RegWorld Infocore Hiring Regulatory Affairs Trainee | B.Pharm & M.Pharm Freshers Eligible | 4-Month Internship with PPO Opportunity
RegWorld Infocore Hiring Regulatory Affairs Trainee | B.Pharm & M.Pharm Freshers Eligible
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(RegWorld Infocore Hiring Regulatory Affairs Trainee) |
Introduction
Regulatory Affairs is one of the fastest-growing career domains in the pharmaceutical industry, offering opportunities to work on drug approvals, regulatory submissions, compliance management, and global pharmaceutical documentation. For pharmacy graduates looking to enter this field, RegWorld Infocore Pvt. Ltd. has announced an excellent opportunity for freshers through its Regulatory Affairs Trainee program.
This opening is suitable for B.Pharm and M.Pharm candidates who want practical exposure to pharmaceutical regulations, documentation management, regulatory compliance, and submission processes. The company is offering a structured 4-month internship program along with a potential Pre-Placement Offer (PPO) based on performance.
Candidates interested in building a long-term career in Regulatory Affairs can consider this opportunity as a strong entry point into the pharmaceutical regulatory sector.
About RegWorld Infocore Pvt. Ltd.
RegWorld Infocore Pvt. Ltd. is a pharmaceutical regulatory consulting and technology-driven services company that supports global pharmaceutical organizations in regulatory compliance, regulatory operations, submissions management, labeling, publishing, and life sciences consulting.
The company works with pharmaceutical, biotechnology, and healthcare organizations to help them navigate complex global regulatory requirements and maintain compliance across international markets.
Company Details
- Company Name: RegWorld Infocore Pvt. Ltd.
- Industry: Pharmaceutical Regulatory Affairs & Life Sciences Consulting
- Headquarters: India
- Business Area: Regulatory Affairs, Compliance, Publishing, Labeling & Regulatory Operations
- Employee Strength: Growing Global Team
- Clients: Pharmaceutical, Biotechnology & Healthcare Companies
RegWorld is known for providing regulatory support services that help pharmaceutical companies accelerate product approvals and maintain regulatory compliance across various markets.
Job Overview Summary
The Regulatory Affairs Trainee position is designed for fresh pharmacy graduates who wish to gain practical industry exposure in pharmaceutical regulatory affairs.
Selected candidates will undergo a structured internship program where they will learn about regulatory documentation, submission processes, pharmaceutical compliance requirements, and regulatory operations. Candidates demonstrating strong performance during the internship may receive a Pre-Placement Offer (PPO) for future employment opportunities.
This role offers valuable exposure to the documentation-driven side of the pharmaceutical industry and can help candidates build a foundation for future careers in Regulatory Affairs, Regulatory Operations, Dossier Preparation, and Compliance Management.
Vacancy Details
| Particular | Details |
|---|---|
| Company | RegWorld Infocore Pvt. Ltd. |
| Position | Regulatory Affairs Trainee |
| Department | Regulatory Affairs |
| Qualification | B.Pharm / M.Pharm |
| Preferred Specialization | Pharmaceutics, Regulatory Affairs, Chemistry |
| Experience | 0–6 Months |
| Freshers Eligible | Yes |
| Internship Duration | 4 Months |
| PPO Opportunity | Yes (Performance Based) |
| Application Mode | |
| hr@regworldinfocore.com |
Job Role Explanation
The Regulatory Affairs department plays a critical role in ensuring pharmaceutical products meet regulatory requirements before reaching the market.
As a Regulatory Affairs Trainee, candidates will gain exposure to various pharmaceutical regulatory functions including:
Regulatory Documentation
Preparing and organizing technical and regulatory documents required for compliance activities.
Regulatory Compliance
Learning how pharmaceutical companies comply with national and international regulatory requirements.
Submission Support
Assisting teams involved in preparing regulatory submissions and maintaining supporting documentation.
Data Management
Managing regulatory records while maintaining accuracy and document integrity.
Learning Global Guidelines
Understanding regulatory expectations associated with pharmaceutical product approvals and lifecycle management.
This role is ideal for candidates interested in regulatory science, pharmaceutical compliance, and global drug registration activities.
Key Responsibilities
The selected candidates may support activities such as:
- Understanding pharmaceutical regulatory requirements.
- Assisting with regulatory documentation activities.
- Supporting preparation of regulatory submissions.
- Reviewing and organizing technical documents.
