Supplier Quality Engineer
Company: Merrimack Manufacturing
Location: Manchester
Posted on: February 14, 2026
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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 position will help manage
and improve the overall quality of our supply chain partners, and
help ensure that we are compliant to ISO 13485 and FDA requirements
as relates to our suppliers and supplied parts. This position will
be part of our Quality team, and will work extremely closely with
our Incoming Inspection, Engineering and Material Management team.
This role will be the primary driver of disposition and closure of
Supply based NCR activity. This role will also weigh in on all
matters pertaining to quality, engineering and continuous
improvement throughout the product lifecycle. RESPONSIBILITIES:
Assist inspection with evaluating cosmetic specifications and other
intricate component requirements requesting input and communication
with QE/ME as needed. Interface with Incoming Inspection, discuss
results, document disposition and required approvals to ensure
timely closure of Nonconformance Reports. Serve as key contributor
at weekly Incoming Inspection NCR MRB meeting. Utilize
relationships with MMC incoming inspection group and the supplier
to investigate differences between measurements. Communicate
failures to suppliers, request SCARs where necessary and document
effectiveness of corrective actions. Work with Supply Chain to
attain RMA numbers, ensure dispositions are carried out per NCR
approval. Generate and Distribute Scorecards to suppliers Conduct
ASL updates in MMC PLM system for new suppliers, Supplier Change
Notifications etc. Interface with suppliers, Manufacturing
Engineers and Quality Engineers to evaluate potential component
issues. Walk down MMC processes vs supplier processes and determine
root cause. Work with Supplier Development and Sr. SQE to schedule
telecons, investigate process control issues or breakdowns,
identify high-risk suppliers, schedule for cause audits, etc.
Facilitate the review and approval of supplier-initiated changes
requests, and communicate the approved changes through Quality and
to the appropriate departments. Look for opportunities to drive
preventive actions and continuous process improvement with our
suppliers. Assist as needed with customer audits and regulatory
audits. Provide recommendations for improvements and help drive
best practices to SOPs pertinent to QA GMP Compliance activities.
QUALIFICATIONS AND SKILLS: 2 years of experience in a Quality
Assurance role, or with a medical device manufacturing company
Experience as a certified quality auditor or supplier auditor is a
plus Familiarity with ISO 13458:2016 and FDA 21 CFR Part 820
Detail-oriented with strong verbal and written communications
skills; demonstrated ability to manage multiple projects/tasks A
demonstrable ability to work with cross-functional teams comprised
of members within and outside of our organization Ability to work
with CAD files and interpret mechanical drawings Ability to analyze
data for accuracy and correctly interpret results Microsoft Office
proficiency Willingness to travel both domestically and
internationally to suppliers as needed, estimated to be 20% travel
EDUCATION: Bachelor’s in Engineering or related experience Powered
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Keywords: Merrimack Manufacturing, Nashua , Supplier Quality Engineer, Engineering , Manchester, New Hampshire