(Executive) Director, Regulatory Affairs, CMC

Dispatch Bio • Philadelphia, PA

2d

About The Position

Our purpose at Dispatch is to help create a world where all cancer patients can be cured. We’re humbled by the opportunity to work together as a team on some of the most pressing medical challenges of our time. To achieve our purpose, we are dedicated to engineering a universal treatment across solid tumors. We’re committed to the development of novel therapies, leveraging first-in-class technologies in viral vectors, universal targets, and novel cytokine biology. Our therapeutic approach has the potential to enable us to treat significant numbers of cancer patients and make a real and lasting impact on the world. Our company was founded on pioneering work carried out in the laboratories of Dr. Carl June (University of Pennsylvania), Dr. Kole Roybal (University of California, San Francisco), Dr. Christopher Garcia (Stanford University) and Dr. Andy Minn (Memorial Sloan Kettering Cancer Center). At our company, you would become one of our early team members— not only playing a role in meeting our ambitious mission but also building our thriving culture. We are determined to deliver with urgency to discover new solutions and we always stay dedicated to scientific rigor; we have an ownership mindset because each and every one of us is integral to our success. Collaboration is core for us because we believe that by bringing people together with diverse perspectives, we make a stronger whole. And, we show we care about our work and each other by sharing feedback - ultimately in service of our vision to empower people to continue forward with their lives – cancer free.

Requirements

• Bachelor's degree in life sciences, chemistry, engineering, or a related discipline
• Minimum of 10 years of regulatory CMC experience within the biotechnology or pharmaceutical industry
• Direct, hands-on experience authoring and managing CMC sections of IND, BLA, or MAA submissions
• Direct experience with cell therapy, viral vector, or other advanced therapy medicinal product (ATMP) manufacturing
• Deep working knowledge of FDA and ICH CMC regulations and guidelines applicable to biologics; cell and/or gene therapy experience
• Demonstrated experience leading CMC-focused health authority interactions and correspondence
• Track record managing complex manufacturing regulatory strategy, including comparability assessments and post-approval/process changes
• Strong leadership skills with the ability to influence and align cross-functional stakeholders without direct authority
• Excellent written and verbal communication skills, with strong attention to detail
• Ability to operate effectively and independently in a fast-moving, resource-constrained startup environment

Nice To Haves

• Advanced degree (MS, PhD, PharmD)
• Experience with global CMC regulatory submissions (e.g., EMA or other ex-U.S. agencies)
• Prior experience supporting solid tumor drug development
• People management experience, with a track record of developing regulatory talent

Responsibilities

• Lead the development and execution of global regulatory CMC strategies Dispatch programs, from early development through licensure
• Author, review, and approve CMC sections of regulatory submissions, including INDs, CTAs, BLAs/MAAs, amendments, annual reports, and responses to health authority questions
• Serve as the primary regulatory CMC liaison to health authorities (e.g., FDA, EMA, TGA), leading preparation for and participation in CMC-focused meetings and other health authority interactions
• Partner closely with Process Development, Manufacturing, Analytical Development, and Quality to ensure regulatory compliance and submission readiness across the product lifecycle
• Provide strategic regulatory guidance on manufacturing changes, process validation, comparability protocols, and facility qualification/licensure activities
• Assess regulatory risk associated with CMC and manufacturing decisions, and advise senior leadership on mitigation strategies and health authority engagement
• Track, interpret, and communicate evolving global CMC regulatory guidance and policy trends relevant to cell and gene therapy manufacturing
• Manage regulatory CMC aspects of relationships with CDMOs, contract testing laboratories, and other external manufacturing partners
• Build, mentor, and develop regulatory CMC talent as the team and pipeline grow
• Contribute to and help scale regulatory CMC processes, tools, and templates appropriate for a growing organization
• Represent Regulatory CMC on cross-functional program teams and provide regular updates to senior leadership

Benefits

• Highly competitive compensation package with meaningful ownership through equity
• Excellent coverage for medical, vision, and dental
• 401(k) with generous contribution
• Life insurance
• Flexible PTO policy
• Additional substantial benefits

What This Job Offers

• Job Type: Full-time
• Career Level: Executive