Haemonetics Software Solutions
Night Shift Manufacturing Operations Manager
Haemonetics Software Solutions, Phila, Pennsylvania, United States
Night Shift Manufacturing Operations Manager page is loaded## Night Shift Manufacturing Operations Managerlocations:
Clinton, PAtime type:
Full timeposted on:
Posted Todayjob requisition id:
R9871We are constantly looking to add to our core talent. If you are seeking a career that is challenging and rewarding, a work environment that is diverse and dynamic, look no further — Haemonetics is your employer of choice.## Job DetailsAt Haemonetics we manufacture critical disposable medical devices and are scaling to meet demand while continuously driving excellent product quality. We’re adding a Night Shift Manufacturing Operations Manager to lead overnight production, safeguarding quality, compliance, and output while keeping people safe.**Job Summary**Own end-to-end night-shift operations. Lead supervisors, group leaders, and hourly teams to hit plan, protect quality, maintain compliance (21 CFR 820/ISO 13485/GMP/GDP), and drive continuous improvement. You’ll set the pace on safety, OEE, schedule attainment, FPY, scrap, and labor productivity—and ensure clean, tight handoffs to the day shift.Key Responsibilities* Safety & Compliance
+ Champion a zero-injury culture; enforce LOTO, PPE, and cleanroom/gowning standards.
+ Ensure strict adherence to FDA, ISO 13485, GMP, and Good Documentation Practices; audit batch records/travelers for completeness and accuracy.
+ Lead incident investigations and near-miss reviews; implement corrective and preventive actions (CAPA).* People Leadership
+ Lead and develop supervisors, group leaders, and operators: staffing, onboarding, coaching, performance management, and recognition.
+ Set clear expectations and standard work; hold the line on accountability and attendance.
+ Maintain morale and discipline on the night shift; resolve conflicts and escalate appropriately.* Production Control
+ Own the shift schedule to meet plan; manage changeovers, start-ups, and shutdowns.
+ Monitor line health in real time (Overall Equipment Effectiveness, cycle times, yields); remove bottlenecks fast.
+ Coordinate with Maintenance and Engineering for break-fix, PM compliance, and downtime reduction; manage call-in/escalation.* Quality Assurance
+ Ensure products meet or exceed specifications; oversee in-process checks, line clearance, and lot control.
+ Drive first-pass yield and scrap reduction; contain defects immediately with documented NCE/NCR and disposition.
+ Partner with Quality on deviations, investigations, and change control.* Materials & Readiness
+ Align with Planning/Materials on kitting, WIP flow, and inventory accuracy; prevent line starves/stops.
+ Verify tooling/fixtures availability and readiness; manage consumables and 5S standards.* Continuous Improvement
+ Identify waste and variability; lead Kaizen/PDCA to improve throughput, cost, and stability.
+ Promote and lead quick, easy Kaizens, 5S, and GEMBA walks.
+ Standardize best practices across crews; update work instructions and training as processes evolve.* Communication & Reporting
+ Run crisp tier meetings; communicate priorities, issues, and countermeasures.
+ Deliver nightly KPIs (OEE, FPY, scrap, attainment, downtime, safety) and next-shift risks.
+ Execute disciplined shift handoff to days/evenings with clear actions and owners.* General Supervisory Duties
+ Interview, hire, train, schedule, assign work, evaluate performance, reward/discipline, and resolve grievances in accordance with company policy and law.**Qualifications*** Bachelor’s degree in industrial engineering, or related field.* MBA preferred.* 5+ years leading production teams (medical devices or other regulated manufacturing preferred).* Working knowledge of GMP, ISO 13485, and FDA 21 CFR 820; CAPA, NCR/NCE, change control familiarity.* Proven results improving OEE, FPY, scrap, and schedule attainment.* Strong floor presence, communication, and decision-making—especially under limited off-hour support.* Comfortable with nightshift work and schedule flexibility as business needs evolve. #J-18808-Ljbffr
Clinton, PAtime type:
Full timeposted on:
Posted Todayjob requisition id:
R9871We are constantly looking to add to our core talent. If you are seeking a career that is challenging and rewarding, a work environment that is diverse and dynamic, look no further — Haemonetics is your employer of choice.## Job DetailsAt Haemonetics we manufacture critical disposable medical devices and are scaling to meet demand while continuously driving excellent product quality. We’re adding a Night Shift Manufacturing Operations Manager to lead overnight production, safeguarding quality, compliance, and output while keeping people safe.**Job Summary**Own end-to-end night-shift operations. Lead supervisors, group leaders, and hourly teams to hit plan, protect quality, maintain compliance (21 CFR 820/ISO 13485/GMP/GDP), and drive continuous improvement. You’ll set the pace on safety, OEE, schedule attainment, FPY, scrap, and labor productivity—and ensure clean, tight handoffs to the day shift.Key Responsibilities* Safety & Compliance
+ Champion a zero-injury culture; enforce LOTO, PPE, and cleanroom/gowning standards.
+ Ensure strict adherence to FDA, ISO 13485, GMP, and Good Documentation Practices; audit batch records/travelers for completeness and accuracy.
+ Lead incident investigations and near-miss reviews; implement corrective and preventive actions (CAPA).* People Leadership
+ Lead and develop supervisors, group leaders, and operators: staffing, onboarding, coaching, performance management, and recognition.
+ Set clear expectations and standard work; hold the line on accountability and attendance.
+ Maintain morale and discipline on the night shift; resolve conflicts and escalate appropriately.* Production Control
+ Own the shift schedule to meet plan; manage changeovers, start-ups, and shutdowns.
+ Monitor line health in real time (Overall Equipment Effectiveness, cycle times, yields); remove bottlenecks fast.
+ Coordinate with Maintenance and Engineering for break-fix, PM compliance, and downtime reduction; manage call-in/escalation.* Quality Assurance
+ Ensure products meet or exceed specifications; oversee in-process checks, line clearance, and lot control.
+ Drive first-pass yield and scrap reduction; contain defects immediately with documented NCE/NCR and disposition.
+ Partner with Quality on deviations, investigations, and change control.* Materials & Readiness
+ Align with Planning/Materials on kitting, WIP flow, and inventory accuracy; prevent line starves/stops.
+ Verify tooling/fixtures availability and readiness; manage consumables and 5S standards.* Continuous Improvement
+ Identify waste and variability; lead Kaizen/PDCA to improve throughput, cost, and stability.
+ Promote and lead quick, easy Kaizens, 5S, and GEMBA walks.
+ Standardize best practices across crews; update work instructions and training as processes evolve.* Communication & Reporting
+ Run crisp tier meetings; communicate priorities, issues, and countermeasures.
+ Deliver nightly KPIs (OEE, FPY, scrap, attainment, downtime, safety) and next-shift risks.
+ Execute disciplined shift handoff to days/evenings with clear actions and owners.* General Supervisory Duties
+ Interview, hire, train, schedule, assign work, evaluate performance, reward/discipline, and resolve grievances in accordance with company policy and law.**Qualifications*** Bachelor’s degree in industrial engineering, or related field.* MBA preferred.* 5+ years leading production teams (medical devices or other regulated manufacturing preferred).* Working knowledge of GMP, ISO 13485, and FDA 21 CFR 820; CAPA, NCR/NCE, change control familiarity.* Proven results improving OEE, FPY, scrap, and schedule attainment.* Strong floor presence, communication, and decision-making—especially under limited off-hour support.* Comfortable with nightshift work and schedule flexibility as business needs evolve. #J-18808-Ljbffr