Executive Role at Sun Pharm| Pharma Graduates Eligible
A Sun Pharma regulatory job opportunity is available for aspiring professionals to join Sun Pharmaceutical Industries Ltd as an Executive/Sr. Executive in Gurgaon. This role within the Regulatory & Business Continuity unit calls for candidates with a B. Pharma or M. Pharma degree and 4-6 years of relevant experience. Interested applicants are encouraged to apply before the deadline.
About Sun Pharmaceutical Industries Ltd
Sun Pharmaceutical Industries Ltd is a leading global pharmaceutical company headquartered in India. It specializes in the development, manufacturing, and marketing of a wide range of pharmaceutical formulations and active pharmaceutical ingredients. The company is dedicated to improving the quality of life through innovative medicines and has a strong presence in various therapeutic segments.
- Company: Sun Pharmaceutical Industries Ltd
- Location: Gurgaon – R&D
- Job Title: Executive/Sr. Executive
- Business Unit: Regulatory & Business Continuity
- Job Grade: G12A / G11B
Sun Pharma Regulatory Job Description
The selected candidate will be responsible for reviewing and compiling product registration dossiers, preparing responses to deficiency letters from health authorities, and providing regulatory support to cross-functional departments. This Sun Pharma regulatory role is crucial in ensuring compliance with regulatory requirements across various regions, including the US, Canada, Europe, and Japan.
Key Responsibilities
- Review all data and documents related to product registrations for various health authorities.
- Compile registration dossiers for submission to various health authorities like US-FDA, Health Canada, Europe, Australia/New Zealand, Japan, and Israel.
- Prepare responses to deficiency letters received from various agencies.
- Maintain life-cycle/post-approval changes for drug product registration dossiers.
- Provide regulatory support to cross-functional departments.
- Prepare and submit scientific advice to various health authorities.
- eCTD compilation, verification, and submission through electronic gateway.
- Review, preparation, and submission of annual reports to US FDA.
- Review, preparation, and submission of post-approval supplements to US FDA.
Eligibility for This Regulatory Affairs Role
- Educational Qualification: B. Pharma / M. Pharma
- Experience: 4-6 Years
Documents Required
- Resume
- Cover Letter
- Educational Certificates
- Experience Certificates
CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE
Additional Information
At Sun Pharma, your success and well-being are top priorities. The organization provides robust benefits and opportunities to foster personal and professional growth. Every day is an opportunity to grow, collaborate, and make a lasting impact.
Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employees 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).
Qualified candidates are encouraged to seize this Sun Pharma regulatory job opportunity at Sun Pharmaceutical Industries Ltd and apply before the deadline. This role promises a chance to contribute significantly to the organization’s mission while advancing one’s career in the pharmaceutical sector.
