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Manager - Regulatory Affairs

Abbott

Legal Jobs

Manager - Regulatory Affairs

full-timePosted: Jan 12, 2026

Job Description

Primary Job Function: 
 

With Manager Support:-

1. Product registrations / Submissions
-Actively leads product registrations by preparing/ requesting documentation needed for complex filings
-Employs project management skills to monitor activities and meet deadlines
-Prepares registration packages for routine filings
-Identifies and collects data needed
-Seeks expert advice and technical support for complex filings
-Prepares responses to deficiency letters
 

2. Relationships & Cross Functional team work
-Represents Regulatory CMC at relevant project meetings and communicates agreed RA position 
-Monitors and communicates actual versus planned regulatory activities and timelines
-Identifies and communicates risks and issues impacting project progression


3. Affiliate Coordination
-Maintains strong working relationships with Regional Product Leads and Affiliate colleagues


4. Compliance across Life-Cycle
-Assesses and approves change requests and updates files accordingly 
-Maintains awareness of legislation and current developments within specific area of business
-Works to assure products remain in compliance
 

5. Strategy
-Develops Regulatory CMC strategies for assigned products and projects
-Identifies, communicates, and mitigates Regulatory CMC risks
 

6. Process Improvement
-Identifies opportunities and suggests improvements
-Supports the development of position papers & work aids etc
 

7. Health Agency Interaction
-Attends Health Agency meetings as appropriate


8. Licensing Reviews
-Provides CMC Regulatory support for due diligence activities
 

9. Technical competency
-Has general knowledge of technical/scientific principles and develops specific knowledge of allocated products 
-Has general knowledge of global and regional regulatory requirements 
-Has specialist regulatory knowledge of assigned country or product-class requirements

CORE COMPETENCIES

Adaptability
-Effectively prioritizes mid-term (weeks) to longer-term (months) work tasks 
-Regularly reviews commitments and re-prioritises activities or negotiates timelines as necessary 
-Reacts quickly to solve problems and issues when they arise
 

Initiative
-Starts to learn new aspects of the business and understand the roles of other functions
-Proactively anticipates, mitigates and avoids problems and issues
-Proactively seeks feedback from manager and team members and adapts behaviour to improve performance
 

Innovation
-Has an intrapreneurial mindset to identify new or unique ways to address work problems or opportunities
 

Integrity
-Delivers high quality results. 
-Meets agreed deadlines. 
-Exhibits honesty and presents complete impartial information.
-Displays consistency between words and actions.
-Acknowledges and responds constructively to failures and mistakes.
-Expresses dissatisfaction constructively, without over-reacting.
 

Teamwork
-Actively interacts with colleagues to drive completion of team and shared goals
 

LEADERSHIP COMPETENCIES

Set Vision and Strategy
-Clearly articulates Regulatory CMC strategies and obtains alignment and agreement from key stakeholders
 

Build Organization and Inspire People
-Mentors junior team members
-Provides training and support on areas of subject matter expertise
-Proactively strengthens own leadership skills and actively uses these skills in day to day work
 

Drive Results
-Encourages others to complete goals


Make Difficult Decisions
-Interacts with cross-functional and department colleagues to help drive efficient decision-making


Encourage an Open Environment and Knowledge Sharing
-Provides honest, accurate feedback to managers, whether positive or negative
-Not afraid to challenge peers and managers and be challenged
-Openly shares information with peers
Supervisory/Management Responsibilities:

Direct Reports:     None (individual contributor)
Indirect Reports:    None (individual contributor)

Minimum Education:

Bachelor's Degree in pharmacy, biology, chemistry, pharmacology, or related subject

Minimum Experience/Training Required:

A minimum of 10 years of experience in Regulatory Affairs, R&D, Manufacturing or related areas

Locations

  • Mumbai, India

Salary

Estimated Salary Rangemedium confidence

100,000 - 160,000 INR / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • adaptabilityintermediate
  • initiativeintermediate
  • innovationintermediate
  • integrityintermediate
  • teamworkintermediate
  • project management skillsintermediate
  • technical/scientific principles knowledgeintermediate
  • global and regional regulatory requirements knowledgeintermediate

Responsibilities

  • Leads product registrations and prepares documentation
  • Prepares registration packages and responses to deficiency letters
  • Represents Regulatory CMC in project meetings
  • Monitors regulatory activities and timelines
  • Coordinates with affiliates
  • Assesses and approves change requests
  • Develops Regulatory CMC strategies
  • Identifies process improvements
  • Interacts with Health Agencies
  • Provides CMC Regulatory support for licensing reviews

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Answer 10 quick questions to check your fit for Manager - Regulatory Affairs @ Abbott.

