Project Engineer I
Athens, TX
Job Type
Full-time
Description
Company Overview
Biomerics is a world-class manufacturer and innovative polymer solutions provider for the medical device and biotech industries. As a vertically integrated company, we specialize in the design, development, and production of medical devices for diagnostic and interventional procedures. We are focused on next-generation solutions for the vascular access, electrophysiology, cardiac rhythm management, neurovascular, structural heart, and cardiovascular markets.
At Biomerics, we are dedicated to our diverse employee base. We understand that a strong, skilled, and engaged workforce is the foundation of our continued success as a business. We strive to live up to the Biomerics values in all our interactions. It is an exciting time to be part of our collective team. There is no limit to the impact that can be achieved here at Biomerics. We improve and advance our employees' lives, and the lives of the patients that depend on our products.
At Biomerics we believe in integrity, partnership, empowerment & accountability, trust, agility, teamwork, excellence, and we care. Our team-oriented, customer-focused corporate culture places a premium on building strategic, mutually beneficial partnerships with customers as well as our team members.
Job Summary:
As a Project Engineer I at Biomerics, you will support cross-functional engineering and manufacturing projects related to medical device development and production. This is an entry-level role ideal for recent graduates or professionals with limited experience who are eager to grow in a regulated, fast-paced environment.
Responsibilities:
Assist in project planning, documentation, and execution.
Coordinate with cross-functional teams including R D, Quality, and Manufacturing.
Support validation and verification activities for new and existing products.
Maintain and update technical documentation in compliance with FDA and ISO regulations.
Conduct data collection and analysis to support engineering decisions.
Participate in design reviews and risk assessments.
Requirements
Education / Certifications:
Education: Bachelor's degree in Mechanical, Biomedical, or related engineering field.
Qualifications:
1-2 years of engineering experience, preferably in a medical device or regulated environment.
Understanding of engineering principles, FDA QSR, and ISO 13485.
Strong organizational and communication skills.
Proficient in CAD and MS Office.
Benefits: Medical/Dental/Vision Insurance, Short-Term Disability, Long-Term Disability, Life Insurance, Paid Vacation Days, Paid Holidays, 401k
Athens, TX
Job Type
Full-time
Description
Company Overview
Biomerics is a world-class manufacturer and innovative polymer solutions provider for the medical device and biotech industries. As a vertically integrated company, we specialize in the design, development, and production of medical devices for diagnostic and interventional procedures. We are focused on next-generation solutions for the vascular access, electrophysiology, cardiac rhythm management, neurovascular, structural heart, and cardiovascular markets.
At Biomerics, we are dedicated to our diverse employee base. We understand that a strong, skilled, and engaged workforce is the foundation of our continued success as a business. We strive to live up to the Biomerics values in all our interactions. It is an exciting time to be part of our collective team. There is no limit to the impact that can be achieved here at Biomerics. We improve and advance our employees' lives, and the lives of the patients that depend on our products.
At Biomerics we believe in integrity, partnership, empowerment & accountability, trust, agility, teamwork, excellence, and we care. Our team-oriented, customer-focused corporate culture places a premium on building strategic, mutually beneficial partnerships with customers as well as our team members.
Job Summary:
As a Project Engineer I at Biomerics, you will support cross-functional engineering and manufacturing projects related to medical device development and production. This is an entry-level role ideal for recent graduates or professionals with limited experience who are eager to grow in a regulated, fast-paced environment.
Responsibilities:
Assist in project planning, documentation, and execution.
Coordinate with cross-functional teams including R D, Quality, and Manufacturing.
Support validation and verification activities for new and existing products.
Maintain and update technical documentation in compliance with FDA and ISO regulations.
Conduct data collection and analysis to support engineering decisions.
Participate in design reviews and risk assessments.
Requirements
Education / Certifications:
Education: Bachelor's degree in Mechanical, Biomedical, or related engineering field.
Qualifications:
1-2 years of engineering experience, preferably in a medical device or regulated environment.
Understanding of engineering principles, FDA QSR, and ISO 13485.
Strong organizational and communication skills.
Proficient in CAD and MS Office.
Benefits: Medical/Dental/Vision Insurance, Short-Term Disability, Long-Term Disability, Life Insurance, Paid Vacation Days, Paid Holidays, 401k
Job ID: 479418657
Originally Posted on: 6/2/2025
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