Analyst - QC

Eli Lilly and CompanyUs, IN
Onsite

About The Position

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 Technician – QC – IAPI performs accurate and timely testing of routine lab samples in accordance with appropriate GMP and safety guidelines. The Technician – QC - IAPI also participates in second person verification (SPV) of analytical data, laboratory investigations, equipment calibrations and maintenance by executing well-defined protocols and procedures. The Technician – QC –IAPI identifies and communicates opportunities for improvement within the lab.

Requirements

  • Associate degree (2 yr College degree) in a science field related to the lab in which they are placed (e.g., chemistry for chem. Labs or micro or biology for micro lab) or 5+ years of demonstrated relevant experience in a GMP (analytical chemistry or microbiology) lab.
  • Proficiency with computer systems including Microsoft Office products, LIMS, etc.
  • Ability to work in a lab environment, including wearing appropriate PPE and other safety required equipment and considerations.
  • Ability to work in a highly regulated environment.
  • Demonstrated strong math and documentation skills including (but not limited to) sample prep and data review.
  • Demonstrated strong oral and written communication and interpersonal interaction skills.
  • Ability to work in a fast-paced analytical lab running HPLC, UPLC and GC methods.
  • 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

  • Previous experience with Lilly deviation and change control process.
  • Analytical chemistry experience.

Responsibilities

  • Accurately and safely perform analytical test methods or related support activities as per procedures or protocols and reviews that results conform to standards.
  • Perform data entry and reviews own work for accuracy in accordance with laboratory procedures, standards, and GMP requirements.
  • Recognizes when a deviation from procedures, etc has occurred and initiates an investigation.
  • Verify (SPV) analytical data of other analysts within the lab as required.
  • Identifies and communicates opportunities for improvement initiatives in daily work activities.
  • Troubleshoot equipment and methods as required.
  • Training and mentoring others within lab, where applicable.
  • Executes notification to management when required by procedures or standards.
  • Perform routine equipment qualifications/calibrations or maintenance through execution of well-defined protocols.
  • Participate in laboratory investigations

Benefits

  • 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 (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)
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