Education * Bachelor's Degree in Mechanical Engineering, Biomedical Engineering, Industrial ... Continuous improvement mindset Work Methodology: * 100% on site job * Full time job * Location:
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Education * Bachelor's Degree in Mechanical Engineering, Biomedical Engineering, Industrial ... Continuous improvement mindset Work Methodology: * 100% on site job * Full time job * Location:
Biomedical Engineering * Chemical Engineering * Microbiology or related scientific/engineering ... Remote work reporting to the Juncos, PR site. * Full Time Job * Shift: Administrative Shift, but ...
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Biomedical Engineering * Chemical Engineering * Microbiology or related scientific/engineering ... Remote work reporting to the Juncos, PR site. * Full Time Job * Shift: Administrative Shift, but ...
$89K - $122K/yr
A degree in Mechanical Engineering, Chemical Engineering, Biomedical Engineering, Bioprocess ... Full on site job in Juncos, PR * Full time job * Expected project duration: 5 months for the first ...
Quick apply
$89K - $122K/yr
A degree in Mechanical Engineering, Chemical Engineering, Biomedical Engineering, Bioprocess ... Full on site job in Juncos, PR * Full time job * Expected project duration: 5 months for the first ...
Full Time Mri Biomedical Engineer information
What is the difference between Full Time Mri Biomedical Engineer vs MRI Technologist?
| Aspect | Full Time Mri Biomedical Engineer | MRI Technologist |
|---|---|---|
| Credentials | Bachelor's degree in biomedical engineering or related field; certifications may vary | Certification as MRI Technologist (ARRT or equivalent); associate's or bachelor's degree in radiologic technology |
| Work Environment | Designing, testing, and maintaining MRI equipment; R&D labs; hospitals; medical device companies | Operating MRI machines; capturing images; patient positioning; working directly with patients in hospitals or imaging centers |
| Employer & Industry | Medical device manufacturers, research institutions, hospitals | Hospitals, imaging centers, clinics |
While both roles involve MRI technology, Full Time MRI Biomedical Engineers focus on equipment design, development, and maintenance, whereas MRI Technologists operate MRI machines to acquire diagnostic images. The roles differ in responsibilities, credentials, and work settings but are both essential in the MRI field.
What are popular job titles related to Full Time Mri Biomedical Engineer jobs in Puerto Rico? For Full Time Mri Biomedical Engineer jobs in Puerto Rico, the most frequently searched job titles are:
What job categories do people searching Full Time Mri Biomedical Engineer jobs in Puerto Rico look for? The top searched job categories for Full Time Mri Biomedical Engineer jobs in Puerto Rico are:
What cities in Puerto Rico are hiring for Full Time Mri Biomedical Engineer jobs? Cities in Puerto Rico with the most Full Time Mri Biomedical Engineer job openings:
Job description
Summary:
The Product Development Engineer supports the design, development, and continuous improvement of medical device products by implementing engineering changes, maintaining design documentation, and ensuring compliance with quality and regulatory requirements. This role collaborates with cross-functional teams including Engineering, Manufacturing, Quality, Planning, and Materials to develop design solutions that improve product performance, manufacturability and operational efficiency.
Responsibilities
Education
The Product Development Engineer supports the design, development, and continuous improvement of medical device products by implementing engineering changes, maintaining design documentation, and ensuring compliance with quality and regulatory requirements. This role collaborates with cross-functional teams including Engineering, Manufacturing, Quality, Planning, and Materials to develop design solutions that improve product performance, manufacturability and operational efficiency.
Responsibilities
- Support product design, development, and engineering change activities throughout the product lifecycle.
- Prepare and maintain engineering documentation, specifications, and technical records in accordance with company quality standards.
- Initiate and process engineering change documentation, including:
- Product Change Notices (PCH)
- Revision Change Notices (RCH)
- Design Change Notices (DCH)
- Quality Change Notices (QCH)
- Manufacturing Change Specifications (MCS)
- Execute engineering changes using Agile MAP, SAP, and Design Control systems.
- Review product development requirements to ensure compatibility with manufacturing processes and product design outputs.
- Collaborate with Product Development, Manufacturing, Quality, Materials, Tooling, and Planning teams to ensure design feasibility and manufacturability.
- Modify existing product designs and components to improve product functionality, manufacturing efficiency, and field performance.
- Develop and maintain CAD models, drawings, and engineering documentation using approved design software.
- Coordinate design requirements with cross-functional teams to optimize manufacturing processes, material availability, tooling, and contractual requirements.
- Ensure engineering documentation and product development activities comply with applicable quality systems and regulatory standards.
- Identify opportunities for process improvements and recommend solutions to enhance engineering efficiency and product quality.
- Participate in technical projects and support new product development initiatives.
- Provide technical guidance and mentoring to junior engineers when required.
- Support project execution while meeting timelines, quality objectives, and business priorities.
Education
- Bachelor's Degree in Mechanical Engineering, Biomedical Engineering, Industrial Engineering, or a related Engineering discipline.
- Advanced degree is a plus.
- Minimum of 2 years of engineering experience in product development, design engineering, or manufacturing engineering.
- Experience in regulated industries such as Medical Device, Pharmaceutical, or Life Sciences preferred.
- Experience managing engineering changes and design documentation.
- Agile MAP / Product Lifecycle Management (PLM)
- SAP
- Design Control Systems
- CAD software (SolidWorks, CATIA, Creo/ ProEngineer, Siemens NX, AutoCAD, or similar)
- Engineering documentation and technical specifications
- Product Design & Development
- Engineering Change Management
- Design for Manufacturability (DFM)
- Quality Systems and Design Controls
- Product Lifecycle Management (PLM)
- Medical Device Design Controls
- Engineering Change Order (ECO) processes
- Manufacturing processes
- Root Cause Analysis
- Process Improvement
- Project Management fundamentals
- Regulatory compliance (FDA, ISO 13485)
- Strong verbal and written communication skills
- Bilingual (English & Spanish)
- Excellent analytical and problem-solving skills
- Strong organizational and documentation abilities
- Quality-focused mindset
- Ability to work independently with minimal supervision
- Cross-functional collaboration and teamwork
- Ability to manage multiple priorities in a fast-paced environment
- Leadership, coaching, and mentoring skills
- Continuous improvement mindset
Work Methodology:
- 100% on site job
- Full time job
- Location: Juncos, PR
- Administrative shift (willing to work Weekend when needed).
- Type of industry: Medical devices
- Expected hiring month: July 2026
- Timeframe: July 2027
About CIS International
Sourced by ZipRecruiter
Company size
11 - 50 Employees
Headquarters location
Gardena, CA, US
Year founded
1991