Qa Executive – Regulatory / Documentation Pharma Manufacturing Ahmedabad Vejalpur (India)

Qa Executive – Regulatory / Documentation Pharma Manufacturing Ahmedabad Vejalpur (India)

18 Sep
|
Prime Placement
|
India

18 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:
Valuable knowledge of Pharma QA & Regulatory Affairs.
Practical exposure to CDSCO / State FDA documentation.
Knowledge of Artwork & Packaging Material Verification.
Good documentation and coordination skills.
Positive communication skills, especially for client coordination.
Robust attention

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

Work Location: In person

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

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