Associate Director - Quality Engineer

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life‑changing medicines, strengthen how health is understood and managed, and support the communities we serve.

This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

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 39,000 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 Engineer – FUME is responsible for providing technical guidance and leadership to the Richmond, Virginia API/Fill finish Operations and Richmond Facilities Management sites regarding the quality standards employed to maintain and improve site operations. The area of focus is utilities, including bulk distributed materials (BDMs), but will require backup in facilities, systems and equipment management.

• Provide direct quality oversight of production, engineering, automation, and laboratory operations.
• Review and approve documents including, but not limited to, procedures, change control proposals, deviations, equipment/system qualification/validation, analytical methods, and computerized system validations as business FUME.
• Provide quality guidance and recommendations regarding manufacturing, materials, utilities, maintenance, and laboratory issues.
• Participate in aberrant data investigations (i.e., deviation investigations).
• Conduct analytical data review including stability data.
• Disposition API Intermediates and raw materials, as appropriate.
• Provide coaching, feedback and mentoring to engineering and FUME as it relates to execution of quality systems.
• Maintain and improve facility, utility, maintenance, and equipment (FUME) quality systems.
• Contribute to and review Annual Product Reviews (APR), Quarterly Product and Process Self-Assessments (QPPA), Asset qualification maintenance system strategies and equipment/computer system periodic reviews, as appropriate.
• Conduct gap assessments of global requirements and ensure implementation of the governing standards.
• Participate in and/or lead, support self‑inspection activities and regulatory inspections.
• Assist business partners in the interpretation of regulatory and corporate requirements.

• BS in Engineering or a science‑related field or equivalent experience.
• Must have hands‑on experience with ADC (Antibody Drug Conjugate) processes.
• Minimum of 8 years of relevant experience in engineering or quality roles.

• Experience in API or finished product manufacturing, FUME or Engineering.
• Experience with system and equipment qualifications.
• Demonstrated strong written and verbal communication skills.
• Strong attention to detail.
• Proficiency with computer system applications.