QC Lab Supervisor I

AbbVie; North Chicago (IL); On-site; USD 75,000 - 143,000; Full time

Benefits offered by this job

Comprehensive benefits package

401(k) plan

Job summary

AbbVie seeks a QC Lab Supervisor I to organize and supervise Lab Analysts, ensuring timely release of raw materials, in-process, and finished products in compliance with quality criteria and deadlines.

The role emphasizes leading a high-performance team, managing laboratory resources, and implementing continuous improvements while maintaining cGMP and safety standards.

Qualifications

• Bachelor’s degree in a scientific field.
• 2+ years of QC Lab experience.
• Thorough knowledge of chemistry, technical writing, investigations, analytical lab equipment, and laboratory operations.
• General knowledge in cGMPs and regulatory requirements.
• Strong problem-solving, decision-making, teamwork, and communication skills.
• Ability to work cross-functionally and interpret lab data for action.
• Ability to identify and implement corrective actions.

Responsibilities

• Lead and develop a high-performing QC Lab team while prioritizing shop floor presence.
• Oversee laboratory operations and scheduling for raw materials, in-process, and finished products.
• Review and approve analytical data and support investigations.
• Ensure QC activities comply with cGMP and safety standards; drive process improvements.
• Assist with equipment maintenance and qualification; plan instrument needs.

Skills

QC Lab experience

Problem solving

Teamwork

Cross-functional collaboration

Decision making

Communication of data

Leadership and coaching

Education

Bachelor’s Degree in Science

Job description

• Compensation: USD 75,000 - USD 142,500 - yearly

Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube.

Job Description

The QC Lab Supervisor I is responsible for the organization, administration, and supervision of Lab Analysts and other Lab employees; properly overseeing the day-to-day operations by prioritizing shop floor presence and receiving guidance and direction from more senior leaders. Oversees the processes of the 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

• Responsible for leading and developing a high performing team while prioritizing shop floor presence. This includes hiring, setting performance expectations, providing continuous and on-time performance feedback, coaching staff, assisting in problem-solving, and handling employee matters. Ensures that the department has the appropriate talent and level of performance to meet business objectives. Monitors administration of training, identifies training needs, and ensures development of team.
• Oversees the operation and functions of the laboratory group which may include Raw Materials, Finished Products, Projects/validation samples, MEC, and stability samples. Organizes laboratory activity by coordinating the activity of personnel depending on the demands of planning. Controls the products (raw materials, intermediates, and finished products) by following procedures (general, specific, of analysis and use, and qualification of equipment) to meet the lab testing schedule. Oversees s
• Identifies aspects of the tests or results warranting further attention and implements corrective actions.
• Reviews and approves Analytical data (may relate to analytical product release depending on regional regulatory requirements).
• Supports laboratory investigations, including out-of-specification test results, and ensures effective corrective actions are implemented.
• Effectively understands, communicates, and presents QC Metrics. Attends and leads Tier meetings.
• Ensures appropriate procedures are in place and that QC activities are executed in line with internal procedures, requirements of cGMP, and relevant safety standards. Assists in implementing continuous improvement actions to lab processes.
• Assists analysts with analytical/microbial instrumentation. Assures instrumentation availability to achieve schedule and improves capacity by ensuring that preventive and repair maintenance as well as material qualifications are carried out in a timely matter. Plans the needs of instruments by maintaining permanent technical and technological intelligence. Applies systematic corrections and/or corrective actions that mitigate the risk of recurrent instrumentation failures.
• Assists in the periodic inspection of laboratory facilities to ensure that they are operated and administered according to Good Manufacturing Practices (GMP) and Good Laboratory Practices, maintaining laboratory audit readiness. When required, support supplier, internal, and regulatory audits
• May serve as a backup when the Lab Manager is unavailable. Generates and manages non-hazardous and hazardous waste, according with the internal operating procedures and in compliance with local and federal regulations.

Qualifications

• Bachelor’s Degree required, preferably in a Scientific field (Chemistry, Microbiology, or Biology)
• 2+ years of QC Lab experience required.
• Demonstrated thorough scientific knowledge and technical expertise in chemistry, technical writing, investigations, analytical laboratory equipment, and laboratory operations required.
• General knowledge in cGMPs, compendia, and regulations required
• Effective problem-solving, decision-making, teamwork, influence, negotiation, and conflict resolution skills required. Ability to foster an inclusive environment.
• Ability to work cross-functionally and coordinate work both within the department and with other departments.
• Ability to interpret the impact of laboratory data for appropriate and effective actions.
• Ability to identify, develop, communicate, and follow through to completion necessary corrective action plans to resolve problems.

Shift:Monday- Friday, 2pm-10:30pm CT

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law:

• The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this role at thetimeofthis posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographiclocation,andwemayultimatelypaymore or less than the posted range. This range may bemodifiedin thefuture.
• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees.
• This job is eligible toparticipatein our short-term incentiveprograms.

Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.Theamountandavailabilityof anybonus,commission, incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employeeremainsin the Company'ssoleandabsolutediscretion unless and until paid andmay bemodifiedat the Company’s sole and absolute discretion, consistent withapplicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.