Executive - Regulatory Affairs
Sun Pharmaceutical Industries, Inc., Chicago, IL, United States
Company: Sun Pharmaceutical Industries Ltd
Job Title:
Executive – Regulatory and Business Continuity
Business Unit:
R&D1 Regulatory Affairs
Job Grade
G12A
Location :
Baroda
Key Responsibilities:
Compilation, review of dossier for US, EU, AU, Canada & IL market for both solid oral and non-oral dosage form
Review of query response prepared and compiled by regulatory associates
Manage all the activities pertaining to dossier submission for aforesaid markets.
Meet the dossier submission and query response timeline as per given target
Review of all the documents received from stake holder for dossier compilation, Query response and Life cycle management
Allocation of projects to regulatory associate & manage the team for all the regulatory submission activities
Lifecycle management for US, EU, Canada & IL market
Single point contacts for all the regulatory submission activities for IL and Palestine markets
NA
Job Requirements Educational Qualification
M.Pharm
Experience
Your Success Matters to Us
At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together!
Disclaimer:
The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).
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Job Title:
Executive – Regulatory and Business Continuity
Business Unit:
R&D1 Regulatory Affairs
Job Grade
G12A
Location :
Baroda
Key Responsibilities:
Compilation, review of dossier for US, EU, AU, Canada & IL market for both solid oral and non-oral dosage form
Review of query response prepared and compiled by regulatory associates
Manage all the activities pertaining to dossier submission for aforesaid markets.
Meet the dossier submission and query response timeline as per given target
Review of all the documents received from stake holder for dossier compilation, Query response and Life cycle management
Allocation of projects to regulatory associate & manage the team for all the regulatory submission activities
Lifecycle management for US, EU, Canada & IL market
Single point contacts for all the regulatory submission activities for IL and Palestine markets
NA
Job Requirements Educational Qualification
M.Pharm
Experience
Your Success Matters to Us
At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together!
Disclaimer:
The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).
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