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Hiring Associate Regulatory Operations
Abbott
Mumbai
5+ Years
Regulatory Affairs
🏢 About Abbott
Abbott is a global healthcare leader focused on improving lives through medical devices, diagnostics, nutrition, and branded generic medicines. It offers strong opportunities in regulatory affairs and global drug development.
📋 Job Overview
- Role: Associate Regulatory Operations
- Location: Mumbai
- Experience: 5+ Years
- Qualification: Pharmacy / Life Sciences
- Deadline: April 18, 2026
📌 Key Responsibilities
- Manage regulatory documents in DMS
- Handle version control & workflows
- Format documents (MS Word styles)
- Prepare submission-ready PDFs
- Perform QC checks
- Compile regulatory dossiers
- Support non-eCTD submissions
- Coordinate with global teams
- Maintain trackers & reports
🎓 Eligibility Criteria
- Bachelor’s in Pharmacy / Life Sciences
- 5+ years in Regulatory Affairs / Ops
- Experience in dossier management
- Knowledge of DMS & publishing tools
💻 Required Skills
- Regulatory submission lifecycle
- Document formatting & QC
- Global regulatory workflows
- Time management & collaboration
💰 Salary & Benefits
- ₹10 – ₹18 LPA
- Global exposure
- Career growth in Regulatory Affairs
- Stable corporate role
📚 Internal Resources (Must Read)
🎯 Interview Tips
- Understand regulatory submission lifecycle
- Revise dossier structure
- Prepare DMS & publishing questions
- Focus on QC & compliance
📚 Practice:
📌 Note Before You Apply:
Ensure your experience matches regulatory operations before applying.
Ensure your experience matches regulatory operations before applying.
🚀 Job Application Link
📌 Important Note Before You Apply:
Kindly read the full job description carefully before applying. Ensure your profile and core qualifications align with Regulatory Operations workflows, electronic submission publishing (eCTD/neES formats), regulatory dossier compilation, lifecycle management support, document management systems, and global health authority data compliance standards before proceeding with your application on the Abbott portal.
Kindly read the full job description carefully before applying. Ensure your profile and core qualifications align with Regulatory Operations workflows, electronic submission publishing (eCTD/neES formats), regulatory dossier compilation, lifecycle management support, document management systems, and global health authority data compliance standards before proceeding with your application on the Abbott portal.
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