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Junior Regulatory Associate

Navitas Life Sciences
Navitas Life Sciences
2+ years
₹4.5 LPA – ₹6.5 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 – Publishing and Submissions
Location: [Not specified]
Experience Required: Experience in Publishing and Submissions is required
Job Type: Full-Time


Job Description:
We are currently seeking a Junior Regulatory Associate to support our Publishing and Submissions team. The ideal candidate will contribute to the preparation of regulatory submissions in CTD/eCTD formats and assist in ensuring compliance with global regulatory standards. This is an excellent opportunity to develop your regulatory operations skills in a high-growth, global environment.


Key Responsibilities:

Regulatory Submission Support:

  • Understand regulatory requirements and submission formats including IND, ANDA, NDA, and DMF in CTD/eCTD for global regulatory agencies (e.g., US FDA, EMA, Health Canada).

  • Assist Regulatory Associates/Senior Regulatory Associates in document-level publishing activities such as:

    • Bookmarking

    • Hyperlinking

    • Table of Contents creation

    • Document formatting to comply with agency-specific requirements.

Publishing & Archiving:

  • Perform submission publishing support, including:

    • Same-day dispatch of submissions

    • Handling complex or major submissions

    • Archiving submission packages post-dispatch

    • Conducting basic quality checks to ensure submission-readiness.

Compliance & SOP Adherence:

  • Ensure full compliance with client-specific SOPs and policies, as well as internal organizational standards.

  • Maintain documentation as per regulatory submission protocols and version control practices.


Desirable Skills and Experience:

  • Prior experience in Publishing and Submissions within a regulatory affairs or regulatory operations environment is mandatory.

  • Familiarity with eCTD software tools such as Lorenz DocuBridge, Extedo, eCTD Express, pharmaREADY, etc. is a plus.

  • Basic understanding of global regulatory submission standards and guidance.

  • Good knowledge of Microsoft Office Suite (Word, Excel, Outlook, PowerPoint).

  • Strong attention to detail, ability to meet tight deadlines, and willingness to learn.


Estimated Salary: ₹4.5 LPA – ₹6.5 LPA (based on experience and publishing tool proficiency)