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Sr. Quality Engineer

Sr. Quality Engineer

Merrimack ManufacturingManchester, NH, US
30+ days ago
Job type
  • Full-time
Job description

Job Description

Job Description

COMPANY OVERVIEW :

Merrimack Manufacturing is a medical device manufacturer located in the Manchester Millyard. We are a growing manufacturing company that will play a crucial part in bringing innovative and life changing products to life.

POSITION OVERVIEW :

This positon will support manufacturing quality operations in a dynamic, fast-paced, medical device-manufacturing environment. This environment includes the manufacture, inspection, and test of devices for design verification, design validation, and commercial production.

RESPONSIBILITIES :

  • Working under the direction of the Quality Manager, ensure all product, processes, and components are within specifications.
  • This position may also serve as a member on collaborative cross-functional teams, to support new product development efforts, commercial production, material-related design changes, and manufacturing and process changes, risk management activities, and other compliance projects.
  • Work in compliance with applicable standards and regulations such as 21 CFR 820 and ISO 13485 : 2016.
  • Lead the Device History Records (DHR) review and approval process.
  • Lead nonconformance reports (NCR) and CAPA investigations.
  • Lead the development and implementation of PFMEAs and control plans.
  • Lead process and equipment validation activities (IQ, OQ, PQ / PV, TMV).
  • Lead manufacturing and quality system improvements.
  • Lead customer feedback process and investigations.
  • Author Engineering Change Orders (CO); support CO implementation tasks
  • Use experience with engineering and technology to ensure compliance with applicable standards and regulations.
  • Position requires daily contact with members of Production, Engineering, Materials, and Quality departments.
  • Routine contact with design authority and customers; occasional contact with auditors

QUALIFICATIONS AND SKILLS :

  • 5+ years of experience related to the manufacturing of medical devices in a QMS environment while being in a Quality Control or Engineering role
  • Experience with compliance, with applicable standards and regulations such as 21 CFR 820 and ISO 13485 : 2016 is required
  • Experience with Microsoft Office software (Word, Outlook, Excel) required
  • Experience participating in internal and external audits
  • Strong project management, prioritization and leadership skills are required
  • Must be able to manage multiple priorities
  • Performing statistical data analysis using Minitab or equivalent
  • Presenting and leading meetings with an audience of peers and senior management level
  • Use critical thinking and deductive reasoning to make risk based decisions
  • Knowledge and comprehensive understanding of CAPAs, root cause analysis, and the 8D method
  • Excellent oral communication and technical writing skills
  • High level of attention to detail and accuracy
  • EDUCATION : Bachelor’s degree or equivalent experience in Manufacturing, Mechanical or related engineering / life sciences related discipline.

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