Quality Control Inspector II – Medical Devices

IPG Photonics Corporation

Marlborough (MA)

On-site

USD 26,000 - 30,000

Full time

7 hours ago
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Benefits offered by this job

Medical insurance
Dental insurance
Vision insurance
401(k) plan with Company matching
Employee Stock Purchase Plan (ESPP)
Tuition Reimbursement Program
Paid vacation time
EAP

Job summary

IPG Photonics Corporation, including its IPG Medical subsidiary in Marlborough, MA, is seeking a Quality Inspector to support manufacturing by performing incoming inspections and reviewing documentation for conformity. You will help ensure GMP and quality practices across the facility and assist in calibration activities and audits.

The role requires 1–3 years in a quality function, familiarity with ISO13485 and CFR 21-820, and strong Word/Excel skills.

Qualifications

  • High School Diploma or equivalent required.
  • 1–3 years in a Quality role (medical device preferred).
  • Strong MS Word and Excel skills.
  • Familiarity with ISO13485, ISO14644, and CFR 21-820.
  • Experience with QMS, PLM and CMMS systems.

Responsibilities

  • Perform incoming inspection of materials and documentation.
  • Review DHRs with release of finished goods.
  • Maintain GMP and documentation practices.
  • Assist engineers with calibration activities.
  • Participate in internal/external audit preparation.
  • Support in CAPAs / NCRs to improve processes.

Skills

MS Word
MS Excel
Reading drawings
ISO13485 knowledge
CFR 21-820 knowledge
QMS PLM CMMS familiarity
Attention to detail

Education

High School Diploma or equivalent

Tools

QMS software
PLM software
CMMS software

Job description

IPG Photonics Corporation, including its IPG Medical subsidiary in Marlborough, MA, is seeking a Quality Inspector to support manufacturing by performing incoming inspections and reviewing documentation for conformity. You will help ensure GMP and quality practices across the facility and assist in calibration activities and audits.

The role requires 1–3 years in a quality function, familiarity with ISO13485 and CFR 21-820, and strong Word/Excel skills.

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