If you’re looking for a career in Regulatory Affairs in India, here’s a great opportunity to join a leading global CRO hiring for three roles — from entry-level to senior publishing expertise. Whether you prefer working onsite or remotely, these roles offer a strong pathway to growth in regulatory compliance, EUCTR submissions, eCTD publishing, and document lifecycle management.
These openings are ideal for professionals with 1 to 5+ years of experience in pharmaceutical regulatory documentation, electronic submissions, Veeva Vault, RIMS, and regulatory project coordination.
📍 Available Positions
1️⃣ Principal Regulatory Affairs Assistant (Onsite – Bangalore)
Key Responsibilities:
- Support EUCTR documentation and regulatory submissions
- Maintain SOP awareness and apply current regulatory guidance
- Coordinate project deliverables, timelines, and stakeholder communication
- Support bids, proposals, and documentation lifecycle management
Qualifications:
- Bachelor’s or Master’s degree in Life Sciences / Pharmacy
- 1+ years regulatory affairs or documentation experience
Best For: Entry-level to intermediate candidates wanting onsite collaboration and EUCTR hands-on experience.
2️⃣ Regulatory Affairs Specialist (Remote – India)
Key Responsibilities:
- Support EUCTR submission processes and regulatory deliverables
- Manage RIMS and document workflows
- Ensure compliance with agency and SOP requirements
- Communicate with global project teams and regulatory stakeholders
Qualifications:
- Bachelor’s/Master’s degree in Pharmacy or Life Sciences
- 2+ years regulatory affairs experience
- Knowledge of RIMS, SOP alignment, documentation auditing
Best For: Candidates seeking remote regulatory affairs careers in India.
3️⃣ Senior Regulatory Publishing Specialist (Remote – India)
Key Responsibilities:
- Prepare submission-ready dossiers per ICH/eCTD requirements
- Perform publishing quality review, lifecycle management, and validation
- Work with Veeva Vault, Adobe, templates, macros, and advanced formatting
- Train and mentor publishing team members
- Work independently on high-complexity global submissions
Qualifications:
- Bachelor’s degree (Life Science preferred)
- 5+ years experience in regulatory publishing
- Expertise in eCTD, CSR, IB, modules, and document formatting
Best For: Senior candidates with ePublishing and submission experience.
🎯 Benefits of Joining
- Work with a global regulatory and publishing team
- Competitive salary with performance opportunities
- Skill growth in EUCTR, eCTD, regulatory compliance and software tools
- Remote options available for eligible roles
📌 How to Apply
Application Link for RA Assistant
Application Link for Regulatory Affairs Specialist
Application Link for Sr. Regulatory Publishing Specialist
