Manufacturing Engineer II

2 months ago


Tilton NH, United States Michael Page Full time

  • Great opportunity to join an industry leader with global reach
  • New opportunity created due to growth

    About Our Client

    My client is a global CMO in the Medical Equipment Manufacturing industry. From concept to commercialization, my client offers end-to-end capabilities to help bring their customers' medical technology solutions to life.

    Job Description

    The Manufacturing Engineer II will report directly into the Engineering Manager and be responsible for:

  • Develop and optimize manufacturing processes for new and existing medical devices to ensure efficiency, quality, and cost-effectiveness.
Design and implement production layouts, tooling, and fixtures to enhance manufacturing capabilities.Conduct root cause analysis and implement corrective actions to resolve production issues and improve product quality.Collaborate with R&D, quality, and production teams to support new product development and launch activities.Perform process validation and verification activities, including IQ, OQ, and PQ, to ensure compliance with regulatory requirements.Develop and maintain standard operating procedures (SOPs), work instructions, and other process documentation.Identify and implement continuous improvement initiatives to enhance manufacturing performance and reduce waste.Support the implementation and maintenance of lean manufacturing principles and Six Sigma methodologies.



Apply today for immediate consideration 

MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.

The Successful Applicant

Bachelors Degree in Mechanical Engineering or a related field3-5+ years of experience in a contract manufacturing industry (Medical Device preferred)Knowledge of continuous improvement, lean and six sigma tools (greenbelt preferred)Working knowledge of ISO 9001, ISO 13485 and FDA regulationsStrong communication skills and ability to work in cross-collaborative teamsAbility to prioritize tasks, solve problems, and make sound decisions in a fast-paced environmentProficiency in CAD software (SolidWorks, AutoCAD) and statistical analysis tools (Minitab)

What's on Offer

Competitive compensationComprehensive benefits planCareer growth opportunitiesAccess to high level management401K matchExcellent work life balance
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