Join Us in Tackling Autoimmune Disease at Its Root
At Vor, we believe science can do more than manage symptoms. It can change the course of disease. By advancing telitacicept, a first- and potentially best-in-class dual BAFF/APRIL inhibitor, we are silencing upstream survival signals and stopping downstream autoimmune cascades. Together, we are addressing disease at its root cause and rewriting what is possible for patients worldwide.
When you join Vor, you’re not just working on a medicine. You’re part of a mission to redefine the future of autoimmune care.
Why Work at Vor?
Impact: Contribute directly to a medicine with best-in-disease Phase 3 results in myasthenia gravis and expansion into multiple autoimmune diseases.
Growth: Be part of a rapidly scaling company with opportunities to grow your career in science, clinical development, commercial strategy, and beyond.
Innovation: Work on a platform with potential beyond one indication — a therapy that has already shown consistent results across lupus, IgA nephropathy, and Sjögren’s syndrome.
Belonging: Join a culture where every voice is heard, and where our shared mission unites us across functions and geographies.
Vor Bio is seeking an exceptional and highly motivated CMC leader Director/Sr Director Regulatory CMC to join our team. The qualified candidate will work cross-functionally to lead development and implementation of robust regulatory CMC strategies & tactics across programs and lifecycle stages to support our company objectives. As a result, the candidate will play a vital role in helping to progress our lead program, telitacicept, a first- and potentially best-in-class dual BAFF/APRIL inhibitor, through clinical development and global registration.
The candidate must be a highly effective leader as they will be relied upon to drive robust CMC strategic plans throughout development. This individual should also have strong interpersonal skills and a demonstrated track record with regulatory agencies.
Extensive experience in the development of biologics and combination biologic/device products is a must.
Key areas of responsibility:
· As a member of the CMC project teams, act as Regulatory CMC Lead for assigned programs providing strategic guidance to development team(s) on complex regulatory CMC topics.
· Responsible for leading negotiations with regulators as applicable for initial INDs/CTAs, amendments and future marketing registration applications.
· Accountable to establish and execute high-quality CMC related submissions including INDs/CTAs or amendments working in collaboration with other stakeholders (ie., research process & analytical development, manufacturing, and other SME’s).
· Keep abreast of and communicate CMC regulatory requirements to ensure all development activities follow applicable regulations and guidelines.
· Provide regulatory strategic and tactical support for CMC aspects such as change control & inspection management. Assess proposed manufacturing process changes, provide expertise on raw materials management, DP/DS specifications and release, process characterization & validation, methods development & validation and provide strategic regulatory guidance to enable implementation.
· Participate in regulatory intelligence activities as they pertain to global CMC regulations and guidance and integrate into program plans.
· Maintain responsibility for all CMC Regulatory timelines, that also includes managing contract staff and vendors relevant to CMC activities.
· Build and maintain strong relationships with internal and external stakeholders.
Skills and requirements:
· PharmD or PhD preferred with ≥8 years of industry experience in Regulatory CMC biologics. Strong scientific background and training in manufacturing processes and development and development of combination biologic/device products are required. Small molecule and medical device experience are a plus. Experience working with FDA sCDER is required.
· A strong background & track record in filing regulatory submissions from early development to pre and post approval submissions and product lifecycle management in the area of biologic medicinal products.
· A broad understanding of all aspects of CMC including process development, regulatory and quality requirements, analytical development, formulation and drug product technologies, distribution in US/ex-US.
· Experience interfacing with FDA, and other global health authorities.
· Demonstrated risk identification and critical thinking skills.
· Strong understanding of the global pharmaceutical drug development and regulatory environment, including anticipating future trends and opportunities in biologics.
· Ability to interact effectively across all levels of the organizations; integrates functional expertise with business knowledge to solve problems, meet priorities and deadlines in alignment with corporate goals and objectives.
· Recognized as an influential leader who possesses a cross-functional collaborative skill set.
· Strong oral and written communication skills with strong attention to detail and the ability to coordinate multiple activities in a faced paced biotech environment.
· Able and willing to author regulatory documents as needed and provide guidance to subject matter experts on authoring regulatory appropriate CMC reports and assessments.
The salary range for the Director, Regulatory CMC is expected to be between $200,000 and $220,000 per year. Individual pay may vary based on multiple factors including but not limited to relevant job-related skills, experience, education or training, market factors, and work location.
The salary range for the Senior Director, Regulatory CMC is expected to be between $250,000 and $265,000 per year. Individual pay may vary based on multiple factors including but not limited to relevant job-related skills, experience, education or training, market factors, and work location.
At Vor, we support our team with robust benefits, including comprehensive health coverage, flexible paid time off, generous parental leave, and a competitive 401(k). From education assistance to wellness resources and financial security, we invest in your well-being so you can thrive at work and beyond.
As an equal opportunity employer, we at Vor Bio know that diversity inspires innovation, inclusiveness, and creativity. We invite you to come as you are. All applicants will be considered for employment agnostic to race, age, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.
Please visit our website at https://www.vorbio.com/ for more information.
Skills Required
- Minimum 8 years industry experience in Regulatory CMC biologics
- PharmD or PhD
- Extensive experience in development of biologics and combination biologic/device products
- Experience working with FDA CDER (sCDER)
- Proven track record filing regulatory submissions from early development through pre/post-approval
- Broad understanding of CMC: process development, analytical development, formulation, drug product technologies, quality and regulatory requirements
- Experience interfacing with FDA and other global health authorities
- Ability to assess manufacturing changes, provide guidance on specifications, validation, and methods development
- Demonstrated risk identification, critical thinking, and strong oral and written communication skills
- Ability and willingness to author regulatory documents and guide SMEs on CMC reports and assessments
- Experience managing contract staff and external vendors relevant to CMC activities
- Recognized influential leader with cross-functional collaboration skills
What We Do
Vor Bio is a clinical-stage cell and genome engineering company that aims to change the standard of care for patients with blood cancers by engineering hematopoietic stem cells to enable targeted therapies post-transplant.
