Regulatory Affairs Consultant
A company is looking for a Regulatory Affairs Specialist - Consultant.
Key Responsibilities
• Review new certificate requests and manage submissions to FDA
• Project manage multiple requests to ensure deadlines are met and maintain communication with stakeholders
• Support reputed company improvement of regulatory processes and deliver product license maintenance portfolio
Required Qualifications
• 3+ years of regulatory experience
• Experience with US Annual Report submissions
• Demonstrated ability to support international product approval
• Bachelor's degree or equivalent work experience
• Familiarity with pharmaceutical organizational structures
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