QC Inspector II

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, diverse, and thriving workforce that drives a sustainable future for our company and society.

 

QA/QC Inspector Technician II is responsible for verification of product quality and conformity through direct product and component inspection, production record review, and environmental monitoring.

 

Duties and Responsibilities

• Support manufacturing operations through the timely review of components, finished assemblies, and associated production records to ensure compliance with applicable requirements and procedures; this includes executing basic calculations and accurately recording inspection results.
• Perform incoming inspection and physical measurement of materials for conformity to specifications; including the creation and completion of records for received materials.
• Support Quality-critical manufacturing processes such as label generation and environmental monitoring.
• Perform internal process audits as needed to ensure compliance with applicable standards, requirements, and procedures.
• Support document control and records management as needed; this includes scanning, filing, and overall documentation management.
• Perform other duties as assigned to support Quality initiatives and projects

Qualifications

Requirements

• 1-3 years’ experience of Quality inspection in a medical device or regulated environment; preferably high-volume manufacturing
• Excellent attention to detail when performing inspections and documenting results.
• Strong knowledge of Microsoft Word and Excel.
• Working knowledge of 21 CFR 820 and ISO 13485, or other applicable standards and regulations
• Ability to read drawings and prints.
• Ability to work in a cross-functional team environment with competing priorities.
• Ability to cooperate as part of the Quality team to meet department goals.
• High School Diploma or equivalent