Amneal Pharmaceuticals, Inc. (NYSE: AMRX) is a global pharmaceutical company dedicated to making healthy possible through the development, manufacturing, and distribution of a diverse portfolio of over 270 high-quality medicines. With a team of 7,500+ colleagues, we are committed to innovation and excellence in the pharmaceutical industry.
Position Available
Role: Regulatory Affairs – Post Approval
Job Location: Ahmedabad
We are looking for candidates with the following qualifications and experience:
- Department: Regulatory Affairs
- Designation: Executive/Senior Executive
- Location: Ahmedabad
- Qualification: B. Pharm/M. Sc./M. Pharm
- Experience: 2-7 Years
Required Skills:
- Good knowledge of ANDA submission activities and post-approval procedures, including related ICH and USFDA guidelines.
- Experience with API DMF review concerning USFDA regulatory requirements.
- Exposure to Solid oral dosage forms, Sterile dosage forms, complex dosage forms, and topical/Inhalation dosage forms, including a basic understanding of the manufacturing process and key regulatory aspects.
- Ability to review change cases concerning ICH quality/post-approval USFDA guidance, with an understanding of post-approval submission guidelines and procedures for Annual Reports, CBE 0, CBE 30, and PAS filing.
- Proficient in drafting Annual Reports with required submission data as per USFDA guidance.
- Experience in drafting controlled correspondence and Briefing Packages to FDA on specific cases as needed for assigned projects.
- Awareness of FDA recommendations regarding commercial marketing status notifications, including content and time frames.
How to Apply:
Interested candidates can share their CV with the following email addresses:
- kavitriy@amneal.com
- yash.ojha@amneal.com

Disclaimer
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