Skip to main content
Tallo logoTallo logo
Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

R&D Advanced Therapeutics Manager

Job

Innovative Health LLC

Scottsdale, AZ (In Person)

Full-Time

Posted 4 weeks ago (Updated 3 weeks ago) • Actively hiring

Expires 7/13/2026

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
77
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job Description

R D Advanced Therapeutics Manager Innovative Health
LLC - 3.3
Scottsdale, AZ Job Details Full-time 17 hours ago Qualifications Developing medical devices Product development research management Bachelor's degree in mechanical engineering Electrical compliance testing Managing medical device teams Staff supervision Strategic management Product development project management Resource allocation (project management tasks) Replacing parts Requirements design Bachelor's degree in electrical engineering Electronics component replacement Medical device testing Coaching Engineering Research and development in electrical engineering Talent management Regulatory compliance Bachelor's degree in biomedical engineering Mechanical Engineering Electrical system design Process design Biomedical Engineering Talent acquisition strategy Performance management Electronics test specifications 8 years System design for system development Team development Full Job Description The R D Advanced Therapeutics Manager role is responsible for leading the development of advanced medical device reprocessing platforms, including Class III devices and complex electromechanical systems. This role provides both strategic and hands-on leadership across advanced therapeutic device reverse engineering and process development, with a focus on system-level architecture, disassembly/reassembly processes, component replacement strategies, and validation of functional equivalence.
Essential Duties and Responsibilities:
StrategicTechnical Leadership Define system-level architecture across different therapeutics platforms. Establish engineering requirements framework in compliance with FDA, ISO, and internal design controls. Define electrical performance criteria, functional equivalence requirements, and acceptance criteria for reprocessed devices. Lead cross-platform engineering strategy to ensure reuse of validation frameworks. Advanced Reprocessing Development Develop and implement disassembly, component replacement, and reassembly strategies for complex devices. Lead reverse engineering and second-life device design approaches. Define critical-to-function components and replacement thresholds. ValidationTest Architecture Build validation architecture covering: Electrical performance Mechanical performance System-level functional equivalence Oversee development of test methods, protocols, and design verification and validation strategies. Program Execution Lead R D programs from concept through production. Manage timelines, technical risk, and resource allocation. Partner with RA/QA to define regulatory pathways and validation expectations. Team Development Lead, mentor, and develop engineering team (Sr Engineers, Engineers, Technicians). Support hiring strategy aligned with technical roadmap. Foster a collaborative, high-performance culture.
Supervisory Responsibilities:
Direct supervision of R D engineering team members Responsible for hiring, coaching, and performance management
Education, Qualifications and Skills:
Bachelor's degree in engineering (Electrical, Mechanical, Biomedical or related); advanced degree preferred 8 - 10+ years of experience in medical device R D Strong experience in Class III medical device development Experience with system-level architecture and electromechanical systems Deep understanding of design controls, risk management, and validation for FDA-regulated products Strong leadership, problem-solving, and communication skills Ability to work in a fast-paced, collaborative environment