2nd-Shift Senior Manufacturing Engineer, Sustaining

Cirtec Medical

Lowell (MA)

On-site

USD 100,000 - 140,000

Full time

43 hours ago
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Benefits offered by this job

Training and career development
Healthcare (medical, dental, vision)
Wellness programs
Paid Time Off
401(k) with company match

Job summary

Cirtec Medical Corp. is seeking a Sr. Manufacturing Engineer – Sustaining (2nd shift) based in Lowell, MA.

This hands-on role leads sustaining engineering on 2nd shift, guiding production lines, resolving issues, and driving continuous improvement on the floor to meet quality and output goals. The ideal candidate has a BS in a STEM field, 5+ years in medical device manufacturing, and strong experience with ISO 13485/GMP, MES/ERP, and CAD tools (SolidWorks).

Qualifications

  • This role requires a Bachelor’s degree in a STEM engineering discipline and 5+ years of medical device manufacturing or a regulated industry.
  • Experience in sustaining engineering, manufacturing support, and process troubleshooting with floor-based production exposure.
  • Demonstrated ability to perform root cause analysis and implement corrective actions.
  • Working knowledge of ISO 13485 and GMP requirements; experience with MES and ERP systems.

Responsibilities

  • Provide hands-on engineering support to 2nd shift manufacturing operations and serve as primary engineering contact for assigned lines.
  • Troubleshoot manufacturing and product issues, perform root-cause analysis, and implement CAPA actions.
  • Maintain and improve process documentation, work instructions, and SOPs.
  • Monitor metrics (yield, scrap, efficiency) and drive continuous improvement with cross-functional teams.

Skills

Sustaining engineering
Root cause analysis
Cross-functional collaboration
Troubleshooting
Verbal and written communication

Education

Bachelor's degree in STEM engineering

Tools

CAD (SolidWorks)

Job description

Cirtec Medical Corp. is seeking a Sr. Manufacturing Engineer – Sustaining (2nd shift) based in Lowell, MA.

This hands-on role leads sustaining engineering on 2nd shift, guiding production lines, resolving issues, and driving continuous improvement on the floor to meet quality and output goals. The ideal candidate has a BS in a STEM field, 5+ years in medical device manufacturing, and strong experience with ISO 13485/GMP, MES/ERP, and CAD tools (SolidWorks).

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