Nevakar Careers

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.

Job Openings

Technical Operation Manager/Sr. Manager

The candidate must be solution-oriented, operationally savvy, creative, highly organized, flexible, and adept at handling multiple projects with tight deadlines via multiple stakeholders.

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Principal Scientist

The Group Leader will lead a group of analytical scientists that is responsible for design and development of analytical test methods for raw materials and drug products.

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Clinical Portfolio Strategy

Identify potential product concepts for pipeline in the clinical unmet space that aligns with Nevakar's strategy.

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Research Scientist LC/MS

The Research Scientist will support Nevakar R&D by developing liquid chromatography- mass spectrometry (LC/MS) test methods, generating impurity profiles for raw materials and developmental products, elucidating degradant structures and degradation mechanisms.

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Associate Program Management

Incumbent will independently manage and coordinate complex drug development activities for cross functional development projects, including the project management of clinical and regulatory activities. Manages strategy development, project planning, execution and delivery oversight.

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Senior Associate CMC QA - (Microbiologist)

Incumbent will work with a cross functional team to provide Chemistry and Manufacturing Controls (CMC) Quality Assurance (QA), coordination and support during development, technical transfer, clinical materials production, regulatory filing, and commercial manufacturing activities.

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Senior Director Marketing

Responsible for leading and developing strategic and tactical marketing plans to launch new products in the hospital marketplace and ensures appropriate processes are in place for successful launch execution.

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Regulatory CMC Strategist - Labeling Lead

This position will support and manage the regulatory activities associated with the Chemistry, Manufacturing and Controls for licensed and development products.

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