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Our employees are our most valuable asset. Our ability to bring new medicines to the market depends on the knowledge, skills, and experience of Navinta employees. We are committed to engaging a diverse workforce of exceptionally talented people and developing them professionally. Navinta provides a challenging environment that offers employees opportunities to enhance their technical and managerial skills through continued exposure to new technologies, products, and business practices. As part of our team, you will have the opportunity to collaborate with talented business leaders and world-class scientists while continuously developing your career in an exciting work environment.



Co. seeks Quality Assurance Chemist responsible for marketed products. Review & establish the acceptance criteria & quality defects (AQL) for Injectables, tablets, capsule products. Review & approve batch records & other product related documents for batch release, bioequivalence & clinical study reports for regulatory submissions. Participate in approval & site audits of raw & packaging material vendors, contract manufacturing, packaging & clinical research organizations. Review & approve Quality system related protocols & reports. Review & finalize process-related change controls, deviations, out-of-specification by following cGMP & SOPs & in-process quality assurance standards. Provide cGMP training to QA personnel & supervise overall activities. Send resume to:, or to HR Dept., Navinta LLC, 1499 Lower Ferry Rd., Ewing, NJ 08618.

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