PHARMA STUFF

Sun Pharma Recruitment – Regulatory Affairs Jobs for M.Pharm

Written by

Sudheer vanguri

in

Sun Pharmaceutical Industries Ltd. are inviting applications for opportunities in their India Regulatory Affairs team at the Vadodara site.
Candidates with an M.Pharm and 4 to 10 years’ relevant Regulatory Affairs experience are eligible.
Applicants should have a good understanding of CDSCO licensing, BA/BE study permissions, import licences and Indian regulatory submissions.
Any interested candidates with experience in regulatory compliance and pharma regulatory affairs are invited to send in their most up to date CVS via email.

Sun Pharma Recruitment – Job Overview

Sun Pharma are currently seeking experienced pharma professionals to join their India Regulatory Affairs team in Vadodara, Gujarat.

This is for M.Pharm graduates with experience in Indian regulatory affairs (regulatory licensing, clinical study permissions, regulatory submissions etc). Should be familiar with CDSCO requirements and the relevant Indian pharma laws.

Job Details

Particulars Details
Company Sun Pharmaceutical Industries Ltd.
Department India Regulatory Affairs
Job Role Regulatory Affairs
Qualification M.Pharm
Experience 4–10 Years
Job Location Vadodara, Gujarat
Application Mode Email
Email

Sun Pharma Regulatory Affairs Job Responsibilities & Requirements

Candidates should have relevant experience in Indian Regulatory Affairs and an understanding of pharma regulatory processes.

Regulatory Affairs – Key Requirements

  • Experience in CDSCO licensing.

  • Handling BA/BE study permissions.

  • Experience of import licences for pharmaceuticals.

  • Prepare and manage regulatory submissions in India.

  • Strong understanding of the NDCTR 2019.

  • Knowledge of the Drugs and Cosmetics Act and Rules.

  • Familiarity with CDSCO procedures and import licensing requirements.

  • Experience in dealing with queries from regulatory authorities.

  • Coordination with cross-functional stakeholders.

  • Ability to effectively manage the regulatory activity and the requirements of stakeholders.

Required Skills

Candidates should possess the following professional skills:

  • Regulatory Affairs and Compliance

  • CDSCO Regulatory Procedures

  • Indian Pharmaceutical Regulations

  • BA/BE Study Permission Requirements

  • Import Licensing

  • Regulatory Documentation and Submissions

  • Regulatory Query Management

  • Cross-functional Stakeholder Management

  • Planning and Coordination

  • Communication and People Management

Eligibility & Qualifications

Educational Qualification

Candidates must possess the following qualifications:

  • M.Pharm (Master of Pharmacy)

Experience Requirements

  • 4 to 10 years’ relevant experience in Regulatory Affairs.

  • Significant exposure to CDSCO licensing.

  • Experience of dealing with BA/BE study permits and import licences.

  • Practical experience in Indian regulatory submissions.

  • Understanding of NDCTR 2019 and the Drugs and Cosmetics Act and Rules.

  • Experience dealing with queries from regulatory authorities and co-ordinating with other functions.

Job Location – Sun Pharma Vadodara

The position is based at the Vadodara site in Gujarat as part of the India Regulatory Affairs function.

Candidates with relevant Indian regulatory experience are invited to apply.

How to Apply for Sun Pharma Recruitment

Eligible candidates for this Regulatory Affairs position should feel free to send their up to date CVS directly to the recruitment email address.

Application Process

  1. Prepare your updated resume with details of your Regulatory Affairs experience.

  2. Highlight your experience in CDSCO licensing, BA/BE study permissions and import licences.

  3. Mention your knowledge of the NDCTR 2019 and the Drugs and Cosmetics Act and Rules.

  4. Include your current title and relevant professional experience.

  5. Just send your updated CV to the email address given below.

Email for Application: Rosemary.varghese@sunpharma.com

Important Instructions

  • M.Pharm qualification is required.

  • Candidates must have 4 to 10 years of relevant Regulatory Affairs experience.

  • Experience in Indian regulatory submissions is absolutely essential.

  • Knowledge of CDSCO procedures and the import licensing requirements is expected.

  • Highlight your relevant regulatory experience right up front in your CV.

Frequently Asked Questions

1. What qualification is required for Sun Pharma Regulatory Affairs jobs?

Candidates must hold an M.Pharm.

2. How much experience is required?

Applicants should have 4 to 10 years of relevant Regulatory Affairs experience.

3. What’s the job location?

The position is based at Sun Pharma’s Vadodara facility in Gujarat.

4. What regulatory experience is required?

Candidates should have experience in CDSCO licensing, BA/BE study permissions, import licences and Indian regulatory submissions.

5. What regulatory knowledge is expected?

Candidates should be familiar with NDCTR 2019, the Drugs and Cosmetics Act and Rules, CDSCO procedures and import licensing requirements.

6. How can candidates apply?

Interested parties can email their updated CVS to Rosemary.varghese@sunpharma.com

7. What’s the final date to apply?

The recruitment info doesn’t state an application deadline.

Job Summary

Category Details
Company Sun Pharmaceutical Industries Ltd.
Vacancies Regulatory Affairs – India Regulatory Affairs
Required Education M.Pharm
Experience 4–10 Years

More posts