Chemist - Quality Control

BioSpace; Indianapolis (IN); On-site; USD 65,250 - 148,500; Full time

Benefits offered by this job

401(k) plan

Medical benefits

Pension plan

Flexible benefits

Vacation benefits

Job summary

A leading radiopharmaceutical company in Indianapolis is seeking a Chemist – Quality Control. The successful candidate will perform analytical tests in compliance with GMP standards, verify results, and contribute to quality system improvements. Ideal applicants hold a Bachelor’s in a science field and have experience in analytical laboratories. This role involves a 4-day workweek, with competitive compensation offered between $65,250 and $148,500 annually.

Qualifications

• 1+ years of experience in a GMP analytical lab preferred.
• Experience with radioactive materials a plus.
• Ability to work in a lab environment including safety considerations.

Responsibilities

• Perform sample analysis and verify analytical data.
• Assist in continuous improvement of quality systems.
• Train and mentor other lab personnel.

Skills

Analytical test methods

Problem-solving

Communication skills

Documentation skills

Education

Bachelor’s degree in a science field

Tools

LIMS

Empower

Chromeleon

UHPLC

pH meters

ICPMS

Job description

Chemist – Quality Control

The Chemist – Quality Control in Indianapolis Radioligand Therapy (IRLT) group performs accurate and timely testing of routine and some non‑routine radioactive lab samples in accordance with appropriate GMP and safety guidelines. The chemist completes second person verification of others’ results, participates in laboratory analytical investigations, equipment evaluations and qualifications, and quality system improvement initiatives by executing well‑defined protocols and procedures. The chemist shares technical information and best practice within plant sites or groups.

Responsibilities

• Sample Analysis and Reporting
• Verify (SPV) analytical data of other analysts within the lab as requested.
• 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 conformances to procedures, standards, 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.
• May perform holistic review of data for release of data from the laboratory.
• Problem Solving
• Recognizes when a deviation from test methods and procedures has occurred and initiates analytical investigations and participates in root cause investigations.
• Participates, including lead investigator duties, in investigations for deviations.
• Assists in troubleshooting equipment and methods as required.
• Continuous Improvement Initiatives
• 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.
• Reviews SOPs for executable as written.
• Shares technical information and best practice within plant sites or group.
• Lab Operations
• Assist with drafting protocols for non‑routine testing or validation with appropriate guidance.
• Assist in developing equipment qualification protocols with appropriate guidance.
• Perform routine equipment calibrations or maintenance.
• Comply with and assist with implementing safety standards.
• Execute notification to management when required by procedures or standards.
• Initiate lab deviations.
• Train and mentor others. Assist with developing training materials.

Basic Requirements

• Bachelor’s degree in a science field related to the lab (e.g., chemistry, biochemistry, biology, etc.)
• Preferred 1+ years of experience in a GMP analytical lab

Additional Skills/Preferences

• Experience with radioactive materials a plus.
• Proficiency with computer systems LIMS, Empower, Chromeleon, Excel, etc.
• Proficiency with UHPLC, pH meters, ICPMS, Rad detectors, Dose calibrators, and Gamma detectors, among others, a plus.
• Ability to work in a lab environment, including wearing appropriate PPE and other safety required equipment and considerations.
• Demonstrate strong math and documentation skills.
• Demonstrate strong oral and written communication and interpersonal interaction skills.

Additional Information

• Position supports a 4 day, 10 Hour shift (Saturday‑Wednesday) or (Wednesday‑Sunday) with both day and night shifts available. Night shift preferences will be considered favorably.
• Tasks may require repetitive motion and standing for long periods of time.
• Must be able to lift at least 5 liters of liquid.
• Overtime work required, as necessary.

Compensation

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $65,250 - $148,500.

Benefits

Lilly offers a comprehensive benefit program to eligible employees including a company‑sponsored 401(k), pension, vacation benefits, medical, dental, vision, and prescription drug benefits, flexible benefits, life insurance, death benefits, leave of absence benefits, and well‑being benefits.

Equal Employment Opportunity

Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.