Associate - Incoming Materials Disposition - FDE

Lilly • Concord, NC

2d

About The Position

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.
​Organization Overview:
At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.
Responsibilities:
The QA Associate - Incoming Materials Disposition will report to the QA Materials Incoming/Disposition Manager. This person will support release of incoming materials utilizing SAP and Lab systems.
Key Objectives/Deliverables:
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.

Requirements

• Associate degree required (minimum)
• Knowledge of cGMP practices including good documentation practices, data integrity and regulatory compliance.
• Demonstrated ability to communicate with cross-functional teams including good oral and written communication skills.
• Strong attention to detail.
• Ability to work independently with minimal supervision.
• Qualified candidates must be 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.

Nice To Haves

• Bachelor's degree in a science, engineering, computer, or pharmaceutical related field of study, preferred.
• Previous experience in GMP production and warehouse environments.
• Understanding of statistical tools and analysis.
• Experience in inventory management systems (EWM, SAP, etc.)

Responsibilities

• 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.

Benefits

• Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance).
• Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: Associate degree
• Number of Employees: 5,001-10,000 employees