Quality Inspector - Marlborough, MA

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.

Do you want to be successful with opportunities to learn new skills and have career development? Then, please send us your application!

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 documentation for conformity to specifications.
• Support manufacturing operations through timely review of DHR'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.
• Perform quarterly Air Sampling / Particle Testing in the Clean Room.
• Other duties as assigned.

• 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 ISO 13485, ISO 14644, and CFR 21-820.
• User experience of QMS, PLM and CMMS systems.
• Organizational skills and attention to detail.
• Ability to read drawings and prints.