QA Executive – Regulatory / Documentation - Pharma Manufacturing - Ahmedabad (India)

QA Executive – Regulatory / Documentation - Pharma Manufacturing - Ahmedabad (India)

16 Sep
|
Prime Placement
|
India

16 Sep

Prime Placement

India

Job Title: QA Executive – Regulatory Affairs

Location: Shyamal, Ahmedabad
Experience: 1–2 Years
Qualification: B.Pharm / M.Pharm / relevant Pharma qualification

Job Overview:
We are looking for a QA Executive with exposure to Regulatory Affairs, Artwork Verification and Pharma Documentation. The candidate will coordinate with domestic/international clients and support regulatory approvals, product permissions and export-related compliances.

Key Responsibilities:

- Coordinate with domestic & international clients for regulatory requirements.
- Prepare and verify pharma artwork, labels and packaging components.
- Ensure artwork matches approved dossiers and maintain proper version control.
- Perform text checks and documentation verification.
- Ensure compliance with FDA and CDSCO guidelines.
- Handle documentation related to Product Permissions, CoPP and NOC.




- Support export clearances and manufacturing approvals.
- Coordinate with CDSCO / State FDA and other regulatory authorities.
- Coordinate with internal QA, regulatory and technical teams.
- Maintain accurate regulatory records and documentation.

Required Skills:

- Good knowledge of Pharma QA & Regulatory Affairs.
- Practical exposure to CDSCO / State FDA documentation.
- Knowledge of Artwork & Packaging Material Verification.
- Good documentation and coordination skills.
- Good communication skills, especially for client coordination.
- Solid attention

Apply Now - +91-XXXXXXXXXX

Pay: ₹25,000.00 - ₹30,000.00 per month

Work Location: In person

📌 QA Executive – Regulatory / Documentation - Pharma Manufacturing - Ahmedabad (India)
🏢 Prime Placement
📍 India

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