×
Register Here to Apply for Jobs or Post Jobs. X

Quality Operations Specialist

Job in Manchester, Hillsborough County, New Hampshire, 03103, USA
Listing for: Merrimack Manufacturing
Full Time position
Listed on 2026-09-12
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Production QC/QA
  • Manufacturing / Production
    Quality Engineering, Production QC/QA
Salary/Wage Range or Industry Benchmark: 60000 - 85000 USD Yearly USD 60000.00 85000.00 YEAR
Job Description & How to Apply Below

COMPANY OVERVIEW:

Merrimack Manufacturing is amedical device manufacturer located in the Manchester Millyard. We are a growing manufacturing company thatwill 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.

To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary