Group Manager

5 days ago

Vizianagaram, India Pfizer Full time

Use Your Power for Purpose Every day everything we do is driven by an unwavering commitment to delivering safe and effective products to patients Our quality culture rooted in science and risk-based compliance is both flexible and innovative always putting the customer first Whether you are engaged in development maintenance compliance or analysis through research programs your contributions have a direct impact on patients This commitment to quality and safety ensures that our products meet the highest standards making a real difference in the lives of those who need them Your role is crucial in maintaining this standard and together we strive to innovate and improve ensuring that our patients receive the best possible care What You Will Achieve In this role you will Drive the investigations for Quality robustness within the timelines Review of investigation for root cause analysis and appropriate corrective actions implemented Compliance to site investigations procedures Facilitate investigations and implement corrective actions ensuring timely closeout Undertake and implement improvement plans to meet the Quality department s goals and Key Performance Index KPI Liaise and influence the cross functional team to drive the site investigations to meet the supply reliability Monitor review develop and implement the action plan for investigation program metrics sustenance Derive appropriate training methodologies to improve and maintain the capability and competency of investigators and approvers Undertake and implement improvement plans to meet the Quality department s goals Evaluate data and trends report results to management Here Is What You Need Minimum Requirements Preferably 8-10 years of experience in Quality Assurance Quality Control function of Sterile manufacturing facility Solid background in people management Expertise in handling investigations through a Quality Tracking system Well-versed in GMP Manufacturing as well as QA QC Laboratory environments Project management experience Strong interpersonal and influential skills to effectively lead and collaborate with teams Ability to analyze information using various statistical tools Know the processes and procedures including the principles and practices of good data management ALCOA and be able to guide advise and coach the team Bonus Points If You Have Preferred Requirements Master s degree coupled with relevant pharmaceutical experience Comprehensive expertise and familiarity with all facets of biologic manufacturing including cell culture fermentation purification microbiology and chemistry Robust understanding of DMAIC methodology and Method 1 coaching training or similar Experience in developing team capability and skills through continuous support and one-on-one coaching Ability to review develop and introduce systems practices and cultural changes Strong organizational and time management skills Work Location Assignment On Premise Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates Quality Assurance and Control

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