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Senior General Manager

Job in 400601, Thane, Maharashtra, India
Listing for: rubicon research limited
Full Time position
Listed on 2026-06-08
Job specializations:
  • Management
    Healthcare Management
Job Description & How to Apply Below
Purpose

This position will lead and be accountable for the pre-approval regulatory efforts in the US

market.

Position / Job Title Senior General Manager/General Manager Department Regulatory Affairs Reporting To

Director – Regulatory Affairs & IP

Location Thane Years of Exp

20+ years

Dosage Form

Know-how of all dosageforms

Job Responsibilities / Deliverables

Prepare Regulatory Strategies for US market.
Review and submit quality dossiers in the US market in line with regulatory strategy and expectations including Abbreviated New Drug Applications (ANDAs), New Drug Applications (NDAs) or 505(b)(2) applications.
Plan and manage all pre-approval submissions including pre-IND, IND, pre-NDA, pre-ANDA, CGT requests and query responses.
Manage various filings including submission of meeting requests, teleconference requests or controlled correspondence.
Plan all the regulatory workto meet the filing schedule.
Interact with the regulatory agencies and manage meetings with them as necessary.
Coordinate with various stakeholders including Development Centers, Manufacturing Units, Quality Units, Supply Chain for needful documentation for timely and quality filings.
Provide necessary regulatory clearances and assessments during the product development process including inactive ingredient clearances, biowaiver and size and shape clearances.
Address any queries from the stakeholders regarding regulatory filings.
Advise and guidethe team on regulatory matters.
Support organizational initiatives and manage the team to meet thedeliverables.
Ensure business growthand operational excellence within Regulatory Set up.

Qualifications & Pre-Requisites

Proficiency in Regulatory Affairs.
Knowledge of Pharmaceutical Development and Manufacturing.
Excellent leadership, analytical, communication, planning, interpersonal skills and act as a solution provider.
Experience working with USFDA
Manage 100+ submissions annually including original filings and queryresponses.

Additional notes
-Willneed to work in different shifts
Position Requirements
10+ Years work experience
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