Merrimack Manufacturing logo

Quality Engineer

Merrimack Manufacturing

On-site
Manchester, NH
Full-time
Mid Level
3+ yrs
Salary not listedPosted 4w ago

Real job — pulled straight from Merrimack Manufacturing’s careers page · Verified July 13, 2026 · No reposts.

Job description

Merrimack Manufacturing is hiring a Quality Engineer — a full-time, based in Manchester, NH role. Apply directly on Merrimack Manufacturing's careers page below.

Quality Engineer

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 test of devices for design verification, design validation, and commercial production.

RESPONSIBILITIES:
  • Work cooperatively with other team members and in compliance with applicable standards and regulations such as 21 CFR 820 and ISO 13485:2016 to transition products from development to manufacturing.
  • Use experience within medical devices, to provide guidance and assistance in the development of new production processes
  • Drive the development, implementation, and approval of PFMEAs and control plans.
  • Develop inspection processes and sampling plans according to the risk level of the components, material and devices
  • Use experience with engineering and technology to ensure compliance with applicable standards and regulations.
  • Ensure all product, processes, and components are within specifications and work with internal team and with customers to resolve any nonconformance issues
  • Facilitate the development, implementation, and approval of Device Master Records and Device History Records.
  • Review existing procedures and for continuous improvement and improved workflow
  • Lead investigations resulting in root cause and corrective actions through use of data analysis, inductive and deductive reasoning, and problem solving skills.
  • Use critical thinking and deductive reasoning to make risk based decisions.
  • Develop and approve technical documents to plan work, such as Master Validation Plans, Quality Plans, and Qualification Protocols; support execution of work product.
  • Collect and evaluate data, lead system and process improvements using six sigma tools
  • Provide reliability and statistical analysis of data for investigations, qualifications, test method validations and other Quality related activities.
  • Participate in ISO 13485 audits and assist in FDA and other regulatory inspections Will use Microsoft Office software (Word, Outlook, Excel).

QUALIFICATIONS AND SKILLS:
  • 3 + years of experience in occupation related to Quality Control of medical devices.
  • Experience with compliance, with applicable standards and regulations such as 21 CFR 820 and ISO 13485:2016 is required.
  • Experience participating in internal and external audits.
EDUCATION: Bachelor’s degree or equivalent experience in Industrial, Mechanical or related engineering / life sciences related discipline.

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Frequently asked questions

What skills are required for Quality Engineer at Merrimack Manufacturing?

The required skills for Quality Engineer at Merrimack Manufacturing include: Six Sigma, Microsoft 365, Word, Outlook, Excel.

What is the seniority level for Quality Engineer at Merrimack Manufacturing?

Quality Engineer at Merrimack Manufacturing is a Mid Level level position.

How do I apply for Quality Engineer at Merrimack Manufacturing?

You can view the full description and apply for Quality Engineer at Merrimack Manufacturing on EchoJobs: https://echojobs.io/job/merrimack-manufacturing-quality-engineer-gqh3p.