Director/Senior Director, Regulatory Affairs Strategy

Oruka Therapeutics • Waltham, MA

1d • $213,000 - $286,000 • Hybrid

About The Position

Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka’s mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com
As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture.
The Director / Senior Director, Regulatory Affairs Strategy will serve as the Global Regulatory Lead for one or more development programs and will report to the Vice President, Regulatory Affairs. This individual will define and execute regulatory strategies that support rapid, high-quality global development of Oruka’s biologics portfolio, with an emphasis on differentiated programs in immunology and dermatology.
This is a highly visible, cross-functional leadership role for a regulatory strategist who can translate an ambitious product profile into actionable development and registration plans. The successful candidate will lead health authority interactions, shape key development milestones, guide major submissions, and proactively identify regulatory risks and opportunities to support corporate objectives.
At Oruka, this role offers the opportunity to help shape regulatory strategy for potentially best-in-class antibodies intended to redefine treatment expectations in psoriasis and related diseases, including programs with the potential for very infrequent dosing, deep efficacy, and durable responses.

Requirements

• Bachelor’s degree in a life sciences discipline required; advanced degree preferred; RAC a plus
• Director: 10+ years of progressive Regulatory Affairs experience in biotechnology or pharmaceuticals
• Senior Director: 12+ years of progressive Regulatory Affairs experience, including broader program leadership and significant health authority interaction
• Strong experience developing and executing global regulatory strategy for drugs and/or biologics in clinical development
• Direct experience authoring and/or leading major regulatory submissions and briefing packages
• Demonstrated experience leading interactions with FDA and international health authorities
• Deep knowledge of global regulatory requirements, including FDA, ICH, and ex-US development considerations
• Strong grasp of development-stage regulatory strategy for biologics
• Ability to interpret evolving regulatory guidance and apply it in a practical, risk-based way
• Excellent leadership, communication, influencing, organizational, and project management skills
• Strong scientific and business judgment, with the ability to connect regulatory strategy to program and company goals
• Ability to manage multiple priorities and thrive in a fast-paced, collaborative environment
• Willingness to travel up to 20%

Nice To Haves

• Experience in dermatology, immunology, or inflammation considered advantageous
• Experience in fast-paced biotech settings and comfort operating in a lean, hands-on environment strongly preferred

Responsibilities

• Serve as Global Regulatory Lead on multidisciplinary program teams for one or more investigational products
• Develop, drive, and continuously refine global regulatory strategies aligned with program goals, development timelines, and corporate priorities
• Provide regulatory leadership across the product lifecycle, from early development through registration planning and lifecycle management
• Assess regulatory precedent, competitor actions, and evolving global guidance to identify strategic risks, opportunities, and options
• Partner closely with Clinical, Clinical Operations, Nonclinical, CMC, Quality, Medical, Biometrics, and Program Leadership to ensure regulatory strategy is integrated into overall development planning
• Lead regulatory scenario planning for key inflection points, including dose selection, indication strategy, expedited development opportunities, pediatric requirements, and regional filing considerations
• Lead the preparation, strategy, and execution of key health authority interactions, including FDA and ex-U.S. agency meetings, scientific advice, and other formal engagements
• Serve as primary regulatory contact for assigned programs and represent Oruka externally with health authorities, consultants, and partners, as applicable
• Lead the development of briefing documents, meeting requests, responses to regulatory questions, and other agency-facing communications
• Translate agency feedback into clear strategic recommendations and cross-functional action plans
• Lead or oversee preparation of high-quality global regulatory submissions, including INDs/CTAs and amendments, annual reports, investigator brochure updates, briefing packages, and components of future marketing applications, as applicable
• Ensure submission plans, timelines, content strategies, and review processes support efficient execution
• Partner with Regulatory Operations and external vendors to support dossier planning, publishing, and e-submissions
• Ensure regulatory documentation is scientifically sound, compliant, and aligned with the target product profile and overall development strategy
• Monitor and interpret relevant global regulations, guidance, and policy developments, and communicate implications to cross-functional teams
• Support regulatory inspection readiness and compliance with applicable regulations, ICH guidelines, and company procedures
• Contribute to the development and continuous improvement of SOPs, templates, and internal regulatory processes
• Track and help ensure fulfillment of regulatory commitments for assigned programs
• Influence cross-functional teams through strong strategic thinking, sound judgment, and clear communication in a dynamic biotech environment
• May mentor junior regulatory staff or oversee consultants and external resources supporting assigned programs

Benefits

• A chance to be part of a vibrant startup culture where your work can directly impact bringing new medicines to patients.
• Competitive salary and benefits package.
• A supportive and inclusive team environment where everyone is encouraged to bring their authentic selves to work.
• Opportunities for professional growth and development.

What This Job Offers

• Job Type: Full-time
• Career Level: Director
• Number of Employees: 1-10 employees