Work with Us
Nevakar is a great place to begin and advance your career. We are passionate about what we do and recognize that success will depend on entrepreneurship, innovation and integrity of the team. We are a group of individuals that represent diversity in thought, approach, and innovation in our work.
We are located in Bridgewater, NJ and are creating a diverse and inclusive environment which reflects our culture and values. If you are interested in joining our dynamic team, we have opportunities for careers in pharmaceutical research and development, health care, medicine, manufacturing, commercial and more.
Equal Opportunity Employer Minorities/Women/Veterans/Disabled
Social Responsibility at Nevakar
Not only are we dedicated to bringing better healthcare to patients who need it, we also believe that we have a social responsibility to our employees. We believe that employees who look forward to their work every day, who feel like they are a member of a team of collaborators, and who know they will also receive support in a variety of ways, will make Nevakar a better company. We help ensure the future of Nevakar by investing in those who help build it – and that could be you.
Clinical Study Manager (Operations)
Lead execution of clinical studies in various therapeutics areas, in adherence to Good Clinical Practices (GCPs), Standard Operating Procedures (SOPs), Food and Drug Administration (FDA) regulations, and International Conference on Harmonization (ICH) guidelines.Apply Now
Quality Systems Associate
Ideal candidate would possess a background in electronic and or paper based Quality Systems. Minimum 3 years of experience in pharmaceutical industry or at least 2 years in QA or regulatory affairs role. BS degree Life Sciences is preferred; however, equivalent experience will be considered.Apply Now
Principal Scientist – Analytical (Chromatography)
Principal Scientist will support Nevakar R&D by designing, developing, and optimizing analytical test methods for drug products. The primary focus of this position will be on chromatographic methods utilizing different types of separation and detection techniques.Apply Now
Preclinical Development – R&D
Preclinical Development is responsible for conducting toxicology, pharmacokinetic, ADME, safety pharmacology and pharmacology studies in support of repurposing and repositioning drugs. This group represents the company in all nonclinical activities, and assists clinical and regulatory in support of 505(b)(2) submissions.Apply Now
Sr. Associate CMC QA
The focus of the position is to ensure CMC QA document review and approvals are performed in a detailed and timely fashion to ultimately support clinical release, regulatory approval, and commercialization of sterile drug product programs.Apply Now