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Quality Operations Specialist

Merrimack Manufacturing
Posted 2 days ago, valid for 21 days
Location

Manchester, NH, US

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • Merrimack Manufacturing, a medical device manufacturer in Manchester Millyard, is seeking a candidate to support manufacturing quality operations.
  • The role requires a minimum of 2 years of experience in manufacturing or quality control related to medical devices and offers a salary of $50,000 to $70,000 per year.
  • Responsibilities include supporting quality engineers, conducting Device History Record reviews, and ensuring compliance with internal and regulatory requirements.
  • Candidates should possess strong organizational and communication skills, along with proficiency in Microsoft Office software.
  • An associate degree or equivalent experience in a related field is required for this position.
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.



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