Position Details
About this role
This role involves developing and validating computational models for medical devices, supporting regulatory submissions, and managing vendor relationships to ensure high-quality simulation outputs.
Key Responsibilities
- Develop computational models
- Validate simulation results
- Prepare regulatory reports
- Manage vendor relationships
- Build reusable simulation frameworks
Technical Overview
The technical environment includes finite element analysis using Abaqus and ANSYS, simulation framework development, model validation, and regulatory documentation within healthcare or medical device sectors.
Ideal Candidate
The ideal candidate is a mid-level engineer with 3+ years experience in computational modeling and finite element analysis, skilled in simulation frameworks, model validation, and regulatory documentation, preferably with experience in medical device or pharmaceutical industries.
Must-Have Skills
Nice-to-Have Skills
Tools & Platforms
Required Skills
Hard Skills
Soft Skills
Industry & Role
Keywords for Your Resume
Deal Breakers
Lack of FEA or simulation experience, No experience with Abaqus or ANSYS, No regulatory modeling knowledge
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