The pharmaceutical and healthcare sector in India continues to create exciting career opportunities for skilled professionals in regulatory affairs. If you have experience in DMF documentation, AMV activities, and CTD submissions, this latest opening in Ahmedabad could be the next step in your pharma career journey.
A leading pharma recruitment consultancy is currently hiring for the position of Regulatory Affairs Executive – DMF & AMV at Shantipura, Ahmedabad. Candidates with 1–2 years of experience in regulatory affairs and strong knowledge of documentation, product registration, and international regulatory markets are encouraged to apply.
📍 Job Details
| Particulars | Details |
|---|---|
| Position | Regulatory Affairs Executive – DMF & AMV |
| Location | Ahmedabad, Gujarat |
| Openings | 3 |
| Industry | Pharmaceutical / Healthcare |
| Salary | ₹25,000 – ₹30,000 per month |
| Experience | 1–2 Years |
| Qualification | B.Pharm, M.Pharm, B.Sc, M.Sc |
This opportunity is ideal for professionals looking to build a successful career in international regulatory affairs and pharmaceutical documentation management.
🧪 Key Responsibilities
The selected candidates will be responsible for managing multiple regulatory documentation and compliance activities. The role demands technical expertise along with strong coordination and communication skills.
Main Responsibilities Include:
- Preparation of M3, QOS, QIS, M5, DMF, and PDR documentation
- Managing stability data and regulatory submissions
- Working on CTD and ACTD dossier formats
- Product registration for ROW, LATAM, SEA, Africa, and Pacific countries
- Supporting lifecycle management activities for pharmaceutical products
- Coordinating with clients and regulatory authorities
- Maintaining accurate documentation and compliance records
Candidates with prior exposure to international regulatory markets will have an added advantage.
✅ Required Skills
To succeed in this role, applicants should possess the following skills and expertise:
📌 Regulatory Documentation Knowledge
Experience in preparing and reviewing:
- Drug Master Files (DMF)
- QOS and QIS documents
- PDR reports
- Stability documentation
- CTD / ACTD dossiers
📌 Pharmacovigilance & AMV Understanding
Candidates should have working knowledge of:
- PVP activities
- PVR documentation
- AMV processes
📌 International Regulatory Exposure
Understanding of pharmaceutical product registration requirements in:
- ROW markets
- LATAM countries
- South East Asia
- African regions
- Pacific countries
📌 Technical & Soft Skills
- Strong MS Office knowledge (Word, Excel, PowerPoint)
- Excellent communication and coordination abilities
- Attention to detail and analytical thinking
- Ability to manage multiple projects effectively
🎓 Educational Qualification
Applicants with the following educational backgrounds can apply:
- Bachelor of Pharmacy (B.Pharm)
- Master of Pharmacy (M.Pharm)
- Bachelor of Science (B.Sc)
- Master of Science (M.Sc)
Candidates with pharmaceutical regulatory affairs experience will be preferred.
🌍 Why Choose a Career in Regulatory Affairs?
Regulatory affairs is one of the fastest-growing career domains in the pharmaceutical industry. Professionals working in this field ensure that medicines and healthcare products comply with international quality and safety standards.
Major Benefits of a Career in Regulatory Affairs
- High demand in pharma companies worldwide 🌎
- Opportunities in global product registration
- Excellent long-term career growth 📈
- Exposure to international compliance systems
- Strong learning opportunities in documentation and quality processes
With expanding pharmaceutical exports from India, skilled regulatory professionals are becoming increasingly valuable in the global healthcare industry.
🏢 About the Recruitment Consultancy
The hiring is being managed by Medi Pharma Konnect, a recruitment consultancy specializing in healthcare and pharmaceutical hiring solutions. The consultancy focuses on connecting pharma companies with qualified professionals across multiple domains.
Important Note ⚠️
The recruiter has clearly stated that no fees are charged from job applicants during the recruitment process. Candidates are advised to stay alert and avoid fraudulent agencies demanding money for interviews or placements.
📩 How to Apply
Interested candidates can directly contact the recruiter using the details below:
Contact Person: Swapna Niel
Email: medipharma.cv2@gmail.com
Phone / WhatsApp: 6353266231
Applicants should send their updated resume along with relevant regulatory affairs experience details.
💡 Tips Before Applying
Before submitting your application, make sure your resume highlights:
- Regulatory affairs experience summary
- Knowledge of CTD/ACTD submissions
- International market exposure
- Documentation handling skills
- Software and MS Office proficiency
A professional and updated resume can significantly improve your chances of shortlisting.
🔗 Related Pharma & Regulatory Jobs
You may also like these opportunities:
- Wipro Hiring Medical Writers in Pune
- Clinical Research Associate (CRA) Work From Home Jobs
- Clinical Document Management Specialist I at Ora
- Zydus Lifesciences Apprentice Business Strategy Jobs
- Product Management Trainee Jobs for B.Pharm Freshers
📌 Final Thoughts
This Regulatory Affairs Executive job in Ahmedabad is an excellent opportunity for pharma professionals aiming to grow in global regulatory operations. Candidates with expertise in DMF preparation, AMV activities, and international dossier submissions should apply as early as possible.
As the pharmaceutical industry continues expanding globally, regulatory affairs professionals remain at the center of product approvals, compliance, and international business growth. If you are passionate about pharmaceutical regulations and documentation management, this role could be an important step toward long-term career success.
