United States onlyLet’s build the future of medicine - together.
Join Enveda as a Sr. Quality Operations Manager in a Remote capacity 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 | Competitive Salary
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.
We’re proud of the momentum we’ve built.
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:
--Newsweek: Top 100 Global #MostLovedWorkplaces (2025)
--Forbes: America’s Best Startup Employers (2024 & 2025)
--Newsweek: America’s Greatest Startup Workplaces (2025)
--LinkedIn: Top Startups to Watch (2024)
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 a Sr. Quality Operations Manager, you’ll be at the forefront of delivering hope to patients everywhere. Your expertise in quality and regulatory compliance will be critical in accelerating our mission to integrate quality from the ground up because every breakthrough starts with bold questions and brave actions.
What You’ll Do
- Collaborate with cross-functional teams to ensure quality is integrated into all aspects of drug development
- Provide quality and compliance support to all functions ensuring GCP, GLP, and cGMP compliance
- Provide quality oversight for outsourced activities and conduct vendor audits of Enveda’s suppliers
- Develop and implement GXP standardized operating procedures
We’re Looking For
- Bachelor’s degree in life sciences, pharmaceutical sciences, or a related field
- In-depth knowledge of GCP, GMP, and GLP regulations and ICH guidelines
- Strong analytical and problem-solving skills
- Excellent communication and leadership abilities.
- Flexible to travel up to 20%
If you’re passionate about innovation and impact, we encourage you to apply even if you don’t meet every requirement.
Our Values: Curiosity | Agency | Journey | Charity | Unity
Benefits: 90% Medical, Dental, Vision | 401k Match | Flexible PTO | Adoption Assistance
Enveda is protecting Job Seekers:
We care deeply about creating a safe, respectful experience for every applicant, so we wanted to share a few guidelines to help you spot anything that doesn’t feel right.
--You’ll always meet real Enveda team members through video or in-person conversations before receiving an offer.
--All communication from us will come from an @enveda.com or @envedabio.com email address.
--We’ll never ask you to purchase equipment, send money, or share sensitive banking details as part of any step in our recruiting process.
If something feels off or you’re unsure whether a message is truly from Enveda, please reach out at anytime at recruiting@enveda.com.
At Enveda, we’re building a place where everyone can do the best work of their life. We are an equal opportunity employer and value diversity in all its forms. Apply now and join a team committed to shaping the future of drug discovery.
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