The Associate Vice President – Quality Control will provide strategic leadership and operational oversight for the Quality Control function across sterile injectable manufacturing facilities. The incumbent will be responsible for ensuring that all analytical, microbiological, and stability testing activities comply with global regulatory requirements, current Positive Manufacturing Practices (cGMP), and internal quality standards.
The role involves leading a high-performing QC organization, driving operational excellence, strengthening compliance systems, supporting regulatory inspections, and fostering a culture of quality and continuous improvement.

Key Responsibilities
Strategic Leadership
Develop and execute the Quality Control strategy in alignment with the organization's business objectives.
Provide leadership for Chemical, Instrumentation, Microbiology, Stability, Environmental Monitoring, and Incoming Material laboratories.
Establish long-term quality objectives and performance metrics for the QC function.
Drive a culture of quality, accountability, innovation,



and operational excellence.
Build and mentor future leaders within the Quality Control organization.

Quality Control Operations
Oversee testing of raw materials, packaging materials, in-process samples, finished products, water systems, gases, and environmental monitoring samples.
Ensure timely batch release through effective laboratory operations and optimal resource utilization.
Review and approve analytical methods, specifications, SOPs, protocols, reports, and laboratory documentation.
Ensure compliance with approved testing procedures and validated analytical methods.
Monitor laboratory productivity and implement initiatives to improve turnaround time without compromising quality.

Regulatory Compliance
Ensure full compliance with cGMP, GLP, Data Integrity requirements, and applicable global regulatory guidelines.
Maintain inspection readiness for global regulatory agencies

📌 Avp Quality Control Baddi (India)
🏢 Venus Remedies
📍 India