Uzma Khan

Fathers Name: Qamaruzzaman Khan DOB: 9th September, 1987 Nationality: Pakistani Languages: Fluent in English &, Urdu Contact: House # R-754 Sector-9, North Karachi 0334-3815518 uzkan1987@gmail.com

OBJECTIVE

Seeking a challenging and rewarding position in a dynamic organization to contribute my skills, knowledge and experience of working in different local and multinational organizations with an opportunity to promote the status of the organization and my professional development and career growth as well.

QUALIFICATION

2010 Pharm D University of Karachi

2005 Intermediate (Pre Medical) BAMM P.E.C.H.S Govt. college for women 2003 Matriculation (Science) Usman Public School

EXPERIENCE

Bayer Pakistan (Private) Limited March 2013 to September 2015 Position: Quality Assurance Officer – GMP Documentation

Main Responsibilities –

Compilation of executed batch records, executed laboratory control records, Production control records and associated (executed) records

Release of batch record for:

Preparation and revision of SOPs as per procedure, distribution of approved copies and maintenance of master SOP files.

Responsible for GMP in-process of Plant and submission of weekly report to QA Manager. Conducting follow up of rectification of Observations.

Preparation and maintenance of Master Batch Record. Issuance of Batch Documents to Production department. Recording and Compilation of Product Quality Reviews. To do Process validation, method validation. Updation and Maintenance of Site Master File. GMP Documentation and record Retention as per Bayer Directives. Deviation Management and related Corrective and Preventive Actions. Conduct employee training sessions about GMP, SOP trainings and drug laws. Participation in the investigation of complaints, deviations, discrepancies etc. related to the quality of the

product as well as counterfeit issues. Participate in conducting internal audit (self inspection) as per GMP guidelines. Preparation of internal audit report submitted to QAM Participate in preparation of TAC Audit. Participate in preparation of audits of local drug regulatory officers. Implementation of 6S within department.

Spencer Pharma (Private) Limited January 2012 to February 2013

Position: Product Development Officer Main Responsibilities –

Develop Product Process plans for New or under development products. Develop BMRs for new develop products. Develop SOPs for dispensing, manufacturing, packaging and storage of raw materials and finish goods. Improve current BMRs as per GMP. Implementation of GMP Standards on work place. Implement Process and control Check Sheets. To do Process validation, method validation. Improve Finish Good Monographs. Preparation of drug master file. Software Documentation.

Geofman Pharmaceuticals March 2011to December 2011

Position: Production officer Department: Penicillin Cream and Ointments

Main Responsibilities –

Manage and supervise the manufacturing of quality products as per GMP standards. Manage and plan the work for maximum production. Manage the labor for encouraging them to give their maximum output for quality production. Manage the production floor as per GMP standards. Detail report on the production work. Manage the Packaging Department for Solid, Liquid Dosage Forms. Manage the Packaging Department for Injectables. Maintain all documentation of Manufacturing and Packaging Department. Prepare Monthly Statement Report for Packaging Department. Maintain BMRs for Production Department.

Liaquat National Hospital 1st June 2010- 30th June 2010 Position: Internship

TRAININGS

Internal training on 6S Internal training on Drug Law 1976 External training from PIMS on Effective Letters, Reports and Presentations

SKILLS

SAP Microsoft Office (Excel, Word, Power Point) PDF Writer

EXTRA SKILLS

Leadership skills.

Multi tasking skills

Good communication skills.

Emergency/Crises management skills

Good decision making skills

Good time management skills.

Able to perform actively in group task.

INTERESTS Reading books & novels, traveling and cooking.