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Technical Line Lead - Medical Devices

Job in Vandalia, Montgomery County, Ohio, 45377, USA
Listing for: Johnson Electric
Full Time position
Listed on 2026-07-09
Job specializations:
  • Quality Assurance - QA/QC
    Production QC/QA, Regulatory Compliance Specialist
  • Manufacturing / Production
    Production QC/QA, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

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 accuracy

    Ability 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 — We can’t wait to meet you!

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