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Sr.Executive Regulatory Affairs || Immediate joinner || New Delhi
2-5 years
New Delhi
1 vacancy
Sr.Executive Regulatory Affairs || Immediate joinner || New Delhi
Zuche Pharmaceuticals
posted 16d ago
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Fixed timing
Key skills for the job
Job Description
🔑 Key Responsibilities:
Prepare and review CTD, ACTD, and TCF dossiers with precision.
Review critical technical documents such as:
Process Validation Report (PVR) Specifications (SPEC) Standard Testing Procedure (STP) Certificate of Analysis (COA)
🎓 Requirements:
Minimum of 1 year of experience in regulatory affairs for medical devices.
Educational qualification: M.Pharma or B.Pharma.
📩 Ready to make an impact?
Apply now or share this opportunity with your network! hrm@zuchepharma.in
Employment Type: Full Time, Permanent
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Anonymous · Regulatory Affairs
in Green Park
An organisation to learn and work with. A very supportive team and environment and work culture.
Read 1 reviewExecutive Regulatory Affairs salary at Zuche Pharmaceuticals
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Zuche Pharmaceuticals Benefits
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