CIS International LLC

Product Development Engineer

CIS International LLC  •  Juncos, PR (Onsite)  •  3 days ago
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Job Description



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
CIS International LLC

About CIS International LLC

Founded on November 2010, CIS International is servicing companies within the Medical Device, Pharmaceutical, Biotechnology, Food and Beverage, Chemical, Manufacturing industry, and others.

As part of our process of adaptation to the changes that the market represents, our company has been studying the international market for approximately 3 years. With this, we seek to support new and existing customers outside Puerto Rico, such as the United States, India and Dominican Republic.

Industry
Chemicals & Materials
Company Size
11-50 employees
Headquarters
San Lorenzo, PR
Year Founded
2015
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