Quality Control Inspector II (Temp / 2nd Shift 3 - 11PM) - Marlborough, MA

IPG Photonics; Marlborough (MA); On-site; USD 30,000 - 47,000; Full time

Job summary

IPG Photonics, headquartered in Marlborough, MA, seeks a detail‑oriented Quality Inspector to support incoming inspection and documentation control for medical device products. The role requires basic quality experience and familiarity with ISO13485 standards.

Responsibilities include reviewing DHRs, assisting with GMP and documentation practices, and contributing to CAPA activities. On-site position with growth in a technology-forward laser solutions environment.

Qualifications

• High School Diploma or equivalent required.
• Quality focus; medical device knowledge preferred.
• 1-3 years in a Quality role (medical device preferred).
• Strong MS Word and Excel skills.
• Familiarity with ISO13485, ISO14644, CFR 21-820.
• Experience with QMS, PLM and CMMS systems.
• Excellent organizational skills and attention to detail.
• Ability to read drawings and prints.

Responsibilities

• Perform incoming inspection of materials and receiving documentation for conformity to specifications.
• Support manufacturing operations through timely review of DHRs including release of finished goods.
• Adhere to good manufacturing practices and good documentation practices.
• Participate in CAPAs to improve company practices and systems.
• Other duties as assigned.

Skills

Attention to detail

Reading drawings

Education

High School Diploma or equivalent

Tools

QMS

PLM

CMMS

Job description

Are you looking for a rewarding career in manufacturing? If so, IPG Photonics may be the place for you! Working with IPG Photonics you can expect interesting tasks and challenging projects as well as a motivating and friendly environment. You will be working with teams that influence the future of laser technologies.

IPG Medical, a wholly owned subsidiary of IPG Photonics (NASDAQ: IPGP), is focused on developing next-generation products based on IPG Medical's state-of-the-art laser technology. Headquartered in Marlborough, MA, we aspire to work together with our employees and customers to apply light in ways that improve life.

Our mission is to develop innovative medical device laser solutions that make the world a better place. To accomplish this mission, we are committed to attracting and retaining the best talent and an engaged and thriving workforce that drives a sustainable future for our company and society.

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
• Participate in NCMRs / CAPA's to better improve company practices and systems
• Other duties as assigned

Qualifications:

• High School Diploma or equivalent is required.
• Additional training inQuality 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, andCFR 21-820.
• User experience of QMS, PLM and CMMS systems.
• Organizational skills and attention to detail.
• Ability to read drawings and prints.