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Kickstart your career in Regulatory Affairs with an exciting opportunity at Flamingo Pharmaceuticals. This role is ideal for fresh graduates and aspiring regulatory professionals looking to build expertise in pharmaceutical documentation, global submissions, and compliance while working in a dynamic and growth-oriented environment.
Job Title
Regulatory Affairs Trainee
Company
Flamingo Pharmaceuticals
Location
Mumbai, Maharashtra
Employment Type
Full-Time
Qualification
* B.Pharm / M.Pharm (Preferred)
Experience
* Freshers are encouraged to apply.
Estimated Salary
* ₹3.2 LPA – ₹4.5 LPA (Estimated and may vary based on company policy and candidate profile.)
Key Responsibilities
* Assist in the preparation and compilation of regulatory dossiers.
* Support CTD/eCTD documentation and submission activities.
* Maintain regulatory documentation and product registration records.
* Ensure compliance with national and international regulatory guidelines.
* Coordinate with cross-functional teams to facilitate regulatory submissions.
* Stay updated with current pharmaceutical regulatory requirements.
Required Skills
* Basic understanding of Regulatory Affairs and pharmaceutical documentation.
* Knowledge of CTD/eCTD concepts is an added advantage.
* Familiarity with ICH Guidelines, CDSCO, USFDA, WHO, and MHRA regulations is preferred.
* Strong documentation, analytical, and communication skills.
* Attention to detail and willingness to learn.
Why Apply?
* Excellent opportunity to start a career in Regulatory Affairs.
* Exposure to global regulatory submissions and compliance.
* Learn from experienced regulatory professionals.
* Career growth in the pharmaceutical industry.
Disclaimer: FYND Talent Solutions is an independent recruitment platform. This job is shared for informational purposes only and is not an official communication from the hiring company unless explicitly stated.
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