info@arvantamedtech.com

Why Join Arvanta?

Innovation at the Core

Be part of a team pushing the boundaries of medical technology

Meaningful Impact

Create solutions that directly improve patient care and outcomes

Growth Opportunities

Develop your career in a rapidly expanding field

Collaborative Culture

Work alongside talented professionals in a supportive environment

Open Positions

Clinical Data Scientist

Remote

Analyze complex clinical and healthcare data to drive product improvement and development. You'll work closely with research, engineering, and commercial teams to extract meaningful insights that shape our technology roadmap.

Key Responsibilities:
  • Design and implement data collection protocols for clinical studies
  • Develop algorithms to process and analyze medical data from our devices
  • Generate insights to improve product performance and patient outcomes
  • Create visualization tools to communicate findings to various stakeholders
Qualifications:
  • MS or PhD in Data Science, Biostatistics, or related field
  • 3+ years experience working with healthcare or clinical data
  • Proficiency in Python, R, or similar programming languages
  • Experience with machine learning techniques applied to medical data
Apply Now

Regulatory Affairs Specialist

Hybrid

Guide our medical devices through global regulatory approval processes. You'll develop and implement regulatory strategies to ensure our innovative products reach the market efficiently while maintaining compliance with all applicable regulations.

Key Responsibilities:
  • Prepare and submit regulatory documentation to FDA, EU MDR, and other global authorities
  • Monitor and interpret regulatory changes affecting our product portfolio
  • Collaborate with cross-functional teams to ensure compliance throughout product development
  • Represent the company in interactions with regulatory bodies
Qualifications:
  • Bachelor's or Master's degree in a scientific, engineering, or related field
  • 4+ years of experience in medical device regulatory affairs
  • Knowledge of FDA, EU MDR, and international regulatory requirements
  • Strong project management and communication skills
Apply Now

Benefits & Perks

Competitive salary and equity packages

Comprehensive health, dental, and vision insurance

401(k) matching program

Generous paid time off and parental leave

Professional development budget

Not seeing the right fit?

We're always looking for talented individuals to join our team. Send your resume to careers@arvantamedtech.com with a brief description of your interests and expertise.