Elevatia Solutions Hiring Regulatory Affairs Executive in New Delhi
If you’re planning to start or grow your career in the pharmaceutical industry, this latest opportunity from Elevatia Solutions could be worth checking out. The company is currently hiring for the position of Regulatory Affairs Executive at its New Delhi office.
This role is open to both freshers and candidates with up to 2 years of experience, making it a great option for those who want to build a career in regulatory affairs, clinical research, and pharmaceutical compliance. With increasing demand for professionals in regulatory operations, opportunities like this can help you gain valuable industry experience early in your career.
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🏢 About Elevatia Solutions
Elevatia Solutions is a growing organization involved in pharmaceutical and healthcare regulatory support services. The company works closely with clients to manage compliance requirements and ensure that products meet regulatory standards.
Their work mainly focuses on:
- Regulatory submissions and approvals
- Product registrations and licensing
- Compliance management
- Documentation and technical support
For candidates interested in regulatory affairs, working in such an environment can provide practical exposure to real industry processes.
📋 Role Overview
Here are the key details of the job:
- Position: Regulatory Affairs Executive
- Company: Elevatia Solutions
- Location: Sarojini Nagar, New Delhi
- Qualification: B.Pharm, M.Pharm, or related Life Sciences field
- Experience: 0–2 years
- Department: Regulatory Affairs
This role is ideal for candidates who want to gain hands-on experience in regulatory documentation, submissions, and compliance management.
💼 Key Responsibilities
As a Regulatory Affairs Executive, your responsibilities will focus on documentation, submissions, and ensuring compliance with industry standards.
✅ Main Responsibilities Include:
- Preparing, reviewing, and submitting regulatory applications, dossiers, and technical documents
- Maintaining compliance with regulatory guidelines, SOPs, and laws
- Supporting product registrations, approvals, and licensing processes
- Coordinating follow-ups with regulatory authorities
- Assisting in audits, inspections, and safety reporting activities
- Handling documentation tasks and responding to regulatory queries
- Supporting compliance-related operations within the organization
This role will give you a clear understanding of how pharmaceutical products move through regulatory approval processes.
🎓 Eligibility Criteria
Before applying, make sure you meet the basic requirements.
✅ Educational Qualification:
- B.Pharm or M.Pharm
- Or any related Life Sciences degree
✅ Experience:
- Freshers are eligible
- Candidates with up to 2 years of experience can apply
This flexibility makes the role suitable for both beginners and those with some industry exposure.
🧠 Skills Required
You don’t need advanced expertise, but having the right foundational skills can help you succeed in this role.
💡 Important Skills:
- Basic understanding of regulatory affairs and documentation
- Knowledge of CTD/eCTD submissions (preferred)
- Good communication skills
- Coordination and teamwork abilities
- Strong attention to detail
- Ability to manage documentation and compliance processes
Even if you’re a fresher, showing interest and basic knowledge in regulatory processes can improve your chances.
🌱 Why This Job is a Good Opportunity
For freshers and early-career professionals, finding the right starting point is important. This role offers multiple benefits.
🔹 1. Entry into Regulatory Affairs
Regulatory Affairs is an essential function in the pharmaceutical industry. This role provides a direct entry into this field.
🔹 2. Practical Learning Experience
You’ll gain hands-on experience in documentation, compliance, and submission processes.
🔹 3. Career Flexibility
After gaining experience, you can move into roles such as:
- Regulatory Affairs Specialist
- Clinical Research Associate (CRA)
- Pharmacovigilance roles
- Quality Assurance and Compliance
🔹 4. Skill Development
You will develop key skills such as:
- Regulatory documentation
- Compliance management
- Communication with authorities
- Audit and inspection support
💰 Salary and Benefits
The expected salary for this role is:
💵 ₹2.5 LPA to ₹4.5 LPA
The final salary may vary depending on your qualifications, skills, and interview performance.
🎁 Additional Benefits:
- Exposure to pharmaceutical regulatory operations
- Opportunities for professional growth
- Industry-standard work environment
- Learning and development in compliance and submissions
For freshers, gaining this type of exposure is often more valuable than just the salary.
📍 Job Location
📌 Sarojini Nagar, New Delhi
New Delhi is an important center for pharmaceutical regulatory activities, making it a good place to build your career in this domain.
💡 Who Should Apply?
This role is best suited for:
- Pharmacy and Life Science graduates
- Freshers interested in regulatory affairs
- Candidates with basic knowledge of pharmaceutical documentation
- Individuals who are detail-oriented and organized
If you’re looking for a job that involves structured work, documentation, and compliance, this could be a good fit.
📝 How to Apply
Interested candidates can apply by sending their updated resume via email.
📧 Email ID: Reachus@ElevatiaSolutions.com
✅ Important Tip:
Mention “Application for Regulatory Affairs Executive” in the subject line while sending your email. This helps your application get noticed by the recruitment team.
🔗 Explore Similar Opportunities
- Explore more opportunity in Regulatory affairs
- Novotech Hiring Document Management Associate
- Labcorp Hiring Clinical Project Coordinator
- Syneos health hiring for CRA-future roles
- Thermo Fisher Hiring Coding Specialist
- Glenmark hiring for PV Trainee
📚 Career Guide
- Best career option after B.pharm
- Guide on how to create resume for fresher
- Common interview mistake and how to avoid this
