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Actalent

QC Supervisor

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What they do

A Quality Assurance Supervisor supervises quality assurance staff and oversees processes involved in the prevention of faults in manufactured products and solutions.

$74,747 / year median in Illinois

-0% projected decline

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Job Description

at Actalent in
Morton Grove, Illinois, United States Job Description Job Title:
QC Lab Supervisor - 3rd Shift Job Description The QC Supervisor oversees all quality control laboratory activities on the 3rd shift, ensuring accurate analytical support for routine processes and new products in a regulated GMP environment. This role accepts full responsibility for laboratory management during the shift, including equipment oversight, documentation control, and approval or rejection of materials and samples. The QC Supervisor leads a small team of analysts, promotes compliance with quality and safety systems, and drives continuous improvement within the laboratory. Responsibilities + Manage the QC laboratory during the 3rd shift and serve as the primary point of contact for all quality control activities. + Oversee the maintenance and calibration of laboratory equipment to ensure accurate and reliable performance. + Manage documentation related to raw materials, intermediates, in-process controls (IPCs), stability, and cleaning samples in accordance with GMP and data integrity requirements. + Review existing standard operating procedures (SOPs) and SOP qualifications (SOPQs), and write or update new procedures to reflect new equipment, technologies, and methods. + Participate in the description of technical procedures and the review of analytical methods, ensuring they are current, clear, and compliant. + Initiate and manage change controls in documentation and systems, including quality control laboratory reports and related records. + Support the introduction and implementation of new work procedures within the laboratory, ensuring proper training and adherence. + Approve or reject raw materials, intermediates, IPCs, stability samples, and cleaning samples based on analytical results and applicable specifications. + Prepare and review analytical records in accordance with current SOPs and SOPQs for subsequent approval or rejection decisions. + Maintain order, cleanliness, and organization within the laboratory to support safe and efficient operations. + Oversee data entry and calculations in laboratory systems, ensuring accuracy and completeness, and generate analytical records and bulletins as needed. + Control and maintain the sample library, ensuring proper storage, traceability, and retrieval of samples. + Write and investigate deviations, out-of-specification ( OOS ), out-of-trend ( OOT ), out-of-expectation ( OOE ) results, and other laboratory events, documenting root causes and corrective actions. + Promote To view full details and how to apply, please login or create a Job Seeker account