Location: Visakhapatnam (Vizag)

We seek a highly experienced Senior Executive/Assistant Manager - Quality Control Documentation & QMS to lead our critical QC Documentation Management and Quality Management System (QMS) initiatives at Synnat Pharma. If you have 10 to 12 years in Pharmaceutical Quality Control, a solid grasp of US FDA Regulations, EU GMP, and ICH Guidelines, and a passion for ensuring Data Integrity, this role is for you.

Roles & Responsibilities:

QC Documentation Management
Lead the development, review, and approval of all Quality Control (QC) documentation, including SOPs, specifications, test methods, and protocols.
Ensure all QC documentation adheres to regulatory guidelines (US FDA, EU GMP, ICH) and internal quality standards.
Oversee the lifecycle management of QC documents, including version control, archiving, and retrieval processes.
Implement and maintain robust documentation practices to ensure data integrity across all QC activities.
Prepare and present QC documentation during internal and external audits,



demonstrating compliance and control.

Quality Management System (QMS) Implementation & Oversight
Contribute to the overall QMS framework, aligning QC processes with company-wide quality objectives.
Facilitate incident management processes within QC, ensuring proper documentation, investigation, and reporting.
Lead Corrective And Preventive Actions (CAPA) initiatives, including root cause analysis, action plan development, and effectiveness verification.
Manage and track all deviations, out-of-specification (OOS) results, and out-of-trend (OOT) events, ensuring timely investigation and resolution.
Drive the implementation and continuous improvement of Quality Management System (QMS) activities within the Quality Control department.

Compliance and Regulatory Affairs
Collaborate with regulatory affairs and quality assurance teams to ensure seamless integration of QC processes into global reg

📌 Senior Executive Visakhapatnam
🏢 Synnat Pharma
📍 Visakhapatnam