C V (updated 2016)

ZEESHAN SOHAIL
PERSONAL INFORMATION
Address House # 48/A ,Project no 2, Pakistan Railway Society, Block #10-a ,Gulshan-e-Iqbal, Karachi
,Pakistan.
Telephone: (Mobile) +92-333-3497470
(Postal code) 75290
E-mail shani04june87@hotmail.com
zeeshan.sohail57@skype.com
Gender Male
Religion Islam
Marital status
Date of birth
married
4th
June 1987
Place of birth
C.N.I.C#
U.A.E ( Al-Ain)
42401-4655008-1
EDUCATION
2015
2011
2010
 MBA (Marketing)
 MSc (Chemistry)
 BSc(honours) (Chemistry)
Preston university.(H.E.C recognized) continue
University of Karachi 1st
division
University of Karachi 1st
division
2006  HSSC (Pre-medical) Government Dehli College 1st
division
2004  SSC (Science) Rakhshinda Public Secondary School 1st
division
RELEVANT COURSES ATTENDED
Courses undertaking in B.S  Major INORGANIC CHEMISTRY with BIOSTATISTICS and BIOCHEMISTRY as
subsidiaries.
 COMMUNICATION SKILLS (Assignment: report, presentation on multimedia.)
 ENGLISH LITERATURE.
Scientific Research
at
Govt. Of Pakistan Ministry of Science &
Technology (P.C.S.I.R)
 INFORMATION TECHNOLOGY (Assignment: report ,search work ,presentation on multimedia)
 COMMUNITY DEVELOPMENT (Assignment: report, search work from books and internet)
 ECONOMICS (Assignment: report ,search work from books and internet)
Pakistan Council of Scientific & Industrial Research Laboratories Complex, Karachi
(P.C.S.I.R)
 Synthesis of Derivatives of 4-Amino -5-Hdroxy-2, 7-Naphthalenedisulfonic Acids and
investigate their properties.
 Analytical techniques : (1) thin layer Chromatography
(2) HPLC
(3)UV-Visible Spectroscopy
Page 1

WORLD HEART DAY
28TH
September 2011
Attend different Youth Seminars related to Health & Medicines
Risk factor of Heart Disease with certificate is awarded.
Session based on Bloom's Taxonomy & VARK Learning Style Theory-
6.5 Credits Hours.
Executive Quality Assurance (Validation)
 Arrange and deliver cGMP Training of staff, departmental SOPs training etc
 Ensure timely execution of all validation/qualification activities at plant as per Quality
Standards.
 Plan, prepare protocols, get approved and perform the all plant validation activities
(periodic as well as new ones) along with my supporting team.
 Random GMP inspection of factory premises.
 Area monitoring of sterile area.
 Inspection of Production area, warehouse, packaging store and Raw material store.
 Batch record review/Audit.
 Responsible for the implementation and maintenance of validation master plan.
 Handling all activities related to validation.
 Preparation and reviewing of validation protocols and reports..
 Responsible for the IQ/OQ/PQ for new machines and re-validation for the existing ones.
 Reviewing and assessing the impact of any changes in process or equipment on the
corresponding validation status.
 Provides technical support in resolving validation-related exceptions or deviations.
Provide validation support to plants for new projects assigned.
Workshop
On
Effective Communication
Skills
Employment History
Healthtek (Pvt.) Ltd.
(2nd
may 2015 – present)
Responsibilities:
Brookes Pharma (Private) Limited.
(24th
March 2014 –28th
April 2015) Quality Assurance Officer (sterile area)
Page 2

Responsibilities:  Ensure the compliance and GMP during manufacturing and packaging processes and
ensure the product quality, safety and efficacy throughout the product life cycle.
 In process checks during Manufacturing, ampoules Washing, Filling, filtration, autoclaving
& leak testing
 Verification of integrating test for bubble point of bulk product.
 Verification & assurance of area monitoring & particle count
 Manual optical of vials/ampoules
 Sampling (Bulk, Intermediate & Finished Products and stability samples
 Verification of return packaging materials (Physically & on BIMS)
 Verification of F.O / inventory lot returns
 Record inserting electronically, Updating record of daily activities
 Record of deviation during processes & rectifications
 Verification of activities related log books, and process related documents
 Calibration of processing vessels / volume rod
 Environmental monitoring (Temp., R.H, Diff. pressure, air velocity)
 Calibration of weighing scales, and process control equipment through 3rd
party and its
record keeping,)
 APQR (APR)
 Expended Investigation, Deviation
 ICSSR (Inspection of market return goods and reworking slips and its disposition) or rework
 Checking / verification SOPs, MOs and Directions
 Record updating, disposition of retention samples/Batch documents
 Conduction of self-inspection
 Monthly inspection of Fire extinguishers and fire buckets
 Preparation & verification of records i.e. Narcotics/psychotropic products
Barrett Hodgson Pakistan Pvt. Ltd.
(Feb. 2013 – March 2014) Quality Assurance Officer (sterile and non-sterile area)
Responsibilities:  Arrange and deliver cGMP Training of staff, departmental SOPs training etc.
 To monitor the dispensing activity in the warehouse during dispensing of raw material.
 To carry out the inspection and sampling of following as per standard operating procedure
of solid, semi solid, capsule, ophthalmic/ ear, liquid, and clean area of the manufacturing
plant.
 Intermediate products (granules).
 Bulk products
 Finished products
 Product supplied from contract manufacture or imported products
 Returned goods
 Packaging components.
 To submit the samples to laboratories for testing purpose.
 To ensure that in-process checks are carried out for each batch of each product during
manufacturing and packaging, according to standard operating procedure.
 To ensure that in-process rejections are inspected and certified before disposal.
 To ensure that the reference samples of each batch of each product during packing or
imported product /contract manufactured products are collected according to standard
operating procedure.
 To audit the batch record of production and packing of each product for completeness and
correctness, before the batch release. If batch yield is not within limits, proper investigation
have been carried out and documented with batch record before batch release.
 To ensure that the destruction of rejected products, packaging components and returned
goods are being carried after proper authorization according to standard operating procedure.
Elko Organisation (Private) Ltd.
(Aug.2011 –Jan.2013) Quality control Analyst
Page 3

Responsibilities:  Writing and reviewing the Standard Operating Procedures (SOPs) and Testing Methods in
compliance with cGMP, Pharmacopoeias and other International References.
 Carry out daily inspection in the factory.
 Auditing the Batch Manufacturing Records.
 Sampling and Testing of Packaging Materials & Commodities.
 Inspect any deviation against cGMP rules and ISO procedures, raise deviation/ non-
conformity report, maintain their records and identify root causes and corrective / preventive
actions.
 Knowledge about Instruments:
 HPLC
 Dissolution Apparatus
 Spectrophotometer
 Potentiometer
 Karl’ Fisher
 D.T Apparatus
 Hardness Tester
 Friability Tester
 Melting Point Apparatus
 Conductivity Meter
 pH Meter
TECHNICAL SKILLS  MS Word, Excel, PowerPoint
 BIMS (Data entry Oracle base software) used in Brookes pharma Pvt. Ltd.
 J.D Edward (data entry C++ base software)used in Barrett Hodgson Pakistan
 Accounting Program (Data entry version 6.0 software ) used in Elko Organisation Pvt. Ltd.
REFERENCES To be furnished upon request.
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C V (updated 2016)

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C V (updated 2016)