Transglobal Odyssey Pvt. Ltd. is hiring for the position of Regulatory Affairs Executive in New Delhi, India. Candidates with qualifications such as B.Pharm, M.Pharm, B.Sc, M.Sc in Life Sciences, Biotechnology, Biology, or Microbiology can apply for this exciting pharmaceutical regulatory affairs opportunity.
This Regulatory Affairs Executive job in Delhi is ideal for freshers and experienced professionals with up to 2 years of experience who are looking to build a career in pharmaceutical regulatory affairs, CTD dossier preparation, ACTD submissions, and pharmaceutical documentation.
About Transglobal Odyssey Pvt. Ltd.
Transglobal Odyssey Pvt. Ltd. is involved in pharmaceutical regulatory and healthcare-related services. The company is expanding its Regulatory Affairs team and seeking candidates with strong documentation, coordination, and regulatory compliance skills.
Job Details
| Job Position | Regulatory Affairs Executive |
|---|---|
| Company | Transglobal Odyssey Pvt. Ltd. |
| Location | Okhla Phase 2, New Delhi, India |
| Job Type | Full-Time |
| Experience Required | 6 Months – 2 Years |
| Department | Regulatory Affairs |
| Qualification | B.Pharm / M.Pharm / B.Sc / M.Sc |
| Mode of Work | On-site |
Regulatory Affairs Executive Job Responsibilities
The selected candidate will be responsible for:
- Preparation and compilation of CTD and ACTD dossiers
- Reviewing regulatory documents such as COA, specifications, labels, PIL, artworks, and packaging materials
- Coordinating with internal departments for regulatory documentation
- Managing pharmaceutical product registration activities
- Responding to regulatory queries from health authorities and clients
- Preparation and review of Module 1 to Module 5 documents
- Maintaining submission trackers and regulatory databases
- Coordinating with third-party consultants and vendors
- Ensuring compliance with pharmaceutical regulatory guidelines
Required Qualifications
Candidates applying for this Regulatory Affairs Executive job should have:
- B.Pharm or M.Pharm degree
- OR B.Sc / M.Sc in Life Sciences, Biology, Biotechnology, or Microbiology
- 6 months to 2 years of experience in pharmaceutical regulatory affairs preferred
- Basic understanding of CTD/ACTD dossier preparation
- Strong documentation and communication skills
- Proficiency in MS Office tools including Word, Excel, and PowerPoint
Preferred Skills
- Knowledge of pharmaceutical regulatory documentation
- Understanding of pharmaceutical registration processes
- Good organizational and coordination skills
- Strong attention to detail
- Ability to manage multiple tasks in a fast-paced environment
Why Join Transglobal Odyssey?
Working with Transglobal Odyssey Pvt. Ltd. offers candidates an opportunity to gain hands-on exposure in:
- Pharmaceutical Regulatory Affairs
- CTD and ACTD dossier preparation
- Product registration activities
- Regulatory compliance processes
- Pharmaceutical documentation management
This role is especially beneficial for candidates looking to grow in international pharmaceutical regulatory affairs and regulated market submissions.
How to Apply
Interested candidates can send their updated CV to:
Candidates are advised to mention “Application for Regulatory Affairs Executive – Pharmabharat” in the subject line while applying.
Official Website:
www.tgody.com
