Regulatory Affairs Specialist

Enovis Corporation (NYSE: ENOV) is an innovation-driven medical technology growth company dedicated to developing clinically differentiated solutions that generate measurably better patient outcomes and transform workflows. Powered by a culture of continuous improvement, global talent and innovation, the Company’s extensive range of products, services and integrated technologies fuels active lifestyles in orthopedics and beyond. For more information about Enovis, please visit

At Enovis™ we pay attention to the details. We embrace collaboration with our partners and patients and take pride in the pursuit of scientific excellence — with the goal of transforming medical technology as we know it. Because that’s how we change the lives of patients for the better. And that’s how we create better together. Why work at Enovis? See for yourself

As a key member of the Enabling Tech team you will play an integral part in helping Enovis drive the medical technology industry forward through transforming patient care and creating better patient outcomes.

Regulatory Affairs Specialist

Regulatory Affairs Manager

Austin, TX

Enabling Technologies

Orthopedic Medical Devices & Digital Health

We are looking for an experienced Regulatory Affairs Specialist to join our global Regulatory Affairs team. In this role, you will develop and execute regulatory strategies for innovative medical devices, software, and AI-enabled technologies, helping bring them to market across the US, Europe, and Australia.

• Develop and execute regulatory strategies for new and existing medical devices and software.
• Lead and support regulatory submissions, including FDA 510(k), EU MDR technical documentation, and TGA submissions.
• Work closely with Engineering, Clinical, Quality, and Product Development teams throughout the product lifecycle.
• Provide regulatory guidance on product development, risk management, clinical evidence, testing, labeling, and product changes.
• Interact with FDA, Notified Bodies, and TGA and support pre-submission meetings.
• Support post-market activities, regulatory assessments, audits, CAPAs, and product changes.
• Help develop regulatory strategies for emerging technologies, including AI and machine learning.
• Monitor regulatory changes and advise the business on new requirements.

• Bachelor’s degree in Science, Biomedical Engineering, Regulatory Affairs, or a related field.
• 5+ years of experience in medical devices, healthcare, or a related industry.
• Experience with regulatory submissions in the US and Europe; TGA experience is a plus.
• Strong knowledge of FDA regulations, EU MDR, ISO 13485, and ISO 14971.
• Experience with software/SaMD, AI, or machine learning is a strong advantage.
• Excellent communication, analytical, and problem-solving skills.
• Ability to work independently while collaborating effectively with international, cross-functional teams.

• This is an exciting opportunity to work at the intersection of medical devices, orthopedic innovation, software, and AI.
• You’ll have the opportunity to influence innovative products from development through market launch and help deliver technologies that improve surgical precision and patient outcomes.

• Primarily office-based
• Occasional travel to manufacturing and clinical sites and surgeon workshops
• Hands-on exposure to surgical instruments, navigation systems, and innovative medical technologies

• Must be able to travel up to 10% of the time.

• Experience with software/SaMD, AI, or machine learning is a strong advantage.
• Excellent communication,…