- Maintaining documentation accuracy.
- Learning pharmaceutical compliance processes.
- Supporting regulatory operations teams.
- Coordinating documentation-related activities.
- Managing records according to company procedures.
- Assisting senior Regulatory Affairs professionals.
Actual responsibilities may vary based on assigned projects and business requirements.
Eligibility Criteria
Candidates should meet the following requirements:
Educational Qualification
- B.Pharm
- M.Pharm
Preferred M.Pharm Specializations
- Pharmaceutics
- Regulatory Affairs
- Chemistry
Experience
- 0–6 Months
- Freshers can apply
Additional Preference
Candidates with academic exposure to:
- Regulatory Affairs
- Pharmaceutical Documentation
- Drug Registration
- Regulatory Guidelines
- Compliance Management
may have an advantage during the selection process.
Skills Required
Successful candidates should ideally possess:
Technical Skills
- Basic Regulatory Affairs knowledge
- Documentation skills
- Pharmaceutical compliance understanding
- Technical document review ability
- Regulatory submission awareness
Soft Skills
- Strong communication skills
- Attention to detail
- Analytical thinking
- Time management
- Learning attitude
- Team collaboration
These skills are highly valued in pharmaceutical regulatory careers and can significantly improve long-term career growth.
Estimated Salary / Stipend
The company has not officially disclosed internship stipend or salary details.
Based on similar Regulatory Affairs trainee opportunities in India:
Estimated Internship Stipend: ₹8,000 – ₹20,000 per month
Estimated Entry-Level Salary After PPO: ₹2.5 LPA – ₹4.5 LPA
Actual compensation may vary depending on company policy, location, qualifications, and candidate performance.
Interview Details
This recruitment process is not a walk-in drive.
Selection Process
- Resume Submission
- Application Screening
- Shortlisting
- HR Interview
- Technical Discussion
- Final Selection
- Internship Joining
Only shortlisted candidates are expected to receive communication from the company regarding further interview rounds.
Required Documents
Candidates should prepare:
- Updated Resume/CV
- B.Pharm/M.Pharm Mark Sheets
- Degree Certificate
- Internship Certificates (if available)
- Academic Project Details
- Government ID Proof
- Passport Size Photograph
- Regulatory Affairs Certifications (if available)
Having a well-prepared professional resume can improve selection chances.
How to Apply
Eligible candidates can apply by sending their updated resume to:
Email: hr@regworldinfocore.com
Suggested Email Subject
Application for Regulatory Affairs Trainee – Pharma Duniya Candidate
Candidates should ensure that their resume clearly highlights:
- Educational qualifications
- Regulatory Affairs knowledge
- Academic projects
- Documentation skills
- Internships
- Certifications
Frequently Asked Questions (FAQs)
Q1. Are freshers eligible for this Regulatory Affairs Trainee role?
Yes. Fresh B.Pharm and M.Pharm graduates are eligible to apply.
Q2. What is the internship duration?
The internship duration is 4 months.
Q3. Is there a PPO opportunity?
Yes. Candidates may receive a Pre-Placement Offer based on performance during the internship.
Q4. Which M.Pharm specialization is preferred?
Pharmaceutics, Regulatory Affairs, and Chemistry specializations may receive preference.
Q5. Is prior Regulatory Affairs experience mandatory?
No. Candidates with 0–6 months of experience can apply.
Q6. What skills are important for selection?
Documentation skills, communication skills, attention to detail, and basic Regulatory Affairs knowledge are important.
Q7. Is this opportunity suitable for long-term career growth?
Yes. Regulatory Affairs is one of the most stable and growing career paths in the pharmaceutical industry.
Final Conclusion
The RegWorld Infocore Regulatory Affairs Trainee opportunity provides an excellent starting point for B.Pharm and M.Pharm graduates interested in building careers in pharmaceutical regulatory affairs. The structured internship program offers practical exposure to regulatory documentation, compliance activities, submission support, and pharmaceutical regulations.
For freshers looking to enter a specialized pharmaceutical domain with strong long-term growth potential, this internship can serve as a valuable stepping stone toward careers in Regulatory Affairs, Regulatory Operations, Drug Registration, Compliance Management, and Global Pharmaceutical Documentation.
Candidates interested in regulatory science and pharmaceutical compliance should consider applying early and ensure their resumes highlight relevant academic knowledge and documentation skills.
Disclaimer
Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
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