Senior Executive US Injectable Regulatory Affairs at Cadila Pharmaceuticals Ltd.
Cadila Pharmaceuticals Ltd. is currently hiring for the position of Senior Executive US Injectable Regulatory Affairs in the Regulatory Affairs department within the Pharmaceutical industry.
Roles & Responsibilities
Senior Executive US Injectable Regulatory Affairs Job in Ahmedabad – Cadila Pharmaceuticals Ltd.
Cadila Pharmaceuticals Ltd. is looking for a Senior Executive – US Injectable Regulatory Affairs for its Ahmedabad, Gujarat location. This pharmaceutical industry opportunity is suitable for professionals with 2 to 5 years of experience in regulatory affairs, ANDA submissions, injectable dossiers, and regulatory compliance. Candidates with an M.Pharm qualification can apply for this full-time role.
Location
Ahmedabad, Gujarat, India
Employment Type
Full-time
Experience Required
2 to 5 Years
Educational Qualification
M.Pharm
Key Responsibilities
- Prepare and review US injectable regulatory submissions.
- Support ANDA filing activities.
- Compile regulatory dossiers and responses.
- Coordinate with cross-functional teams.
- Track regulatory commitments and timelines.
- Review technical and quality documentation.
- Monitor regulatory updates and requirements.
- Support agency correspondence activities.
- Ensure compliance with global regulations.
- Maintain regulatory databases and records.
Required Skills & Competencies
- US regulatory affairs expertise.
- ANDA submission experience.
- Injectable product knowledge.
- Regulatory documentation skills.
- Strong analytical abilities.
- Attention to detail.
- Project coordination skills.
- Communication abilities.
- Problem-solving mindset.
- Regulatory compliance knowledge.
Why Join Cadila Pharmaceuticals Ltd.?
- Exposure to global regulatory projects.
- Career growth in regulatory affairs.
- Learning-focused environment.
- Professional development opportunities.
- Work with experienced industry experts.
How to Apply
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