
- Evaluating temperature excursions on shipments received at the warehouse.
- Identifies and assists in resolving issues on inbound shipments (i.e. Incorrect quantity or product, contamination, etc.).
- Performs appropriate transactions in SAP to ensure system represents appropriate status of material (QI, blocked, scrapped, etc.).
- Initiates complaints/remarks to supplier for materials not meeting Lilly expectations.
- May participate in investigations regarding materials or service complaints.
- Authors/revises SOPs, materials specifications, as needed.
- Interacts with other quality functions and supports material related Supplier Change Notifications.
- Participates in/supports regulatory inspections, as needed.
- Required: Knowledge of cGMP practices including good documentation practices, data integrity and regulatory compliance.
- Required: Demonstrated ability to communicate with cross-functional teams including good oral and written communication skills.
- Required: Strong attention to detail.
- Required: Ability to work independently with minimal supervision.
- Required: Legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for employment positions on the R path.
- BA/BS degree required
- Understanding of regulatory compliance and data integrity principles
- Experience with SAP and inventory management systems (e.g., EWM, SAP)
- Ability to work with cross-functional teams
- This position is not permanent. It is for a fixed term position through 2026.
- This position is Sunday - Thursday, but additional flexibility may be required based on business needs.
- Overtime and off-shift support may be required.
- May be required to respond to operational issues outside of core business hours and days.
- May be subject to post-offer physical and vision exam.
- Job is exposed to repetitive movements such as:
Walking, Sitting, Bending, Twisting.
Position Requirements
10+ Years
work experience
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