Shape regulatory strategies for innovative medical products and oversee U.S. FDA submissions, impacting global market access for transformative treatments.
About Panther:
Panther is unlocking the tremendous biological powers of our skin to deliver a wide range of shelf-stable treatments. Panther’s precisely engineered microarray patches (MAPs) are focused on: i) Skin Health, treating coloration, wrinkles, scars, wounds, etc.; and ii) Therapeutics, treating ailments along the immunological spectrum, including infectious diseases, cancer, allergies and autoimmune diseases.
Panther’s MAPs are designed to deliver superior efficacy and high levels of usage/adherence, and enable automated data integration across its ecosystem of consumers, providers and treatment developers. Panther’s AI enabled platform provides personalized customer care and accelerated treatment discovery. Via advanced GMP manufacturing, direct-to-consumer distribution and consumer self-application, Panther’s MAPs are affordable, simultaneously enabling universal access and commercial success. Panther is led by accomplished tech, biotech and health professionals
The Opportunity
Panther Life Sciences is seeking a senior regulatory affairs manager to shape the future of its regulatory strategy across an ambitious portfolio spanning cosmetics, medical devices, and therapeutics. This is a high-impact leadership role at the intersection of science, strategy, and innovation, managing one of Panther’s most critical areas of investment while architecting the regulatory roadmap that will bring transformative, shelf-stable, patient-centric treatments to market.
This role is central to Panther’s success.The direction will architect the regulatory frameworks required to bring transformative, shelf-stable, patient-centric treatments to global markets, spanning cosmetics, medical devices, and therapeutics. As a key member of the leadership team, you will drive U.S. FDA and international submissions, every stage of product development from concept to global launch. This individual brings a rare combination of ambition, humility, precision, and deep collaboration, paired with a passion for next-generation medical products and improving the patient experience. The right leader will help unlock Panther’s full potential.
Some travel may be required approximately 10%.
Responsibilities
Regulatory Strategy (U.S. & Global)
Define and execute regulatory pathways for devices, therapeutics, cosmetics, and platform submissions.
Lead FDA filings (including RFD and IND pathways) and guide parallel global filings.
Ensure tight integration between regulatory strategy, R&D, clinical, and commercial teams.
Strategic Company Initiatives
Lead medical device approval for Panther’s device(s), including at least one parallel global agency.
Lead clinical trial preparation and documentation
Support quality initiatives in accordance with ISO 9001
Qualifications
6–12+ years of medical device regulatory experience, with at least 3 years in a lead role at a company developing a novel, non-predicate device
Direct experience navigating novel device classification pathways with FDA CDRH (De Novo, PMA), including preparation of classification arguments and special controls frameworks
Working knowledge of 21 CFR 878 and familiarity with CDRH reviewers in the aesthetic/dermatology device space
Proven ability to independently own Pre-Submission (Q-Sub) meetings with FDA
Experience operating under quality system (e.g. ISO 13485, and ISO 9001)
Experience reviewing or designing clinical study protocols for medical devices
Preferred Qualifications
Prior experience with clinical trials outside the US
Familiarity with aesthetic device submissions
Demonstrated experience navigating FDA device designations
Background at an early-stage or Series A/B device company where regulatory strategy is built from the ground up
Understanding of how novel device classification intersects with IP strategy
Working knowledge of the MoCRA framework
Experience working on Software as a Medical Device (SaMD)
Benefits
Equity in the form of Stock Options
Robust Health Insurance includes Medical, Dental, Vision
Life, AD&D, and Short-Term Disability Insurance
In-person company events
Fully-stock kitchen
In-office lunch twice a week
Working with a world-class team in technology and healthcare on the most innovative solutions
Paid time off and Paid Company Holidays.
Equal Opportunity Employer
Panther Life Sciences is an equal opportunity employer committed to building a diverse and inclusive workplace. We welcome applicants from all backgrounds and do not discriminate based on race, color, religion, gender, gender identity or expression, sexual orientation, pregnancy, marital or partnership status, age, national origin, citizenship, veteran or military status, disability, medical condition, genetic information, caregiver status, or any other characteristic protected by law.
Health Insurance
Robust Health Insurance includes Medical, Dental, Vision
In-office lunch twice a week
Paid Time Off
Paid time off and Paid Company Holidays.
Panther Life Sciences develops innovative microarray patches (MAPs) that tap into the biological potential of our skin to provide effective, shelf-stable treatments. We focus on skin health and therapeutic solutions, targeting a variety of conditions, including skin coloration, wrinkles, scars, and immunological ailments.
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