About the job
As a Quality Control Lab Supervisor I, you will play a pivotal role in managing and guiding Lab Analysts and laboratory personnel to ensure the smooth functioning of day-to-day operations. Your expertise will be crucial in overseeing the chemical analysis and release processes of raw materials, in-process, and final products, ensuring compliance with quality standards while adhering to deadlines and controlling costs. You will also be responsible for optimizing laboratory resources and support activities for maximum efficiency.
- Lead and nurture a high-performing team, emphasizing a strong presence on the shop floor. This encompasses recruiting talent, setting performance goals, providing timely feedback, coaching team members, and addressing employee-related issues. You will ensure the department is well-equipped to meet business objectives through effective performance management and training development.
- Direct the operations of laboratory groups, including Raw Materials, Finished Products, Projects/validation samples, MEC, and stability samples, while coordinating activities based on planning demands. You will ensure product compliance by following established procedures for testing and analysis, meeting the required testing schedule.
- Identify any test-related issues or results that require further investigation and implement necessary corrective actions.
- Review and approve analytical data, ensuring compliance with regional regulatory requirements for product release.
- Support laboratory investigations, particularly those related to out-of-specification test results, ensuring that effective corrective measures are enacted.
- Communicate and present Quality Control metrics effectively, leading discussions in Tier meetings.
- Ensure QC activities align with internal procedures, cGMP requirements, and safety standards, contributing to continuous improvement initiatives in laboratory processes.
- Assist analysts with instrumentation related to analytical and microbial testing, ensuring equipment is maintained, qualified, and available to meet operational schedules. You will proactively plan for instrument needs and implement corrective actions to prevent recurring failures.
- Participate in routine inspections of laboratory facilities to ensure compliance with Good Manufacturing Practices (GMP).

