Lilly

healthcare

Technician-QC-IAPI

$0–0k Indianapolis, Indiana, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid candidates.

The Brief

“Technician - QC - IAPI at Lilly. Skills: QC testing, GMP compliance, Data integrity. Perform accurate, timely testing of routine lab samples. Identify and communicate opportunities for improvement”

What You'll Achieve.

Meet sample TAT; Meet site priorities; Ensure inspection readiness

Industry & Context.

healthcare
Problems you'll solve

Troubleshooting of analytical methods; Troubleshooting laboratory issues

Eligibility Requirements

Ability to work in a lab environment, Ability to work in a highly regulated environment, Must be able to lift at least 5 liters of liquid, Carry equipment up flights of stairs, Tasks may require repetitive motion, Standing for long periods of time, Schedule 12 hours 3-2-2-3 NIGHT SHIFT, On-call coverage may be needed, Holiday coverage may be needed, Overtime or weekend work required

What They're Looking For.

Must Have

Ability to work in a lab environment, Ability to work in a highly regulated environment, Demonstrated math and documentation skills, Demonstrated oral and written communication and interpersonal interaction skills, Must be able to lift at least 5 liters of liquid and carry equipment up flights of stairs, Tasks may require repetitive motion and standing for long periods of time, Qualified applicants must be authorized to work in the United States on a full-time basis

Nice to Have

3 years+ of relevant experience, Associate’s degree, Proficiency with computer systems, including Microsoft Office products, LIMS, etc., Proficiency with HPLC, UPLC, GC, and Karl Fischer

What You'll Do.

timely testing of routine lab samples

Identify and communicate opportunities for improvement

Ensure work is completed in a timely manner

Adhere to EHS requirements and safety procedures

Maintain cleanliness and contamination control

Execute activities in compliance with SOPs

Execute activities in accordance with data integrity standards

Identify and escalate atypical results

Communicate with QC Team

Share context regarding non-routine samples

Identify and communicate opportunities for improvement

Support implementation of improvements

Handle samples to prevent contamination

Document sample collection

Perform routine equipment checks

Report equipment malfunctions

Assist with basic troubleshooting

Escalate complex issues

How You'll Work.

Team & Collaboration

Communicate with QC Team; Participate in cross-functional teams; Communicate clearly with Operations; Work together to ensure samples are collected; Inform Operations and QC promptly; Provide on-site support during audit/inspections

Communication Scope

Oral communication; Written communication; Interpersonal interaction

Full Job Description

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. **_Position Brand Description:_** The Technician – QC – IAPI performs accurate, timely testing of routine lab samples in accordance with applicable GMP and safety guidelines. The Technician – QC –IAPI identifies and communicates opportunities for improvement within the lab. **_Key Objectives/Deliverables:_** \- **Timeliness:** Ensure work is completed in a timely manner to meet sample TAT (Turnaround Time) and site priorities. \- **Safety and GMP Compliance** : Adhere to Environmental Health and Safety (EHS) requirements and laboratory safety procedures. Maintain cleanliness and contamination control, in alignment with cGMPs, chemical hygiene, and biosafety guidelines. **\- Compliance and Documentation** : Execute activities in compliance with applicable standard operating procedures (SOPs), methods/protocols, good documentation practices (GDP), and regulatory guidelines. **\- Data Recording and Data Integrity** : Execute activities in accordance with data integrity standards and ALCOA+ principles. \- **Deviation Identification and Investigation** : Identify and escalate any atypical results and potential deviations. Communicate with QC Team. Share context regarding non-routine samples and ensure analysts are aware of time sensitive samples. \- **Continuous Improvement:** Identify and communicate opportunities for improvement as well as supporting those implementations. \- **Cross-functional Participation** : Participate in cr

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