Genedrift is inviting applications for the position of Trainee Intern – Regulatory Affairs in Uttarakhand, India. This opportunity is ideal for B.Pharm and M.Pharm freshers or candidates with up to 6 months of experience looking to start a career in pharmaceutical regulatory affairs.
Candidates with strong communication skills, attention to detail, and interest in global compliance documentation can apply for this pharma internship opportunity. The role offers hands-on exposure to regulatory documentation, compliance management, and coordination with internal teams.
Job Overview
| Details | Information |
|---|---|
| Position | Trainee Intern – Regulatory Affairs |
| Company | Genedrift |
| Location | Uttarakhand, India |
| Experience | Freshers / 3–6 Months |
| Qualification | B.Pharm / M.Pharm |
| Industry | Pharmaceutical Regulatory Affairs |
| Employment Type | Internship / Trainee |
Key Responsibilities
Candidates selected for the Regulatory Affairs Trainee Intern role will be responsible for:
- Coordinating with internal departments for document reviews and submissions
- Supporting project updates and regulatory documentation processes
- Ensuring compliance with internal SOPs and client documentation standards
- Managing document translations and maintaining internal records
- Following team leader instructions to achieve project timelines and quality standards
- Assisting in regulatory operations and compliance activities
Eligibility Criteria
Applicants applying for the Genedrift Regulatory Affairs Internship 2026 should meet the following criteria:
- Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm)
- Freshers are eligible to apply
- Candidates with up to 6 months of experience may also apply
- Excellent written and verbal communication skills
- Strong attention to detail
- Ability to work collaboratively in team environments
Why Join Genedrift?
Working with Genedrift offers fresh pharmacy graduates an opportunity to gain industry exposure in pharmaceutical regulatory affairs and compliance.
Benefits of This Opportunity
- Entry-level pharma regulatory affairs experience
- Exposure to global compliance documentation
- Collaborative work environment
- Skill development in SOP compliance and document management
- Career growth opportunities in pharmaceutical regulatory affairs
How to Apply
note : self introduction vidio is mandatory
