| Role Title: |
Regulatory Affairs Executive |
| Reports to Role (Title): |
General Manager |
| Location: |
Office in Pune (MH), India |
| Scope: |
Develop expertise in regulatory requirements for registration of pharma and agrochemicals. |
ROLE PURPOSE
To assist the General Manager on projects and matters with regards to registration of drugs, cosmetics ,medical devices and agrochemicals in India.
ACCOUNTABILITIES
- Preliminary research about the molecules based on the query of clients
- Close cooperation with the manager during strategy finalization
- Follow-up with clients up to finalization of project plan
- Contacting laboratories for quotations and follow-up of status of studies placed
- Maintain good customer relations and manage projects to full customer satisfaction
- Visit to the CIBRC and CDSCO offices as and when required
- Follow-up with authorities to check the updates of submissions
- Work as an effective team member and provide responsive support to the team on all matters pertaining to
- Maintain and develop personal capabilities and expertise to become a creditable partner in the view of
KNOWLEDGE SKILLS & EXPERIENCE
Critical Knowledge:
- Master Degree in Regulatory Pharmacology from reputed Institute in India
- Knowledge about regulatory bodies like CDSCO,ECHA,MHRA,FDA,CIBRC & EFSA
- Fluent in English is must
