Biologist-QC Micro at Eli Lilly and Company

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:

At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.

Position Brand Description:

The microbiologist/biologist performs accurate and timely testing of routine and some non-routine lab samples in accordance with appropriate GMP and safety guidelines.  The microbiologist/biologist completes second person verification of others results, participates in laboratory root cause investigations, equipment evaluations and qualifications, and some quality system improvement initiatives by executing well-defined protocols and procedures.  The microbiologist/biologist shares technical information and best practice within plant sites or group.

Responsibilities:

• Accurately and safely perform analytical test methods or related support activities as per procedures or protocols. Uses technical knowledge in the review and interpretation of data for conformance to procedures, standards, and protocols and/or real-time recognition of aberrant data and results.
• Perform data entry and reviews own work for accuracy in accordance with laboratory procedures, standards and GMP requirements.
• Verify (SPV) analytical data of other analysts within the lab as requested.
• May perform holistic review of data for release of data from the laboratory.
• Recognizes when a deviation from procedures has occurred.
• Executes notification to management when required by procedures or standards.
• Performs investigations for deviations.
• Troubleshoot equipment and methods as required.
• Assist in improvement of quality systems by creating or revising worksheets and other lab documentation systems.
• Identifies and communicates opportunities for improvement initiatives in daily work activities.
• Shares technical information and best practice within plant sites or group.
• Perform routine equipment calibrations or maintenance through execution of well-defined protocols.
• Comply with and implement safety standards.
• Train and mentoring others.

Basic Requirements:

• Bachelor degree in scientific field related to the lab (Biology/Microbiology/Biochemistry/Chemistry).

Additional Skills/Preferences

• Laboratory experience in GMP QC Laboratory environment
• Ability to working in a lab environment including wearing appropriate PPE and other safety required equipment and considerations.
• Ability to work independently and accurately with minimal supervision.
• Ability to make decisions based on knowledge, experience, best practices and requirements.
• Ability to multitask, prioritize and coordinate work to meet customers needs.
• Demonstrated strong math and documentation skills.
• Demonstrated strong oral and written communication and interpersonal interaction skills.
• Demonstrated problem solving and investigative skills.
• Proficiency with computer systems including Microsoft Office products

Additional Information:

• Ability to work 8 hour days – Monday through Friday
• Ability to cover weekends, holidays, and company shutdowns as needed.
• Minimal travel required.
• Applicant will work in various areas within the Parenteral Plant.  Some allergens are present in the parenteral plant. Mobility requirements and exposure to allergens should be considered when applying for this position.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

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.

Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women’s Network, Working and Living with Disabilities. Learn more about all of our groups.

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