OmniSonics Medical Technologies, Inc., based in Wilmington, MA, is a venture-backed medical
device company focused on developing breakthrough products for the treatment of vascular
Our core hiring principle is to find and acquire motivated people who have a desire to
contribute at the highest possible technical levels. This mission enables us to provide our
employees with challenge and opportunities for personal and professional growth, while also
providing for a work/life balance that so many desire.
We are searching for individuals who will be responsible for leading the transformation
process for our growing business, individuals that want to make meaningful contributions and
participate actively in the pursuit of highly complex solutions. The advanced nature of our
products create an environment that demands people constantly drive towards innovative
solutions and push themselves beyond what they think they are already capable of.. Not a day
goes by that there doesn’t exist the possibility of making a difference.
At Omnisonics, you'll find the expectations are high—as are the rewards. We offer very
competitive salaries, stock options, and the opportunity to participate in a very
comprehensive and generous benefit program that addresses virtually all of your personal needs
including Medical, Dental, Vision, Paid Time Off, 401K, and participation in our Stock Option
We are currently in search of a Senior Manufacturing Engineer to perform a variety of tasks
Plans, develops, and implements manufacturing processes .
Conducts Process Characterization via. Design-of-Experiments and creates Process
Specifications and Manufacturing Instructions.
Maximizes efficiency by analyzing layout of equipment, workflow, assembly methods, and
Leads Cross-Functional Teams in the creation of Process Failure Mode and Effects Analysis
Analyze manufacturing processes and identify areas for improvement in yield, efficiency,
quality, and cost reduction programs. Utilizes and conducts Process Control studies, Cp/Cpk
analysis, Descriptive Statistics, Lean Mfg Analysis, and applies Six Sigma applications.
Implements Process Improvements and revisions into production.
Leads and /or participates in project teams supporting new product development and product
transfer into manufacturing.
Creates Project Plans, schedules and executes detailed phases of engineering work in part of a
major project or in total project of moderate scope.
Writes Process Qualification/Validation Plans and Reports, executes relative activities,
performs data analysis, and optimizes Specifications and Processes as required.
Evaluates and determines need for Statistical Process Control, implements as required.
Prepares Project updates and Presentations to communicate status.
Provide guidance in equipment selection, overall operations and capacity expansion.
Requires a Bachelor’s degree in Manufacturing/Industrial Engineering or equivalent and at
least 5-10 years experience in a FDA regulated medical device manufacturing environment.
Experience with the assembly of medical devices
Must be proficient with GMP’s, CE’s and ISO standards.
Extensive Experience with CNC machining, Grinding, and Welding.
Familiar with a variety of the field’s concepts, practices, and procedures.
Product and Process Validation and IQ, OQ and PQ experience.
Transfer of New Products and Processes into Manufacturing.
PFMEA and Risk Analysis
Additional Experience in these areas would be a plus:
DFM, Lean Manufacturing, and Six-Sigma
Packaging engineering certificate and/or related packaging experience
Plastics and Injection Molding
Work Cell Development and Layout
Time Studies and Standard Development