Production Supervisor - 3rd Shift
Thermo Fisher Scientific
- Location
- Meriden, Connecticut, United States of America
- Employment
- Full Time
- Work model
- On-Site
- Level
- Mid
- H-1B history
- 76 approvals (FY2023)
- Posted
- 1d ago
About this role
Work Schedule Third Shift (Nights) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description Production Supervisor - 3rd Shift At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Our teams enable our customers to make the world healthier, cleaner, and safer by delivering innovative technologies, products, and services that support life-changing scientific discoveries and improve patient outcomes. At our Meriden, CT manufacturing site, you'll join a team committed to safety, quality, operational excellence, and employee development. We invest in our people by providing opportunities to learn, grow, and build rewarding careers while making a meaningful impact every day. We are seeking an experienced and motivated 3rd Shift Production Supervisor to lead manufacturing operations on our overnight shift. In this role, you'll provide hands-on leadership to a team of production employees, driving a culture centered on safety, quality, continuous improvement, and employee engagement. 3rd Shift Hours: Sunday – Friday: 11:00 PM – 7:00 AM , including rotating weekend on-call coverage.
What You'll Do
Lead daily manufacturing operations to safely meet production schedules, quality standards, and customer commitments. Foster a culture where safety is the top priority by modeling safe behaviors, conducting safety meetings, leading audits, and ensuring compliance with all safety procedures. Supervise, coach, mentor, and develop a team of hourly production employees while building engagement, accountability, and strong team performance. Manage daily workforce activities including staffing, attendance, overtime, vacation scheduling, timekeeping, and shift communications. Provide ongoing coaching, performance feedback, recognition, and employee development to help team members succeed. Coordinate production priorities, assign resources, and adjust workflows to maximize productivity while maintaining product quality. Partner with Quality, Engineering, Planning, Maintenance, and other departments to quickly resolve production challenges and improve operational performance. Drive continuous improvement initiatives using Lean Manufacturing, Practical Process Improvement (PPI), Six Sigma, and structured problem-solving tools. Monitor production metrics and analyze operational data to identify opportunities to improve safety, quality, delivery, productivity, and cost. Ensure compliance with GMP, ISO, FDA, company quality systems, and standard operating procedures. Support process improvements that reduce waste, improve efficiency, and enhance overall manufacturing performance. Build positive working relationships within a union manufacturing environment by consistently administering the collective bargaining agreement and promoting respectful employee relations.
What We're Looking For
Required Qualifications: High School Diploma or GED. Three (3) or more years of manufacturing experience. One (1) or more years of supervisory, team lead, or other manufacturing leadership experience. Strong communication, organizational, and problem-solving skills. Ability to lead by example and motivate teams in a fast-paced manufacturing environment.
Preferred Qualifications
Higher level education or certifications. Experience supervising employees in a union manufacturing environment. Experience interpreting and administering a collective bargaining agreement. Experience in medical device, pharmaceutical, food, life sciences, or other regulated manufacturing environments. Knowledge of GMP, FDA, and ISO quality systems. Experience with Lean Manufacturing, Six Sigma, Kaizen, or Practical Process Improvement (PPI). Experience