Manufacturing Supervisor

Stryker; Ventura (CA); Sur place; USD 98 000 - 164 000; Plein temps

Résumé du poste

Stryker in Ventura, CA is seeking a Manufacturing Supervisor to lead daily ops, ensuring safety, quality, and on-time delivery in a regulated medical device setting. You will manage labor, equipment, capacity, and partner with Planning, Supply Chain, Engineering, Quality, and Materials to resolve issues while driving Lean and continuous improvement.

The role requires a bachelor’s degree in a related field or 10 years of leadership in manufacturing, with 2+ years in Lean/Kaizen, GMP experience,

Qualifications

• Bachelor's degree in a related field with 4+ years of leadership in manufacturing, or 10+ years of leadership without a degree.
• 4+ years leading teams in a regulated manufacturing environment.
• 2+ years leading Lean Manufacturing, Kaizen or continuous improvement initiatives.
• Experience with regulated quality systems and compliance.

Responsabilités

• Lead daily manufacturing operations to meet safety, quality, delivery, productivity, yield, and cost objectives.
• Monitor performance metrics and implement corrective actions to address gaps and improve results.
• Ensure regulatory and GMP compliance, including audit readiness activities.
• Manage labor, equipment, and production capacity to meet customer demand and production schedules.
• Partner with Planning, Supply Chain, Engineering, Quality, and Materials to resolve production issues and support operational goals.
• Lead recruiting, onboarding, performance management, coaching, and development activities for production employees and supervisors.
• Drive Lean Manufacturing, Kaizen, and continuous improvement initiatives to improve quality, increase capacity, reduce waste, and optimize efficiency.
• Manage operating expenses, support budget execution, and identify cost-saving opportunities while maintaining quality and compliance standards.

Connaissances

Leadership

Lean Manufacturing

Kaizen

Regulatory compliance

Audit readiness

Team development

Formation

Bachelor's degree in Engineering/Science/Business/Supply Chain

Description du poste

Join a manufacturing leadership role with broad responsibility across production, quality, compliance, people leadership, and continuous improvement in a regulated medical device environment. The Manufacturing Supervisor oversees daily manufacturing operations, ensuring products are produced safely, efficiently, and in compliance with applicable quality and regulatory requirements while supporting operational performance and team development.

What You Will Do

• Lead daily manufacturing operations to achieve safety, quality, delivery, productivity, yield, and cost objectives.
• Monitor operational performance metrics and implement corrective actions to address gaps and improve results.
• Ensure compliance with applicable regulatory, quality system, GMP, and company requirements, including audit readiness activities.
• Manage labor, equipment, and production capacity to meet customer demand and production schedules.
• Partner with Planning, Supply Chain, Engineering, Quality, and Materials teams to resolve production issues and support operational goals.
• Lead recruiting, onboarding, performance management, coaching, and development activities for production employees and supervisors.
• Drive Lean Manufacturing, Kaizen, and continuous improvement initiatives to improve quality, increase capacity, reduce waste, and optimize efficiency.
• Manage operating expenses, support budget execution, and identify cost-saving opportunities while maintaining quality and compliance standards.

What You Will Need

Required Qualifications

• Bachelor's degree in Engineering, Science, Business, Supply Chain, or a related field and minimum 4 years of leadership experience in manufacturing; OR minimum 10 years of manufacturing leadership experience in lieu of a degree.
• Minimum 4 years of experience leading teams within a regulated manufacturing environment.
• Minimum 2 years of experience leading Lean Manufacturing, Kaizen, or continuous improvement initiatives.
• Experience working within regulated quality systems and compliance requirements.

Preferred Qualifications

• Minimum 2 years of experience in medical device manufacturing.
• Experience working with Good Manufacturing Practices (GMP), FDA regulations, and quality system requirements.
• Experience managing operating budgets, capital projects, and workforce planning.
• Lean Manufacturing certification or continuous improvement certification.

$98,200 - $163,700 USD Annual