Argon Medical Devices, Inc.

Manufacturing Engineer

WHEELING, ILPosted 30+ days ago

Job summary

  • Job post source

    This job is directly from Argon Medical Devices, Inc.

  • Job overview

    The Manufacturing Engineer at Argon Medical Devices leads efforts to improve manufacturing efficiency and supports production of medical products, impacting overall product quality and operational effectiveness.

  • Responsibilities and impact

    The role involves providing engineering support for product development and manufacturing, evaluating designs for manufacturability, implementing cost-saving initiatives, developing process qualification protocols, performing root cause analysis, optimizing workforce and workspace, collaborating with vendors and management, applying statistical methods, troubleshooting, and leading teams.

  • Compensation and benefits

    The salary range is $90,000 to $115,000 depending on experience and location, with benefits including medical, dental, vision, life insurance, 401K with employer match, and eligibility for bonuses.

  • Experience and skills

    Candidates need a Bachelor's degree in Mechanical or Industrial Engineering, 6+ years in FDA/GMP regulated industries, proficiency in AutoCAD, SolidWorks, Minitab, Microsoft Office, Project, knowledge of MRP systems, experience in production planning, manufacturing methods, statistical techniques, and qualification protocols (IQ/OQ/PQ).

  • Career development

    The position offers mentoring opportunities for junior engineers and involvement in cross-functional project leadership, supporting professional growth in manufacturing engineering and project management.

  • Work environment and culture

    Argon Medical Devices values a mission-driven, family-oriented culture with strong organizational values guiding decisions and fostering a collaborative environment.

  • Company information

    Argon Medical Devices is a global manufacturer headquartered in Plano, Texas, specializing in specialty medical devices for interventional procedures with a reputation for best-in-class products that improve patient outcomes.

  • Job location and travel

    The company is headquartered in Plano, Texas, with the role likely based there; travel requirements are minimal at 5%.

  • Unique job features

    The job features involvement in regulatory-compliant manufacturing processes, use of advanced engineering software, and leadership in process improvement projects within a medical device manufacturing context.

Company overview

Argon Medical Devices Inc. is a global manufacturer of specialty medical products, focusing on devices used in interventional procedures, vascular surgery, and oncology. They generate revenue by selling a diverse range of medical devices, including biopsy needles, drainage catheters, and vascular access products, to hospitals, clinics, and healthcare providers worldwide. Founded in 1972, Argon has a history of innovation and growth, marked by strategic acquisitions and a commitment to improving patient outcomes through high-quality, reliable medical solutions.

How to land this job

  • Position your resume to highlight your experience in FDA/GMP regulated industries, focusing on manufacturing engineering roles that demonstrate your ability to support product development and production processes.

  • Emphasize your proficiency with AutoCAD, SolidWorks, Minitab, and MRP systems, along with your expertise in statistical process control, design of experiments, and root cause analysis to align with the job’s technical requirements.

  • Apply to the Manufacturing Engineer position through Argon Medical Devices’ corporate career site and LinkedIn to maximize your application visibility and ensure it reaches the relevant hiring teams.

  • Connect with manufacturing engineering and operations staff at Argon Medical Devices on LinkedIn; start conversations by referencing recent Argon Medical innovations or asking about their approach to manufacturing process improvements as ice breakers.

  • Optimize your resume for ATS by incorporating keywords from the job description such as 'manufacturing engineering,' 'FDA/GMP,' 'process qualification,' 'statistical process control,' and 'value improvement projects' to pass initial automated screenings.

  • Use Jennie Johnson’s Power Apply feature to automate tailored resume submissions, identify multiple application channels, and find LinkedIn contacts to network with, allowing you to focus your energy on preparing for interviews and skill development.

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