Research And Development Specialist

R&D SPECIALIST (MEDICAL DEVICES)

About Consure Medical:

Consure Medical is a fast-growing, innovation-first medical device company that is redefining critical care. We've built a portfolio of first-of-its-kind products in incontinence management, skin health, infection prevention, and critical care—technologies that deliver measurably better clinical outcomes, lower healthcare costs, and broader patient access. Our solutions are sold globally, protected by strong intellectual property, supported by rigorous regulatory clearances and comprehensive clinical evidence, and manufactured to the highest quality standards.

We're not a large bureaucracy or a small local player with limited reach. We're at the perfect scale: agile enough for rapid iteration, backed by the resources to launch globally in 4–6 quarters, and focused exclusively on products that genuinely transform patient care.

The Opportunity:

This is a rare chance to join as a hands-on R&D Specialist and own meaningful medical device development from bold concept to commercial launch. You'll work in a fast-paced, high-ownership environment with minimal supervision—exactly the kind of role that rewards engineers, product designers, and technically minded medical professionals who love turning ideas into reality.

If you're currently stuck in a large organization where real product development feels distant, or at a smaller company that may never see global scale, or a motivated individual breaming with vision to transform healthcare, this is your opportunity to make an outsized impact. You'll design, prototype, test, and help launch pioneering Class I and II devices that will reach patients worldwide—while collaborating directly with clinical, quality, regulatory, marketing, and commercial teams across the US, Europe, and Asia.

Key Responsibilities:

• Drive end-to-end product development: from concept and system-level design through verification, validation, regulatory submission, and successful commercialization.
• Own 3D CAD modeling, detailed drawings, assemblies, and BOMs; rapidly iterate designs using state-of-the-art tools.
• Lead hands-on prototyping efforts—including rapid prototypes, functional builds, injection-molded components, catheter assemblies, and iterative improvements.
• Support design verification & validation, risk management (ISO 14971), biocompatibility (ISO 10993), and all required documentation (DHF, DMR, Technical Files) in full compliance with global medical device regulations.
• Collaborate cross-functionally with Quality, Manufacturing, Regulatory, and Clinical teams to ensure seamless transfer to production and global market readiness.
• Provide technical expertise for regulatory submissions and approvals across multiple international markets.
• Contribute to post-market surveillance, product enhancements, and continuous improvement initiatives.
• Stay ahead of the curve by evaluating new materials, technologies, and processes that can accelerate development and elevate product performance.

Requirements (Bare Minimum – We Hire for Talent & Mindset):

· Bachelor's or Master's degree in Mechanical Engineering, Electronics Engineering, Biomedical Engineering, or a closely related discipline.

· 3–5 years of hands-on experience in medical device design and development for Class I and/or Class II products.

· Demonstrated proficiency in CAD (SolidWorks or equivalent), rapid prototyping, injection molding, catheter assembly, and the full medical device development lifecycle.

· Familiarity with basic embedded software or firmware used to design and operate basic medical devices.

· Strong working knowledge of design controls, Design History Files (DHF), Device Master Records (DMR), risk management, biocompatibility studies (ISO 10993), and regulatory requirements for global markets.

· Proven ability to move quickly from idea to functional prototype with minimal supervision.

· Superior communication skills—able to dream up innovative designs, clearly articulate technical concepts, and collaborate effectively with diverse global stakeholders.

· A doer's mindset: you believe in your ideas, execute with tactical excellence, and thrive in an entrepreneurial, non-hierarchical culture.

Why You'll Love Working Here:

• Real Impact, Real Speed: Take products from concept to global launch in 4–6 quarters—not years.
• Ownership & Autonomy: Minimal bureaucracy, maximum freedom to innovate and own outcomes.
• Global Stage: Work on technologies that are already selling worldwide and will continue to expand rapidly.
• Intrapreneurial Environment: Build, test, and scale your ideas alongside a passionate team that values results over titles.
• Purpose-Driven Work: Every prototype and every launch directly improves patient lives and transforms critical care.

Location & Work Schedule: QNQ Design and Development Pvt Ltd, 253, Okhla Phase 3, New Delhi- 110020, India

Work Days and Timings: Mon to Sat – 9:00 AM to 6:00 PM. Second & Fourth Saturdays and Sundays are off.

If you're a hands-on builder who gets excited by turning cutting-edge ideas into market-ready medical breakthroughs, we want to hear from you.

Apply now and help shape the future of patient care at Consure Medical.