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Quality Operations Specialist
Quality Operations SpecialistMerrimack Manufacturing • Manchester, NH, US
Quality Operations Specialist

Quality Operations Specialist

Merrimack Manufacturing • Manchester, NH, US
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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 position will support manufacturing quality operations in a dynamic, fast-paced, medical device manufacturing environment.
  • This environment includes the manufacture, inspection, and testing of devices for process validation and commercial production.

    • RESPONSIBILITIES :

  • Working under the direction of Quality Engineers support, drive, and coordinate final inspection and acceptance of medical devices.
  • Support quality engineers in processing nonconformances, deviations, and rework authorizations by gathering data, updating logs, or drafting documentation.
  • Perform Device History Record (DHR) reviews for completeness, accuracy, and compliance to internal and regulatory requirements.
  • Identify and document errors or missing information in DHRs and coordinate with production or quality teams for timely correction.
  • Work cooperatively with team members on commercial production lines to support quality requirements and projects.
  • Provide administrative and technical support for change orders, training records, and CAPA follow-up as assigned.
  • May perform inspections for components, materials, devices and documents.

    • Position requires daily contact with members of Production, Engineering, Materials, and Quality departments and occasional contact with auditors and customers QUALIFICATIONS AND SKILLS :

  • 2 + years of experience in occupation related to Manufacturing or Quality Control of medical devices.

    • Experience with compliance, with applicable standards and regulations such as 21 CFR 820 and ISO 13485 :

  • 2016 is preferred.
  • Experience with Microsoft Office software (Word, Outlook, Excel) required.
  • Self-starter and independent individual with strong organizational, time management and communication skills.
  • Ability to drive assigned tasks to closure Must be able to manage multiple priorities.
  • Use critical thinking and deductive reasoning to make risk based decisions.

    • EDUCATION :

  • Associate degree or equivalent experience in Manufacturing, Quality, Mechanical or related engineering / life sciences related discipline.   Powered by JazzHR
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