Executive, Regulatory Affairs
Amneal Pharmaceuticals
- Location
- Ahmedabad, Gujarat, India
- Job type
- Full-time
About the role
Amneal Pharmaceuticals
Website:
amneal.com
Job details:
Job Description
- Good knowledge of ANDA submission activities and post-approval procedures and related ICH and USFDA guidelines.
- Exposure of the Solid oral dosage form / Sterile dosage form / complex dosage form / topical-Inhalation dosage form and brief manufacturing process and key regulatory aspects.
- Ability to preliminary review the change cases with respect to ICH quality / post approval USFDA guidance and aware for Post approval submission guideline and procedure for Annual report/CBE 0/CBE 30 and PAS filling
- Drafting of the Annual Report with required submission data as per USFDA guidance.
- Preliminary review of entire submission package.
- Awareness about the FDA recommendation on the commercial marketing status notification submission in terms of content and time frames and submissions.
- Coordination with Cross Functional teams for the documents availability as per regulatory submission plan.
- Ensure the no delay in drafting and compiling the regulatory submission.
- Maintain regulatory information as per allocated task.
- Having good Regulatory CTD modules drafting & preliminary review skills.
Education
QUALIFICATIONS
- B. Pharm B. Pharm - Required
- M. Pharm M. Pharm - Preferred
Experience:
- 5 years or more in 5 - 8 Years
Specialized Knowledge: Licenses:
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