Raptim Research has announced an opening for its Regulatory Affairs – DCGI team at Mahape, Navi Mumbai, Maharashtra. This opportunity is suitable for M.Pharm professionals with 1–4 years of relevant Regulatory Affairs experience and practical knowledge of the SUGAM portal.
Candidates searching for Regulatory Affairs jobs in Navi Mumbai, DCGI jobs for M.Pharm candidates, or pharma regulatory affairs jobs in Maharashtra can review the eligibility criteria and application process below.
Raptim Research Regulatory Affairs Vacancy – Overview
| Particular | Details |
|---|---|
| Company | Raptim Research |
| Department | Regulatory Affairs – DCGI |
| Job Location | Mahape, Navi Mumbai, Maharashtra |
| Qualification | M.Pharm – Pharmaceutics/Pharmaceutical Sciences |
| Experience | 1–4 years |
| Key Skill | SUGAM Portal |
| Job Category | Pharmaceutical Regulatory Affairs |
| Application Mode | |
| Salary | Not disclosed by employer |
About Raptim Research
Raptim Research Private Limited is a Contract Research Organization (CRO) established in 2005. The company provides clinical research, BA/BE, in-vitro and other drug-development services. Its official website lists its India head office at TTC Industrial Area, Mahape MIDC, Navi Mumbai.
The current Raptim Research Regulatory Affairs job offers eligible pharmaceutical professionals an opportunity to work on DCGI regulatory submissions and associated compliance activities.
Job Responsibilities
Selected candidates for the Regulatory Affairs DCGI vacancy at Raptim Research will be responsible for:
- Preparing and reviewing DCGI applications for BENOC, Test Licence, Working Standard import licence and Clinical Trial applications.
- Preparing responses to regulatory queries concerning BENOC, Test Licence, Working Standard and Clinical Trial applications.
- Reviewing and submitting information to the Clinical Trials Registry – India (CTRI).
- Handling quota allocation, import applications and query responses involving Narcotic Drugs and Psychotropic Substances (NDPS).
- Managing quarterly returns for NDPS substances to the Central Bureau of Narcotics (CBN) and State FDA.
- Handling NDPS-2 and NDPS-6 licences with the State FDA.
- Supporting DCGI-related regulatory documentation and submission activities.
Qualification and Experience
Candidates applying for this Regulatory Affairs DCGI job in Navi Mumbai should meet the following requirements:
Educational Qualification: M.Pharm in Pharmaceutics or Pharmaceutical Sciences.
Experience: 1–4 years of relevant professional experience.
Essential Skill: Candidates should be well versed with the SUGAM portal.
Previous hands-on exposure to DCGI applications, CTRI submissions, Test Licence applications, BENOC documentation, import licences or NDPS regulatory activities would be directly relevant to the responsibilities described by the employer.
Why Consider This Regulatory Affairs Role?
This opening may be particularly relevant for early-career Regulatory Affairs professionals looking to build experience across multiple Indian regulatory processes. The responsibilities cover DCGI submissions, SUGAM portal activities, CTRI, import-related documentation and NDPS compliance.
The position is based in Mahape, Navi Mumbai, making it relevant for candidates searching for M.Pharm jobs in Navi Mumbai, SUGAM portal jobs, DCGI Regulatory Affairs jobs, and pharmaceutical regulatory careers in the Mumbai region.
Note: The employer has not specified salary, incentives, insurance, leave, transport or other employment benefits in the supplied recruitment notice. Candidates should confirm compensation and benefits directly with Raptim Research during the recruitment process.
How to Apply for Raptim Research Jobs
Interested and eligible candidates should send their updated resume/CV by email.
Email: rakesh.talwatkar@raptimresearch.com