Liaquat Ali
Assistant Manager Qa Compliance @GSK
Signup · Get unlimited contacts
WORK HISTORY
Assistant Manager Qa Compliance @GSK
Managing of internal quality complaints and timely resolution, developing solutions to complex problems.Managing the Deviation Investigation for OOS and OOT.Monitor and evaluate the level of cGMP compliance for the product manufacture, packaged, tested and released at local and third parties key Quality indicators.Assessment of deviation management as per QA & compliance prospective.Risk Assessment of Production Process, complaint as well as deviation. Audit readiness. Managing the Third parties deviation and complaints.
EDUCATION
Anglia Ruskin University
Master of Business Administration (M.B.A.)
University of the West of Scotland
Master's degree
ABOUT LIAQUAT ALI
I have finished my MSc in Quality Management from University of West of The Scotland in 2021 MBA from Anglia Ruskin University UK & B-Pharmacy University of Sindh Jamshoro Pakistan. I worked as Assistant Manager QA Compliance \"GSK OTC Pakistan” where Leading and managing the site internal audit program & Self-Inspection program, CAPA, Deviation, Complaints, Quality Alerts, Quality Council, Local Management of Product Incidents & Recalls and Regulatory Inspections. I am certified GSK Auditor. Super User in QWF (Quality Work Flow for managing all Deviations, Complaints, Regulatory inspection reports, CAPA\'s) and Now it is now as Carisma-C-3. Data base. Performed GMP audit of Third party Manufacturing.Ensure that GMP audits are performed as per annual audit schedule and conduct due diligence audits if required. •Manage the site Complaints Handling & Deviation processes and ensure that all product quality complaints/deviations are adequately investigated, reported and any follow-up activities as per requirement. Ensure adequate trending of product quality complaints & deviations to initiate proper product improvement activities. Support the regular product reviews with product quality complaints information. Ensure timely and complete product quality investigations related to Product Recall, Counterfeit and/or Withdrawals in close interaction with global and country QA functions. •Perform gap assessment of all applicable QMS documents in the compliance department and assure adherence to QMS documents and regulatory requirements.• Managing the CAPA (preventing & corrective actions) to eliminate “clusters” and reoccurrence. Check all feedback for plausibility and completeness and CAPAs. •Maintain the (KPIs) and GMP-compliance/pro-active follow-up of actions. Manage the Quality Management review (QMR) at per defined frequency. Product Release.Internal Audits CAPA logging in QWF and closure of CAPA\'S. Prior to this work, I have been involved in many other organizations including National and Multinational Pharmaceuticals Industry and worked as production officer in Novartis Consumer Health Care jamshoro and Senior Production officer in Atco laboratories Pvt Limited. My current interests including travelling, watching cricket and also involved in social activities.
This profile is compiled from publicly available professional sources. Unifers is not affiliated with or endorsed by LinkedIn. Request removal of this profile.