Supervisor, Sr. Team Leader
Join a global pharmaceutical leader committed to improving lives through innovation and a shared mission to deliver better health outcomes. At our company, change isn't something we wait for-it's something we create. Be part of a collaborative culture where your expertise and values help shape meaningful progress.
Position: Supervisor, Senior Team Leader - 2nd Shift (2:30 PM - 11:00 PM)
We're seeking a dedicated Senior Team Leader to oversee production operations during the second shift in our Medical Device manufacturing division. This role is pivotal in managing personnel, optimizing workflow, and ensuring efficient use of equipment, materials, and labor.
Key Responsibilities:
- Lead and support production teams, ensuring smooth product flow and timely resolution of technical issues.
- Meet production deadlines and efficiency targets while maintaining high standards of quality.
- Recommend and implement improvements to production processes and product quality in alignment with company policies.
- Enforce safety protocols and interpret company policies with accuracy.
- Ensure completeness and accuracy of Device History Records for all completed production.
- Develop staffing and training plans based on forecasted production schedules.
- Conduct regular performance evaluations and support employee development.
- Participate in New Product Introduction (NPI) initiatives.
- Collaborate with Planning, QA, Engineering, and other departments to resolve production challenges and meet schedule requirements.
- Maintain safety and housekeeping standards in the production area.
- Assist with hiring, training, and managing employee relations, including attendance tracking and performance management.
- Drive continuous improvement initiatives and cross-functional collaboration.
Supervision & Reporting:
- Operates independently with minimal supervision.
- Reports directly to the Manufacturing Manager.
Qualifications:
- Minimum 5 years of experience in medical device manufacturing, preferably in a high-mix, low-volume environment.
- At least 3 years of supervisory experience in a GMP-regulated setting.
- Bachelor's degree required.
- Strong computer skills (Word, Excel, PowerPoint); ability to learn new systems (e.g., MS Project, Visio, ERP).
- Excellent interpersonal, organizational, and analytical skills.
- Proven problem-solving capabilities.
- Preferred: formal supervisory training.
- Lean/Six Sigma certification (Greenbelt or Blackbelt) is a plus.
- Solid understanding of GMP and FDA regulatory requirements.
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