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Zuche Pharmaceuticals

Compare

3.5

based on 23 Reviews

5 Zuche Pharmaceuticals Jobs

Sr.Executive Regulatory Affairs || Immediate joinner || New Delhi

Zuche Pharmaceuticals

3.5

based on 23 Reviews

2-5 years

New Delhi

1 vacancy

Sr.Executive Regulatory Affairs || Immediate joinner || New Delhi

Zuche Pharmaceuticals

posted 25d ago

Job Role Insights

Fixed timing

Key skills for the job

Transcription Regulatory Affairs Drug Regulatory Affairs Export Documentation Medical Devices

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

Read full job description

Prepare for Executive Regulatory Affairs roles with real interview advice

What people at Zuche Pharmaceuticals are saying

Executive Regulatory Affairs salary at Zuche Pharmaceuticals

reported by 2 employees

₹2 L/yr - ₹2.6 L/yr

47% less than the average Executive Regulatory Affairs Salary in India

View more details

What Zuche Pharmaceuticals employees are saying about work life

based on 23 employees

75%

60%

54%

100%

Strict timing

Monday to Saturday

No travel

Day Shift

View more insights

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