Sr. Principal Associate - GQA Advisor

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. The Sr. Principal Associate – GQA Advisor is part of the Global Quality Auditing (GQA) team and represents a corporate quality‑compliance interface supporting global GXPs. The position assures that the processes and procedures are in accordance with company requirements, current regulations, and guidelines. The Sr. Principal Associate - GQA Advisor will perform internal investigations, which may be for‑cause or human resources quality related in support of the HRQ program as well as perform GXP audits. This role supports the process for escalation, investigation, and reconciliation and trending of compliance‑related investigations with potential impact to Quality coming from the HR function, and will assist in the assessment and investigation of Quality‑related deviations and applicable audits. GQA is operating as a valued business partner to Manufacturing, Research & Development, Human Resources, Legal, and others in taking a proactive approach to further enhance the quality status of business operations and regulatory compliance. Key Objectives/Deliverables Business/Technical Leadership/Compliance Manages sensitive information in accordance with Lilly Policies. Supports and participates in triage discussions to assess potential impact to quality and investigates accordingly and collaborates with cross functional partners to ensure procedural escalation and documentation requirements are met. Provides investigation guidance, can conduct root cause analysis to ensure consistency to sites for quality‑related investigations associated with human relations or in cases of potential conflict of interest in the Quality unit (e.g., allegations against the Quality unit or Quality Leader). Conducts audits, root cause and trend investigations for GQA per established processes. Collaborates with the Quality Culture, Data Integrity, and GMP Training teams to identify/develop/deliver initiatives to address common themes across the programs. Consulting/Mentoring Consults with cross functional partners to ensure investigations with potential human relations Quality impact are escalated per program requirements and drive consistent execution of GQS104. Consults with members of GQA for broader quality and compliance gaps and deviations and trending. Personal Development and Shared Learning Attend training courses, conferences, or association meetings to continue to gain knowledge. Share such information with other members of the team or company to increase awareness and to train others in the implementation of these practices. Be continually aware of current industry trends and regulatory agency interpretation of GxP and other relevant requirements. Continue to gain knowledge necessary to provide a greater understanding of GxP requirements. Divisional/Global Quality Organization Support Participate in projects that support or enhance GxP Compliance and continuous improvement. Minimum Requirements Minimum Bachelor’s Degree in Pharmacy, Chemistry, Biology, Engineering Microbiology or other technical areas of study; minimum of 10 years relevant industry experience in areas that must include: Quality Assurance or Quality Control. Experience in Quality Assurance or GxP function with strong compliance knowledge with demonstrated ability to influence others, negotiate, and investigate. Experience and demonstrated ability to perform GXP audits for various modalities; including but not limited to parenteral. Demonstrated critical thinking, root cause analysis, and complex investigation management experience. Demonstrated ability to communicate and deliver constructive feedback, including excellent oral and written communication and oral presentation skills. Demonstrated ability to interpret and apply standards to different situations by understanding subject needs and applying good problem‑solving skills. Ability to work independently and as part of a team with minimal supervision. Education Requirements BA, BS, MS or Ph.D. in a technical field, such as Biology, Chemistry, Engineering, Pharmacy or Microbiology. Other Information Must be able to work in a GxP environment. Must be able to travel 10‑50%, including international travel. Position is located at Indianapolis Corporate Center or another Lilly US site. 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. 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 B or S paths or at levels M1‑M2 or P1‑P4. #J-18808-Ljbffr BioSpace