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18 часов назад

Sr. Drafter (Medical Devices)

Формат работы
hybrid
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Philippines
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Мэтч & Сопровод

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Описание вакансии

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TL;DR

Sr. Drafter (Medical Devices): Create and maintain high-quality SolidWorks CAD models and manufacturing documentation for regulated medical device products with an accent on GD&T application, revision control, and PDM administration. Focus on producing inspection-ready drawings, coordinating with vendors and quality teams, and enforcing drafting standards for consistency and compliance.

Location: Hybrid Manila, PH

Company

hirify.global is a leading digital healthcare company that creates wearable biosensors and cloud-based analytics to detect and predict cardiac arrhythmias.

What you will do

  • Create and maintain SolidWorks part/assembly models and 2D drawings with complete packages including dimensions, tolerances, BOMs, and manufacturing notes.
  • Apply and interpret GD&T per ASME Y14.5 to support functional requirements, manufacturability, and inspection strategies.
  • Own document and revision control using PDM/PLM tools, execute ECO/ECN changes, and ensure configuration accuracy.
  • Coordinate with purchasing, external vendors for prototypes, tooling, RFQs, and resolve production issues.
  • Administer SolidWorks PDM system, maintain component library, templates, and enforce drafting standards organization-wide.
  • Mentor junior drafters and drive continuous improvement in documentation quality.

Requirements

  • 7+ years mechanical drafting experience, preferably in medical devices or regulated industry
  • Advanced proficiency in SolidWorks (parts, assemblies, drawings, configurations)
  • Strong GD&T knowledge and tolerance practices per ASME Y14.5
  • Experience with inspection/metrology, materials, manufacturing processes, and post-processing
  • Document/revision control expertise (ECO/ECN, PDM/PLM systems)
  • Strong organizational skills for managing priorities, vendor interactions, and cross-functional collaboration

Nice to have

  • SolidWorks PDM Admin experience (vault governance, workflows, permissions)
  • ISO 13485 and/or FDA 21 CFR 820 familiarity
  • Experience with prototypes/tooling orders and supplier coordination

Culture & Benefits

  • Collaborative environment focused on innovation, patient impact, and rapid growth.
  • Opportunities for career advancement and skill development in a global team.
  • Inclusive workforce celebrating diverse backgrounds and perspectives.
  • Reasonable accommodations for disabilities in application process.

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