Mohammad Wasif Bari

Experience

• 

  Novartis Pakistan

  Aug 2013 - Jun 2014

  IPC Monitor
• 

  Novartis

  Jul 2014 - May 2016

  QMI Associate

  •Coordinate and monitor all the activities of Quality Modules / Quality directives authorization and implementation received from Corporate.•Distribution of Quality Modules / Quality Directives received from Corporate to concerned department for timely gap assessment so that module/directives can be authorization for use at site with in global due date.•Assure timely completion of all corrective actions defined in the gap assessment so that module can be implemented at site with in global due date.•Assure timely posting of gap assessments, modules/directives authorization and implemented on QSS SharePoint.•Comply and ensure compliance to Health, Safety and Environment, Policies, guidelines and requirement as applicable by law and Novartis corporate guidelines.•Comply and ensure compliance to GMP (Good Manufacturing Practices), Quality and other related polices guidelines and requirement as applicable by law and Novartis corporate guidelines.•Review all local SOPs to ensure that SOP is in accordance with the respective Quality Manuals, Global SOPs and Quality Systems SOPs for Jamshoro Site and Head Office.•Co-ordinate and support all departments for the creation and revision of Local SOPs.•Any other job assigned by QSS lead.•Issue Manufacturing Instructions and Packaging Instructions as per production plan in the absence of Documentation Coordinator. Show less

• 

  GSK

  Jun 2016 - Apr 2022

  Lead Projects deployed for Computerised System including Control Systems, Analytical Systems and Information Technology Systems.Lead Validation activities for Control Systems, Analytical Systems, Information Technology Systems and Excel Spreadsheets, including vendor quality reports through release of system for use.Lead project for System Assessment of Analytical Systems, Manufacturing System and Information Technology SystemsExecution of external and internal assessments and audits of CSV status.Maintain System Register and CSV master plans. Conduct Training for associates from Site Leadership team to First Line Leader on Data Integrity Detection, Prevention and Data Integrity in Deviation Management.Assuring active and appropriate level of energy directed to ensure progress against the Site Data Integrity PlanLead Investigation of all Data Integrity issues at Site with appropriate reporting to regional Quality Head and Data Integrity Lead with effective CAPAs.Maintain Data Integrity Story Board for Inspections and Audits readiness.Act as a SPOC (single point of contact) for eCompliance on assigned computerized systems initiatives.Attend weekly Team calls with Global eCompliance Team for Global communication.Monthly Report CSV Progress Dashboard to Global Head of eCompliance and Data Integrity Lead.Monthly Report Data Integrity Progress Dashboard to Central Data Integrity Team. Show less

  • Team Lead Packaging

    Jan 2021 - Apr 2022

  • eCompliance Specialist

    Jan 2020 - Aug 2021

  • eCompliance and Data Integrity Lead

    Mar 2017 - Jan 2020

  • QMS Associate

    Jun 2016 - Feb 2017
• 

  Abbott

  Apr 2022 - Jun 2023

  Production Manager
• 

  Pfizer

  Jun 2023 - now

  Manager Quality Assurance