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Reg Affairs Senior Specialist; Documentation

Sandoz
Sandoz
3-6 years
Not Disclosed
10 Dec. 29, 2025
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

Regulatory Affairs Senior Specialist – Documentation

Company: Sandoz
Location: Telangana, India
Job Type: Full-Time, Regular
Experience Required: 3–6 Years
Job ID: REQ-10024332
Date Posted: 26th December 2025


Job Overview

Sandoz is seeking a Regulatory Affairs Senior Specialist – Documentation to join our Development team in Telangana, India. This role plays a critical part in supporting the preparation, review, and submission of CMC (Chemistry, Manufacturing, and Controls) documentation throughout the drug lifecycle. The ideal candidate will combine technical expertise in Module 3, regulatory knowledge, and strong documentation skills to ensure high-quality submissions aligned with global regulatory standards.

The position reports to the Regulatory Affairs Lead and requires close collaboration with cross-functional teams, including development, quality, and global regulatory counterparts.


Key Responsibilities

Regulatory Document Preparation & Submission

  • Plan, author, and submit regulatory CMC documents in compliance with relevant Health Authority guidelines and corporate timelines.

  • Compile drug master files, dossier parts, and submission packages, applying current regulatory strategies and trends.

  • Ensure technical congruency and compliance in all submissions, maintaining accuracy and consistency across documents.

  • Prepare responses to regulatory questions during development, registration, and post-approval lifecycle stages.

Regulatory Review & Assessment

  • Review CMC documentation to ensure adequate information for Sandoz to maintain full quality responsibility for medical products, including control of mutagenic impurities per ICH M7 guidelines.

  • Ensure compliance with ICH Q11 and related Q&A documents, reviewing starting material designation, manufacturing, and control procedures.

  • Assess regulatory impact of changes in CMC information and determine required documentation to meet applicable guidelines.

Collaboration & Knowledge Transfer

  • Establish and maintain strong working relationships with internal teams, partners, and external stakeholders.

  • Provide regulatory guidance to cross-functional teams under supervision, supporting global regulatory initiatives and projects.

  • Contribute to internal regulatory SOPs, guidance documents, and knowledge transfer initiatives.

  • Continuously update regulatory expertise through training and professional development.

Quality & Compliance

  • Work according to internal and external guidance, SOPs, and established timelines.

  • Ensure all documentation supports business continuity and audit readiness.


Required Qualifications & Skills

  • Education: Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Chemistry, or related field.

  • Experience: 3–6 years in regulatory affairs, documentation, or CMC submissions in the pharmaceutical or biotech industry.

  • Strong skills in scientific/technical writing, documentation, and presentations.

  • Solid knowledge of Module 3 (CMC) and basic understanding of global regulatory guidelines.

  • Proficiency in MS Word, Excel, and regulatory submission tools.

  • Ability to follow written procedures with precision and maintain high attention to detail.


Why Sandoz?

Sandoz, a global leader in generic and biosimilar medicines, reaches nearly 500 million patients annually. With investments in new development capabilities, modern production facilities, and global partnerships, Sandoz offers a dynamic environment for career growth and impactful work.

We foster an open, collaborative culture where diversity, innovation, and personal growth are valued. Employees benefit from flexible hybrid working options, professional development opportunities, and a supportive, entrepreneurial environment.

Join Sandoz to contribute to high-quality, affordable medicines and shape the future of global healthcare.