Head of TDO & Strategy

Head of TDO & Strategy

Here at Kelonia Therapeutics, we aren't just a clinical company; we're trailblazers in viral engineering, pushing the boundaries of in vivo lentiviral gene and cell therapy. We're not just a team; we're dreamers on a mission to bring the promise of cell and gene therapy to every patient in need.

At Kelonia, we've gathered a group of pioneers in cell and gene therapy to lead our journey, with extraordinary scientific founders at the helm, providing the cutting-edge technology that sets us apart. We're not just building a company; we're cultivating a culture that values both skill and care.

Are you ready to be a part of our remarkable journey? We're looking for someone exceptional to join our growing team as Head of Technical Development Operations & Strategy. We're seeking an inspiring leader to architect and scale Technical Operations across the development lifecycle, including process, analytical, formulation development, internal manufacturing and MSAT, and CDMO management, while ensuring cGMP compliance and advancing critical regulatory submissions. This is an opportunity to shape groundbreaking therapies, build a company from the ground up, and make a transformative impact on patients' lives. The ideal candidate pairs deep technical expertise with strategic vision and a collaborative spirit. Join us at the forefront of innovation and help write the next chapter in gene therapy.

What You Will Do :

• Drive the overall TDO Strategy, Vision and Strategic Growth to enable success, ensuring alignment with program and corporate milestones including control strategy, PPQ / validation path, and BLA / MAA readiness.
• Establish trusted Partnership and Collaboration with Regulatory CMC and Quality.
• Lead upstream, downstream, analytical, formulation and fill-finish activities; oversee tech transfer to CDMOs, set phase-appropriate specs / method lifecycle / stability, and lead comparability / bridging.
• Own and optimize clinical supply (DS / DP / F&F, packaging / labeling, release / testing, cold-chain distribution) to ensure on-time, in-spec lots.
• Own the preparation, review, and submission of CMC sections for global filings (IND / IMPD / CTA, NDA / BLA); author / defend content and lead FDA / EMA / HA meetings.
• Partner with QA to run change control, deviations / CAPA, data integrity, and inspection readiness across internal and external sites.
• Lead a high-performing, collaborative TDO Strategy team, fostering accountability, speed, and quality.
• Cultivate and manage relationships with CDMOs / CMOs via QTAs / TTAs, audits, and KPI dashboards to ensure best-in-class capabilities.
• Govern the TDO Strategy budget; model options for throughput, COGS, and yield improvements; communicate trade-offs and recommendations to the exec team and Board.

What You Will Bring :

At Kelonia, we are dedicated to promoting a healthy work-life balance, and our benefits are designed to reflect that commitment. Alongside Flexible Time Off, we offer a flexible scheduling environment that empowers employees to work in a way that aligns with both their needs and our company's objectives. We also provide a team-focused environment with a competitive benefits package, including health, dental, commuter benefits, and more. At Kelonia, we foster a collaborative and inclusive workplace where you can join a small team that values both talent development and achieving company goals. Kelonia Therapeutics is an equal opportunity employer. We do not discriminate on the basis of race, color, gender, gender identity, sexual orientation, age, religion, national or ethnic origin, disability, protected veteran status or any other basis protected by applicable law. Kelonia does not accept unsolicited resumes from any source other than directly from candidates. Job Type : Full-time Work Type : On-Site M-F Location : Boston, MA