Abbott is hiring a Specialist Regulatory Affairs professional for its Medical Devices (MD) division in New Delhi, India. This full-time Regulatory Affairs opportunity is suitable for experienced professionals with knowledge of regulatory submissions, product registrations, regulatory strategy, and product lifecycle management.
The selected candidate will support regulatory activities for medical devices and work as a regulatory liaison throughout the product lifecycle. The role involves coordinating product registration submissions, communicating with regulatory agencies, supporting regulatory approvals, and advising internal teams on applicable regulations.
Candidates with at least 1 year of relevant experience are encouraged to apply for this Abbott Regulatory Affairs job in New Delhi.
Job Highlights
- Company: Abbott
- Job Role: Specialist Regulatory Affairs
- Job Family: Regulatory Operations
- Division: MD Medical Devices
- Job Type: Full-Time
- Location: New Delhi, India
- Work Location: New Friends Colony, New Delhi
- Experience Required: Minimum 1 Year
- Qualification: Associate Degree or relevant equivalent qualification
- Job Requisition ID: 31160383
- Posted: September 9, 2026
About the Role
The Specialist Regulatory Affairs will work as an experienced individual contributor under limited supervision. The role requires strong subject matter knowledge in Regulatory Affairs and the ability to apply regulatory knowledge according to specific product and business requirements.
The professional will contribute to the development and management of regulatory submissions and support the timely approval and continued compliance of Abbott’s medical device products.
This Regulatory Affairs role provides an opportunity to work across different stages of the medical device product lifecycle, including product registration, regulatory strategy, risk management, manufacturing changes, labeling, and interactions with regulatory authorities.
Key Responsibilities
As a Specialist Regulatory Affairs at Abbott, the selected candidate may be responsible for:
- Supporting the development of product registration submissions.
- Preparing and coordinating regulatory progress reports, supplements, amendments, and periodic reports.
- Interacting with regulatory agencies to help expedite approvals for pending registrations.
- Serving as a regulatory liaison throughout the product lifecycle.
- Supporting product planning and implementation activities.
- Participating in the development and execution of regulatory strategies.
- Contributing to regulatory risk management activities.
- Supporting activities related to Chemistry, Manufacturing and Controls (CMC) where applicable.
- Helping ensure timely approval of new products and continued approval of marketed products.
- Representing Regulatory Affairs in interactions with marketing, research, development, and regulatory agencies.
- Advising internal development and marketing teams regarding manufacturing changes.
- Supporting regulatory requirements for line extensions and technical labeling.
- Interpreting relevant regulations and providing regulatory guidance to internal stakeholders.
Qualifications and Eligibility
Education
Abbott has listed the following educational requirement:
- Associate Degree (approximately 13 years of education)
Candidates with relevant educational backgrounds and qualifications related to Regulatory Affairs, Life Sciences, Pharmacy, Medical Devices, Biomedical Sciences, or related disciplines may find this opportunity relevant. Applicants should carefully review the official job posting before applying.
Experience
- Minimum 1 year of relevant experience
Experience in areas such as Regulatory Affairs, Regulatory Operations, medical device registration, product registration, regulatory submissions, or medical device compliance may be beneficial.
Skills That May Be Valuable
Candidates applying for this Abbott Regulatory Affairs job may benefit from knowledge or experience in:
- Regulatory Affairs
- Regulatory Operations
- Medical Device Regulations
- Product Registration
- Regulatory Submissions
- Product Lifecycle Management
- Regulatory Strategy
- Risk Management
- Technical Documentation
- Product Labeling
- Regulatory Compliance
- Manufacturing Change Assessment
- Communication with Regulatory Authorities
- Cross-functional Collaboration
Why Consider This Opportunity?
Working in Regulatory Affairs provides exposure to the processes that support the approval and continued availability of healthcare products. In this role, professionals may gain experience working with cross-functional teams and supporting regulatory requirements across the product lifecycle.
Potential professional benefits of this opportunity include:
- Experience in the medical device industry
- Exposure to Regulatory Affairs and Regulatory Operations
- Cross-functional collaboration with research, development, and marketing teams
- Experience supporting product registrations and regulatory submissions
- Opportunity to develop knowledge of medical device regulations
- Full-time employment with a global healthcare organization
Specific employee benefits, compensation, and policies may vary based on Abbott’s employment terms and location.
Salary for Specialist Regulatory Affairs at Abbott
Abbott has not disclosed the salary for this position.
Based on the role level, location, required experience, and the Indian Regulatory Affairs job market, a realistic estimated salary range could be approximately:
₹4 LPA – ₹9 LPA
Actual compensation may vary depending on the candidate’s experience, qualifications, skills, previous compensation, internal salary structure, and other factors.
Note: This is an independent market-based estimate and is not an official salary disclosed by Abbott.
Job Location
Abbott – Medical Devices Division
New Friends Colony
New Delhi, India
This position is based in New Delhi and is listed as a full-time opportunity.
How to Apply
