Project Engineer

Catalyst Life Sciences; New Hampshire; On-site; USD 115,000 - 130,000; Full time

Job summary

Catalyst Life Sciences is seeking a Project Engineer to join a dynamic Medical Device company in New Hampshire. The role involves leading product development, managing project documentation, and ensuring compliance with safety and quality standards. Ideal candidates will have a Bachelor's degree in a relevant field and extensive experience in medical device manufacturing.

Qualifications

• 7+ years of experience in medical device manufacturing.
• Knowledge of FDA regulations, ISO 13485, and GMP.

Responsibilities

• Lead new product development and manufacturing processes.
• Manage project documentation, schedules, and budgets.

Skills

Project Management

Collaboration

Risk Assessment

Education

Bachelor’s degree in Mechanical Engineering

Bachelor’s degree in Biomedical Engineering

Bachelor’s degree in Systems Engineering

Tools

SolidWorks

Job description

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Catalyst Life Sciences provided pay range

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

Base pay range

$115,000.00/yr - $130,000.00/yr

Catalyst is seeking a Project Engineer to join an exciting Medical Device company. You will work with a range of devices, from Class I-III, from inception to manufacturing, serving various clients.

The role is based in New Hampshire.

Responsibilities:

• Lead new product development and manufacturing processes.
• Manage project documentation, schedules, budgets, and conduct risk assessments.
• Collaborate with suppliers to identify cost-saving and process improvement opportunities.
• Ensure safety, quality, and accurate documentation throughout all project phases.

Qualifications:

• Bachelor’s degree in Mechanical, Biomedical, Systems Engineering, or related field.
• 7+ years of experience in medical device manufacturing.
• Experience with project management tools and SolidWorks.
• Knowledge of FDA regulations, ISO 13485, GMP, and medical device manufacturing processes.

Seniority level

• Mid-Senior level

Employment type

• Full-time

Job function

• Engineering, Project Management, and Design

Industries

• Medical Equipment Manufacturing

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