Materials Management Quality Assurance

. Serve as a materials management expert, mentoring and advising MMQA, Foundry Materials Management, and PR&D .

Posted 10/15/2026full-timeLebanon • United StatesMid-LevelSenior💰 $66,000 - $171,600 per yearWebsite

Key responsibilities & impact

Serve as a materials management expert, mentoring and advising MMQA, Foundry Materials Management, and PR&D
Develop processes and strategies for timely release of raw materials, excipients, GMP consumables, packaging components, and supplier qualifications
Oversee and support qualification of suppliers of purchased materials for GMP operations
Conduct or assist with risk assessments and recommend Supplier/Service Provider approval
Participate in periodic supplier performance reviews
Write and coordinate Supplier, Service Provider, and Affiliate Quality Agreements
Represent quality on material management and supplier certification committees
Provide operational oversight for incoming receipt, sampling, and testing
Perform batch disposition of incoming materials and consumables
Perform SAP data steward functions
Review and redline GMP documents, including specifications and procedures
Track and report materials management metrics to supplier relationship meetings, supplier committees, and the Materials Management Governance Committee
Support regulatory inspections with documentation and subject matter expertise
Evaluate product quality impact of GMP-related deviations or change controls and support investigations, root cause analysis, and CAPA
Notify management about critical departures and ensure resulting issues are managed
Maintain audit readiness and participate in internal and external inspections
Perform other related duties as assigned

What you’ll need

Bachelor’s degree in a science, engineering, computer-related, or pharmaceutical field, or equivalent industry experience
3+ years working in the pharmaceutical industry in Quality Assurance roles
Authorized to work in the United States on a full-time basis
Lilly will not provide support for or sponsor work authorization or visas for this role
Previous experience working with and managing suppliers and materials in a regulated environment
Previous experience with SAP or other inventory/materials management systems
Demonstrated knowledge and use of US, EU, Japanese and other regulations as they pertain to pharmaceutical manufacturing and material/supplier management
Experience supporting facility or area start up preferred
Skilled in handling deviation and change management records, overseeing evaluation, approval, and complex quality events
Good oral and written communication skills
Strong problem solving and decision-making skills
Technical writing experience, including authoring, reviewing, and approving complex GMP documents and quality system procedures
Technical aptitude and ability to train and mentor others

Comp & perks

Company bonus depending in part on company and individual performance
Company-sponsored 401(k)
Pension
Vacation benefits
Medical, dental, vision and prescription drug benefits
Flexible benefits, including healthcare and/or dependent day care flexible spending accounts
Life insurance and death benefits
Certain time off and leave of absence benefits
Well-being benefits, including employee assistance program, fitness benefits, and employee clubs and activities