Production Team Lead - Medical Devices

Johnson Electric; Vandalia (OH); On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Recognition Programs

Community Engagement Opportunities

Access to Innovation Hubs

Job summary

Johnson Electric is seeking a Technical Line Lead for its Medical Devices Operations in Vandalia, OH. In this onsite role, you will lead a team focused on the assembly of wearable medical devices, ensuring compliance with FDA regulations and quality standards.

The ideal candidate has extensive experience in medical device manufacturing and proven leadership abilities. You will train operators, enforce safety and quality standards, and support continuous improvement initiatives.

Qualifications

• 2–3 years of experience working in medical device manufacturing.
• 2–3 years of experience in a Line Lead or leadership role.
• Minimum 1 year of experience working in compliance with FDA regulations.

Responsibilities

• Oversee assembly of medical devices per quality standards.
• Train production operators on processes and equipment.
• Monitor production performance for efficiency and compliance.

Skills

Leadership

Problem solving

Attention to detail

Technical capability

Job description

Join Our Team as a Technical Line Lead – Medical Devices at Johnson Electric!

Location: Vandalia, OH (Onsite)

Facility: Medical Devices Operations

Department: Production / Operations

Vacancy Type: Existing Position

Why You’ll Love Working Here

• Recognition Programs: Programs that recognize and reward employee achievements and contributions.
• Community Engagement: Opportunities to participate in community service and corporate social responsibility initiatives.
• Strong Leadership: Work under experienced and visionary leaders who guide the company towards success.
• Innovation Hubs: Access to state-of-the-art facilities and innovation hubs that foster creativity and development.

What You’ll Be Doing

• Performing and overseeing assembly of wearable medical devices in accordance with approved work instructions, Device Master Records (DMRs), and quality system procedures
• Assigning production operators to tasks, balancing workloads, and coordinating quick changeovers while maintaining quality and traceability
• Training and coaching production operators on manufacturing processes, equipment use, quality requirements, and Standard Operating Procedures (SOPs)
• Ensuring compliance with FDA Quality System Regulations (21 CFR Part 820), ISO 13485 requirements, and internal quality policies
• Verifying adherence to Good Documentation Practices (GDP), including accurate and timely completion of production records
• Enforcing safety standards, lean manufacturing principles, and 5S workplace organization
• Monitoring production performance to maximize efficiency, minimize waste, and support on‑time delivery targets
• Identifying, documenting, and escalating quality issues, non‑conformances, equipment concerns, and resource needs to the Supervisor
• Supporting corrective and preventive actions (CAPA), root cause analysis, and continuous improvement initiatives
• Participating in and recommending GK (continuous improvement) activities to enhance quality, efficiency, and compliance
• Actively performing hands‑on line work to maintain production flow, troubleshoot issues, and meet production commitments

What We’re Looking For

• 2–3 years of experience working in medical device manufacturing
• 2–3 years of experience in a Line Lead or leadership role
• Minimum 1 year of experience working in compliance with FDA regulations
• Strong attention to detail and commitment to quality and documentation accuracyAbility to understand, follow, and train others on technical assembly processes and quality standards
• Proven ability to lead by example and support a compliant, quality‑focused culture
• Strong problem‑solving and analytical skills
• Comfort working in regulated environments with GMP and GDP requirements

Key Competencies

• Leadership and team support
• Technical capability and process understanding
• Attention to detail and thoroughness
• Problem solving and root cause analysis
• Regulatory and quality compliance awareness

Work Environment

• Climate‑controlled medical device manufacturing environment
• Strict adherence to cleanliness, safety, GMP, and regulatory standards
• Hands‑on production floor role

How To Apply

Apply online at www.johnsonelectric.com — We can’t wait to meet you!