Genedrift is inviting applications for the position of Trainee Intern – Regulatory Affairs (DIN11) in India. This is an excellent entry-level opportunity for B.Pharm and M.Pharm freshers who want to begin a career in pharmaceutical Regulatory Affairs.
The role focuses on regulatory document coordination, submission support, SOP compliance, document management, project tracking, and maintaining internal regulatory records. The provided vacancy lists the position as WFH, with candidates from Uttarakhand preferred.
Publicly available listings matching job code JP8 – Trainee Intern – Regulatory Affairs (DIN11) identify the employer as Genedrift.
Genedrift Regulatory Affairs Job Overview
| Details | Information |
|---|---|
| Company | Genedrift |
| Position | Trainee Intern – Regulatory Affairs |
| Job Code | JP8 |
| Reference No. | RV73 |
| Department | Regulatory Affairs (DIN11) |
| Qualification | B.Pharm / M.Pharm |
| Experience | Fresher |
| Location Codes | Uttarakhand |
| Country | India |
| Preferred Joining | Within 30 days |
| Age Bracket | 18–24 Years |
| Uttarakhand Candidates | Preferred |
About the Regulatory Affairs Trainee Intern Role
The Genedrift Regulatory Affairs Trainee Intern will support internal teams involved in regulatory documentation and submission-related activities.
Freshers joining this role will work under the guidance of the team leader and learn the guidelines, practices, documentation requirements, and internal standards followed during different regulatory activities and submissions.
This makes the opportunity particularly relevant for pharmacy graduates searching for Regulatory Affairs fresher jobs in India, B.Pharm Regulatory Affairs jobs, or M.Pharm Regulatory Affairs internships.
Key Responsibilities
Selected candidates will be responsible for:
- Coordinating with internal teams for the review of documents and regulatory submissions.
- Maintaining compliance with internal and client document-management SOPs.
- Coordinating with different teams to obtain updates regarding projects, activities, and submissions.
- Supporting internal teams in finalizing document translations.
- Following the team leader’s guidance regarding regulatory practices, standards, and submission requirements.
- Ensuring internal records and activities remain properly updated.
- Supporting timely completion of assigned regulatory documentation activities.
- Maintaining quality while working within defined timelines.
Qualification & Eligibility
Candidates applying for the Genedrift Trainee Intern – Regulatory Affairs position should have:
Educational Qualification:
- Bachelor of Pharmacy (B.Pharm), or
- Master of Pharmacy (M.Pharm)
Experience: Freshers can apply.
The matching vacancy information specifically lists B.Pharm and M.Pharm candidates and identifies the opportunity as suitable for freshers.
Skills Required
Genedrift is looking for candidates with:
- Excellent written and verbal communication skills.
- Strong interpersonal abilities.
- Effective presentation skills.
- Good computer skills.
- Comfort working with online office applications.
- Willingness and enthusiasm to learn.
- Flexibility and adaptability.
- Ability to work under pressure.
- Strong focus on timely delivery.
- Ability to produce quality work within tight timelines.
- Good coordination and documentation skills.
Who Should Apply?
This Regulatory Affairs trainee opportunity is particularly suitable for B.Pharm and M.Pharm freshers interested in starting their careers in pharmaceutical regulatory operations.
Candidates interested in regulatory documentation, submission coordination, document management, SOP compliance, and pharmaceutical regulations can consider applying.
Candidates from Uttarakhand are preferred, according to the provided vacancy details.
Work Location & Mode
The provided vacancy specifies the employment type as:
Work Mode: Work From Home (WFH)
Location Codes: DEL IN, DED IN
Country: India
A matching public listing associates the location codes with Delhi and Dehradun and provides a Dehradun address in Uttarakhand.
Candidates should confirm the exact work arrangement and reporting-location requirements with Genedrift during the recruitment process.
Estimated Salary
The employer has not disclosed an official salary in the supplied job description.
Based on comparable entry-level Regulatory Affairs trainee opportunities, an indicative range may be approximately:
₹2.0 – ₹3.0 LPA
This is an estimated range only and not an employer-confirmed salary. A matching third-party listing also reports approximately ₹3 lakh per year for this position.
Benefits of This Opportunity
Candidates joining a Regulatory Affairs trainee position can potentially gain practical exposure to:
- Regulatory document management.
- Pharmaceutical submission processes.
- Internal and client SOP compliance.
- Regulatory project coordination.
- Submission tracking.
- Document review workflows.
- Cross-functional communication.
- Regulatory documentation standards.
- Professional experience in the Regulatory Affairs domain.
These are role-related learning opportunities inferred from the responsibilities; specific employee benefits were not stated in the supplied vacancy.