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Executive/Senior Executive- Global Ra

Enzene Biosciences Ltd.
Enzene Biosciences Ltd.
4-7 years
Not Disclosed
10 Jan. 14, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Executive / Senior Executive – Global CMC Regulatory Affairs

Location: Pune, Maharashtra, India
Employment Type: Permanent
Department: Global CMC – Regulatory Affairs
Industry: Biopharmaceutical / Pharmaceutical

Job Overview

We are looking for a skilled Executive / Senior Executive – Global CMC Regulatory Affairs to support global regulatory submissions across the US and European regions. This role focuses on the preparation, review, and lifecycle management of CMC documentation, ensuring compliance with FDA, EMA, and ICH requirements for pharmaceutical and biosimilar products.

The position requires strong collaboration with cross-functional teams and a solid understanding of global regulatory frameworks, eCTD publishing standards, and submission strategy.


Key Responsibilities

CMC Documentation & Global Submissions

  • Review, finalize, and maintain CMC (Chemistry, Manufacturing, and Controls) documents for US FDA and EMA regulatory submissions.

  • Draft, compile, and review eCTD modules, ensuring compliance with current regulatory, technical, and formatting standards.

  • Author and review key regulatory documents including INDs, IMPDs, Briefing Books (BBs), and supporting CMC sections.

Cross-Functional Collaboration

  • Work closely with cross-functional teams (Quality, Manufacturing, Analytical, Clinical, and Supply Chain) to collect technical data and align submission content with regulatory strategy.

  • Ensure consistency, accuracy, and appropriate regulatory language across all submission documents.

Regulatory Compliance & Intelligence

  • Ensure all documents meet PDF publishing standards and technical specifications required for eCTD submissions.

  • Maintain up-to-date knowledge of ICH guidelines, regional regulatory requirements (US/EU), and biosimilar-specific regulations.

  • Support regulatory strategy development, health authority interactions, and preparation of responses to agency queries.


Education & Experience Requirements

  • Educational Qualification: M.Pharm, M.Sc, M.Tech, or equivalent degree in Pharmacy, Biotechnology, Life Sciences, or related discipline.

  • Experience Required: 4–7 years of hands-on experience in Global CMC Regulatory Affairs, with direct exposure to US FDA and EMA submissions.


Key Skills & Competencies

  • Strong expertise in CMC documentation and global regulatory submissions.

  • Working knowledge of eCTD structure, publishing requirements, and lifecycle management.

  • Sound understanding of ICH guidelines and global regulatory frameworks.

  • Experience supporting biosimilar or complex biologics submissions is highly desirable.

  • Excellent technical writing, communication, and stakeholder coordination skills.


Why Join This Role

This role offers an opportunity to work on global regulatory submissions, collaborate with diverse technical teams, and contribute to the successful approval and lifecycle management of innovative pharmaceutical and biopharmaceutical products.