Technical Lead

Overview

On Site
$40+
Contract - W2
Contract - Independent
100% Travel

Skills

ISO 13485
ISO 9000
OQ
NPI
PQ
Six Sigma
DFA
IQ
Manufacturing
Medical Devices
SolidWorks
Root Cause Analysis
Supply Chain Management
Technical Writing
Electrical Engineering
Mechanical Engineering
Risk Management
Design For Manufacturability
Lean Manufacturing
Design Controls
Biomedicine
Plant Lifecycle Management
Product Design

Job Details

Role: Technical Lead

Location: Arlington, TN

Key Responsibilities:

  • Lead technical planning and execution of NPI projects from concept through commercialization.
  • Collaborate with R&D, Quality, Regulatory, Manufacturing, and Supply Chain teams to ensure smooth product transition.
  • Own the technical documentation including design history files (DHF), product specifications, and risk assessments.
  • Apply Design for Manufacturability (DFM), Design for Assembly (DFA), and process validation (IQ/OQ/PQ) principles.
  • Serve as the main technical contact for suppliers, contract manufacturers, and internal stakeholders.
  • Support regulatory submissions (e.g., 510(k), PMA) with technical data and validation reports.
  • Drive root cause analysis and implement corrective actions during product design and pilot runs.
  • Ensure all development activities comply with ISO 13485, FDA QSR (21 CFR Part 820), and other relevant standards.

Qualifications:

  • Bachelor s or master s degree in mechanical, Biomedical, Electrical Engineering, or related field.
  • 7+ years of engineering experience in the medical device industry, with 3+ years in an NPI or technical lead role.
  • Strong knowledge of medical device product lifecycle, especially development and manufacturing transfer phases.
  • Proven experience with design controls, risk management (ISO 14971), and validation protocols.
  • Familiarity with CAD software (e.g., SolidWorks), PLM systems, and ERP tools.
  • Excellent leadership, communication, and project management skills.

Preferred Qualifications:

  • Experience with Class II or Class III medical devices.
  • Six Sigma or Lean Manufacturing certification.
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