Assistant Manager, Regulatory Affairs

Preferred Qualification: M. Pharm. Preferred Experience: 8-12 yrs (for AM/DM level) Job Description: Preparation, scientific review, coordination & finalization of ANDA/NDA CMC modules for oral solid, oral liquid, injectable & other dosage form as per the business goals. Working on due diligence projects for US, EU & Canada markets as per the business agreement. Managing pre-approval portfolio including original submission, deficiency response, final approval request & any other submissions.

Preparation of project status, discussion slides & white papers as required for escalation & decision at different stages of the projects. Assessment of change controls & providing necessary regulatory comments/approval. Provide support in developing/updating regulatory tools, checklists, databases as per dept. needs. Participate in project meetings, communication & coordination with CFTs.

Knowledge of relevant regulatory guidelines & updates is must. Ability to perform under changing priorities, deadlines & regulatory expectations.  Skills like, technical writing, presentation, training, effective communication/coordination is preferred. Experience of Nitrosamine risk assessment report review will add value. A positive learning orientation to quickly adapt Amneal systems, RA tools & processes will add value.

Knowledge of using AI tools in routine work will add value.