Temporary Quality Control Inspector

Are you looking for a rewarding career in Quality? 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
• 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

• 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.

Are you looking for a rewarding temporary career opportunity in Quality? 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.

This is a temporary position supporting IPG Medical's Quality organization.

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 DHRs, including release of finished goods.
• Adhere to Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
• Assist Quality Engineers and manufacturing personnel in the execution of calibration activities, including review and retrieval of calibrated equipment for processing.
• Maintain 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 and CAPAs to improve company practices and systems.
• Perform other duties as assigned.

• High School Diploma or equivalent required.
• Additional training in Quality and/or medical devices preferred.
• 1-3 years of experience in a Quality role; medical device experience preferred, although experience in other regulated industries will be considered.
• Strong working knowledge of Microsoft Word and Excel.
• Understanding of ISO 13485, ISO 14644, and 21 CFR Part 820.
• Experience using QMS, PLM, and CMMS systems.
• Strong organizational skills and attention to detail.
• Ability to read and interpret drawings and prints.