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Princeton, New Jersey, United States
Onsite
About Us: this is who we are
At Cyprotex US, an Evotec company, we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team, we thrive on challenging the status quo, learning from each other, and pushing the boundaries of what’s possible. We're on a mission to create a place where curiosity isn't just encouraged—it’s celebrated. Are you someone who asks questions, seeks answers, and isn't afraid to go deeper? #BeCureious with us and see where your curiosity can take you!
Cyprotex US specializes in ADME-Tox and Biosciences including both in vitro (laboratory experiments) and in silico (computer modelling) approaches. Cyprotex was founded in 1999. The Company serves the Pharmaceutical and Biotech, Cosmetics/Personal Care and Chemicals Industries as well as academia and not-for-profit organizations. Over 1700 organizations trust Cyprotex for their ADME-Tox and Bioscience research needs.
The Role: Your challenge…in our journey
We’re looking for a passionate and curious Senior Scientist to join our team. If you’re excited by new challenges, solving complex problems, and learning every step of the way, you might just be the perfect fit. In this role, you’ll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories.
As a Senior Scientist at Cyprotex, you'll have the freedom to ask the hard questions, think outside the box, and find creative solutions that push us forward. It’s a role where your curiosity will fuel both your personal growth and the success of the team.
What You'll Do:
We are seeking a Senior Scientist to be responsible for conducting routine ADME assays as well as participating in experimental design, performing experiments, troubleshooting, and performing data analysis and interpretation.
Perform routine in-vitro ADME assays
Responsible for planning, performing and reporting in vitro metabolism ADME studies for discovery and development stage compounds.
Actively participate in experimental design, perform experiments as well as critically analyze, interpret and report the data to design next steps.
Ability to perform high-impact as well as high throughput studies to completion in a fast paced environment, while managing multiple projects to meet the timelines
Provides scientific knowledge and responsible in establishing new ADME assays as well as contribute to the continuous improvement of the current ADME assays
Guide junior scientists within the department
Assist in data analysis and interpretation
Laboratory support including ordering, equipment calibration and validation Working to a high standard and adhering to our Quality System
Work closely with the Project Managers to ensure the requirements of our clients are met
Assist in running and maintaining robotic systems to support processes.
Perform Quality Review of peer data and assist in consolidating assay control and validation criteria
Work closely with the Project Managers to ensure the requirements of our clients are met
Who You Are:
PhD in a scientific relevant field with experience in contract research organizations, pharmaceutical industries or academia. (Ph.D. preferred) or Masters with 6 years plus experience.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Industry/academic experience in DM/PK and a strong record of scientific achievement
Experience in drug discovery/development
Broad understanding of ADME, in vitro drug metabolism and DDI
Knowledge of bioanalytical sciences including LC-MS/MS, GC-MS, biotransformation and physical organic chemistry
Experienced in cell based or biochemical assays.
Ability to work in a team environment, remaining attentive to ideas, recognizing responsibilities, and actively participating with others to accomplish assignments and achieve desired goals.
Excellent oral and written communication skills
Knowledge and proficiency with Microsoft Word and Outlook
Strong attention to detail
Ability to communicate with peers and all levels of management
Ability to manage time and works independently
Perform other duties as assigned
Desirable
Plate based screening.
Cell culture experience.
LC-MS/MS experience.
Why Join Us:
Growth Opportunities: We’re a company that believes in continuous learning and development. Whether it’s professional courses, mentorship, or new projects, we’ll help you grow.
Flexible Work Environment: We offer flexible work options to help you balance your professional and personal life. Site based.
Inclusive Culture: We’re committed to building a diverse and inclusive environment where everyone’s voice is valued, and curiosity is encouraged.
Innovative Projects: You’ll have the chance to work on groundbreaking initiatives and cutting-edge technology in an atmosphere where your curiosity is the key to success.
A Place for Big Ideas: We don’t just talk about thinking outside the box—we throw the box away. If you’ve got ideas, we want to hear them.
Are You Still Curious?
If you’ve read this far, then chances are you’ve got a curious mind—just like us. So, what are you waiting for? Take the leap and apply today. We can’t wait to see where your curiosity leads you—and how it will shape the future of Evotec.
Let your curiosity guide your career—#BeCurious and explore the endless possibilities at Evotec!
The base pay range for this position at commencement of employment is expected to be $80,750 to $109,250. This is a salaried exempt role. Base salary offered may vary depending on the individual’s skills, experience and competitive market value. Additional total rewards include discretionary annual bonus, comprehensive benefits to include Medical, Dental and Vision, short-term and long-term disability, company paid basic life insurance, 401k company match, flexible work, generous paid time off and paid holiday, wellness and transportation benefits.
Evotec (US) Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, gender, age, disability, genetic information, gender expression, gender identity, national origin, religion, sexual orientation, or veteran status.