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Ra Officer (Associate Consultant)

PLG groups
3+ years
Not Disclosed
Remote, India, India
10 June 2, 2026
Job Description
Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, 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, mRS and EQ-5D-5L, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: RA Officer (Associate Consultant)

Domain: Regulatory Affairs & Operations (Life Cycle Management)
Location: India (Remote work possible)
Employment Type: Permanent Contract


Role Overview

The RA Officer (Associate Consultant) supports regulatory affairs activities for pharmaceutical, biological, and medical device products in the Australia, New Zealand, and broader JAPAC region. The role focuses on regulatory submissions, dossier preparation, compliance support, and lifecycle maintenance of product registrations in alignment with regulatory authorities such as TGA and Medsafe.


Key Responsibilities

1. Regulatory Submissions & Registrations

  • Support product registration and listing for pharmaceuticals, biologics, and medical devices in Australia and New Zealand

  • Assist in maintaining existing product registrations and listings

  • Prepare, review, and submit regulatory dossiers to:

    • TGA (Therapeutic Goods Administration, Australia)

    • Medsafe (New Zealand)

2. eCTD Publishing & Documentation

  • Provide support for eCTD (electronic Common Technical Document) publishing

  • Prepare, review, and update regulatory and quality documentation

  • Ensure accuracy and compliance of submission documents

3. Regulatory Compliance Support

  • Ensure submissions comply with:

    • TGA legislation and guidelines

    • Medsafe regulations and procedures

  • Maintain high standards of confidentiality in regulatory documentation

4. Authority Interaction & Query Handling

  • Assist clients in responding to regulatory queries from TGA and Medsafe

  • Support senior team members in addressing complex regulatory questions

5. Project & Client Support

  • Assist in project management and client coordination tasks

  • Support senior consultants in preparing complex regulatory applications

  • Contribute to lifecycle management of regulated products

6. GMP & Quality Documentation

  • Prepare GMP clearance applications for submission to regulatory authorities

  • Review and update quality-related regulatory documents


Required Qualifications

  • Undergraduate degree in Pharmaceutical Sciences or a related scientific discipline

  • Minimum 3 years of experience in Regulatory Affairs

  • Preference for experience in Australia and New Zealand regulatory markets (commercial environment)


Key Skills & Competencies

Regulatory Knowledge

  • Strong understanding of:

    • TGA (Australia) regulations

    • Medsafe (New Zealand) guidelines

    • Regulatory submission processes

  • Knowledge of pharmaceutical, biological, and medical device regulatory frameworks

Technical & Documentation Skills

  • Experience with eCTD publishing systems

  • Strong documentation, review, and submission skills

  • Ability to prepare structured regulatory dossiers

Analytical & Problem-Solving Skills

  • Ability to interpret regulatory guidelines

  • Strong attention to detail

  • Ability to manage complex regulatory requirements

Project Management Skills

  • Ability to work under deadlines

  • Experience handling multiple regulatory projects simultaneously

  • Coordination with clients and internal teams

Communication Skills

  • Excellent written and verbal communication in English

  • Strong interpersonal skills for client interaction

  • Ability to handle regulatory authority queries professionally

Professional Attributes

  • High level of confidentiality handling

  • Strong learning mindset and adaptability

  • Interest in consulting environment


Working Environment

  • Remote work possible (India-based role)

  • Exposure to international regulatory systems (Australia, New Zealand, JAPAC)

  • Client-facing consulting environment


Role Impact

  • Ensures timely approval and maintenance of life-saving pharmaceutical and medical products

  • Supports regulatory compliance across international markets

  • Plays a key role in enabling product availability in Australia and New Zealand healthcare systems

  • Contributes directly to global regulatory success of pharmaceutical companies