Apply for Associate Regulatory Operations at Abbott Mumbai. Check eligibility, experience, responsibilities, salary details and apply online before deadline now today.
Introduction
Professionals with experience in regulatory affairs and document management now have a strong opportunity to grow in a global healthcare company. The Associate Regulatory Operations at Abbott role focuses on submission support, document management, and regulatory compliance across multiple regions. This position is ideal for candidates looking to build expertise in regulatory operations and global dossier handling.
Job Overview
| Job Title | Associate Regulatory Operations |
|---|---|
| Company Name | Abbott |
| Location | Mumbai, India |
| Employment Type | Full-Time |
| Department | Regulatory Operations (EPD) |
| Experience Required | 5+ Years |
| Education | Bachelor’s in Pharmacy / Life Sciences |
| Salary | As per company standards |
Company Overview
Abbott is a leading global healthcare organization known for its innovative products in diagnostics, medical devices, nutrition, and pharmaceuticals. With a strong global presence, Abbott offers excellent career opportunities in regulatory affairs, R&D, and manufacturing, along with exposure to international markets and compliance standards.
Job Location & Employment Type
- Location: Mumbai Development Center, India
- Employment Type: Full-Time
- Work Schedule: Standard (Monday–Friday)
Open Positions / Department Details
This role is part of the Established Pharma Division (EPD) Regulatory Affairs team, responsible for managing regulatory documentation, submission processes, and compliance activities across global markets.
Key Roles & Responsibilities
Document Management & Submission Support
- Manage and maintain documents in regulatory document management systems
- Ensure proper workflow, version control, and formatting of documents
- Prepare submission-ready documents using MS Word and PDF tools
- Support compilation of submission dossiers and binders
Regulatory Operations & Compliance
- Handle country-specific dossier structures, especially for non-eCTD markets
- Perform quality checks on documents for formatting and compliance
- Maintain trackers for reporting and submission activities
- Ensure compliance across product lifecycle stages
Stakeholder Coordination
- Collaborate with regional product leads, affiliates, and global regulatory teams
- Support submission activities for different regions
- Participate in project meetings and communicate timelines
Process Improvement & Risk Management
- Identify process gaps and suggest improvements
- Monitor timelines and highlight risks or delays
- Support continuous improvement initiatives
Training & Support
- Train new users on regulatory systems like DARIUS
- Provide operational support for ad-hoc regulatory activities
Eligibility Criteria
Education
- Bachelor’s degree in Pharmacy, Biology, Chemistry, Pharmacology, or related field
Experience
- Minimum 5+ years of experience in Regulatory Affairs, R&D, or related domain
Skills Required
- Strong knowledge of regulatory operations and submission processes
- Experience with document management systems (e.g., DARIUS)
- Proficiency in MS Word and PDF tools for document formatting
- Attention to detail and quality-focused approach
- Strong communication and teamwork skills
- Ability to manage multiple tasks and deadlines
Salary & Benefits
- Salary: As per company standards
- Opportunity to work on global regulatory submissions
- Exposure to international regulatory environments
- Career growth in regulatory affairs and operations
- Learning and development opportunities
- Collaborative and professional work culture
Selection Process
The hiring process generally includes:
- Online application submission
- Resume shortlisting
- Technical interview
- HR discussion
- Final selection
How to Apply
Candidates interested in the Associate Regulatory Operations at Abbott role can apply through the official Abbott careers portal. Ensure your resume highlights relevant regulatory and documentation experience.
Important Dates
- Last Date to Apply: April 18, 2026
Why Apply for This Job?
- Work with a globally recognized healthcare company
- Gain expertise in regulatory operations and submissions
- Exposure to global markets and compliance requirements
- Strong career growth in regulatory affairs
- Opportunity to collaborate with international teams
- Develop skills in document management and regulatory systems
FAQs
1. Who can apply for this job?
Candidates with a Bachelor’s degree in life sciences and 5+ years of regulatory experience can apply.
2. Is experience in regulatory systems required?
Yes, experience with systems like DARIUS or document management tools is preferred.
3. What is the salary for this role?
Salary is not disclosed and will be as per company standards.
4. What type of submissions will I handle?
You will support regulatory submissions across multiple regions, including non-eCTD markets.
5. How can I apply for this job?
You can apply online through the official Abbott careers website.
Conclusion
The Associate Regulatory Operations at Abbott role is an excellent opportunity for experienced professionals to strengthen their careers in regulatory affairs. With exposure to global submissions, compliance systems, and cross-functional collaboration, this position offers strong professional growth in the pharmaceutical industry. Apply before the deadline to secure your opportunity.
Disclaimer
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