Regulatory Affairs Manager

The Ritedose Corporation; Columbia (SC); On-site; USD 96,000 - 125,000; Full time

Job summary

The Ritedose Corporation in Columbia, SC is seeking a Regulatory Affairs Manager to lead regulatory strategies for ANDA submissions and provide CDMO support for customer-led submissions (FDA and global). This role ensures compliance and lifecycle management in line with the Director of Regulatory Affairs.

Responsibilities include authoring and editing technical documents, serving as RA lead on teams, and publishing to FDA for lifecycle submissions while guiding junior staff and monitoring

Qualifications

• Bachelor of Science in Biology, Chemistry, Engineering, Pharmaceutical Sciences, or related field.
• 5+ years regulatory affairs experience; FDA submission experience required, device/drug-device combo experience preferred.
• Highly detail-oriented with problem-solving and organizational skills.
• Ability to work on complex projects with initiative and minimal guidance.
• Experience with eCTD publishing software and MS Office.

Responsibilities

• Support writing/editing technical documents for internal ANDA and customer-led submissions.
• Act as primary RA contact on project teams to support product development.
• Format, publish, and submit documentation to FDA for initial and lifecycle submissions.
• Respond to FDA queries and deficiencies.
• Develop regulatory strategies for product development, registration, and maintenance across markets.
• Monitor evolving regulations and assess impact on products.
• Oversee adverse event reporting process and ensure compliance with requirements.
• Support due diligence, licensing, and partnerships.

Skills

Detail-oriented

Problem solving

Organization

Communication

Education

Bachelor of Science in Biology, Chemistry, Engineering, Pharmaceutical Sciences, or related field

Tools

eCTD publishing software

Electronic document control system

Microsoft Word

Microsoft Excel

PowerPoint

Adobe Acrobat

Job description

Job DetailsJob Location: The Ritedose Corporation - Columbia, SC 29203Education Level: 4 Year DegreeSalary Range: $96,000.00 - $125,000.00 Salary/yearJob Shift: Day

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.

Qualifications

• 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