Sr. Drafter (Medical Devices)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
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
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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