Job Title: Senior Executive – India Regulatory Affairs (Manager II – India Regulatory & Business Continuity)
Location: Baroda (Tandalja – R&D), India
Business Unit: R&D1 – Regulatory Affairs
Company: Sun Pharmaceutical Industries Ltd
Employment Type: Full-Time
Experience Required: 8–10 Years
Education Required: M.Pharm (Master of Pharmacy)
Senior Executive – India Regulatory Affairs | ND, SND & FDC Submissions
Sun Pharmaceutical Industries Ltd is seeking an experienced Regulatory Affairs professional to support India regulatory strategy and lifecycle management activities for new drugs, subsequent new drugs (SND), and fixed-dose combinations (FDCs). This role is responsible for dossier compilation, regulatory evaluation, SUGAM portal submissions, and cross-functional coordination to ensure successful approvals within India.
This opportunity is ideal for regulatory professionals with strong experience in CDSCO submissions, CMC document review, clinical trial documentation, and Indian regulatory pathways.
Role Overview
The Senior Executive – India Regulatory Affairs will evaluate regulatory strategies, review technical documentation, and coordinate cross-functional inputs to prepare and submit high-quality regulatory dossiers for Indian market approvals. The role requires strong expertise in CMC documentation, clinical trial and bioequivalence (BE) data review, safety and efficacy justification, and regulatory submission processes through the SUGAM portal.
The candidate must demonstrate a thorough understanding of Indian regulatory guidelines and ensure compliance throughout the submission lifecycle.
Key Responsibilities
India Regulatory Strategy & Submission Planning
Evaluate regulatory strategies for products to be registered in India.
Develop submission roadmaps for ND, SND, and FDC applications.
Prepare executive summaries for Subject Expert Committee (SEC) referrals for products not approved in India.
Dossier Compilation & Regulatory Documentation
Compile and review complete regulatory dossiers in line with Indian regulatory guidelines.
Coordinate with cross-functional teams to obtain finalized CMC, Clinical Trial (CT), and Bioequivalence (BE) documents.
Review and validate CMC documents prior to submission.
Review specifications for bulk drugs and finished formulations as per regulatory expectations.
Clinical & Safety Documentation
Review clinical trial and bioequivalence study reports for regulatory submissions.
Conduct literature searches to support regulatory application strategies.
Prepare scientific rationale for safety and efficacy of new drugs and FDCs using published data.
Regulatory Filing & Portal Management
File ND, SND, and FDC applications through the SUGAM portal.
Submit applications for domestic manufacturing permission, marketing authorization, and clinical trial approval.
Ensure regulatory timelines are met and track application progress.
Labeling & Prescribing Information
Review draft specimen labels, cartons, and packaging materials.
Prepare prescribing information aligned with international reference labeling.
Ensure labeling compliance with Indian regulatory requirements.
Business Continuity & Compliance
Support regulatory business continuity planning.
Maintain documentation accuracy and audit readiness.
Ensure compliance with internal SOPs and CDSCO regulatory standards.
Required Qualifications
M.Pharm (Master of Pharmacy).
8–10 years of hands-on experience in India Regulatory Affairs.
Proven experience in ND, SND, and FDC regulatory submissions.
Strong knowledge of CDSCO guidelines and SUGAM portal filing processes.
Experience reviewing CMC, CT, and BE documentation.
Strong understanding of Indian regulatory approval pathways.
Excellent scientific writing and documentation skills.
Effective cross-functional coordination and communication skills.
Technical Competencies
Expertise in India regulatory dossier preparation and compilation.
Knowledge of Indian Drugs and Cosmetics Act and CDSCO regulatory requirements.
Experience preparing SEC referral documents.
Proficiency in literature search and safety-efficacy justification writing.
Ability to critically review pharmaceutical specifications and regulatory documentation.
Travel Requirement
Not Applicable.
Why Join Sun Pharmaceutical Industries Ltd
Sun Pharma is one of the world’s leading specialty generic pharmaceutical companies with a strong domestic and global footprint. This role offers the opportunity to contribute to high-impact regulatory submissions within India, collaborate with cross-functional R&D teams, and support business continuity initiatives in a dynamic regulatory environment.
Disclaimer
This job description outlines the general nature and scope of responsibilities associated with this role. It is not intended to be a comprehensive list of all duties and may evolve in accordance with business needs.
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