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Regulatory Submissions & QA Specialist

GForce Life Sciences, San Francisco, California, United States, 94199

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A leading life sciences company is looking for a Regulatory Affairs & Quality Assurance Analyst. The role involves supporting regulatory compliance activities through submissions to regulatory agencies such as the FDA. Responsibilities include managing regulatory documentation, collaborating with cross-functional teams, and providing regulatory guidance. Ideal candidates should have a Bachelor's degree in a relevant field and 2-3 years of experience in an FDA-regulated industry, along with strong organizational and problem-solving skills. #J-18808-Ljbffr