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Posted 18 days ago

Production Manager

@ Kelly Services

Ontario

$62/hrFull-time10+ years experience
Apply now
SIGNALS

Overview

Kelly Services is hiring a Production Manager on a temp-to-perm basis for a medical-device manufacturer in North York, ON. The role leads manufacturing operations from procurement through shipment, enforces ISO 13485, GMP and FDA/Health Canada compliance, and leads a production team. Pay is $60-$65/hour plus 4% vacation pay, Monday to Friday onsite.

Pay:

$62 an hour

Responsibilities:

  • Lead all manufacturing operations, from planning through shipment
  • Ensure ISO 13485, GMP and FDA compliance
  • Oversee quality, CAPA and continuous improvement
  • Lead and develop a multidisciplinary production team
  • Drive cost reduction and Lean initiatives

Requirements summary:

  • Bachelor's in engineering or operations, or equivalent experience
  • 10+ years of production management in regulated industries
  • Knowledge of ISO 13485, GMP, FDA and Health Canada regulations
  • Experience with NetSuite, SAP, Oracle or equivalent ERP/MRP
  • Proven cross-functional leadership

Tools & skills

Benefits mentioned

Vision
Source and dates

Employer career site / ATS feed · careerpage

Employer posting date
2026-10-19
First seen by our source
2026-10-11
Source record updated
2026-10-26

These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.

Job details

SenioritySenior
DepartmentPharmacy
Experience10+ years
Manages peopleYes
Hours per week40
Scheduleday
Work settingPlant or factory, Office
PositionSitting and standing
Physical demandsphysical low · computer high
LanguagesEnglish
EducationBachelor’s degree (required)
Fields of studyEngineering, Manufacturing, Operations Management
Perks mentionedGenerous paid time off

Summary and details written by AI from the posting; the employer’s posting is the authority.

Kelly Services

FieldValue
Open jobs on Jobsy103
Job description

Kelly Services’ has partnered with a client in North York, ON to recruit for a medical-device manufacturing company

Temp to perm role

Monday to Friday onsite

Pay rate: $60-$65/hour + 4% vacation pay

Key Responsibilities

Production Operations & Manufacturing

  • Lead all aspects of manufacturing operations, including production planning, scheduling, procurement, materials management, assembly, testing, packaging, inventory control, deployment, and logistics.
  • Ensure production schedules are achieved while maintaining quality, cost, and delivery objectives.
  • Monitor production capacity and develop strategies to support future business growth.
  • Optimize manufacturing workflows to improve productivity, efficiency, and throughput.
  • Oversee inventory management, production forecasting, and material availability.
  • Manage supplier relationships to ensure quality, on-time delivery, and resolution of material quality issues.
  • Coordinate production priorities across engineering, purchasing, service, and customer support teams.
  • Drive Design for Manufacturing (DFM) initiatives in collaboration with Engineering.

Quality, Regulatory & Compliance

  • Ensure compliance with ISO 13485, GMP, FDA, Health Canada, and other applicable regulatory requirements.
  • Maintain world-class manufacturing quality standards.
  • Develop, implement, and continuously improve Standard Operating Procedures (SOPs), work instructions, and production documentation.
  • Oversee non-conformance investigations, corrective and preventive actions (CAPA), and continuous quality improvements.
  • Monitor manufacturing metrics including yield, defect rates, rework, scrap, and overall equipment effectiveness.
  • Support internal and external quality audits.

Strategic Manufacturing Leadership

  • Develop and execute Cellview’s manufacturing strategy in alignment with corporate growth objectives.
  • Support new product introduction (NPI) activities, ensuring smooth transition from engineering into production.
  • Identify opportunities for automation, process improvements, and manufacturing scalability.
  • Collaborate with EssilorLuxottica on long-term manufacturing strategy, operational alignment, and best practice implementation.
  • Lead manufacturing readiness for future product releases and production expansion.

Operational Excellence & Continuous Improvement

  • Establish KPIs and production dashboards to monitor operational performance.
  • Lead Lean Manufacturing and continuous improvement initiatives.
  • Drive cost reduction initiatives while maintaining product quality.
  • Improve manufacturing efficiency through process optimization and waste reduction.
  • Develop roadmaps for operational maturity and scalable manufacturing systems.

Leadership & Team Development

  • Recruit, develop, mentor, and lead a multidisciplinary production team, including technicians, assemblers, inventory personnel, and manufacturing support staff.
  • Foster a culture of accountability, collaboration, quality, and continuous improvement.
  • Conduct performance reviews, coaching, and employee development planning.
  • Promote a safe, organized, and productive manufacturing environment.

Cross-Functional Collaboration

  • Partner closely with Engineering, Regulatory Affairs, Quality Assurance, Supply Chain, Service, and Finance.
  • Support engineering change implementation and production readiness activities.
  • Participate in executive planning and operational review meetings.
  • Provide regular production reporting, forecasts, risks, and improvement recommendations to senior leadership.

Required Qualifications

  • Bachelor’s degree in Engineering, Manufacturing, Operations Management, or a related technical discipline (or equivalent industry experience).
  • 10+ years of progressive manufacturing or production management experience within medical devices, optics, electronics, precision manufacturing, or similarly regulated industries.
  • Demonstrated experience managing full-cycle manufacturing operations from procurement through production, quality assurance, and shipment.
  • Strong understanding of:
  • ISO 13485
  • GMP
  • FDA Quality System Regulations
  • Health Canada Medical Device Regulations
  • Proven leadership experience managing cross-functional teams.
  • Experience implementing and improving manufacturing processes within regulated environments.
  • Proficiency with ERP/MRP systems (NetSuite, SAP, Oracle, or equivalent).
  • Excellent analytical, organizational, communication, and problem-solving skills.
  • Strong decision-making and project management abilities.

Preferred Qualifications

  • Experience scaling manufacturing from early-stage product development to commercial production.
  • Experience working within a high-growth or startup environment.
  • Lean Manufacturing and/or Six Sigma certification or equivalent experience.
  • Optical, ophthalmic, imaging, or medical device manufacturing experience.
  • Experience supporting Design for Manufacturing (DFM) initiatives.
  • Familiarity with manufacturing automation and process optimization.
  • Experience collaborating with international manufacturing organizations.

10294722

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