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Genesee Biomedical, Inc.

Production Manager Medical Devices

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Job Description

Production Manager - Medical Devices Genesee Biomedical, Inc. - 3.0 Denver, CO Job Details Full-time $95,000 - $140,000 a year 4 hours ago Benefits Dental insurance 401(k) Paid time off 401(k) matching Retirement plan Qualifications Customer communication Manufacturing management Operations management Manufacturing budget management Labor cost analysis Manufacturing facility experience Team development Supervising experience Production management software Leading team collaboration initiatives Regulatory/legal compliance standards in production Quality standards in production Biomedical regulatory compliance Managing projects Managing manufacturing teams Productivity software Legal compliance Cross-functional team management
ISO 13485
Cross-functional communication FDA regulations Capital budget management Full Job Description About the Role Genesee BioMedical, Inc. is looking for an experienced Production Manager to lead manufacturing operations at our Denver, CO facility. You'll own daily production performance, regulatory compliance, and the growth of a team of supervisors, leads, and operators across our cleanroom, packaging, and metal manufacturing areas. This is a hands-on leadership role for someone who thrives on building strong teams, hitting targets, and making processes better every day. What You'll Do Direct daily production across all shifts and product lines to meet schedule, output, cost, and quality targets. Own the production plan, capacity, and staffing model in line with the master schedule and customer demand. Own on-time delivery and ERP/MES data integrity; report performance to senior leadership and represent production in S&OP and customer meetings. Ensure compliance with
FDA 21 CFR
Part 820, ISO 13485, GMP, and company SOPs, including cleanroom gowning and environmental protocols. Keep batch records, device history records (DHRs), and production logs accurate and audit-ready; lead production's role in internal, customer, and regulatory audits. Partner with Quality, Engineering, Maintenance, and Supply Chain on root cause investigations and CAPAs. Own production KPIs (OEE, yield, scrap, labor efficiency, schedule attainment) and lead Lean, Six Sigma, 5S, and kaizen initiatives. Manage the department budget, labor costs, and capital equipment and process improvement projects. Lead, coach, and develop Production Supervisors and Leads; own hiring, onboarding, training, performance reviews, and succession planning. Build a culture of safety, quality, and continuous improvement. What You Bring 7+ years of progressive manufacturing leadership experience in a regulated environment, including 3-5 years in a supervisory or management role; medical device experience preferred. Strong working knowledge of
ISO 13485, FDA 21 CFR
Part 820, and GMP. Experience managing department budgets, labor costs, and capital or cross-functional improvement projects. Excellent leadership, planning, and communication skills, with the ability to influence across functions. Proficiency with Microsoft Office and ERP/MES systems. Bachelor's degree in Engineering, Operations Management, Life Sciences, or a related field preferred; equivalent combination of education and experience considered. Nice to Have Cleanroom or sterile manufacturing experience (ISO Class 7 or 8). Lean or Six Sigma certification.
Pay:
$95,000.00 - $140,000.00 per year
Benefits:
401(k) 401(k) matching Dental insurance Paid time off Retirement plan Application Question(s): How many years of experience do you have in an FDA- or ISO 13485-regulated manufacturing environment?
Work Location:
In person

Benefits

  • Paid Time Off (PTO)
  • 401(k) Plans
  • Dental Insurance
  • Other Retirement and Savings