
Regulatory Affairs Associate - FDA Submissions
Makro Scientific, Piscataway, New Jersey, United States
A leading staffing solutions provider in New Jersey is seeking a Regulatory Affairs Associate to prepare and submit annual reports to the FDA. The ideal candidate will have a Master’s degree in Science and at least 3 years of experience in the pharmaceutical industry. Key responsibilities include coordinating submissions and maintaining regulatory databases. Strong communication and computer skills are essential for success in this fast-paced environment. Join a dedicated team and contribute to the success of life sciences companies.
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