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Junior Creo Jobs in Puerto Rico (NOW HIRING)

Junior Creo information

What is the difference between Junior Creo vs Junior SolidWorks?

AspectJunior CreoJunior SolidWorks
Required CredentialsBasic CAD certifications, CAD trainingBasic CAD certifications, CAD training
Work EnvironmentEngineering firms, manufacturing, product designEngineering firms, manufacturing, product design
Employer & Industry UsageWidely used in industrial design and engineeringWidely used in product development and engineering
Common Search & ComparisonYesYes

Junior Creo and Junior SolidWorks are entry-level CAD roles requiring similar certifications and working in comparable environments. Both are used in engineering and manufacturing industries, making them common comparison points for those starting their CAD careers.

What are the most commonly searched types of Creo jobs in Puerto Rico?

The most popular types of Creo jobs in Puerto Rico are:

What job categories do people searching Junior Creo jobs in Puerto Rico look for?

The top searched job categories for Junior Creo jobs in Puerto Rico are:

What cities in Puerto Rico are hiring for Junior Creo jobs?

Cities in Puerto Rico with the most Junior Creo job openings:

Infographic showing various Junior Creo job openings in Puerto Rico as of August 2026, with employment types broken down into 93% Full Time, 3% Part Time, 3% Contract, and 1% Nights. Highlights an 94% Physical, 4% Hybrid, and 2% Remote job distribution.

Product Development Engineer

CIS International LLC

Juncos, PR • On-site

Full-time

Re-posted 18 days ago


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