Sr. Principal Chemist

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 position is responsible for technical mentoring of lab staff and sharing technical information and best practices within the work group and across plant sites. Participates and influences the design and installation of systems, procedures, and methods for the Chemical and Device Testing labs at the site.

• Provide analytical support, project leadership, and/or technical direction, and perform laboratory analyses and data review as needed.
• Oversee and participate in the transfer of analytical methods for marketed products, including setting strategic direction, authoring and reviewing method certification documentation, execution of laboratory testing, and investigation of observations.
• Interact with global Quality Labs and other commercial QC Labs to identify and adopt best practices for testing, documentation, and investigations.
• Ensure methods, procedures and practices adhere to Lilly Global Quality Standards and regulatory requirements, including data integrity.
• Supporting Lean Lab and efficient lab operations
• Network with other areas and externally to understand best practices, share knowledge, participate in technical planning, and to ensure customer needs are met.
• Help define and execute inspection readiness activities in the QC laboratories.
• Interact effectively with auditors and business partners.

• Education:
  • Bachelor or Masters in a science or engineering discipline (Chemistry, Biology, Mechanical Engineering, Biomedical Engineering, etc.)
• Experience:
  • GMP Laboratory experience including familiarity with analytical testing, method transfer, and method validation.
  • Previous experience with enterprise chromatography systems and standalone COTS testing instruments.
  • Previous experience with LC instruments.
  • Experience with statistics and data analysis software, especially data visualization.

• Experience with Empower and Lab Vantage LIMS.
• Strong technical aptitude and ability to train and mentor others.
• Understanding of compliance requirements and regulatory expectations.
• Working effectively with a cross functional group.
• Excellent written and oral communication skills and ability to collaborate and interact with management, scientists, engineering, and IT personnel.
• Ability to focus on continuous improvement.

This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. For GMP purposes, the job description should be updated for significant changes. As always, you should consult with your supervisor regarding your actual job responsibilities and any related duties that may be required for the position.

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