Industrial Process Engineer — Med Devices (On‑Site Florida)

Medical Engineering Consultants (MEC)

Ocala (FL)

On-site

USD 70,000 - 110,000

Full time

6 days ago
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Job summary

Medical Engineering Consultants (MEC) seeks an Industrial Engineer for contract to hire in Ocala, FL. The role focuses on process controls, design transfer, and NPD support within a regulated medical-device environment.

On-site collaboration with Product Development, Quality, and Manufacturing teams is essential to drive remediation and scalable improvements. The ideal candidate will have 3+ years in medical devices, strong Lean Six Sigma experience, and a track record of coordinating

Qualifications

  • Bachelor's degree in Engineering or technical field.
  • 3+ years experience in medical device industry, preferably with orthopedic implants or similar devices.
  • Strong knowledge of Production and Process Controls, including process validation and documentation across full life cycle.
  • Experience supporting New Product Development, Design Transfer, DFM, and manufacturability assessments.
  • Experience relating to FDA warning letters and 483 observations remediation.

Responsibilities

  • Support NPD and Production & Process Controls projects as a Process Controls resource.
  • Partner with Product Development teams during design and development with Design Transfer focus.
  • Assess current state manufacturing and identify process improvements using Lean Six Sigma and other IE methods.
  • Support Design for Manufacturability and scalable designs.
  • Collaborate with suppliers and internal teams to ensure manufacturable designs.

Skills

Lean Six Sigma
Kaizen
Project management
Cross-functional teamwork
Process optimization

Education

Bachelor's degree in Engineering

Tools

Process Validation tools
Documentation systems

Job description

Medical Engineering Consultants (MEC) seeks an Industrial Engineer for contract to hire in Ocala, FL. The role focuses on process controls, design transfer, and NPD support within a regulated medical-device environment.

On-site collaboration with Product Development, Quality, and Manufacturing teams is essential to drive remediation and scalable improvements. The ideal candidate will have 3+ years in medical devices, strong Lean Six Sigma experience, and a track record of coordinating

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