Genedrift
In today’s dynamic pharmaceutical landscape, regulatory compliance is more critical than ever. At Genedrift, we are committed to driving quality, innovation, and excellence in every stage of our product lifecycle — and that starts with building a strong Regulatory Affairs team.
Whether you’re an experienced professional with a background in CDSCO regulations, injectables, and biological products, or a recent graduate looking to make your mark, Genedrift invites you to be part of a team that’s shaping the future of healthcare compliance.
🚀 Opportunity Spotlight: Trainee Intern – Regulatory Affairs (DIN11)
This entry-level opportunity is ideal for candidates holding a B.Pharm or M.Pharm degree, who are eager to develop their skills in a real-world regulatory environment. As a Trainee Intern in Regulatory Affairs, you’ll play a vital role in the submission and documentation processes that ensure our products meet national and international regulatory standards.
🔍 What You’ll Be Doing:
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Collaborating with internal teams to review and coordinate documentation for regulatory submissions.
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Assisting in maintaining compliance with document management SOPs, both internal and client-based.
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Supporting the preparation and finalization of document translations.
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Gaining hands-on experience with regulatory procedures under the mentorship of seasoned professionals.
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Keeping internal records and project documentation up to date and aligned with submission timelines.
💡 What We’re Looking For:
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Educational Background: B.Pharm or M.Pharm
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Skills:
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Strong communication skills, both verbal and written
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Effective presentation abilities
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Proficiency with computer systems and online office applications
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A high degree of adaptability, flexibility, and attention to detail
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Eagerness to learn and grow in a fast-paced regulatory environment
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Preferred Candidates: Applicants from Uttarakhand will be given preference, aligning with our commitment to local talent development.
🌱 Why Join Genedrift?
At Genedrift, you won’t just work on documents — you’ll contribute to the safe and effective delivery of life-saving treatments. You’ll be part of a culture that values growth, learning, and excellence. With access to experienced mentors and a collaborative work environment, this is more than a job — it’s the start of a meaningful career in Regulatory Affairs.
📬 How to Apply
If you’re ready to take the next step and believe you have the passion and commitment to thrive in regulatory sciences, we’d love to hear from you.
Applications are now open for both entry-level and experienced positions in our Regulatory Affairs department.
Shape your future. Shape the industry. Join Genedrift.
To apply for this job please visit genedrift.com.
