Genedrift Hiring Regulatory Affairs Trainee

B.Pharm/M.Pharm Regulatory Affairs Trainee – Uttarakhand

Genedrift hiring Regulatory Affairs Trainee Intern in Uttarakhand. B.Pharm/M.Pharm freshers or 6-month experience. Hybrid role.

Genedrift is hiring a Trainee Intern for its Regulatory Affairs team. This role suits B.Pharm and M.Pharm candidates who want to begin a career in regulatory documentation, compliance and global submission processes. Freshers and candidates with up to six months of experience in R&D or F&D can apply. The position follows a hybrid work model and offers exposure to regulatory workflows used across the pharmaceutical and life sciences sectors.

Company Overview

Genedrift is a growing life sciences organisation focused on innovation in product development, regulatory solutions and scientific services. The company supports pharmaceutical and biotech partners with data-driven regulatory documentation, high-quality research inputs and compliance support. By combining scientific expertise with a technology-driven workflow, Genedrift delivers reliable solutions across development, filing and lifecycle management.

Its culture encourages continuous learning, professional development and hands-on involvement in real regulatory submissions, making it an excellent starting point for early-career professionals.

Job Role & Responsibilities

Trainee Intern – Regulatory Affairs

• Assist in preparing, compiling and reviewing regulatory documents.
• Support regulatory submissions for domestic and international markets.
• Coordinate with R&D and F&D teams to collect required technical data.
• Maintain document accuracy, version control and compliance with guidelines.
• Conduct literature searches and gather updated regulatory references.
• Track submission timelines and maintain internal records.
• Learn SOPs, dossier structures and global regulatory standards.
• Communicate effectively with cross-functional teams and support project needs.

This role provides foundational exposure to regulatory compliance, dossier writing and structured data management—key skills for long-term growth in Regulatory Affairs.

Eligibility / Qualifications

• Required Qualification: B.Pharm or M.Pharm.
• Experience: Freshers or candidates with up to 6 months of experience in R&D or F&D.
• Strong communication and documentation skills.
• Basic understanding of pharmaceutical development, formulation and regulatory principles.

Relevant courses (comma-separated): B.Pharm, M.Pharm (Regulatory Affairs), M.Pharm (Pharmaceutics), Diploma in Drug Regulatory Affairs, Certificate Course in CTD/eCTD, Quality Assurance certifications, ICH Guidelines training modules.

Location & Work Mode

• Location: Uttarakhand.
• Work Mode: Hybrid (mix of on-site and remote work).
• Salary: Not disclosed.

Application Process

Apply directly through the official opening link:
https://genedrift.com/openings

Submit your latest resume along with basic contact details. Shortlisted candidates will be contacted by the HR team.

FAQs

Are freshers eligible for this role?

Yes. Fresh B.Pharm and M.Pharm graduates can apply.

Is prior regulatory experience required?

No. Even 0–6 months of exposure in R&D or F&D is acceptable.

What skills are important for Regulatory Affairs?

Strong documentation ability, understanding of guidelines and good communication.

Is this a full-time position?

Yes, with a hybrid working model.

How do I apply?

Apply through the company’s official portal at genedrift.com/openings.

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Summary Table

Category	Details
Company	Genedrift
Vacancies	Trainee Intern – Regulatory Affairs
Required Education	B.Pharm, M.Pharm (Regulatory Affairs, Pharmaceutics, Drug Regulatory certifications)
Experience	Freshers or up to 6 months (R&D/F&D)