Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

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: Apache Spark, Artificial Intelligence (AI), Big Data, Data Governance, Data Literacy, Data Management, Data Quality, Data Science, Data Strategies, Data Visualization, Machine Learning (ML), Master Da, Auditing, Audit Management, Audits Compliance, Communication, Continued Learning, Decision Making, Gmp Procedures, Inspection Readiness, Managing Ambiguity, Organizing, People Management and Leadershi, Bachelor’s Degree (BS) or Master’s Degree (MS) in: Life Sciences Pharmacy Biotechnology Biomedical Sciences Chemistry Regulatory Affairs Or related scientific disciplines, Budget Management, Clinical Trials, Negotiation Skills, Process Improvement, Project Planning, Vendor Management, Waterfall Model, Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Intern, Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Intern, Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Intern, Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Intern, Causality Assessment, Change Control, Continual Improvement Process, Data Analytics and Digital, GDP Knowledge, gmp knowledge, HSE Knowledge, Manufacturing Process, Manufacturing Production, Operational Excellence, Process, Clinical Monitoring, Clinical Research, Clinical Study Reports, Clinical Trial Management Systems, Clinical Trials, Collaboration, Data Integrity, Decision Making Skills, Lifesciences, Clinical Research, Clinical Trials, Curious Mindset, Databases, Drug Development, Job Description, Lifesciences, Medical Communication, Medical Information, Medical Writing, Military Intelligence, Pat, Clinical SAS Programming, Clinical Trials, Cross-Functional Teams, Drug Development, Lifesciences, Negotiation Skills, People Management, Problem Solving Skills, Regulatory Compliance, Risk Management, Strategy Execution, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Clinical Trials, Functional Teams, Literature Review, Management Skills, Medical Information, Medical Records, Medical Strategy, Pharmacovigilance, Regulatory Compliance, Risk Management, Safety Scien, Coaching Skills, Data Science, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Pro, Collaboration, Communication Skills, gmp, GMP Guidelines, Operational Excellence, Problem Solving Skills, Quality Agreements, Quality Compliance, Quality Management, Quality Standards, Regulatory Requ, Communication Skills, Continual Improvement Process, Master Data, Material Requirements Planning (Mrp), Materials Management, People Management, Production Planning, Supplier Relationship Management (Srm), Supply-Chain Man, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines, gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management, 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