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Regulatory Affairs Manager

THE RITEDOSE CORPORATION
Posted 6 months ago, valid for 10 days
Location

Arcadia Lakes, SC, US

Salary

$96,000 - $125,000 per year

Contract type

Full Time

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Sonic Summary

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  • The Ritedose Corporation in Columbia, SC is seeking a Regulatory Affairs Manager with a salary range of $96,000.00 to $125,000.00 per year.
  • Candidates must possess a Bachelor of Science degree in a relevant field and have at least 5 years of regulatory affairs experience, particularly with FDA submissions.
  • The role involves supporting regulatory strategies for ANDA submissions, managing lifecycle activities, and ensuring compliance with regulations.
  • Key responsibilities include writing technical documents, serving as the primary regulatory contact, and overseeing product labeling and adverse event reporting.
  • Strong problem-solving skills, attention to detail, and proficiency in Microsoft Office and electronic document control systems are essential for success in this position.

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




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