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Abbott logo

Manager - Regulatory Affairs

Abbott

Legal Jobs

Manager - Regulatory Affairs

full-timePosted: Jan 12, 2026

Job Description

Primary Job Function: 
 

With Manager Support:-

1. Product registrations / Submissions
-Actively leads product registrations by preparing/ requesting documentation needed for complex filings
-Employs project management skills to monitor activities and meet deadlines
-Prepares registration packages for routine filings
-Identifies and collects data needed
-Seeks expert advice and technical support for complex filings
-Prepares responses to deficiency letters
 

2. Relationships & Cross Functional team work
-Represents Regulatory CMC at relevant project meetings and communicates agreed RA position 
-Monitors and communicates actual versus planned regulatory activities and timelines
-Identifies and communicates risks and issues impacting project progression


3. Affiliate Coordination
-Maintains strong working relationships with Regional Product Leads and Affiliate colleagues


4. Compliance across Life-Cycle
-Assesses and approves change requests and updates files accordingly 
-Maintains awareness of legislation and current developments within specific area of business
-Works to assure products remain in compliance
 

5. Strategy
-Develops Regulatory CMC strategies for assigned products and projects
-Identifies, communicates, and mitigates Regulatory CMC risks
 

6. Process Improvement
-Identifies opportunities and suggests improvements
-Supports the development of position papers & work aids etc
 

7. Health Agency Interaction
-Attends Health Agency meetings as appropriate


8. Licensing Reviews
-Provides CMC Regulatory support for due diligence activities
 

9. Technical competency
-Has general knowledge of technical/scientific principles and develops specific knowledge of allocated products 
-Has general knowledge of global and regional regulatory requirements 
-Has specialist regulatory knowledge of assigned country or product-class requirements

CORE COMPETENCIES

Adaptability
-Effectively prioritizes mid-term (weeks) to longer-term (months) work tasks 
-Regularly reviews commitments and re-prioritises activities or negotiates timelines as necessary 
-Reacts quickly to solve problems and issues when they arise
 

Initiative
-Starts to learn new aspects of the business and understand the roles of other functions
-Proactively anticipates, mitigates and avoids problems and issues
-Proactively seeks feedback from manager and team members and adapts behaviour to improve performance
 

Innovation
-Has an intrapreneurial mindset to identify new or unique ways to address work problems or opportunities
 

Integrity
-Delivers high quality results. 
-Meets agreed deadlines. 
-Exhibits honesty and presents complete impartial information.
-Displays consistency between words and actions.
-Acknowledges and responds constructively to failures and mistakes.
-Expresses dissatisfaction constructively, without over-reacting.
 

Teamwork
-Actively interacts with colleagues to drive completion of team and shared goals
 

LEADERSHIP COMPETENCIES

Set Vision and Strategy
-Clearly articulates Regulatory CMC strategies and obtains alignment and agreement from key stakeholders
 

Build Organization and Inspire People
-Mentors junior team members
-Provides training and support on areas of subject matter expertise
-Proactively strengthens own leadership skills and actively uses these skills in day to day work
 

Drive Results
-Encourages others to complete goals


Make Difficult Decisions
-Interacts with cross-functional and department colleagues to help drive efficient decision-making


Encourage an Open Environment and Knowledge Sharing
-Provides honest, accurate feedback to managers, whether positive or negative
-Not afraid to challenge peers and managers and be challenged
-Openly shares information with peers
Supervisory/Management Responsibilities:

Direct Reports:     None (individual contributor)
Indirect Reports:    None (individual contributor)

Minimum Education:

Bachelor's Degree in pharmacy, biology, chemistry, pharmacology, or related subject

Minimum Experience/Training Required:

A minimum of 10 years of experience in Regulatory Affairs, R&D, Manufacturing or related areas

Locations

  • Mumbai, India

Salary

Estimated Salary Rangemedium confidence

100,000 - 160,000 INR / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • adaptabilityintermediate
  • initiativeintermediate
  • innovationintermediate
  • integrityintermediate
  • teamworkintermediate
  • project management skillsintermediate
  • technical/scientific principles knowledgeintermediate
  • global and regional regulatory requirements knowledgeintermediate

Responsibilities

  • Leads product registrations and prepares documentation
  • Prepares registration packages and responses to deficiency letters
  • Represents Regulatory CMC in project meetings
  • Monitors regulatory activities and timelines
  • Coordinates with affiliates
  • Assesses and approves change requests
  • Develops Regulatory CMC strategies
  • Identifies process improvements
  • Interacts with Health Agencies
  • Provides CMC Regulatory support for licensing reviews

Target Your Resume for "Manager - Regulatory Affairs" , Abbott

Get personalized recommendations to optimize your resume specifically for Manager - Regulatory Affairs. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Manager - Regulatory Affairs" , Abbott

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Answer 10 quick questions to check your fit for Manager - Regulatory Affairs @ Abbott.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.