Great opportunity to join a team committed to creating innovative solutions! |Globally backed by a top 5 healthcare company!
About Our Client
My client is a global leader in medical device manufacturing, committed to enhancing patient care through innovative, high-quality medical devices. With more than 20 million people in over 100 countries relying on their products, my client is a dedicated and trusted partner in the healthcare industry.
Job Description
The Staff Manufacturing Engineer will report directly into the Group Engineering Lead and be responsible for:
Lead manufacturing process development, optimization, and validation activities for medical device production.
Assist/conduct design reviews of product components, product assemblies, manufacturing fixtures and tooling.
Conduct root cause analysis and implement corrective actions to resolve production issues and improve product quality.
Collaborate with cross-functional teams, including R&D, Quality Assurance, and Production, to support new product introductions and process validations.
Prepare and maintain detailed documentation, including work instructions, process flow diagrams, and standard operating procedures (SOPs).
Provide technical support and training to production staff to ensure adherence to manufacturing standards and procedures.
Ensure compliance with regulatory requirements, including FDA, ISO, and GMP standards.
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, Manufacturing, Plastics or Biomedical Engineering
8+ years of experience in medical device manufacturing (NPD preferred)
Knowledge of regulatory requirements (FDA, ISO 13485 and cGMP Standards)
Experienced with Lean Manufacturing (Six Sigma Green Belt preferred)
Proficiency in CAD software (e.g., SolidWorks, AutoCAD)
Sound analytical and problem-solving skills
Experience with FEA analysis tools is a plus
Strong communication skills and ability to work in cross-collaborative teams
What's on Offer
Competitive compensation
Comprehensive benefits plan
Career growth opportunities
Access to high level management
401K match
Excellent work life balance
Contact: Sean Shepardson
Quote job ref: JN-062024-6442557
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Engineering and Information Technology
Industries
Appliances, Electrical, and Electronics Manufacturing, Industrial Machinery Manufacturing, and Manufacturing
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