Join the Enkrisi Team.

SEE OPEN POSITIONS

Together we will drive change.

In a world of rapid innovation, we seek New Pioneers and Brave Inventors who want to impact all aspects of our business, enabling breakthroughs that will affect future generations. 


We encourage you to bring your disruptive thinking, collaborative spirit, and diverse perspective to our organization. We will continue Inventing for Life, Impacting Lives while Inspiring Your Career Growth.

Why work with us?

INNOVATION

At Enkrisi, we foster a culture of innovation and strive to make a meaningful impact in the pharmaceutical industry through cutting-edge drug development and regulatory affairs strategies.

INTEGRITY

Integrity is at the core of everything we do at Enkrisi. We are committed to providing our clients with the highest level of ethical standards and transparency in all aspects of our work, from drug development to regulatory affairs.

COLLABORATION

Enkrisi values collaboration and teamwork, working closely with clients and partners to achieve shared goals in drug development and regulatory affairs. By fostering strong relationships and open communication, Enkrisi ensures that everyone is working towards a common vision, resulting in more efficient and effective solutions for the benefit of patients and the industry.

DIVERSITY & INCLUTION

At Enkrisi, we foster a culture of innovation and strive to make a meaningful impact in the pharmaceutical industry through cutting-edge drug development and regulatory affairs strategies.

“I feel incredibly lucky to work for Enkrisi. The company’s commitment to innovation, integrity, collaboration, and inclusion is inspiring and shows in everything we do. I’m proud to be part of a team making a real difference in the pharmaceutical industry.”

“I feel incredibly lucky to work for Enkrisi. The company’s commitment to innovation, integrity, collaboration, and inclusion is inspiring and shows in everything we do. I’m proud to be part of a team making a real difference in the pharmaceutical industry.”

MADISON PETERSON,
Marketing Specialist

Head of Regulatory CMC Drug Development
Location: USA   |   Type: FULL-TIME
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Regulatory Affairs Consultant
Location: USA   |   Type: FULL-TIME
Apply
General Manager/Head of Project Management
Location: USA   |   Type: FULL-TIME
Apply
Head of Regulatory CMC Drug Development

Location: USA   |   Type: FULL-TIME

Regulatory Affairs Consultant

Location: USA   |   Type: FULL-TIME

General Manager/Head of Project Management

Location: USA   |   Type: FULL-TIME

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The VirtualPharm Podcast is an audio series that covers topics related to compliance and regulatory affairs in the Lifesciences industry. Each episode, hosted by an expert in the topic with decades of experience, offers listeners detailed insight into the changing regulatory environment.

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