Regulatory Affairs Specialist – Regulatory Affairs | APDM Pharmaceuticals Pvt Ltd | Ahmedabad, Gujarat, India
APDM Pharmaceuticals Pvt Ltd is hiring a Regulatory Affairs Specialist for its Ahmedabad operations. Candidates with 4 to 6 years of experience in regulatory submissions, documentation, and compliance within the pharmaceutical industry are preferred. The role involves handling dossiers, coordinating with regulatory authorities, and ensuring adherence to global standards.
Location
Ahmedabad, Gujarat, India
Employment Type
Full-time
Experience Required
4 to 6 Years
Compensation & Benefits
Not Disclosed
About APDM Pharmaceuticals Pvt Ltd
A pharmaceutical company focused on regulatory-compliant product development and manufacturing.
Position Overview
Manage regulatory submissions and ensure compliance with guidelines.
Key Responsibilities
- Prepare regulatory dossiers
- Handle submissions and approvals
- Maintain documentation
- Ensure compliance with guidelines
- Coordinate with authorities
- Support audits
- Track regulatory updates
- Collaborate with cross-functional teams
Required Skills & Competencies
- Regulatory affairs knowledge
- Documentation skills
- Attention to detail
- Communication
- Problem-solving
- Technical understanding
- Planning ability
- Team coordination
Educational Qualification
B.Pharm
About the Project & Industry
Pharmaceutical sector focusing on regulatory compliance and product approvals.
Why Join APDM Pharmaceuticals Pvt Ltd?
Opportunity to grow in regulatory affairs and global compliance roles.
How to Apply
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