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Regulatory Affairs is responsible for reviewing and providing guidance regarding advertisement and promotion. Demonstrates working knowledge of healthcare-related regulations at a high-level. Detail oriented reviewer of documentation. Organized in documentation practices and record keeping. Review statements and associate with appropriate substantiation. Communicates effectively cross-functionally. Collaborates cross-functionally. Annotate files. Manages multiple tasks. Programs: Proficient in: Microsoft word, excel, adobe acrobat editor, and veeva vault Education: BS.B.Sc., BA university degree in a technical or scientific discipline or cumulative related work experience.
Spec 3, Regulatory Affairs • Franklin Lakes, NJ, United States
Regulatory Affairs Project Manager.Established in 1806 as a small soap and candle business in New York City, Colgate-Palmolive is now a truly global company with products sold in over 200 countries... Show more
With a passion for lifeJoin our diverse teams of passionate people and a career that allows you to develop both personally and professionally.At Getinge we exist to make life-saving technology acce... Show more
Regulatory Affairs Clinical-Nonclinical Strategy.At Pacira, innovation meets purpose.Today, we're building on that legacy with next-generation innovations for chronic, postsurgical, and musculoskel... Show more
Bank, we're on a journey to do our best.Helping the customers and businesses we serve to make better and smarter financial decisions and enabling the communities we support to grow and succeed.We b... Show more
Location: Fairfield, NJ (Seppic) - Sales - North America zone.An Air Liquide Healthcare company, subsidiary of the Air Liquide group, Seppic has been designing, manufacturing, and marketing unique ... Show more
QPharma is currently looking for a Regulatory and Compliance Specialist for our Cedar Knolls, NJ location.Responsibilities include but are not limited to:Quality Management Systems:Manages the proc... Show more
Nasdaq: CELU) is a longevity-focused regenerative and cellular medicine company developing and manufacturing allogeneic and autologous cell therapies derived from the postpartum placenta.Celularity... Show more
PREREQUISITES BS/BA degree in Scientific Discipline (Masters or higher preferred) with 5-7 years in the pharmaceutical industry, preferably with 1-3 years CMC regulatory experience.Experience with ... Show more
Program Director of Regulatory Reporting.The Program Director will be leading large regulatory reporting projects for banking organizations in the USA and has preferably led projects related to Cli... Show more
Respected provider of top-quality services.The Company is seeking a Head of Regulatory Affairs to take on a pivotal leadership role in driving U.OTC drugs, cosmetics, and medical devices.The succes... Show more
Senior Specialist, Regulatory Affairs CMC.Education: Bachelor of Science degree (minimum) in science, engineering, or other relevant field (advanced degree preferred).Experience: At least 4 years o... Show more
It is expected that the development of these protocols will involve both the application of scientific principles and rationales and adherence to regulatory requirements.Write clear Standard Operat... Show more
Scientist II, Specialty Formulations R&D, Denville, NJ: Support in the dev.Full understanding of FDA regs.ANDA, IND/NDA processes, & Good Mfg.Ability to prform phrmceutical calculations.CPP & CQAs ... Show more
IRI believes in commitment, integrity and strategic workforce solutions.We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively.Since... Show more
Regulatory Submission Management.At Gilead, we're creating a healthier world for all people.For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer working... Show more
Principal, Regulatory Compliance.Blue Owl (NYSE: OWL) is a leading asset manager that is redefining alternatives.With over $315 billion in assets under management as of March 31, 2026, we invest ac... Show more
Eligibilities and qualifications. Show more
A Partner to Actalent is seeking an experienced Manager of CMC Regulatory Affairs to lead regulatory strategy and execution across both development and commercial programs.This role is responsible ... Show more
Director of Regulatory Affairs - North America.Location: Morristown, NJ, US, 07960.Overview: As Director of Regulatory Affairs - Cluster (North America), you are accountable for in-market regulator... Show more
Director, Regulatory Relations.Iselin, New Jersey, United States.CLS is the trusted party at the centre of the global FX ecosystem.Utilized by thousands of counterparties, CLS makes FX safer, smoot... Show more
