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Regulatory Affairs Specialist Jobs in Princeton, New Jersey

8 jobs

Overview: We currently have an excellent opportunity for a Sr. Regulatory Affairs Specialist located at our Princeton, NJ location. The Sr. Regulatory Affiars Specialist will provide U.S. Regulatory direction and support to brands from concept to launch. Develop practical approaches for regulatory requirements, including complex technical projects. Liaising between company and domestic regulator...
We currently have an excellent opportunity for a Sr. Regulatory Affairs Specialist located at our Princeton, NJ location. The Sr. Regulatory Affiars Specialist will provide U.S. Regulatory direction and support to brands from concept to launch. Develop practical approaches for regulatory requirements, including complex technical projects. Liaising between company and domestic regulatory authoriti...
Job Description: Azzur Group is seeking a talented Regulatory Affairs Specialist for a Life Sciences client in Bridgewater, NJ. The Specialist will be responsible to author Module 3 submission documentations according to eCTD requirements for New Drug Application (NDA), Prior Approval Supplements (PAS), Changes Being Effected (CBE-0 and CBE-30), and annual reports. Other responsibilities include ...
BioPoint is seeking to hire a regulatory affairs specialist with pharmaceutical or biotech experience for a position in Bridgewater, NJ. Successful candidates need to be strong technical writers. Responsibilities: Author Module 3 submission documentation according to eCTD requirements for New Drug Application (NDA) Prior Approval Supplements (PAS), Changes Being Effected (CBE-0 and CBE-30), and ...
Job Description POSITION SUMMARY: Under the direction of Director, Regulatory Affairs, the International Regulatory Affairs Specialist supports worldwide product registrations and regulatory activities including the following duties: Provide a wide variety of documentation related to a broad product line for submission to various worldwide health agencies; Prepare, submit and maintain specific ...
Overview: The Regulatory Affairs Submissions Specialist is responsible for the electronic/paper compilation and submittal of Regulatory submissions and maintaining submission information in the proper RA systems. Responsibilities: Ensure readiness of submission documents in accordance with agency guidance Perform QA/QC for submission documents and deliverables Promote document authoring stand...
The Regulatory Affairs Submissions Specialist is responsible for the electronic/paper compilation and submittal of Regulatory submissions and maintaining submission information in the proper RA systems. Ensure readiness of submission documents in accordance with agency guidance Perform QA/QC for submission documents and deliverables Promote document authoring standards Promote and support RA s...
Integra LifeSciences, a world leader in medical technology, is dedicated to limiting uncertainty for surgeons, so they can concentrate on providing the best patient care. Integra offers innovative solutions in orthopedic extremity surgery, neurosurgery, spine surgery, and reconstructive and general surgery. Integra's orthopedic products include devices and implants for spine, foot and ankle, hand...