Product Development Engineer (Medical Device)

Judge Direct Placement; Michigan; On-site; USD 95,000 - 150,000; Full time

Benefits offered by this job

Medical insurance

Vision insurance

401(k)

Job summary

A leading company in medical device manufacturing is seeking a Manufacturing Engineer to develop and optimize processes. The ideal candidate will have extensive experience in automation and robotics, along with a solid foundation in regulatory compliance. This full-time role targets mid-senior level professionals with a track record in cost-saving projects and launching new products.

Qualifications

• 3-5 years of experience in manufacturing engineering within the medical device industry.
• Proven experience with automation and robotics.
• Strong understanding of regulatory requirements for medical devices.

Responsibilities

• Develop and optimize manufacturing processes for medical devices.
• Lead automation integration into manufacturing.
• Analyze production data and implement corrective actions.

Skills

Problem-solving

Attention to detail

Communication

Interpersonal skills

Education

Bachelor's degree in Manufacturing Engineering

Mechanical Engineering

Job description

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Judge Direct Placement provided pay range

This range is provided by Judge Direct Placement. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$95,000.00/yr - $150,000.00/yr

Direct message the job poster from Judge Direct Placement

We are seeking a highly skilled and innovative Manufacturing Engineer. The ideal candidate will have extensive experience in medical device manufacturing and a proven track record of implementing automation and robotics, leading cost-saving projects, and launching new products into manufacturing.

Key Responsibilities:

• Develop, implement, and optimize manufacturing processes for medical devices to ensure high quality and efficiency.
• Lead projects to introduce automation and robotics into the manufacturing process to improve productivity and reduce costs.
• Identify and implement cost-saving initiatives without compromising product quality or compliance.
• Collaborate with cross-functional teams, including R&D, quality, and production, to successfully launch new products into manufacturing.
• Conduct process validation and verification activities to ensure compliance with regulatory requirements.
• Analyze production data to identify trends, troubleshoot issues, and implement corrective actions.
• Develop and maintain documentation for manufacturing processes, including work instructions, process flow diagrams, and validation protocols.
• Train and mentor production staff on new processes and equipment.
• Participate in internal and external audits to ensure compliance with industry standards and regulations.

Qualifications:

• Bachelor's degree in Manufacturing Engineering, Mechanical Engineering, or a related field.
• Minimum of 3-5 years of experience in manufacturing engineering within the medical device industry.
• Proven experience with automation and robotics in a manufacturing setting.
• Demonstrated success in leading cost-saving projects and initiatives.
• Experience in launching new products into manufacturing.
• Strong understanding of regulatory requirements and quality standards for medical devices (e.g., ISO 13485, FDA regulations).Excellent problem-solving skills and attention to detail.
• Strong communication and interpersonal skills.
• Ability to work independently and as part of a team in a fast-paced environment.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Engineering, Manufacturing, and Production

• Industries

  Medical Equipment Manufacturing, Manufacturing, and Automation Machinery Manufacturing

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Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

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