Associate Principal Scientist

Princeton, NJ · On-site$94k – $115k

About this role

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 Associate Principal 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 an Associate Principal 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:

  • Perform routine in-vitro toxicology assays

  • Responsible for planning, performing and reporting in vitro TOX 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 TOX assays as well as contribute to the continuous improvement of the current TOX 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 at least 3 years of related experience in contract research organizations, pharmaceutical industries or academia.

  • An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

  • Experienced in High Content Assay development

  • Experienced in Imaging based and MEA based assays

  • Experienced in drug discovery/development

  • Broad understanding of TOX

  • 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.

The base pay range for this position at commencement of employment is expected to be $93,500 to $115,000. This is a salaried exempt position. 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.

Company at a glance

Just – Evotec Biologics, a wholly owned subsidiary of Evotec SE, is an innovative and trusted CDMO for complex biologics, incl. mAbs, bi/multispecifics, and biosimilars. We provide our partners with highly differentiated services for the development and manufacturing of biologics. Our world-leading AI-driven in silico molecular optimization and continuous bioprocessing platforms combined with our revolutionary J.POD® facilities, which represent a paradigm shift within the industry, are helping to reduce the cost of goods and expand global access to affordable, high-quality biotherapeutics in addition to providing a highly agile cGMP manufacturing strategy to support rapid ramp up and uncertain demand scenarios.

Founded2014
Team Size501-1,000 employees
WorkspaceOn-site
IndustryBiotechnology Research
Location
Princeton, New Jersey, United States

Top Benefits

  • Discretionary Annual Bonus
  • Medical Insurance
  • Dental Insurance
  • Vision Insurance
  • Short-term Disability
  • Long-term Disability
  • Company Paid Basic Life Insurance
  • 401k Company Match
  • Flexible Work
  • Paid Time Off
  • Paid Holiday
  • Wellness Benefits
  • Transportation Benefits

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