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Supervisor, Manufacturing; Overnight

Job in Scranton, Lackawanna County, Pennsylvania, 18512, USA
Listing for: haemonetics
Full Time position
Listed on 2026-05-31
Job specializations:
  • Manufacturing / Production
    Production Manager
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below
Position: Supervisor, Manufacturing (Overnight)

Job Details

Frontline operations Good Manufacturing Practices (GMP) Supervisor is responsible for delivering safe, compliant, high-quality production results by aligning people, process, and materials to business priorities. This role reports directly to a Production Manager. The GMP Supervisor creates consistent execution against plan through clear direction, real-time performance management, and systematic problem‑solving, while driving continuous improvement that increases throughput, reduces waste, and strengthens process reliability.

In a regulated environment, they ensure adherence to quality systems and regulatory expectations, respond decisively to issues to protect customers and the business, and foster a culture where standards are followed because they’re understood, not because someone is watching. They also build team capability through hiring, onboarding, coaching, and accountability, developing a motivated workforce that can sustain performance over time.

This role is a 2nd Shift (6:30 PM-6:45 AM) Supervisor role and will work a 2/2/3 schedule located onsite in Clinton, MA.

Key Responsibilities Leadership & Workforce Direction
  • Assign and direct daily work across manufacturing lines to ensure safety, quality, and output goals are achieved.
  • Sets clear expectations and priorities; makes the plan understandable at the operator level.
  • Leads with calm authority under pressure, steady presence on the floor.
  • Holds people accountable fairly and consistently.
  • Coaches and develops others daily; builds capability, not dependency.
  • Communicates early and often, up, down, and sideways, with no surprises.
  • Delegates effectively and empowers Area Leaders/lead hands without losing control of outcomes.
  • Manages conflict directly and respectfully.
  • Drives engagement and culture, reinforces standards, recognizes wins, and shuts down unsafe/low‑standard behavior immediately.
Safety
  • Accountable for the health and safety of all personnel and work areas within assigned responsibility.
  • Ensures safety policies, procedures, and regulatory requirements are understood and consistently followed.
  • Enforces safety standards and applies disciplinary actions when required.
  • Supports and leads investigations of health and safety incidents, including root cause analysis and corrective action implementation.
  • Monitors, manages, and reports safety metrics across assigned shifts and areas.
  • Ensures timely documentation, tracking, and resolution of safety issues.
Quality and Compliance
  • Accountable for ensuring production output consistently meets established quality standards.
  • Ensures production processes and employee behaviors comply with FDA, cGMP, ISO 13485, MDD, and applicable country/regional regulations.
  • Monitors, manages, and reports quality metrics such as in‑process defects, scrap, deviations, and in‑process inventory.
  • Develops and maintains systems that improve visibility and control of key quality indicators.
  • Ensures Quality Management System documentation (Manufacturing Instructions, Standard Instructions, training records) accurately reflects current production practices.
  • Owns deviation management within the area, including containment, lot tracing, corrective actions, and timely closure of NCEs.
Manufacturing and Delivery
  • Accountable for execution of production schedules on a daily, weekly, and quarterly basis across assigned shifts, lines, or areas.
  • Directs and prioritizes work through GMP Area Leaders to ensure safe, compliant, and efficient operations.
  • Monitors, manages, and reports key manufacturing performance metrics including output, efficiency, scrap, downtime, and schedule attainment.
  • Ensures effective material flow, equipment availability, and labor utilization to prevent production interruptions.
  • Directs and approves select system transactions including high‑dollar inventory adjustments, scrap adjustments, and inventory corrections in Oracle/SAP.
  • Ensures TPM activities are planned, executed, and sustained through Area Leaders and technical resources.
  • Identifies, escalates, and eliminates root causes of chronic part shortages, material constraints, and recurring production slowdowns.
  • Serves as the escalation point for complex…
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