CMC Director - Drug Product
EnvedaAbout the role
Let’s build the future of medicine - together.
Join Enveda as a CMC Director – Drug Product and help us transform natural compounds into life-changing medicines. We’re a team driven by curiosity and innovation - are you ready to make a difference?
Remote | Full-Time |$215,000-$225,000
What Makes Us Enveda
Life is smart, and we can learn from it. We’re reinventing drug discovery by harnessing nature’s intelligence. Our platform identifies new medicines four times faster than the industry standard because patients can’t wait. What sets Enveda apart isn’t just what we do - it’s how we do it. Our culture is built on creativity, collaboration, and deep respect for each other. We believe “People Create All Value”, and our success is driven by the extraordinary team turning our mission into reality every day.
Our Momentum
- Unicorn status: Achieved following a $150 million Series D funding round in 2025
- Discovery and innovation: Advanced our first drug candidate to Phase 1 trials in 2024
- Award-winning culture:
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- Newsweek: Top 100 Global #MostLovedWorkplaces (2025)
- Forbes: America’s Best Startup Employers (2024 & 2025)
- Newsweek: America’s Greatest Startup Workplaces (2025)
- Fast Company: Most Innovative Companies in 2026
These milestones reflect the impact of our team and we’re just getting started, but they’re only possible because of the diverse talent, perspectives, and relentless drive of our team, and people like you.
Your Role in Our Mission
At Enveda, every role drives impact. As CMC Director - Drug Product, you will play a key role in executing Enveda’s pharmaceutical development and manufacturing initiatives. Your expertise will guide CMC-related activities spanning oral solid dose drug product formulation development, manufacturing, and regulatory submissions. Reporting directly to the VP, CMC, your contributions will be instrumental in executing our development and manufacturing strategies and ensuring the delivery of high-quality products to patients.
What You’ll Do
- Lead the management and oversight of formulation development, scale-up, and tech transfer for small-molecule oral solid dose (OSD) drug product manufacturing, collaborating with external CDMOs and internal development project teams to deliver clinical drug product on established timelines
- Provide technical and strategic leadership for small-molecule OSD development programs
- Own drug product development strategy from pre-IND through Phase 3, ensuring phase-appropriate design, control strategy, and documentation
- Ensure strict adherence to global regulatory guidelines throughout the manufacturing, packaging, and testing processes
- Serve as the technical authority for OSD formulation development and manufacturing within CMC and the primary point of contact during discussions with health authorities worldwide
- Review and approve controlled drug product development and manufacturing documentation
- Lead the preparation and critical review of CMC documents for regulatory submission
- Work cross-functionally with Regulatory Affairs and Quality Assurance to ensure regulatory compliance and seamless implementation of CMC standards and cGMP regulations
- Contribute to the development and oversight of project-level CMC budgets, emphasizing cost-effectiveness without compromising quality
We’re Looking For
- Lead the management and oversight of formulation development, scale-up, and tech transfer for small-molecule oral solid dose (OSD) drug product manufacturing, collaborating with external CDMOs and internal development project teams to deliver clinical drug product on established timelines
- Provide technical and strategic leadership for small-molecule OSD development programs
- Own drug product development strategy from pre-IND through Phase 3, ensuring phase-appropriate design, control strategy, and documentation
- Ensure strict adherence to global regulatory guidelines throughout the manufacturing, packaging, and testing processes
- Serve as the technical authority for OSD formulation development and manufacturing within CMC and the primary point of contact during discussions with health authorities worldwide
- Review and approve controlled drug product development and manufacturing documentation
- Lead the preparation and critical review of CMC documents for regulatory submission
- Work cross-functionally with Regulatory Affairs and Quality Assurance to ensure regulatory compliance and seamless implementation of CMC standards and cGMP regulations
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