Supplier Quality – Medical Devices (Contract Manufacturing)

Eli Lilly and Company • Us, IN

1d • Onsite

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: Indianapolis Device Manufacturing (IDM) is responsible for the development, commercialization, manufacture, and global technical stewardship of delivery devices used to administer many of the therapeutics in Lilly's portfolio. This includes the development and delivery of test systems and test methods in support of design verification, production, and complaint handling.

Requirements

• Bachelor’s Degree - Preferred in STEM discipline
• 1 year industry related experience
• Qualified applicants must be 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, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.

Nice To Haves

• Experience working with contract manufacturers and suppliers
• Knowledge of global medical devices and combination product regulations (e.g. 21CFR820, 21CFR Part 4, Part 11, ISO 13485, ISO 11608, Canadian MDR, EU Medical Devices Directive/Regulation, JPAL, TGA, ANVISA)
• Knowledge of Quality System elements and their application in a manufacturing environment
• Experience with plastic molding/assembly operations
• Experience with Outlook, Microsoft applications, Trackwise, Veeva, SAP, Darwin, and Master Control
• Effective communication, interpersonal, and networking skill
• Self-management skills
• Strong attention to detail
• Ability to work as part of a team
• Problem solving skills
• Meets commitments and deadlines
• Ability to multi-task and manage competing priorities
• Strong technical writing skills and proficiency in technical review of documents
• Strong organizational, time management and planning skills

Responsibilities

• Provides oversight and support to contract manufacturing operations of medical devices and combination products.
• Oversees the quality of the components, sub-assemblies, and finished devices manufactured at the Contract Manufacturers (CM) and supplied to Internal Lilly sites.
• Provides assistance and guidance on deviation investigations, CAPA, change control, batch release, equipment qualification, process validation, audits, complaints, design verification, and design validation.
• Ensure that components, sub-assemblies, and finished devices have been manufactured and released in compliance with cGMPs.
• Evaluate if products manufactured at the CM meet requirements for batch release.
• Review/approve GMP documents for CMs process manufacturing including: protocols, technical reports, deviations, change controls, inspection procedures and specifications, sampling plans, sort/rework procedures, and validation packages.
• Ensure that Root Cause Investigations (RCIs) are complete, corrective or preventive actions are taken, and effectiveness checks are appropriate to address quality related issues at IDM and CMs.
• Provide data (inputs) for management review, monthly metrics, quarterly business reviews, site compliance reporting, and post-launch risk management reporting.
• Participate in Failure Modes and Effects Analysis (FMEA).
• Initiate and support continuous improvement projects.
• Assist with internal audits and supplier audits and maintain supplier management requirements.
• Support molding and non-molded part validation at CMs.
• Support design verification activities.
• Manage CM Quality Agreements and Quality Plans; ensure the expectations are monitored and met at the CM.
• Participate on joint process teams.
• Maintain knowledge and application of CM QMS to enable quicker, risk-based decisions relative to product quality.
• Coordinate process and design changes with assembly sites.
• Verify effectiveness activities.
• Perform GMP reviews for internal procedures (for R3-R4 candidates).
• Conduct GQS gap assessments and establish action plans with controlling mechanism for closure (for R3-R4 candidates).
• Consult/work with Regulatory to assure compliance with applicable registrations and requirements (for R3-R4 candidates).
• Coach and mentor cross-functional peers (for R3-R4 candidates).

Benefits

• company bonus (depending, in part, on company and individual performance)
• 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
• 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: Mid Level
• Number of Employees: 5,001-10,000 employees