Manufacturing Engineer - Medical Device - Amesbury, MA
Michael Page Amesbury
About Our Client
My client is a global innovative medical device manufacturing company, committed to delivering safe, high-quality, and effective products that improve lives. They pride themselves on their dedication to excellence, precision, and compliance in all stages of manufacturing.
Job Description
The Manufacturing Engineer 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 field
- 3-5+ 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 regulations
- Strong communication skills and ability to work in cross-collaborative teams
- Ability to prioritize tasks, solve problems, and make sound decisions in a fast-paced environment
- Proficiency in CAD software (SolidWorks, AutoCAD) and statistical analysis tools (Minitab)
- Competitive compensation
- Comprehensive benefits plan
- Career growth opportunities
- Access to high level management
- 401K match
- Excellent work life balance
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