Senior Manufacturing Engineer Medical Device

Right Hire Consulting

  • Cambridge, Massachusetts
  • 1 day ago

    Highlights

    The Senior Manufacturing Engineer plays a key role in bridging R&D, pilot, and commercial manufacturing for medical devices, ensuring robust and scalable manufacturing processes from early development to commercialization. Create production-level drawings and optimize designs for manufacturability (DFM), cost, and efficiency using Six Sigma and LEAN principles.

    Numbers & Facts

    LocationCambridge, Massachusetts

    Description

    The Senior Manufacturing Engineer plays a key role in bridging R&D, pilot, and commercial manufacturing for medical devices, ensuring robust and scalable manufacturing processes from early development to commercialization. The role emphasizes efficiency, quality, regulatory compliance, and cost-effectiveness while collaborating across departments and with contract manufacturers.

    Key Responsibilities:

    • Develop and validate efficient, cost-effective manufacturing processes for medical devices, including assembly, testing, sterilization, and packaging.
    • Create production-level drawings and optimize designs for manufacturability (DFM), cost, and efficiency using Six Sigma and LEAN principles.
    • Identify, evaluate, and collaborate with contract manufacturers, ensuring quality, cost, and regulatory compliance.
    • Act as a liaison between internal teams and contract manufacturers to coordinate manufacturing activities.
    • Review engineering specifications and CAD drawings to ensure compliance with standards and best practices.
    • Manage part/drawing releases and ensure accuracy of Bills of Materials (BOMs).
    • Plan and execute process characterization and validation, including risk assessments and critical control point identification.
    • Develop and maintain manufacturing documentation, including work instructions, equipment guides, and process validations.
    • Lead or contribute to pFMEA and implement Lean Six Sigma methodologies.
    • Collaborate with cross-functional teams, including engineers, quality specialists, regulatory experts, and suppliers, to achieve project objectives.

    Deliverables:

    • Up-to-date and accurate BOMs, work instructions, and process documentation.
    • Comprehensive pFMEA and validated manufacturing processes.
    • Effective coordination with contract manufacturers and stakeholders.

    Qualifications:

    • Bachelors degree or higher in Mechanical Engineering.
    • 5+ years of experience in medical device manufacturing, including new product development, design transfer, and process validation.
    • Proficiency in SolidWorks for modeling and fixture/tool design.
    • Experience with contract manufacturers, especially in capital equipment or catheter manufacturing.
    • Strong knowledge of DFM, Six Sigma, LEAN, cGMP, and sterilizable polymers.
    • Proficiency in Microsoft Office and statistical software like Minitab or JMP.

    Preferred Skills:

    • Lean and/or Six Sigma certifications.
    • Expertise in catheter fabrication techniques and electronics testing processes.

    This position offers the opportunity to work on innovative medical technologies in a highly collaborative environment.


    Similar Jobs