Abbott, a global leader in healthcare and pharmaceuticals, is inviting applications for the position of Associate Regulatory Operations at its Mumbai Development Center (EPD – Established Pharmaceuticals Division). This opportunity is ideal for regulatory affairs professionals with hands-on experience in document operations, regulatory submissions, and document management systems.
This role plays a critical part in ensuring high-quality regulatory documents, compliance with global regulatory authority standards, and timely submission support across Abbott’s international markets.
Key Responsibilities – Associate Regulatory Operations
As an Associate Regulatory Operations professional at Abbott, you will be responsible for:
- Processing and formatting regulatory submission documents in compliance with Abbott and global regulatory authority standards
- Performing detailed quality checks (QC) on self and team members’ regulatory documents
- Collaborating closely with Regulatory Affairs teams, Operations colleagues, and Publishing partners
- Ensuring timely delivery of high-quality submission packages
- Supporting departmental initiatives and mentoring junior team members
- Contributing to standard setting, SOPs, and training material development
- Driving process improvement, system enhancements, and troubleshooting document management tools
- Using document management systems and MS Word formatting tools efficiently
Eligibility & Qualifications
To be considered for this Abbott Regulatory Affairs job in Mumbai, candidates must have:
- Graduation or higher qualification in Life Sciences / Pharmacy / Biotechnology
- 3–5 years of experience in Regulatory Affairs, Regulatory Operations, R&D, or related pharmaceutical functions
- Familiarity with pharmaceutical regulatory and labeling documents
- Strong written and verbal communication skills in English
- Proven experience in MS Word formatting and document management systems
- High attention to detail and strong process orientation
- Ability to work in a fast-paced, deadline-driven global environment
Salary & Benefits
- Estimated Salary Range: ₹6,00,000 – ₹10,00,000 per annum (CTC)
- Opportunity to work with a global pharmaceutical leader
- Exposure to international regulatory submissions and systems
- Career growth in Regulatory Operations and Document Management
- Collaborative and compliance-driven work culture
Job Location
📍 Mumbai Development Center – EPD, Mumbai, India
How to Apply
