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Process Supervisor

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ClinLab Solutions Group

Toms River, NJ (In Person)

Full-Time

Posted 1 week ago (Updated 1 week ago) • Actively hiring

Expires 5/31/2026

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Job Description

Process Supervisor at ClinLab Solutions Group Process Supervisor at ClinLab Solutions Group in Toms River, New Jersey Posted in 1 day ago.
Type:
full-time
Job Description:
Work Location:
Ocean County, New Jersey Summary:
This role is responsible for overseeing process improvement initiatives, production scheduling, and team leadership within a cGMP-regulated environment. The position requires a strong background in process optimization, compounding, and cross-functional collaboration to ensure operational excellence and continuous improvement.
Responsibilities:
Lead and coordinate the development and execution of short-term production schedules in alignment with forecasts and operational goals. Drive process improvement initiatives by analyzing key performance indicators, identifying opportunities, and implementing solutions for enhanced efficiency and quality. Collaborate with project managers and engineering teams to ensure seamless execution of development and engineering activities. Monitor daily production performance, review metrics, and drive accountability for throughput, downtime, changeovers, and quality events. Support investigations, root cause analysis, and corrective/preventative actions to address operational issues and ensure compliance with GDP and cGMP standards. Provide leadership, coaching, and support to cross-functional teams, fostering a culture of continuous improvement and high performance. Ensure documentation integrity, perform document reviews and approvals, and reinforce data integrity standards. Remain flexible to support team needs, including shift coverage and escalation of events, and collaborate to ensure adequate staffing for operational demands.
Qualifications:
Bachelor's degree or higher in Science or Engineering preferred. Minimum of 5 years of experience in a life sciences or related industry. Demonstrated expertise in cGMP and GDP requirements, with the ability to communicate and apply these standards effectively. Strong background in process improvement and compounding is highly desirable. Excellent leadership, coaching, and project management skills. Proven ability to analyze data, develop visual presentations, and communicate effectively with diverse groups. Strong technical writing, problem-solving, and organizational skills. Ability to work independently, adapt to changing priorities, and collaborate across multiple shifts and teams.

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