Manager Regulatory Affairs
abbott· 1758 Abbott Healthcare Private Limited
About this role
JOB DESCRIPTION:
List the main responsibilities this role regularly performs.
- As the Experienced professional in the Regulatory Affairs Sub-Function, possesses well developed skills in directing development of product registration submission, progress reports, supplements, amendments, or periodic experience reports.
- Interacts with regulatory agency to expedite approval of pending registration.
- Serves as regulatory liaison throughout product lifecycle.
- Participates in some of the following: product plan development and implementation, regulatory strategy, risk management, chemistry manufacturing control (CMC).
- Ensures timely approval of new drugs, biologics or medical devices and continued approval of marketed products.
- Serves as regulatory representative to marketing, research teams and regulatory agencies.
- Advises development and/or marketing teams on manufacturing changes, line extensions, technical labeling, appropriate regulations and interpretations.
For example you may consider to add :
- Policy Tracking: Monitor new or changing laws, regulatory frameworks, and government proposals.
- Impact Analysis: Assess how regulatory shifts affect business operations, products, or company assets.
- Position Development: Draft official policy interpretations, corporate stances, and defense strategies for regulators.
- External Representation: Speak for the organization in industry associations, trade groups, and public policy forums.
Required Skills
- Legal and Political Acumen: Strong understanding of how legislative bodies and regulatory agencies operate.
- Communication: Ability to translate dense legal text into clear, persuasive briefs for executives and external agencies.
- Skill in collaborating with cross-functional teams and external stakeholders.
The base pay for this position is
N/AIn specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Regulatory Operations
DIVISION:
EPD Established Pharma
LOCATION:
India > Mumbai : BKC Building
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Not specified
MEDICAL SURVEILLANCE:
Not Applicable
SIGNIFICANT WORK ACTIVITIES:
Keyboard use (greater or equal to 50% of the workday)
Frequently Asked Questions
Is the salary disclosed for the Manager Regulatory Affairs position at abbott?
The salary for this Manager Regulatory Affairs role at abbott is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the Manager Regulatory Affairs position at abbott located?
This Manager Regulatory Affairs role at abbott is based in India - Mumbai. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the Manager Regulatory Affairs role at abbott full-time or part-time?
This is listed as a Full time position. It is posted as a Manager Regulatory Affairs role in the 1758 Abbott Healthcare Private Limited department at abbott.
Which team or department does the Manager Regulatory Affairs at abbott belong to?
This Manager Regulatory Affairs position is part of the 1758 Abbott Healthcare Private Limited department at abbott. See the full job description for more information about the team structure and responsibilities.
How do I apply for the Manager Regulatory Affairs position at abbott?
Click the "Apply Now" button on this page. You will be redirected to abbott's official application portal hosted on workday where you can submit your application directly.
When was the Manager Regulatory Affairs job at abbott posted?
This Manager Regulatory Affairs position at abbott was posted on Sep 22, 2026. Apply as soon as possible — early applications are often reviewed first.
Manager Regulatory Affairs
abbott
You'll be redirected to abbott's official application page on Workday.