More jobs:
Manufacturing Engineer
Job in
Providence, Providence County, Rhode Island, 02940, USA
Listed on 2026-06-03
Listing for:
Veranex
Full Time
position Listed on 2026-06-03
Job specializations:
-
Manufacturing / Production
Manufacturing Engineer, Quality Engineering -
Engineering
Manufacturing Engineer, Quality Engineering
Job Description & How to Apply Below
About This Role
Veranex has an exciting opportunity to join our team as a Manufacturing Engineer 2. You will be part of a team working to improve lives globally through medical technology innovation. Manufacturing Engineer 2 performs and coordinates broad manufacturing engineering activities in the development and supply of capital and disposable medical devices and instruments.
What You Will Do
Performs manufacturing engineering functional lead duties including engineering and production builds, assembly line/cell layout, process flow development, process development, manufacturing fixture design, operator manufacturing/assembly training, etc.
Provides technical project management through continuous communication with internal design, engineering, quality, and manufacturing personnel, original equipment manufacturing (OEM) factories, suppliers, and clients regarding manufacturing engineering progress and details of multiple projects.
Works with Quality Engineering to execute Good Manufacturing Practices (GMP) and testing procedures to ensure compliance with design output specifications and lifecycle requirements.
Maintains manufacturing files and databases per internal design control procedures.
Defines and generates all required documentation in support of manufacturing products and processes.
Designs and determines manufacturing text fixtures with minimal guidance from senior staff.
Provides support to improve, maintain, or fix manufacturing processes.
Executes training operators for manufacturing/assembly with minimal guidance from senior staff.
Troubleshoots project related manufacturing issues with minimal guidance from senior staff.
Supports the organization in meeting production schedules through resolving technical, equipment, or operational issues.
Supports initiatives to improve safety and compliance to applicable regulations.
Participates in build and release plans.
Required Qualifications
Bachelor's degree in manufacturing or mechanical engineering
2-4 years of relevant work experience
Strong knowledge of overall medical device industry
Strong knowledge of computer-aided design (CAD) packages
Strong knowledge of process development and process validation
Strong written and oral communication skills
Excellent attention to detail
Ability to multi-task and perform a wide range of activities
Ability to work under a timeline
Ability to solve moderate to complex technical problems
Preferred Qualifications
Experience with medical device manufacturing industry.
UDI Labeling experience
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