Team Leader Quality Control

1 week ago

Baddi, India Panacea Biotec Full time

Continuous Improvement Lead (CI) - VDSP, Lalru & VDPP, Baddi Reports To : Strategic Project Manager (SPM) To lead and institutionalize continuous improvement (CI) initiatives across the WHO prequalified vaccine manufacturing facility by driving cost reduction, waste elimination, energy optimization,yield improvement and process excellence. The role promotes a culture of innovation, quality initiatives and operational efficiency aligned with cGMP, WHO, and other global regulatory standards. Identify and execute improvement projects focused on yield improvement, cycle time reduction, cost savings, and resource optimization. Promote Lean, Six Sigma, and Kaizen practices across all manufacturing and support functions. Drive initiatives such as 5S, Visual Management, TPM, to enhance efficiency and reduce variability. Implement SPC(Statistical Process Control0 and SQC ( Statistical Quality Control) Regulatory Compliance & GMP Alignment Support validation and qualification teams in improving process robustness and data integrity. Collaborate with QA, QC, and Regulatory Affairs to maintain compliance while improving systems and procedures. Work closely with manufacturing, QA, QC, RA, Engineering & SCM heads to identify bottle necks and area for improvement. Partner with functional leaders to standardize processes and reduce variation across plants or departments Facility CI project governance, tracking, reporting & escalation to COO CI Project Leadership & Execution Lead cross-functional CI projects across Drug Substance Plant , Drug Product, Formulation, Filling, and Packaging areas. Develop project charters, timelines, and ROI analysis; Capability Building & Cultural Transformation Build CI mind-set across production, quality, engineering, and warehouse teams. Conduct Gemba walks, performance huddles, and innovation forums to engage teams. Performance Monitoring & Reporting Establish CI metrics and dashboards (OEE, Waste %, Yield, Downtime, etc.) Track CAPA effectiveness, deviation trends, and quality improvements as part of the CI program. Qualifications & Experience: Bachelors or Master’s degree in Engineering, Pharmacy, Biotechnology, or Life Sciences. Minimum 6–10 years of demonstrated relevant experience in vaccine/biotech/pharma manufacturing, preferably in a WHO-GMP or global regulatory-compliant facility. Strong understanding of GMP, WHO, and global vaccine manufacturing regulations Analytical, data-driven decision-making Strong facilitation, coaching, and change management skills Proficiency in using CI tools/software (e.g., Minitab, Power BI, etc.)

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