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Senior Regulatory Operations Specialist I

Fortrea
4-8 years
Not Disclosed
Pune, India
1 June 4, 2026
Job Description
Job Type: Hybrid Education: M.Pharm/B.Pharm or M.Sc. Skills: MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology

Senior Regulatory Operations Specialist I

Location: Pune (Hybrid)
Experience: 4–8+ Years
Department: Regulatory Affairs / Regulatory Operations
Industry: Pharmaceuticals


Job Summary

We are seeking a highly motivated Senior Regulatory Operations Specialist I to support global regulatory submissions, product lifecycle management, labeling activities, CMC documentation, and regulatory compliance initiatives. The role involves close collaboration with cross-functional teams, regulatory agencies, suppliers, and global stakeholders to ensure timely and compliant product registrations and post-approval maintenance activities.


Key Responsibilities

Regulatory Documentation & Submissions

  • Prepare, compile, review, and maintain CMC (Chemistry, Manufacturing & Controls) and regulatory documentation for global product registrations and lifecycle management activities.

  • Support regulatory submissions, variations, renewals, and post-approval changes across international markets.

  • Conduct literature searches and prepare supporting regulatory documents for APIs, excipients, and finished drug products.

Product Lifecycle Management

  • Coordinate change control assessments and evaluate regulatory impacts of manufacturing, supplier, formulation, packaging, and process changes.

  • Manage documentation related to OOS (Out of Specification), OOT (Out of Trend), deviations, and product-related investigations.

  • Support implementation strategies for approved changes and ensure regulatory compliance.

Labeling & Compliance Support

  • Assist in creation, review, quality control, and maintenance of global labeling documents.

  • Ensure labeling content complies with regional and international regulatory requirements.

  • Support regulatory correspondence and documentation management activities.

Quality & Technical Support

  • Create and revise raw material, packaging material, and product specifications.

  • Support stability data evaluation, dissolution profile assessment, and preparation of technical reports.

  • Participate in Computerized System Validation (CSV) activities and support system upgrades.

Stakeholder & Supplier Coordination

  • Collaborate with Regulatory Affairs, Quality Assurance, Manufacturing, R&D, Supply Chain, and external partners.

  • Coordinate import license requirements, documentation requests, and investigation reports.

  • Support supplier data management, business plan maintenance, PO creation, and financial data management activities.

Japanese Language & Communication Support

  • Provide Japanese ↔ English translation support for regulatory and supplier-related documentation.

  • Draft and manage Japanese business communications and regulatory correspondence.

  • Coordinate with Japanese regulatory authorities, suppliers, and business stakeholders.


Required Qualifications

  • Bachelor’s or Master’s degree in:

    • Pharmacy (B.Pharm / M.Pharm)

    • Life Sciences

    • Chemistry

    • Biotechnology

    • Related Scientific Discipline