QC Lab Supervisor
Listed on 2026-01-27
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Quality Assurance - QA/QC
Data Analyst, QA Specialist / Manager
QC Lab Supervisor I (Monday-Friday 2pm-10:30pm)
- Full-time
- Salary Min: 64000
- Salary Max: 122000
- Workday Global Grade: 15
- Compensation: USD 64,000 - USD 122,000 - yearly
Abb Vie’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 – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about Abb Vie, please visit us at Follow @abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok.
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.
- Lead and develop a high performing team, 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 the team.
- Oversee the operation and functions of the laboratory group which may include Raw Materials, Finished Products, Projects/validation samples, MEC, and stability samples. Organize laboratory activity by coordinating the activity of personnel depending on the demands of planning. Control the products (raw materials, intermediates, and finished products) by following procedures to meet the lab testing schedule.
- Identify aspects of the tests or results warranting further attention and implement corrective actions.
- Review and approve analytical data (may relate to analytical product release depending on regional regulatory requirements).
- Support laboratory investigations, including out‑of‑specification test results, and ensure effective corrective actions are implemented.
- Effectively understand, communicate, and present QC metrics. Attend and lead Tier meetings.
- Ensure appropriate procedures are in place and that QC activities are executed in line with internal procedures, cGMP, and relevant safety standards. Assist in implementing continuous improvement actions to lab processes.
- Assist analysts with analytical/microbial instrumentation. Ensure instrumentation availability to achieve schedule and improve capacity by ensuring preventive and repair maintenance as well as material qualifications are carried out in a timely manner. Plan the needs of instruments by maintaining permanent technical and technological intelligence. Apply systematic corrections and/or corrective actions that mitigate the risk of recurrent instrumentation failures.
- Assist in the periodic inspection of laboratory facilities to ensure that they are operated and administered according to GMP and GLP, maintaining audit readiness. When required, support supplier, internal, and regulatory audits.
- May serve as a backup when the Lab Manager is unavailable.
- This role is eligible for a 10% shift premium.
- 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.
- General knowledge in cGMPs, compendia, and regulations required.
- Effective problem‑solving, decision‑making, teamwork, influence, negotiation, and conflict resolution skills required. Ability to…
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