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Junior Regulatory Associate

Navitas Life Sciences
Navitas Life Sciences
2-5 years
₹6.5 LPA – ₹10 LPA
10 July 22, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Junior Regulatory Associate
Location: [Not specified]
Experience Required: 2–5 years
Job Type: Full-Time


Job Description:
We are currently seeking a Junior Regulatory Associate to join our expanding Regulatory Affairs team. The ideal candidate will contribute to the preparation, review, and submission of regulatory dossiers for global markets and provide end-to-end regulatory support across the product lifecycle. This role is pivotal in ensuring compliance with global regulations and helping drive timely product approvals.


Key Responsibilities:

Dossier Preparation & Regulatory Support:

  • Prepare and finalize Global Regulatory Strategy Documents and CTD sections for IND, CTA, BLA, NDA, and ANDA submissions.

  • Collaborate with cross-functional teams and global RA counterparts to develop, review, and finalize high-quality regulatory dossiers for pipeline products.

  • Ensure regulatory submissions align with applicable international guidelines and client-specific standards.

Product Lifecycle & Compliance:

  • Manage timelines and documentation for MA transfers, license renewals, product variations, supplements, annual reports, and safety filings.

  • Support responses to Health Authority queries, coordinate strategic global responses, and address deficiency letters in a timely manner.

Risk Management & Strategy:

  • Monitor and communicate regulatory risks, escalate critical issues, and assist in risk mitigation.

  • Provide regulatory advice during technical reviews and regulatory inspections.

  • Remain updated on international regulations, guidance, and customer practices relevant to exported products.

Documentation & Guidance Implementation:

  • Assist in authoring and reviewing CMC documentation, labeling documents, and safety reports across the regulatory lifecycle.

  • Ensure alignment with regional and global regulatory frameworks, and implement regulatory guidance throughout project phases.


Desirable Skills and Experience:

  • 2–5 years of experience in a regulated life sciences environment.

  • Hands-on experience in registration processes, including development, maintenance, and commercialization.

  • Strong knowledge of CMC authoring, labeling, and regulatory submission strategy.

  • Understanding of global and regional regulatory guidelines, including EMA, USFDA, ICH, etc.

  • Strong analytical, logical, and writing skills.

  • Ability to interpret local regulations, manage cross-cultural teams, and handle complex submission tasks.

  • Excellent communication, time management, and coordination abilities.


Estimated Salary: ₹6.5 LPA – ₹10 LPA (based on experience and skill set)