GeneDrift Hiring Freshers – Trainee Intern Regulatory Affairs | Uttarakhand | 2026

✔ Verified by Medical Jobs India

Trainee - Intern Regulatory Affairs 

GeneDrift

Uttarakhand

Freshers

0–6 Months

Regulatory Affairs

Hybrid

📄 About the Company

GeneDrift is a growing pharmaceutical organization focused on research, development, and regulatory-compliant manufacturing.

The company provides hands-on exposure to regulatory documentation, compliance, and pharma guidelines, making it an excellent learning platform for fresh pharmacy graduates.

📌 Job Overview

GeneDrift is inviting applications for the role of Trainee Intern – Regulatory Affairs at its Uttarakhand facility.

This opportunity is ideal for B.Pharm / M.Pharm freshers or candidates with up to 6 months of experience in R&D or Formulation & Development (F&D) who want to build a strong career in Pharmaceutical Regulatory Affairs.

The role offers a hybrid work model and practical exposure to real-time regulatory operations.

🧪 Job Details – Trainee Intern Regulatory Affairs

Company: GeneDrift

Position: Trainee Intern – Regulatory Affairs

Location: Uttarakhand, India

Work Mode: Hybrid

Experience Required: Freshers / Up to 6 Months (R&D / F&D)

Employment Type: Internship / Trainee Role

🧾 Key Responsibilities

• Assist in preparation and compilation of regulatory dossiers
• Support regulatory submissions and documentation activities
• Maintain regulatory records, logs, and internal databases
• Coordinate with R&D, QA, and other departments for document collection
• Ensure compliance with applicable regulatory guidelines
• Assist in review, formatting, and version control of technical documents
• Support regulatory compliance activities under supervision

🎓 Eligibility Criteria

• B.Pharm / M.Pharm (Mandatory)
• Freshers or candidates with up to 6 months experience
• Basic understanding of pharmaceutical regulatory concepts
• Good written and verbal communication skills
• Strong willingness to learn and grow in regulatory affairs

💼 Why Join GeneDrift?

• Excellent entry-level exposure to Regulatory Affairs
• Hybrid work flexibility
• Learning-oriented and supportive work environment
• Hands-on training in regulatory documentation
• Career growth opportunities in pharma regulatory domain

📌 Note Before You Apply:
We use a 15-second timer to encourage candidates to read the job description carefully before applying. Please ensure you meet the B.Pharm / M.Pharm and fresher / 0–6 months eligibility criteria.

🔎 For More Medical Jobs

👇 Apply Online 👇

⏳ Apply link unlocks in:

15

🚀 Apply Now – GeneDrift Careers

📲 Join for Instant Job Updates

📢 Instant Medical Job Alerts

Join our WhatsApp channel

Join Now

🔎 High Paying Medical Jobs You Might Like:

FDA approved pharma companies, ICH GCP training, Regulatory affairs remote jobs, Drug safety associate openings, India to USA job sponsorship pharma, CRO jobs with visa support