QA Representative - Warehouse 3rd Shift

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.

The Lilly RTP warehouse is a fully automated warehouse system with automated pallet conveyors, pallet exchangers, ASRS (Automated storage and retrieval system), and AGV (Autonomous Guided Vehicle) delivery of materials to the line. The Quality Assurance Representative for the Device Assembly, Packaging (DAP), and Warehouse team provides daily oversight, assistance, and guidance to issues such as non-conformance investigations, change control proposals, procedures / master formula revisions, validations, batch disposition, commissioning, and qualification activities, with a focus on Automated Warehouse operations. This role reports directly to the Associate Director Quality - DAP and Warehouse. The Quality Assurance Representative position is essential for maintaining GMP compliance and providing support during preparation for Pre-Approval/General Inspections by various regulatory agencies.

Key Objectives/Deliverables:

• Responsible for adhering to safety rules and maintaining a safe work environment for both yourself and others by supporting HSE corporate and site goals.
• Lead, mentor, and coach operations and support personnel on quality matters.
• Ensure regular presence in warehousing areas, while also supporting device assembly and packaging areas, to monitor GMP programs, and quality systems.
• Active on local process teams with focus on Warehousing operations or indirect participation through project support activities.
• Ability to assess and triage deviations / observations that occur within the warehouse area.
• Work with Lilly support groups and external partners to resolve or provide advice on receiving or shipping issues.
• Participate in self-led inspections and provide support during internal / external regulatory inspections.
• Effectively review and / or redline to ensure quality attributes are met. (i.e, deviations / observations, procedures, technical studies, validation protocols, change controls, and engineering documents).

• Participate in Six Sigma Projects to help improve productivity within the local process team or quality organization.
• Support project and process improvement initiatives for Plant Process Teams as representative of the Quality function, with focus on the warehousing processes (e.g., receiving, shipping, incoming material inspection).
• Approve commissioning qualification / validation documents for computer systems and equipment related to the warehousing operations, to ensure compliance with quality standards.

Minimum Requirements:

• Experience in GMP facility
• Bachelor's degree, (preference in science, engineering, computer, or pharmaceutical related field of study) or equivalent work experience.

Preferred attributes but not required:

• Demonstrate strong oral and written communication and interpersonal skills.
• Demonstrated decision making and problem-solving skills.
• Demonstrate knowledge and understanding of manufacturing process and Quality Systems.
• Proficiency with computer systems including Microsoft office products, inventory management systems, and deviation management systems (i.e., SAP, Trackwise, etc.)
• Strong attention to detail.
• Proven ability to work independently or as part of a team to resolve issues.
• Previous experience in warehousing operations.
• Previous experience with ASRS warehousing, Autonomous Guided Vehicles, and integrated systems.
• Previous work with combination products or devices with experience with US/EU regulations and notified bodies.
• CQE, or CQA certification from the American Society for Quality (ASQ)
• Computer Systems Quality (CSQA) experience
• Previous experience in GMP production environments.
• Previous facility or area start up experience.

Additional Information:

• May be required to respond to operational issues outside of core business hours / days.
• Applicant may work in various areas within the DAP and Warehouse buildings. Mobility requirements should be considered when applying for this position.
• Ability to work 8 hour days - Monday through Friday required 3rd shift
• Ability to work overtime as required.
• Ability to travel up to 10% to Indianapolis, IN for meetings and coordination with global regulatory organizations required

Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively "Lilly") are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( Lilly_Recruiting_Compliance@lists.lilly.com ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. Any other correspondence will not receive a response.

Lilly is an EEO/Affirmative Action Employer and 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.

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