Supervisor I, QC Lab
AbbVie
August 17, 2026
On-site
North Chicago, IL
$75,000 - $142,500 USD yearly
Operations
Job Description
The QC Lab Supervisor I is responsible for the organization, administration, and supervision of Lab Analysts and other Lab employees; overseeing day-to-day operations by prioritizing shop floor presence and receiving guidance from more senior leaders. Oversees chemical analysis and release of raw materials, in-process, and final products in compliance with current quality criteria while respecting deadlines and managing costs. Ensures effective and efficient utilization of laboratory resources through management of laboratory support activities.
Responsibilities
- Lead and develop a high performing team (hire, set expectations, provide feedback, coach, problem-solve, handle employee matters); monitor training needs and ensure team development.
- Oversee laboratory operations for groups including Raw Materials, Finished Products, Projects/validation samples, MEC, and stability samples; coordinate personnel based on planning demands; control products by following analysis procedures and equipment qualification to meet testing schedules.
- Identify test/result issues needing attention; implement corrective actions.
- Review and approve analytical data (may relate to product release depending on regional requirements).
- Support investigations (including OOS results) and ensure effective corrective actions.
- Understand, communicate, and present QC Metrics; attend and lead Tier meetings.
- Ensure QC activities follow internal procedures, cGMP, and safety standards; assist with continuous improvement.
- Assist with analytical/microbial instrumentation; ensure availability via timely preventive/repair maintenance and material qualifications; apply corrections to mitigate recurring failures.
- Assist with periodic inspections for GMP/GLP and audit readiness; support supplier/internal/regulatory audits when required.
- Backup when Lab Manager is unavailable; manage non-hazardous/hazardous waste per internal procedures and local/federal regulations.
Qualifications
- Bachelor’s degree required (preferably Chemistry, Microbiology, or Biology).
- 2+ years QC Lab experience.
- Thorough scientific knowledge in chemistry, technical writing, investigations, analytical lab equipment, and lab operations.
- General knowledge of cGMPs, compendia, and regulations.
- Problem-solving, decision-making, teamwork, influence, negotiation, and conflict resolution; ability to foster an inclusive environment.
- Ability to work cross-functionally.
- Ability to interpret laboratory data for effective actions.
- Ability to develop, communicate, and complete corrective action plans.
Benefits
- Paid time off (vacation, holidays, sick), medical/dental/vision insurance, and 401(k) to eligible employees.
- Short-term incentive program eligibility.
The QC Lab Supervisor I is responsible for the organization, administration, and supervision of Lab Analysts and other Lab employees; overseeing day-to-day operations by prioritizing shop floor presence and receiving guidance from more senior leaders. Oversees chemical analysis and release of raw materials, in-process, and final products in compliance with current quality criteria while respecting deadlines and managing costs. Ensures effective and efficient utilization of laboratory resources through management of laboratory support activities.
Responsibilities
- Lead and develop a high performing team (hire, set expectations, provide feedback, coach, problem-solve, handle employee matters); monitor training needs and ensure team development.
- Oversee laboratory operations for groups including Raw Materials, Finished Products, Projects/validation samples, MEC, and stability samples; coordinate personnel based on planning demands; control products by following analysis procedures and equipment qualification to meet testing schedules.
- Identify test/result issues needing attention; implement corrective actions.
- Review and approve analytical data (may relate to product release depending on regional requirements).
- Support investigations (including OOS results) and ensure effective corrective actions.
- Understand, communicate, and present QC Metrics; attend and lead Tier meetings.
- Ensure QC activities follow internal procedures, cGMP, and safety standards; assist with continuous improvement.
- Assist with analytical/microbial instrumentation; ensure availability via timely preventive/repair maintenance and material qualifications; apply corrections to mitigate recurring failures.
- Assist with periodic inspections for GMP/GLP and audit readiness; support supplier/internal/regulatory audits when required.
- Backup when Lab Manager is unavailable; manage non-hazardous/hazardous waste per internal procedures and local/federal regulations.
Qualifications
- Bachelor’s degree required (preferably Chemistry, Microbiology, or Biology).
- 2+ years QC Lab experience.
- Thorough scientific knowledge in chemistry, technical writing, investigations, analytical lab equipment, and lab operations.
- General knowledge of cGMPs, compendia, and regulations.
- Problem-solving, decision-making, teamwork, influence, negotiation, and conflict resolution; ability to foster an inclusive environment.
- Ability to work cross-functionally.
- Ability to interpret laboratory data for effective actions.
- Ability to develop, communicate, and complete corrective action plans.
Benefits
- Paid time off (vacation, holidays, sick), medical/dental/vision insurance, and 401(k) to eligible employees.
- Short-term incentive program eligibility.