Apply for Regulatory Affairs Trainee at Aculife Healthcare Ahmedabad. Check eligibility, salary, experience, and email application process details today.
Introduction
If you are an M.Pharm graduate looking to enter the pharmaceutical regulatory field, the Regulatory Affairs Trainee at Aculife Healthcare Pvt. Ltd. is a strong career-starting opportunity. This role offers hands-on exposure to global regulatory markets such as LATAM and Europe. Ideal for freshers and early professionals, this position can help you build a solid foundation in regulatory documentation and international submissions.
Job Overview
| Details | Information |
|---|---|
| Job Title | Trainee Officer – Regulatory Affairs |
| Company Name | Aculife Healthcare Pvt. Ltd. |
| Location | Ahmedabad, Gujarat |
| Employment Type | Full-Time |
| Department | Regulatory Affairs |
| Experience Required | 6 Months – 1 Year |
| Education | M.Pharm (RA / Pharmaceutics Preferred) |
| Salary | ₹2.5 LPA – ₹4.5 LPA (Expected) |
Company Overview
Aculife Healthcare Pvt. Ltd., a part of the reputed Nirma Group, is a leading pharmaceutical company specializing in sterile formulations and healthcare products. With a strong global presence, Aculife exports its products to numerous international markets, including Europe, Latin America, and emerging regions. The company is known for its high-quality standards, regulatory compliance, and innovation-driven approach in the pharmaceutical sector.
Job Location & Employment Type
- Location: Ahmedabad, Gujarat
- Employment Type: Full-Time
- Work Mode: Office-based
This role is based at the company’s corporate office, offering direct exposure to regulatory operations.
Open Positions / Department Details
- Department: Regulatory Affairs (RA)
- Role Level: Trainee / Entry-Level
- Focus Areas:
- Global dossier preparation
- EU & LATAM submissions
- Regulatory documentation and lifecycle management
Key Roles & Responsibilities
- Prepare and review registration dossiers as per country-specific guidelines
- Assist in regulatory submissions for LATAM markets (Brazil, Mexico)
- Support EU regulatory documentation and compliance processes
- Review key technical documents, including:
- Drug Master File (DMF)
- Product Development Reports
- Batch Manufacturing Records (BMR)
- Batch Packaging Records (BPR)
- Analytical validation and stability reports
- Draft and respond to regulatory queries and deficiencies
- Assist in managing pending dossiers and submission timelines
- Support post-approval changes and product variations
- Coordinate with global regulatory teams, distributors, and agents
- Review packaging materials and artworks for compliance
- Maintain and update regulatory databases and records
Eligibility Criteria
Education
- M.Pharm (mandatory)
- Specialization in Regulatory Affairs or Pharmaceutics preferred
Experience
- 6 months to 1 year of Regulatory Affairs experience
- Internship or apprenticeship experience is acceptable
Skills Required
- Basic knowledge of CTD/eCTD format
- Understanding of DMF and dossier compilation
- Familiarity with EU and LATAM regulatory guidelines (preferred)
- Strong documentation and attention to detail
- Good communication and coordination skills
- Ability to manage multiple regulatory tasks efficiently
Salary & Benefits
- Salary: ₹2.5 LPA – ₹4.5 LPA (Expected for trainee roles)
- Additional Benefits:
- Exposure to international regulatory markets
- Learning opportunities in global submissions
- Career growth in Regulatory Affairs
- Experience with a reputed pharma organization
Selection Process
The recruitment process may include:
- Resume screening
- HR discussion
- Technical interview (Regulatory Affairs basics)
- Final selection
How to Apply
Interested candidates can apply via email:
Application Tip:
Mention “Application for RA Trainee Officer – Ahmedabad” in the email subject line to increase your chances of shortlisting.
Important Dates
- Job Posted On: April 3, 2026
- Application Deadline: Not specified (Apply as early as possible)
Why Apply for This Job?
- Ideal entry-level opportunity for M.Pharm graduates
- Hands-on experience with global regulatory submissions
- Exposure to EU and LATAM pharmaceutical markets
- Strong foundation in dossier preparation and lifecycle management
- Opportunity to work under a reputed group like Nirma
- Enhances long-term career prospects in Regulatory Affairs
FAQs
1. Who can apply for this job?
M.Pharm graduates with 6 months to 1 year of Regulatory Affairs experience can apply.
2. What is the salary for this role?
The expected salary ranges between ₹2.5 LPA to ₹4.5 LPA.
3. Is this job suitable for freshers?
Yes, candidates with internship or apprenticeship experience in RA are eligible.
4. How can I apply for this position?
You can apply by sending your resume via email to the provided email ID.
5. What skills are required for this job?
Knowledge of CTD/eCTD, dossier preparation, and regulatory guidelines is important.
Conclusion
The Regulatory Affairs Trainee at Aculife Healthcare Pvt. Ltd. is an excellent opportunity for aspiring regulatory professionals to gain international exposure and practical experience. With structured learning and real-world regulatory tasks, this role can serve as a strong launchpad for your career in the pharmaceutical industry. Apply now to secure your place in this growing domain.
Disclaimer
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