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Corona Remedies Hiring Regulatory Affairs Executive | B.Pharm & M.Pharm
🏢 Corona Remedies Ltd.
📍 Ahmedabad, Gujarat
📄 Regulatory Affairs Executive
🧑💻 2–5 Years Experience
Corona Remedies Ltd. has announced an exciting opportunity for experienced Regulatory Affairs professionals at its Corporate Office in Ahmedabad. Candidates with B.Pharm or M.Pharm qualifications and 2–5 years of Regulatory Affairs experience are encouraged to apply.
This role offers excellent exposure to global regulatory submissions, CTD/eCTD dossier preparation, lifecycle management, and product registrations for regulated and semi-regulated markets.
📋 Job Overview
| Particulars | Details |
|---|---|
| Company Name | Corona Remedies Ltd. |
| Position | Regulatory Affairs Executive |
| Department | Regulatory Affairs |
| Location | Ahmedabad, Gujarat |
| Qualification | B.Pharm / M.Pharm |
| Experience | 2–5 Years |
| Employment Type | Full-Time |
| Industry | Pharmaceutical |
| Application Mode | Online |
💰 Expected Salary Range: Based on Experience & Skills
🏢 About Corona Remedies
Corona Remedies is one of India's rapidly growing pharmaceutical companies with a strong presence across multiple therapeutic segments. The company is known for innovation, quality products, and a strong regulatory compliance framework.
Working with Corona Remedies provides professionals an opportunity to gain exposure to global regulatory markets, dossier submissions, and international registration processes.
📌 Key Responsibilities
- Preparation, review, and submission of CTD/eCTD regulatory dossiers.
- Handle documentation for product registration in regulated and semi-regulated markets.
- Coordinate with regulatory authorities regarding submissions, approvals, and deficiency responses.
- Manage regulatory documentation and ensure compliance with international requirements.
- Track regulatory updates and maintain regulatory intelligence databases.
- Support product registration activities across multiple global markets.
- Ensure timely submission of regulatory filings and lifecycle management documents.
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🎓 Eligibility Criteria
Educational Qualification:
- Bachelor of Pharmacy (B.Pharm)
- Master of Pharmacy (M.Pharm)
Experience Required:
- Minimum 2 Years Experience
- Maximum 5 Years Experience
- Experience in CTD/eCTD dossier preparation preferred
- Regulatory submissions experience preferred
💡 Desired Skills
- Strong knowledge of CTD/eCTD dossier compilation.
- Regulatory submissions and lifecycle management.
- Documentation and compliance management.
- Regulatory intelligence and market registration expertise.
- Good communication and coordination skills.
- Understanding of global pharmaceutical regulations.
- Attention to detail and regulatory documentation accuracy.
- Ability to manage multiple regulatory projects simultaneously.
🎁 Why Join Corona Remedies?
- Work with an experienced Regulatory Affairs team.
- Exposure to regulated and semi-regulated international markets.
- Learning and professional growth opportunities.
- Collaborative and innovation-driven culture.
- Opportunity to contribute to a rapidly expanding pharmaceutical organization.
- Hands-on experience with global regulatory submissions and registrations.
📍 Job Location
Corona Remedies Ltd. – Corporate Office
Corona House, Block C, Mondeal Business Park,
S.G. Highway, Apex Street, Near Gurudwara,
Thaltej, Ahmedabad, Gujarat – 380059
Corona House, Block C, Mondeal Business Park,
S.G. Highway, Apex Street, Near Gurudwara,
Thaltej, Ahmedabad, Gujarat – 380059
📄 Resume & Interview Preparation Tips
- Highlight CTD/eCTD dossier preparation experience.
- Mention regulatory submissions, product registration, and lifecycle management projects.
- Showcase experience with regulated and semi-regulated markets.
- Add skills related to documentation, compliance, and regulatory intelligence.
- Keep your resume ATS-friendly and professionally formatted.
🧠 Practice & Learning Resources
👉 Pharmacovigilance Quiz
👉 Aptitude & Logical Reasoning Quiz
👉 Explore More Healthcare Quizzes
📝 How to Apply
- Read the complete job description carefully.
- Prepare an updated ATS-friendly resume.
- Highlight relevant Regulatory Affairs experience and achievements.
- Complete the countdown timer to unlock the application button.
- Apply only if your profile matches the job requirements.
🚀 Job Application Link
📌 Important Note Before You Apply:
Please make sure to read the complete job description, eligibility criteria, and skills required carefully before submitting your application. Aligning your resume with the specific role requirements significantly increases your chances of getting shortlisted by recruiters.
Please make sure to read the complete job description, eligibility criteria, and skills required carefully before submitting your application. Aligning your resume with the specific role requirements significantly increases your chances of getting shortlisted by recruiters.
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