Quality Control Supervisor

Job Responsibilities: 

• Ensure all operations comply with applicable domestic and international regulatory standards, including FDA, ISO, USP, cGMP, and other industry requirements.
• Collaborate across departments to coordinate laboratory testing schedules and support ongoing production timelines.

• Perform and oversee analytical and quality control testing activities as needed.
• Coordinate testing for raw materials, finished products, stability samples, validation studies, and investigational samples.
• Review and maintain controlled documentation, updating procedures and records when necessary to ensure accuracy and compliance.
• Maintain adherence to company policies, quality systems, safety procedures, and operational standards.
• Assist with investigations related to product deviations, process issues, and customer concerns, including preparation and review of investigation documentation.
• Track and ensure timely completion of corrective and preventive actions (CAPAs).
• Promote safe handling practices in regulated laboratory environments, including maintaining exposure levels within established safety guidelines.
• Lead, mentor, and develop team members while promoting accountability, collaboration, and continuous improvement.
• Communicate departmental goals and align team objectives with broader organizational priorities.
• Provide ongoing coaching, training, and performance feedback to support employee growth and operational success.
• Facilitate daily team meetings to review priorities, communicate updates, and monitor performance metrics.
• Monitor team productivity and communicate progress toward operational goals and key performance indicators.
• Manage staffing needs and overtime requirements while ensuring proper documentation and reporting.
• Support workplace organization, cleanliness, and continuous improvement initiatives within the department.
• Ensure all personnel training and qualification requirements remain current and compliant.

Qualifications: 

• Bachelor’s degree in Chemistry, Life Sciences, or a related discipline preferred; equivalent industry experience may be considered.
• Extensive experience in regulated laboratory or quality environments, including prior leadership or supervisory responsibilities.
• Strong background in cGMP laboratory operations and analytical instrumentation.