Cura Healthcare is hiring for the position of Regulatory Affairs Executive at its Vadodara, Gujarat location. Candidates with 3 to 5 years of experience in pharmaceutical regulatory affairs, holding a B.Pharm, M.Pharm, or Life Sciences degree, are invited to apply. Immediate joiners are preferred for this position.
The role involves preparing, reviewing, and submitting regulatory dossiers, coordinating with regulatory authorities for approvals, managing compliance with global guidelines, and supporting product life-cycle management across international markets.
About CURA Healthcare
Established in 2025 and headquartered in Vadodara, Gujarat, CURA Healthcare operates as a partnership firm providing expert pharmaceutical consulting services, guiding companies from drug discovery to market launch.
The organization offers strategic solutions in regulatory affairs, clinical development, and commercialization, ensuring optimal outcomes and maximizing product value. CURA Healthcare is committed to delivering exceptional service and helping clients bring life-changing therapies to patients worldwide.
For more information, visit the official website: https://www.curagroup.in
Regulatory Affairs Executive Vacancy Details
Cura Healthcare is looking for a skilled and detail-oriented Regulatory Affairs professional to join its expanding regulatory team in Vadodara.
Position: Regulatory Affairs Executive
Location: Vadodara, Gujarat
Experience Required: 3–5 Years
Qualification: B.Pharm / M.Pharm / Life Sciences
Preference: Immediate Joiners
Eligibility Criteria and Qualifications
Candidates interested in this opportunity should meet the following requirements:
Educational Qualification: Bachelor’s or Master’s degree in Pharmacy (B.Pharm / M.Pharm) or Life Sciences.
Professional Experience: 3 to 5 years of hands-on experience in pharmaceutical regulatory affairs.
Technical Knowledge: Strong understanding of FDA, EMA, CDSCO, and ICH guidelines.
Core Skills: Expertise in CTD/eCTD dossier preparation, strong documentation, communication, and project management abilities.
Key Responsibilities of the Regulatory Affairs Executive
The role encompasses comprehensive regulatory compliance and dossier management tasks, including:
- Preparing, reviewing, and submitting regulatory dossiers (CTD/eCTD) for product registrations, renewals, and variations.
- Coordinating with regulatory authorities for approvals and query resolution.
- Ensuring compliance with applicable national and international regulatory guidelines.
- Reviewing product labeling, packaging, and promotional materials.
- Collaborating with R&D, QA, Manufacturing, and Marketing teams.
- Monitoring submission timelines, approval status, and regulatory queries.
- Preparing deficiency responses and maintaining regulatory documentation.
- Supporting regulatory audits and inspections.
How to Apply for This Vacancy
Interested candidates can apply by submitting their updated resume through the official application channel:
Application Email: hr@curagroup.in
Contact Number: 9664797177
Ensure your CV clearly details your background in CTD/eCTD dossier preparation and regulatory submissions before sending your application.
Candidates are advised to verify recruitment communications through official channels before sharing sensitive personal or professional information. Avoid engaging with unverified intermediaries or unauthorized entities.
Frequently Asked Questions
1. What qualification is required for this vacancy?
Candidates should hold a B.Pharm, M.Pharm, or Life Sciences degree.
2. How much experience is required for the Regulatory Affairs Executive role?
The requirement is 3 to 5 years of professional experience in pharmaceutical regulatory affairs.
3. Where is the job located?
The position is located in Vadodara, Gujarat.
4. How can candidates apply?
Candidates can email their updated resume to hr@curagroup.in or contact 9664797177.