Top 2 Biomedical engineer Jobs in Guaynabo Municipio Pr

Product Development Engineer
CIS International LLC —Municipio de Juncos, PR
- Full-time
- Spanish
- English
- Mid-level
Quick Apply
Senior Process Engineer
BioPharma Consulting JAD Group —Juncos, PR
- Contract
- Spanish
- Doctoral degree
- Engineering
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Product Development Engineer

CIS International LLC -
Municipio de Juncos, PR

Quick Apply

Job Details

Full-time

Qualifications

Bachelor's degree in engineering
Compliance documentation
Product design
Engineering product development
Design for manufacturability (DFM)
Design controls
Quality systems
SAP ERP
Product design documentation
Mechanical product development projects

Full 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

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.

Requirements:

Education

Bachelor's Degree in Mechanical Engineering, Biomedical Engineering, Industrial Engineering, or a related Engineering discipline.
Advanced degree is a plus.

Experience

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.

Required Technical Skills

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

Preferred Knowledge

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)

Soft Skills

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

Quick Apply

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