QA-QMS

Vizen Life Sciences Pvt Ltd; Hyderabad; On-site; INR 550,000 - 750,000; Full time

Job summary

Vizen Life Sciences Pvt Ltd in Hyderabad is seeking a detail-oriented quality professional to strengthen our compliance and product integrity. You will document, review, and implement GMP-related procedures in a fast-paced pharmaceutical environment.

The role focuses on SOP preparation, deviation handling, change control, and market complaints management to ensure regulatory readiness and product safety. You will coordinate with QA, production, and procurement to maintain approved vendor lists

Responsibilities

• Preparation of Apex Documents such as SMF, Quality Policy etc.
• Handling of Self-inspection.
• Issuance, review and compilation of Deviations, Incidents, Change Control and Root Cause Analysis.
• Preparation and review of SOPs.
• Handling of Market Complaints & Product Recall.
• Initiation, review and proper implementation of Market Complaints.
• Preparation of Approved Vendor List of Raw Material & Packing Material.
• Reviewing of Artworks of finished product Labels and Mono cartons.
• Issuance and retrieval of Formats, Logbooks and Register as per respective procedure.

Job description

Responsibilities

• .Preparation of Apex Documents such as SMF, Quality Policy etc.
• Handling of Self-inspection.
• Issuance, review and compilation of Deviations, Incidents, Change Control and
• Root Cause Analysis.
• Preparation and review of SOPs.
• Handling of Market Complaints & Product Recall.
• Initiation, review and proper implementation of Market Complaints.
• Preparation of Approved Vendor List of Raw Material & Packing Material.
• Reviewing of Artworks of finished product Labels and Mono cartons.
• Issuance and retrieval of Formats, Logbooks and Register as per respectiveprocedure.