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LifeSync - Amphenol

CAD & PDM Administrator

 Modality: Face to face

 Location: LifeSync Amphenol Costa Rica

About the position

Summary Profile 

The CAD & PDM Administrator serves as the primary administrator and subject matter expert for LifeSync's SolidWorks CAD and Product Data Management (PDM) environment. The role is responsible for maintaining engineering design documentation, administering the PDM vault, establishing CAD standards, supporting engineering documentation, training users, and ensuring data integrity across global engineering teams.

Duties & Responsibilities  

  •  Create, modify, and maintain 3D models, engineering drawings, and assemblies using SolidWorks in accordance with established engineering standards.
  •  Maintain engineering documentation within the Product Data Management (PDM) system, ensuring accurate revision control and document organization.
  •  Process and implement Engineering Change Requests (ECRs) and Engineering Change Orders (ECOs) by updating drawings, Bills of Materials (BOMs), and related engineering documentation.
  •  Establish, maintain, and continuously improve CAD, drawing, PDM, and engineering documentation standards, procedures, naming conventions, templates, and best practices. 
  •  Author and maintain procedures, work instructions, engineering standards, templates, and training materials related to CAD, PDM, and engineering documentation processes. 
  •  Support the continued development and expansion of SolidWorks PDM capabilities across LifeSync's global engineering organization. 
  •  Provide technical guidance and training to engineering personnel regarding CAD, PDM, engineering documentation, and configuration management best practices. 
  •  Prepare and maintain engineering documentation required to support product development, sustaining engineering activities, and manufacturing operations.
  •  Collaborate with Engineering, Manufacturing, Quality, and other cross-functional teams to ensure engineering documentation is complete, accurate, and released on time.
  •  Support the creation, revision, and release of Bills of Materials (BOMs), drawings, specifications, and other controlled engineering documents.
  •  Assist in maintaining engineering records in compliance with company procedures and applicable quality system requirements.
  •  Provide day-to-day support to engineering users on CAD and PDM-related activities.
  •  Participate in continuous improvement initiatives related to engineering documentation and document control processes.
  •  Perform other duties as assigned.

ESSENCIAL Requirements:  

  •  Technical Diploma in Mechanical Drafting, Mechanical Design, Electromechanics, or a related technical field; or currently pursuing a Bachelor's Degree in Mechanical, Electromechanical, Mechatronics Engineering, or a related discipline (preferred to have completed at least 70% of the degree).
  •  Minimum of 2 years of experience supporting engineering documentation, CAD drafting, or mechanical design activities in a manufacturing environment.
  •  Hands-on experience using SolidWorks to create and maintain 3D models, assemblies, engineering drawings, and Bills of Materials (BOMs).
  •  Experience working with a Product Data Management (PDM) system or equivalent engineering document management platform.
  •  Experience supporting Engineering Change Requests (ECRs), Engineering Change Orders (ECOs), document revisions, and controlled engineering documentation.
  •  Working knowledge of engineering drawings, Bills of Materials (BOMs), revision control, and engineering documentation practices.
  •  Basic knowledge of Geometric Dimensioning and Tolerancing (GD&T).
  •  Proficiency in both written and spoken English. Minimum B2.
  •  Proficiency with Microsoft Office applications.

PREFFER QUALIFICATIONS: 

  •  Experience in the Medical Device industry or another regulated manufacturing environment.
  •  Familiarity with FDA, ISO 13485, and Design Control requirements.
  •  Experience supporting Sustaining Engineering or New Product Introduction (NPI) activities.
  •  SolidWorks certification (CSWA or CSWP) preferred.
  •  Experience with ERP systems and Adobe Illustrator is a plus.
 
SKILLS & COMPETENCIES  

  • Customer-focused mindset  
  • Professional verbal and written communication  
  • Strong follow-up and organizational skills  
  • Problem-solving and issue-resolution skills  
  • Accuracy and attention to detail  
  • Time management and prioritization  
  • Ability to work cross-functionally  
  • Ability to adapt to changing priorities and customer needs  
  • Accountability and ownership of assigned work  
Technical skills required


Recruitment process

Our Recruitment Process

We strive to provide a positive and transparent recruitment experience. While the process may vary depending on the position, it generally includes:

  • Application Review – We evaluate your qualifications, experience, and alignment with the position requirements.
  • Initial HR Interview – A conversation to learn more about your professional background, career goals, and expectations.
  • Hiring Manager Interview – A technical and role-specific discussion focused on the responsibilities of the position.
  • Final Evaluation – Depending on the role, the process may include additional interviews, technical assessments, or employment reference checks.
  • Background Check – The selected candidate must successfully complete the company’s required background screening process.
  • Employment Offer – Once the recruitment requirements have been completed, the selected candidate will receive a formal employment offer and onboarding information.
Office location
About the company

About LifeSync

LifeSync, an Amphenol company, is a global leader in the design and manufacturing of value-added medical interconnect solutions for the healthcare industry. As a 100% medical-focused division of Amphenol, we partner with leading OEM medical device manufacturers to develop innovative technologies that support patient care around the world.

Our expertise includes ECG leadwires and cables, SpO₂ sensors, EEG solutions, temperature probes, electrosurgical accessories, custom medical cable assemblies, and specialized medical interconnects.

We combine embedded engineering, advanced automation, and ISO-certified manufacturing to deliver OEM-grade quality from concept through full-scale production. Our global manufacturing network provides resilient supply chain solutions, Lean manufacturing practices, value engineering (VAVE), and world-class quality systems.

Costa Rica is an exciting addition to our global footprint, creating opportunities for talented professionals to contribute to advanced medical device manufacturing while collaborating with teams across North America and Asia.

At LifeSync, we are committed to innovation, quality, continuous improvement, and delivering solutions that strengthen every connection in healthcare.

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