Quality Control Inspector II - Medical Device QC

IPG Photonics; West Oxford (MA); On-site; USD 52,000 - 76,000; Full time

Job summary

IPG Photonics is seeking a Quality Inspector to support incoming inspection and documentation control at our Marlborough, MA site. You will work with manufacturing teams to ensure compliance with quality standards and regulatory requirements.

The role emphasizes attention to detail, reading drawings, and assisting in internal and external audits, CAPAs, and calibration activities in a regulated medical device environment.

Qualifications

• High School Diploma or equivalent is required.
• Additional training in Quality and/or a focus in medical device preferred.
• 1-3 years of experience in a Quality role (medical device preferred, other regulated industries considered).
• Strong working knowledge of Microsoft Word and Excel.
• Understanding of ISO13485, ISO14644, and CFR 21-820.
• User experience of QMS, PLM and CMMS systems.
• Organizational skills and attention to detail.
• Ability to read drawings and prints.

Responsibilities

• Perform incoming inspection of materials and receiving documentationfor conformity to specifications.
• Support manufacturing operations through timely review ofDHR's including release of finished goods.
• Adhere to good manufacturing practices and good documentation practices
• Assist Quality Engineers and manufacturing personnel in the execution of calibration activities including review and retrieval of calibrated equipment for processing
• Positive and cooperative communication and collaboration with all levels of employees, contractors and vendors
• Assist in both internal and external audit preparation
• Participate in NCMRs / CAPA's to better improve company practices and systems
• Other duties as assigned

Skills

Quality

Reading drawings

Attention to detail

Organizational skills

Education

High School Diploma or equivalent

Tools

QMS

PLM

CMMS

Job description

IPG Photonics is seeking a Quality Inspector to support incoming inspection and documentation control at our Marlborough, MA site. You will work with manufacturing teams to ensure compliance with quality standards and regulatory requirements.

The role emphasizes attention to detail, reading drawings, and assisting in internal and external audits, CAPAs, and calibration activities in a regulated medical device environment.