Kesar Hiring Regulatory Affairs Executive
- Company Overview
- Job Role & Responsibilities
- Executive – Regulatory Affairs
- Eligibility / Qualifications
- Educational Qualification
- Experience Required
- Key Skills
- Location & Salary
- Application Process
- Why This Opportunity Stands Out
- FAQs
- Who can apply for this Regulatory Affairs role?
- Is USFDA experience required?
- What is the job location?
- How can I apply?
- What skills are important for this role?
- Additional SEO Titles
- Summary Table
BPharm MPharm RA Jobs Kesar Pharma Gujarat
B.Pharm, M.Pharm candidates apply for Regulatory Affairs Executive role at Kesar Pharma Gujarat with 2–3 years experience.
Kesar Pharma Pvt. Ltd. is urgently hiring for the position of Executive – Regulatory Affairs at its Gujarat location. This opportunity is ideal for B.Pharm and M.Pharm professionals with 2–3 years of experience who are looking to build a strong career in regulatory affairs, dossier preparation, and global pharma compliance.
With increasing demand for regulatory affairs jobs in pharma, especially in USFDA, EU, and global submission environments, this role offers direct exposure to compliance-driven pharmaceutical operations. Candidates aiming for high-growth pharma regulatory careers, dossier submission roles, and compliance-focused jobs will find this position aligned with current industry needs.
High CPC keywords such as regulatory affairs jobs, pharma regulatory jobs, USFDA submission jobs, CTD dossier preparation, and pharmaceutical compliance jobs are naturally integrated to improve search visibility and AdSense performance.
Company Overview
Kesar Pharma Pvt. Ltd. is a growing pharmaceutical company focused on delivering high-quality formulations and maintaining strict regulatory compliance across domestic and international markets. The company is known for its structured regulatory processes, documentation accuracy, and adherence to global pharmaceutical standards.
With increasing expansion into regulated markets, Kesar Pharma is strengthening its regulatory affairs team to support product registrations, dossier submissions, and lifecycle management activities. Working here provides hands-on exposure to regulatory frameworks and submission processes critical for global pharma operations.
Job Role & Responsibilities
Executive – Regulatory Affairs
- Prepare and review CTD (Common Technical Document) dossiers for domestic and international submissions
- Handle regulatory submissions for markets such as USFDA, EU, and other semi-regulated regions
- Coordinate with internal departments including QA, QC, and production for documentation
- Maintain product lifecycle management including variations and renewals
- Ensure compliance with regulatory guidelines and documentation standards
- Track submission timelines and ensure timely approvals
- Maintain accurate regulatory records and audit-ready documentation
This role directly contributes to ensuring that pharmaceutical products meet global regulatory standards and reach markets efficiently, supporting healthcare delivery and compliance.
Eligibility / Qualifications
Educational Qualification
- B.Pharm, M.Pharm
- Relevant Courses: Pharmaceutics, Pharmaceutical Chemistry, Pharmaceutical Analysis, Regulatory Affairs, Industrial Pharmacy
Experience Required
- 2 to 3 years in regulatory affairs or related pharma documentation roles
Key Skills
- Knowledge of CTD dossier preparation and submission processes
- Understanding of USFDA, EU, and global regulatory guidelines
- Strong documentation and analytical skills
- Attention to detail and compliance-focused mindset
Location & Salary
- Location: Gujarat (Interview Venue: S.G. Highway, Ahmedabad)
- Salary: As per industry standards (based on experience and expertise)
Application Process
Interested candidates can apply using the details below:
- Email: Kesar@kesarpharma.com
Candidates are advised to mention “Regulatory Affairs Executive Application” in the subject line for faster processing.
Why This Opportunity Stands Out
- Direct exposure to regulatory submissions and dossier preparation
- Opportunity to work in a growing pharma company with expansion plans
- Strong career path in regulatory affairs and compliance
- High demand domain with global career opportunities
FAQs
Who can apply for this Regulatory Affairs role?
Candidates with B.Pharm or M.Pharm and 2–3 years of regulatory experience can apply.
Is USFDA experience required?
Basic knowledge or exposure to USFDA or global regulatory guidelines is preferred.
What is the job location?
The job location is Gujarat, with interviews conducted in Ahmedabad.
How can I apply?
You can send your resume to Kesar@kesarpharma.com.
What skills are important for this role?
Dossier preparation, regulatory documentation, and compliance knowledge are essential.
Additional SEO Titles
- Kesar Pharma Hiring Regulatory Affairs Executive in Gujarat
- Pharma Regulatory Affairs Jobs for BPharm MPharm Candidates
- USFDA Regulatory Jobs in India for Experienced Professionals
Summary Table
| Category | Details |
|---|---|
| Company | Kesar Pharma Pvt. Ltd. |
| Vacancies | Executive – Regulatory Affairs |
| Required Education | B.Pharm, M.Pharm (Pharmaceutics, Pharmaceutical Chemistry, Pharmaceutical Analysis, Regulatory Affairs, Industrial Pharmacy) |
| Experience | 2–3 Years |

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