Regulatory Affairs Manager
The Ritedose Corporation
Columbia, SC
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JOB DETAILS
JOB TYPE
Full-time
SKILLS
Abbreviated New Drug Application, Adobe Acrobat, Adverse Events, Biology, Biotech and Pharmaceutical, Chemistry, Control Systems, Customer Support/Service, Detail Oriented, Document Control, Documentation, Due Diligence, FDA (Food and Drug Administration), Licensing, Maintain Compliance, Microsoft Excel, Microsoft PowerPoint, Microsoft Word, Organizational Skills, People Management, Policy Implementation, Presentation/Verbal Skills, Problem Solving Skills, Product Development, Product Lifecycle, Product Reviews, Product Support, Regulations, Regulatory Compliance, Regulatory Requirements, Team Building, Team Player, Technical Editing, Technical Support, Technical Writing, Writing Skills
LOCATION
Columbia, SC
POSTED
30+ days ago
The Regulatory Affairs Manager is responsible for supporting development and execution of regulatory strategies for ANDA submissions as well as CDMO support for customer-led submissions (FDA and global). The Regulatory Affairs Manager will ensure compliance with regulatory requirements and manage lifecycle activities in alignment with the Director of Regulatory Affairs.
Responsibilities:
- Provide critical support in writing and editing technical documents to support submissions for internal ANDA projects as well as customer-led global submissions.
- Serve as primary RA contact on project teams to support product development.
- Format, publish, and submit documentation to the FDA for initial and lifecycle submissions.
- Respond to FDA queries and deficiencies.
- Provide guidance to RA Associates and aid in development of team.
- Develop and implement regulatory strategies for product development, registration, and maintenance across assigned markets.
- Monitor and interpret new and evolving regulations and assess impact on company products.
- Draft, review, and finalize product labeling for ANDA submissions, including structured product labeling.
- Oversee adverse event reporting process and ensure compliance with reporting requirements.
- Support due diligence activities, licensing, and partnerships.
- Bachelor of Science in Biology, Chemistry, Engineering, Pharmaceutical Sciences, or related field
- 5+ years regulatory affairs experience; FDA submission experience required, experience with device and/or drug/device combination products preferred
- Highly detail-oriented and possess considerable problem-solving and organization skills
- Ability to work on complex projects and take initiative with general direction and minimal guidance
- Ability to be flexible with a change in priorities
- Excellent written, verbal, and listening skills, must work well with others
- Experience using an electronic document control system
- Experience with eCTD publishing software preferred
- Proficient with Microsoft Word, Excel, PowerPoint, and Adobe Acrobat
About the Company
T
The Ritedose Corporation
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