Production Group Lead IV- 2nd Shift at AVC Medtronic Int'l Trading, Inc — Grand Rapids, MI
Full job description
We anticipate the application window for this opening will close on - 22 Aug 2026
# A Day in the Life
At Medtronic, we act boldly, compete to win, move with speed, foster belonging, and deliver results—the right way. This is the Medtronic Mindset, defining how we work and what we value. Our brand is rooted in action, and every team member plays a vital role in bringing our culture to life.
We recognize your extraordinary potential to help ensure future generations live better, healthier lives. A career at Medtronic is purposeful, mission-driven, and unlike any other. We are committed to alleviating pain, restoring health, and extending life for millions worldwide.
We bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We’re working a minimum of 5 days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary.
Responsibilities may include the following and other duties may be assigned.
- Leads production team work process, equipment testing, manufacturing, disassembly, and reassembly as assigned by supervisor.
- Prioritizes use of operators according to build schedule.
- Communicates process issues and provides status updates to team supervisor.
- Coaches operators/assemblers on production and problem solving skills, performing technical review and machinery setup/breakdown as needed.
- Ensures Medtronic company quality and safety standards are upheld.
Required Knowledge and Experience: Requires 5+ years of related experience
Nice to Have:
- Prior quality/inspection experience preferred.
- Demonstrated ability to train others on inspections that you are signed off on
- Excellent in Good Documentation Practices (GDP)
- Proven experience of 3-5 years in Quality within a regulated industry such as medical devices or Pharma is required for this role.
- An ideal candidate should be able to demonstrate a history of strong teamwork, be proficient in problem resolution and skilled in both written and verbal communication.
- Prior medical device experience.
- Excellent quality standards.
- Experience in a clean room environment.
- Experience with handling and inspecting PCBAs
Physical Job Requirements
U.S. Work Authorization & Sponsorship
Recruitment Fraud Alert
# Benefits & Compensation
Salary ranges for U.S (excl. PR) locations (USD):$53,600.00 - $80,400.00
This position is eligible for a short-term incentive called the Operations Incentive Plan (OIP).