Regulatory Affairs Specialist jobs in Murfreesboro, TN

Regulatory Affairs Specialist is responsible for filing necessary applications and handling all government interactions pertaining to the regulation process for products requiring governmental approval. Assists in developing procedures to ensure regulatory compliance. Being a Regulatory Affairs Specialist typically requires a bachelor's degree. Typically reports to a supervisor or manager. To be a Regulatory Affairs Specialist typically requires 2 to 4 years of related experience. Gains exposure to some of the complex tasks within the job function. Occasionally directed in several aspects of the work. (Copyright 2020 Salary.com)

112 Regulatory Affairs Specialist jobs found in Murfreesboro, TN area

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Business Affairs Coordinator
  • Minno
  • Nashville, TN Full-Time
  • We are currently seeking a Business Affairs Coordinator to assist with drafting agreements for Minno’s licensing of vide...
  • 2 Months Ago
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Regulatory Site Coordinator
  • HCA Healthcare
  • Nashville, TN Full-Time
  • Description SHIFT: No Weekends SCHEDULE: Full-time Sarah Cannon is the research arm of HCA’s global cancer enterprise. F...
  • 21 Days Ago
Murfreesboro is a city in, and the county seat of, Rutherford County, Tennessee, United States. The population was 108,755 according to the 2010 census, up from 68,816 residents certified in 2000. In 2017, census estimates showed a population of 136,372. The city is the center of population of Tennessee, located 34 miles (55 km) southeast of downtown Nashville in the Nashville metropolitan area of Middle Tennessee. It is Tennessee's fastest growing major city and one of the fastest growing cities in the country. Murfreesboro is also home to Middle Tennessee State University, the second largest...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Regulatory Affairs Specialist jobs
$64,318 to $90,741
Murfreesboro, Tennessee area prices
were up 1.3% from a year ago

Regulatory Affairs Specialist in Abbott Park, IIL
Participate in risk-benefit analysis for regulatory compliance.
October 10, 2019
Monitor and submit applicable reports to regulatory authorities.
December 21, 2019
Assist with label development and review for compliance before release.
December 22, 2019