Production Supervisor (Full-time)

Accentuate Staffing is assisting a well-established medical device manufacturer who is hiring a Production Supervisor to join their team! This is a direct hire opportunity leading daily production operations and supporting ongoing operational excellence initiatives. This is an exciting opportunity to join an organization focused on quality, continuous improvement, employee development, and delivering products that support critical customer and industry needs. The ideal candidate will bring leadership experience within a regulated manufacturing environment and a proven ability to develop teams, improve processes, and drive performance. This individual will oversee production activities, collaborate with cross-functional departments, support compliance, and quality requirements, and help implement continuous improvement initiatives that enhance productivity, efficiency, and employee engagement. Lead daily manufacturing operations across multiple production areas, ensuring production targets, quality standards, safety expectations, and delivery commitments are consistently met. Supervise, coach, and develop production staff and frontline leaders while fostering a culture of accountability, engagement, and continuous improvement. Drive operational excellence initiatives focused on process improvement, productivity, efficiency gains, waste reduction, and overall manufacturing performance. Partner with Quality, Engineering, Supply Chain, Planning, and other departments to support production readiness, resolve operational challenges, and ensure successful execution of customer requirements. Monitor departmental performance metrics, labor utilization, training effectiveness, and production costs while identifying opportunities for improvement and resource optimization. Support compliance with quality systems, regulatory standards, audits, inspections, training requirements, and corrective action initiatives to maintain operational excellence. Bachelor’s degree or equivalent combination of education and relevant manufacturing leadership experience. Six or more years of experience supervising and developing teams within a medical device regulated manufacturing environment. Demonstrated success leading production operations and implementing Lean Manufacturing, continuous improvement, or operational excellence initiatives. Experience working within quality-driven manufacturing environments governed by standards such as ISO 9001, ISO 13485, FDA, GMP, or equivalent regulatory requirements. Strong leadership, communication, analytical, and problem-solving skills with the ability to manage multiple priorities and drive results. Proven ability to build effective cross-functional relationships, develop employees, identify root causes, and implement sustainable process improvements.