resum

4
SHUMAILA KHAN Career Objective: I am looking forward for a position in Quality Control department. I expect a career which is different yet unique, my intelligence is continuously nourished by challenges and constant quest for knowledge is honed on the newest of technologies. Looking forward to a challenging career in an organization where I can sharpen my professional skills and experience and work at a position where my ability for innovative decision making could be tapped. Professional Strength: Sincere and committed, disciplined, taking initiative and accepts responsibilities cheerfully. Willingness to “Go the Extra Mile” when required. Using assignments for growth and development Professional Attributes: I consider myself to be confident and a strong participator in group ventures. I enjoy working as a team, but can easily work on my own initiative. I look forward to new opportunities and new challenges and look forward to be associated and grow in such an organization. Summary: Over 3 Years of Analytical Experience in Pharmaceutical Industry in quality control department. Work Experience: As a Senior QC Analyst in Cibex pharma Since Aug 2013 to till the date Work profile in Finished Product section. Received the inward sample in the laboratory along with respective entries in the log book To perform the method transfer of the finished products related to HPLC. Page 1 of 4

Upload: shumaila-khan

Post on 15-Apr-2017

43 views

Category:

Documents


0 download

TRANSCRIPT

Page 1: Resum

SHUMAILA KHAN

Career Objective:I am looking forward for a position in Quality Control department. I expect a career which is different yet unique, my intelligence is continuously nourished by challenges and constant quest for knowledge is honed on the newest of technologies.Looking forward to a challenging career in an organization where I can sharpen my professional skills and experience and work at a position where my ability for innovative decision making could be tapped.

Professional Strength:Sincere and committed, disciplined, taking initiative and accepts responsibilities cheerfully. Willingness to “Go the Extra Mile” when required. Using assignments for growth and development

Professional Attributes:I consider myself to be confident and a strong participator in group ventures. I enjoy working as a team, but can easily work on my own initiative. I look forward to new opportunities and new challenges and look forward to be associated and grow in such an organization.

Summary:Over 3 Years of Analytical Experience in Pharmaceutical Industry in quality control department.

Work Experience:

As a Senior QC Analyst in Cibex pharma Since Aug 2013 to till the date

Work profile in Finished Product section. Received the inward sample in the laboratory along with respective entries in the log book To perform the method transfer of the finished products related to HPLC. To perform analysis of finished Products and in-process samples. To perform analysis of stability samples. Preparation of worksheet along with Specification and STP’s. To plan stability of finished product according to guidelines.

Work profile in Raw Materials section. Analysis of Raw material samples with online documentation and calculation sheet

completion

Page 1 of 3

Page 2: Resum

Work Profile in Chromatography Section. Working in Chromatography Section. To perform analysis of API & formulation Products. Handling of Pre-evaluation incidences, System suitability incidences. Reporting of day to day activities immediately to superiors.

Instrument Handled: HPLC System Dissolution Testers UV Spectrophotometer Tablet Hardness Tester Tablet Friability Tester Disintegration Time Apparatus Karl Fischer Apparatus Weighing balance pH meter Polari meter Melting Point Apparatus Conductivity meter Refractometer

Professional Skills: To perform the calibration of lab instruments Planning and work allocation, assurance the completeness of the activity. Review of analytical documents and compilation. Handling of laboratory incidents and deviation. Handling the investigation of OOS/OOT results with Q.C.Head / Concern person. Testing Method Development Validation of Testing Method Manufacturing Process Validation Standardization of Working Standard Criteria for vendor approval GMP & GLP Compliance Documentation Preparation of volumetric and test solution Packaging Art work review Inventory of lab accessories and reagents. Product registration document preparation. Batch Document Review. Basic knowledge of Raw Materials.

Audit faced:In my 3. Years Exp. I have do working with GLP, cGMP, Safety, as per Guidelines and with discipline and faced audits like ISO, DML, GMP, Regulatory audits.

Educational / Projects:

Page 2 of 3

Page 3: Resum

200 hours Internship in Abbasi Shaheed Hospital Karachi. Training of 200 hours in Noa Hemis Pharmaceuticals Karachi in June 2011 which includes

briefing about Packaging Department, Ware house, Solid and Liquid Production Department, Quality Control & quality Assurance.

Training in Centre for Bioequivalence Studies and Bioassay Research (C.B.S.B.R) KU, on clinical Conduction of Bio-availability / Bioequivalence Studies, consisting on Screening and recruitment, Dosing, Sample collection, processing & Storage of Samples.

Personal Profile:Education:

MBA (Pharmaceutical Management) from Dow university of Health Sciences in 2016 (2nd Semester Cont.)

Pharm D from University of Karachi in 2012 (1st Division C.GPA 3.3) Intermediate (Pre-Med) from St. Joseph’s College for Women in 2007 (A Grade) Matriculation from Rehman Children school in 2005 (A-1 Grade)

Computer Skills: Ms Office (Ms Word, Ms Excel, Ms Power Point) Adobe Acrobat, Nitro PDF ERP

Personal Details: Father’s Name: Nawab Ahmed KhanCNIC : 42401-2765138-0Nationality : PakistaniDomicile : Sindh (Urban)Marital Status : UnmarriedCell No: 0332-9268435E-mail: [email protected] Address: House # 1067 Touheed Colony , Sec-11 New “L” Block Orangi Town,

Karachi

Declaration: I hereby declare that, the above given information by me are true and correct to the best of knowledge.

Reference: Reference will be furnished upon request.

Page 3 of 3