Quality Control Supervisor - 2nd Shift - Hours: 3 -11 PM - Marlborough, MA

IPG Photonics

Marlborough (MA)

On-site

USD 70,000 - 100,000

Full time

14 days+
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Job summary

IPG Photonics’ IPG Medical division seeks a Quality Supervisor to lead QA activities and inspection processes for 2nd shift. You will review DHRs, support CAPAs, and ensure compliance with GMP and QMS practices in a medical device environment.

The role requires strong MS Word/Excel skills, ISO13485 familiarity, and ability to read drawings. On-site position in Marlborough, MA with collaboration across teams and vendors.

Qualifications

  • High School Diploma or equivalent required.
  • 5+ years experience in Quality supervisor or equivalent (medical device preferred).
  • Strong MS Word and Excel skills.
  • Familiarity with ISO13485, ISO14644 and CFR 21-820.
  • Ability to read drawings and prints.

Responsibilities

  • Supervise quality inspectors on 2nd Shift to support QA activities.
  • Prioritize inspection of incoming materials and First Article Inspections.
  • Develop inspection and test methods with Manufacturing and Project Engineers.
  • Support improvement processes including nonconformance action.
  • Investigate NCMRs with proper material disposition.

Skills

Quality supervision
Quality assurance
Documentation
Communication
MS Word
MS Excel
Reading drawings

Education

High School Diploma

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:
  • Supervise quality inspectors on 2nd Shift to support QA activities such as Quality Inspections, DHR review, and NCMRs
  • Prioritizing Inspection of incoming materials, components and subassemblies and First Article Inspections upon request
  • Work with Manufacturing and Project Engineers to develop inspection and test methods and related acceptance criteria
  • Support improvement processes that include nonconformance action
  • Investigate NCMR's with proper material disposition, as needed
  • Perform manufacturing Device History Record (DHR) review including sterile product release of finished goods
  • Adhere to good manufacturing practices and good documentation practices
  • Promote awareness, visibility and communication relative to QMS goals and initiatives
  • Improve, support and maintain processes within the Quality Management System
  • Participate in CAPA's to better improve company practices and systems
  • Adhere to a culture of continuous improvement and system efficiencies
  • Maintain accurate and complete equipment calibration tracker and equipment files
  • Assist in external audit preparation
  • High School Diploma or equivalent is required
  • Additional training inQuality and/or a focus in medical device preferred
  • 5 or more years of experience in a Quality supervisor or equivalent 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
  • Positive and cooperative communication and collaboration with all levels of employees, contractors and vendors
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