Production Supervisor 2nd Shift

Production Supervisor, 2nd Shift Woodland, CA | Full-Time | On-Site Shift: Monday through Friday, 1:00 PM to 9:30 PM Salary: $80,000 - $90,000 annually About the Role: We are seeking an experienced Production Supervisor to lead second shift manufacturing operations within a regulated medical device manufacturing environment. Reporting to the Production Manager, this role is responsible for supervising production personnel, ensuring daily production targets are achieved, maintaining product quality, and fostering a safe and efficient manufacturing environment. The ideal candidate has previous leadership experience in medical device manufacturing , with injection molding experience strongly preferred , and a proven ability to lead teams while maintaining compliance with FDA Quality System Regulations, cGMP, and ISO 13485 standards. This position plays a key role in driving productivity, employee development, and continuous improvement across second shift operations. Responsibilities: Supervise second shift production operations to ensure safety, quality, productivity, and on-time delivery objectives are achieved. Lead, coach, mentor, and develop production employees while promoting accountability, teamwork, and continuous improvement. Assign daily workloads and adjust staffing to meet production schedules without compromising quality or regulatory compliance. Monitor production performance, identify operational issues, and implement corrective actions to improve efficiency and throughput. Support manufacturing operations involving medical device assembly, injection molding, and related production processes. Collaborate with Quality, Engineering, Regulatory, Supply Chain, Human Resources, Maintenance, and Operations to resolve production challenges and support manufacturing objectives. Review production schedules, work orders, routers, and manufacturing documentation to ensure accurate execution of production plans. Coordinate employee onboarding, training plans, qualification records, and ongoing skills development for production personnel. Ensure compliance with FDA Quality System Regulations (QSR), cGMP, ISO 13485, and company quality procedures. Partner with Quality and Engineering to support process validations, verification activities, equipment changes, and continuous process improvements. Monitor manufacturing metrics including productivity, scrap, downtime, quality, and labor utilization to identify improvement opportunities. Lead root cause investigations and corrective actions related to production, quality, and equipment issues. Maintain accurate production records, employee documentation, performance evaluations, and timekeeping records. Enforce workplace safety policies and promote a culture of quality, compliance, and operational excellence. Qualifications: Associate's degree in Manufacturing, Engineering Technology, Business, or a related field preferred. Equivalent experience will be considered. Minimum of 5 years of supervisory experience within a medical device manufacturing environment. Medical device manufacturing experience is required. Injection molding manufacturing experience is strongly preferred. Strong knowledge of FDA Quality System Regulations (21 CFR Part 820), cGMP, ISO 13485, and regulated manufacturing environments. Experience supervising production teams in high-volume manufacturing environments. Ability to interpret technical drawings, manufacturing documentation, work instructions, and production schedules. Experience with ERP or manufacturing scheduling systems. Strong leadership, communication, coaching, and employee development skills. Excellent organizational, problem-solving, and decision-making abilities. Proficiency with Microsoft Office applications, including Excel, Word, and Outlook. Desired Qualifications: Experience supervising silicone injection molding , medical device assembly, extrusion, or cleanroom manufacturing operations. Experience supporting Lean Manufacturing, 5S, Kaizen, or continuous improvement initiatives. Knowledge of process validation, equipment qualification, and production change control. Experience working with cross-functional engineering and quality teams to improve manufacturing performance. Previous experience mentoring team leads or developing future production supervisors. Bilingual English/Spanish communication skills are a plus. #J-18808-Ljbffr