Find & Apply For Regulatory Affairs Specialist Jobs In Richland, South Carolina
Regulatory Affairs Specialist jobs in Richland, South Carolina involve ensuring compliance with regulations, preparing submissions, and communicating with regulatory agencies. Responsibilities include tracking and reviewing regulations, conducting research, and collaborating with cross-functional teams. Experience in regulatory affairs and knowledge of FDA regulations are required. Below you can find different Regulatory Affairs Specialist positions in Richland, South Carolina.
Jobs in Richland
Browse jobs from a variety of sources below, sorted with the most recently published, nearest to the top. Click the title to view more information and apply online.
Product Stewardship & Regulatory Expert Medical Applications
Chemours
Richland, SC
Principal Regulatory Affairs Specialist
Cardinal Health
Richland, SC
Associate Director, Global Labeling
Otsuka America
Richland, SC
Associate Director, Global Labeling
Otsuka America
Richland, SC
Latest Jobs in Richland
Salary Information & Job Trends In this Region
Regulatory Affairs Specialists in Richland, South Carolina play a crucial role in ensuring compliance with regulations and guidelines in the pharmaceutical and medical device industries. - Entry-level Regulatory Affairs Specialist salaries range from $50,000 to $60,000 per year - Mid-career Regulatory Affairs Manager salaries range from $70,000 to $90,000 per year - Senior Regulatory Affairs Director salaries range from $100,000 to $120,000 per year The history of Regulatory Affairs Specialists in Richland, South Carolina dates back to the establishment of regulatory bodies such as the FDA, which set standards for safety and efficacy in healthcare products. Over time, the role of Regulatory Affairs Specialists has evolved to encompass global regulatory requirements, risk management strategies, and quality assurance processes to ensure product compliance. Current trends in Regulatory Affairs in Richland, South Carolina include the adoption of electronic submission systems, increased collaboration with international regulatory agencies, and a focus on expedited approval processes for innovative medical products.
