Posted:-1 days ago|
Platform:
Work from Office
Full Time
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 peersSupervisory/Management Responsibilities:
Direct Reports: None (individual contributor)
Indirect Reports: None (individual contributor) Minimum Education:
Bachelors 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
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 : Mumbai Development Center - EPD
ADDITIONAL LOCATIONS:
WORK SHIFT: Standard
TRAVEL: Not specified
MEDICAL SURVEILLANCE: Not Applicable
SIGNIFICANT WORK ACTIVITIES: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)
Abbott
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