AVP-Quality Control

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 Good 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 organizations 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 efficient 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 including USFDA, MHRA, EMA, TGA, ANVISA, WHO-GMP, and other international authorities.
• Lead and represent the Quality Control function during customer audits, regulatory inspections, and corporate audits.
• Ensure timely closure of audit observations, CAPAs, deviations, and quality investigations.

Laboratory Management

• Provide oversight for all QC laboratories, ensuring proper qualification, calibration, and maintenance of analytical instruments.
• Ensure compliance with laboratory data integrity principles and computerized system requirements.
• Oversee qualification and validation of laboratory equipment and analytical methods.
• Optimize laboratory workflows through digitalization, automation, and continuous improvement initiatives.

Quality Systems

• Lead investigations related to OOS, OOT, deviations, laboratory incidents, and customer complaints.
• Ensure robust root cause analysis and implementation of effective CAPA.
• Review and approve change controls, risk assessments, and laboratory investigations.
• Monitor quality trends and implement preventive actions to minimize quality risks.

Stability Program

• Provide strategic oversight for ICH stability studies and stability chamber management.
• Review stability data and ensure timely reporting to Regulatory Affairs and Quality Assurance.
• Ensure compliance with global stability guidelines and product lifecycle management requirements.

Continuous Improvement

• Drive Lean Laboratory, Six Sigma, Kaizen, and Operational Excellence initiatives.
• Establish departmental KPIs and monitor performance through regular reviews.
• Improve laboratory efficiency, cost optimization, and resource utilization while maintaining compliance.
• Promote innovation through adoption of modern analytical technologies and digital solutions.

Cross-Functional Collaboration

• Collaborate closely with Manufacturing, Quality Assurance, Regulatory Affairs, Engineering, Supply Chain, R&D, and Technical Services.
• Support new product introductions, technology transfers, validation activities, and commercial launches.
• Participate in management reviews and provide strategic recommendations related to quality performance.

People Leadership

• Lead, mentor, and develop managers and senior scientists within the Quality Control function.
• Identify training needs and establish competency development programs.
• Conduct performance reviews, succession planning, and talent development initiatives.
• Foster employee engagement and a culture of ownership and continuous learning.

Educational Qualifications

• M.Sc. (Chemistry), M.Pharm., or equivalent qualification in Pharmaceutical Sciences.
• Ph.D. in Analytical Chemistry or Pharmaceutical Sciences will be an added advantage.

Experience

• 20–25 years of progressive experience in Pharmaceutical Quality Control.
• Minimum 10 years of leadership experience in sterile injectable manufacturing.
• Proven experience in leading multidisciplinary QC teams within regulated pharmaceutical environments.
• Hands-on experience in handling global regulatory inspections.

Technical Competencies

• Extensive knowledge of injectable manufacturing and Quality Control systems.
• Strong expertise in analytical chemistry, microbiology, environmental monitoring, and stability studies.
• Thorough understanding of cGMP, GLP, ICH guidelines, pharmacopeial requirements (USP, EP, BP, IP), and data integrity.
• Experience with laboratory systems such as LIMS, CDS (Empower, Chromeleon), SAP, TrackWise, and electronic quality management systems.
• Expertise in laboratory investigations, risk management, CAPA, change control, and analytical method validation.

Leadership Competencies

• Strategic thinking and business acumen.
• Excellent people leadership and mentoring skills.
• Strong decision-making and problem-solving abilities.
• Effective stakeholder management and cross-functional collaboration.
• Excellent communication and presentation skills.
• Change management and organizational development capabilities.
• High level of integrity, accountability, and quality mindset.

Key Performance Indicators (KPIs)

• Laboratory turnaround time (TAT)
• Batch release adherence
• Regulatory inspection outcomes
• Audit observation closure timelines
• OOS/OOT investigation effectiveness
• CAPA implementation effectiveness
• Laboratory productivity
• Data Integrity compliance
• Stability program compliance
• Employee engagement and team development
• Cost optimization and laboratory efficiency

Preferred Candidate Profile

• Proven leadership experience in injectable pharmaceutical manufacturing.
• Strong exposure to global regulated markets including the US, Europe, UK, Australia, Canada, and other international markets.
• Demonstrated success in leading regulatory inspections and driving quality excellence.
• Strong analytical, strategic, and people management capabilities with a commitment to continuous improvement and operational excellence.