Exciting opportunity for B.Pharm/M.Pharm graduates looking to kickstart their career in the pharmaceutical industry!
The Regulatory Affairs Department in Dehradun, Uttarakhand is hiring freshers and candidates with 5 to 6 months of experience. They are looking for immediate joiners who are passionate, detail-oriented, and ready to grow with us.
About Genedrift
Genedrift is a trusted provider of Regulatory and Pharmacovigilance services, specializing in pre and post market approved product safety, complaints management, medical inquiry support, and post market surveillance. The company excels at developing customized solutions to align with clients’ strategic objectives and streamline business processes.
Job Description
This is a full-time hybrid role for a Regulatory Affairs Trainee at Genedrift.
- Coordinating with internal teams for review of documents and submissions.
- Upkeep and compliance with the internal and client document management SOPs.
- Coordinating with internal teams for updates on various activities/ projects/ submissions.
- Work with internal teams to finalize the document translation.
- Closely follow the team leader and understand the guidelines, practices, and standards to be followed for various submissions and activities.
- Ensuring internal records/ activities are updated.
Related Job: Regulatory Affairs Executive at West Coast Pharmaceuticals
Required Profile for RA Role
- Excellent interpersonal skills including oral and written communication with effective presentation skills.
- Excellent computer skills and comfortable with online office applications.
- A keen eye to learn.
- Flexible, Adaptive, Ability to work under pressure, work with a focus on delivery, and provide quality outputs within tight timelines.
- Candidates from Uttarakhand, are preferred.
How to Apply for RA Role at Genedrift?
You can apply for Trainee Intern – Regulatory Affairs role at Genedrift by clicking the below apply button.
Job Code: JP8 – Trainee Intern – Regulatory Affairs (DIN11)