MedTech Manufacturing & Operations Leader

LightForce

Wilmington (MA)

On-site

USD 250,000 - 420,000

Full time

14 days+

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Benefits offered by this job

Unlimited PTO
12 paid holidays
Premium medical/dental/vision
401(k) retirement plan
Parental leave

Job summary

LightForce is seeking an experienced Operations leader to build and scale a fully digital, 3D-printed medtech manufacturing organization in Massachusetts. You’ll own strategy, throughput, yield, capacity and costs, partnering with Engineering, Quality, Finance, and Commercial to drive a high-performing team on a fast-scaling platform.

You will lead NPI and design transfer, build a lean operating system, and establish an automation roadmap while ensuring FDA/ISO25 compliance.

Qualifications

  • 12+ years of progressive manufacturing and ops leadership in FDA-regulated medical devices.
  • Experience scaling manufacturing for high-volume, multi-shift environments.
  • Deep knowledge of ISO 13485, FDA QSR, design transfer, and process validation.
  • Lean manufacturing, automation, and capital budgeting experience.
  • Bachelor's degree; technical degree preferred.

Responsibilities

  • Set multi-year manufacturing strategy and capacity plan.
  • Own throughput, yield, cost, and on-time delivery.
  • Build lean ops and lead a high-performing team.
  • Lead NPI/design transfer for new products.
  • Partner with Quality, Supply Chain and Finance on budgets.

Skills

Strategic leadership
Cross-functional leadership
FDA-regulated manufacturing
Lean / Six Sigma
Budget management

Education

Bachelor's degree in Engineering or related field

Tools

ERP (SAP/Oracle)
MES/Automation tooling

Job description

LightForce is seeking an experienced Operations leader to build and scale a fully digital, 3D-printed medtech manufacturing organization in Massachusetts. You’ll own strategy, throughput, yield, capacity and costs, partnering with Engineering, Quality, Finance, and Commercial to drive a high-performing team on a fast-scaling platform.

You will lead NPI and design transfer, build a lean operating system, and establish an automation roadmap while ensuring FDA/ISO25 compliance.

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