Quality Control Supervisor – Medical Devices (2nd Shift)

IPG Photonics Corporation; Marlborough (MA); On-site; USD 98,000 - 117,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

401(k) with company matching

Tuition reimbursement

Employee Assistance Program (EAP)

ESPP

Job summary

IPG Photonics Corporation is seeking a Quality Control Supervisor for the 2nd shift (3–11 PM) in Marlborough, MA. The role oversees quality inspectors and ensures adherence to GMP and QMS objectives within a medical device context.

The ideal candidate will have 5+ years in quality supervision, strong Microsoft Word/Excel skills, and solid knowledge of ISO13485, ISO14644, CFR 21-820. On-site opportunities include comprehensive benefits and growth potential.

Qualifications

• High school diploma or equivalent required.
• Additional training in quality; medical device focus preferred.
• 5+ years in a quality supervisor or equivalent role (medical device preferred).
• Strong working knowledge of Microsoft Word and Excel.
• Understanding of ISO13485, ISO14644, and CFR 21-820.
• Experience with QMS, PLM and CMMS systems.

Responsibilities

• Supervise quality inspectors on 2nd Shift; support QA activities.
• Prioritize inspection of incoming materials and first article inspections.
• Develop inspection/test methods and acceptance criteria with engineers.
• Support improvement processes including nonconformance action.
• Investigate NCMRs and determine material disposition.

Skills

Attention to detail

Organizational skills

Reading drawings

Communication and collaboration

Education

High School Diploma or equivalent

Quality training / certification (preferred)

Tools

Microsoft Word

Microsoft Excel

QMS

PLM

CMMS

Job description

IPG Photonics Corporation is seeking a Quality Control Supervisor for the 2nd shift (3–11 PM) in Marlborough, MA. The role oversees quality inspectors and ensures adherence to GMP and QMS objectives within a medical device context.

The ideal candidate will have 5+ years in quality supervision, strong Microsoft Word/Excel skills, and solid knowledge of ISO13485, ISO14644, CFR 21-820. On-site opportunities include comprehensive benefits and growth potential.