Join Enveda as a Director, Quality Systems and Engineering in a remote setting 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?
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:
Jan 2024: Named a LinkedIn “Top Startup to Watch”
Mar 2024: Forbes America’s Best Startup Employers
Oct 2024: First drug to Phase 1 Clinical Trials
Dec 2024: Raised a $130M Series C
These milestones reflect the impact of our team, and we’re just getting started. 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 Director, Quality Systems and Engineering, you’ll be at the forefront of delivering hope to patients everywhere. Your expertise in quality systems and regulatory compliance will be critical in accelerating our mission to integrate quality into every aspect of drug development—because every breakthrough starts with bold questions and brave actions.
What You’ll Do
Lead initiatives to advance Enveda’s quality capabilities and instill a culture of quality across the company.
Collaborate with teams to identify automation opportunities and implement validated solutions for drug development programs.
Oversee the administration of Enveda’s electronic quality management system and ensure compliance with GXP regulations.
We’re Looking For:
A Bachelor’s degree in Computer Science, Engineering, Bioinformatics, or a Life Sciences field.
7+ years of experience in the pharmaceutical industry, particularly in a GXP regulated environment.
In-depth knowledge of GXP regulations for software development and a strong desire to apply AI technologies to enhance GXP processes.
If you’re passionate about innovation and impact, we encourage you to apply—even if you don’t meet every requirement.
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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