Associate Principal Scientist - In Vitro Toxicology - Microelectrode Array - Site Based, Prince[...]

Evote; Princeton (NJ); On-site; USD 93,500 - 126,500; Full time

Benefits offered by this job

Discretionary annual bonus

Flexible work

Generous paid time off

Job summary

A leading biotech company located in Princeton, New Jersey, is seeking an Associate Principal Scientist to drive impactful projects and collaborate with talented professionals. The role involves performing innovative in-vitro toxicology assays, with a focus on Microelectrode Array technology. Candidates must possess a PhD and have substantial experience in cell biology and electrophysiology, among other qualifications. Attractive compensation package includes a base salary of $93,500 to $126,500, along with comprehensive benefits.

Qualifications

• At least 3 years of post-PhD experience in contract research organizations, pharmaceutical industries or academia.
• Industry/academic experience in cell biology and electrophysiology.
• Experience in drug discovery/development, especially MEA assays.

Responsibilities

• Perform routine in-vitro toxicology assays, focusing on Microelectrode Array (MEA).
• Plan, perform, and report in vitro Toxicology studies for compounds.
• Guide junior scientists within the department.

Skills

Cell biology

Electrophysiology

Time management

Communication skills

Attention to detail

Education

PhD in a scientific relevant field

Tools

Microsoft Word

Microsoft Excel

Job description

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, with a focus on Microelectrode Array (MEA)
• Responsible for planning, performing and reporting in vitro Toxicology 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
• 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 post PhD 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.
• Industry/academic experience in cell biology and electrophysiology and a strong record of scientific achievement
• Experience in drug discovery/development, especially MEA assays
• Expertise in electrophysiological assays with Microelectrode Array for cardiac and neuro assays is highly desired
• 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 with peers and all levels of management
• Knowledge and proficiency with Microsoft Word and Excel
• Strong attention to detail
• Ability to manage time and work independently
• Ability to train and mentor junior scientists
• Broad understanding of Toxicology, electrophysiology, and cell biology

Benefits & Compensation

The base pay range for this position at commencement of employment is expected to be $93,500 to $126,500. 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.

EEO Statement

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.