Yousef Ahmad Y. Banat is seeking a position in quality assurance in the pharmaceutical industry. He has a B.Sc. in Chemical Technology and over 7 years of experience in quality assurance roles. His experience includes documentation, compliance inspection, batch record review, and finished product testing. He is proficient in MS Office, GMP, and GDP. He is motivated, dedicated, and eager to take on new challenges.

1. Yousef Ahmad Y. Banat
Jarash-Jordan
yab_045@yahoo.com
Tel: 00962 77 2361993
Looking for position in a reputed company that lets me utilize my knowledge,
interpersonal skill and extrovert personality for growth of the company.
PERSONAL PROFILE
Date of Birth : 12th April 1987
Gender : Male
Marital Status : Single
Languages Known : Arabic & English
Nationality : Jordanian
EDUCATION
B.Sc. in Chemical Technology -2011
Tafila Technical University (TTU)
COMPUTER SKILLS
Operating System : Windows 95/98/XP/WIN 7
Packages : MS-Office(Word, Excel, Power Point, etc)
EXPERIENCE:
Employer: Al-Taqadom Pharmaceutical Industry Company
Industry: Pharmaceutical Industry
Position: Quality Assurance Officer/ Documentation Officer
Time period: APR2014- Present
Location: Amman-Almuwqqar
Description of Job:
 Preparation of the manufacturing and packaging batch records upon the
requisition of production departments.
OBJECTIVE

2.  Preparation of the department’s logbooks using the suitable approved
forms based on a requisition from the departments.
 Enter the approved document data to the documentation data base.
 Prepare a copies from the approved documents required to be distributed
to the departments.
 Distribution of the approved documents and calling back the cancelled
and revised documents.
 Filing of the active documents in suitable file based on the type of the
document and the issuance department.
 Keeping the latest version of the cancelled and revised documents for the
suitable retention time.
 Checking of the documents for the appropriateness and compliance with
the internal documentation system before final approval.
 Performing any other activities requested by Quality Assurance Manager
and documentation supervisor regarding Quality Assurance Duties.
Employer: Al-Taqadom Pharmaceutical Industry Company
Industry: Pharmaceutical Industry
Position: Quality Assurance Officer/ Compliance Inspection Technician
Time period: APR2012- APR2014
Location: Amman-Almuwqqar
Description of Job:
 Perform daily tour in the manufacturing packaging areas in addition to
warehouses to check the compliance of the performed activities and
documentation with the approved systems and procedures.
 Write inspection reports regarding noncompliance activities and submit to
area supervisor to do the suitable corrective/preventive actions and then
forward the report to the inspection supervisor.
 Follow up the required action suggested by the departments or by Quality
Assurance supervisor and Quality Assurance Manager.
 Review the batch record documentation and compare the performed steps
and progress of the process with the documented steps on the batch record.
 Perform the acceptance tests of the finished products before final release as
part of finished product inspection procedure.
 Check the cleanliness of the working areas and machines in production and
packaging before starting production daily activities.
 Check the environmental control parameters such as temperature and
humidity in production and warehouses and check the relevant logbooks.
 Performing any other activities requested by Quality Assurance Manager and
supervisor regarding Quality Assurance Duties.

3. Employer: Hayat Pharmaceutical Industry Company
Industry: Pharmaceutical Industry
Position: Quality Assurance Officer
Time period: DEC2011-APR2012
Location: Amman-Sahab
Description of Job:
 Perform daily tour in the manufacturing and packaging areas in addition
to warehouses to check the compliance of the performed activities and
documentation with the approved systems and procedures.
 Write inspection reports regarding non-compliance activities and submit
to area supervisor to do the suitable corrective / preventive actions and
then forward the report to the inspection supervisor.
 Review the batch record documentation and compare the performed
steps and progress of the process with the documented steps on the
batch record.
 Perform the acceptance tests of the finished products before final release
as part of finished product inspection procedure.
 Check the cleanliness of the working areas and machines in production
and packaging before starting production daily activities.
 Check the environmental control parameters such as temperature and
humidity in production and warehouses and check the relevant logbooks.
 Review all documents and records including batch manufacturing
and packaging records in addition to Quality Control Records as
part of Finished Product release
Publications, Courses & Even
GMP: Good Manufacturing Practices.
GDP: Good Documentation Practices.
Manufacture of oral solid dosage forms:
(Granulation & Compression: Current Updates, Practical Issues)
TRAINING
Employer: Hikma Pharmaceutical Industry Company
Industry: Pharmaceutical Industry
Position: Trainee
Time period: FEB2011-APR2011
Location: Amman- Bayader Wadi Al Sir

4.  Trained in Hikma Pharmaceuticals during my studies at the chemical
plant in the Department of QC and I have experience in working on the
devices: HPLC, GC, UV, IR.
STRENGTHS & SKILLS
 I am having a passion to learn and improve all the time.
 Ready to take up new challenges.
 Self-motivated and a quick learner with a good team spirit.
 Dedicated, friendly and a self confident person.
REFERENCES
 Eng. Ahmad abu-Rahma
Quality Assurance Department manager
Al- Taqaddom Pharmaceuticals Industries.
E-mail a.aburahma@tqpharma.com
 Abdulrhman jameel hawwari
Quality Assurance Department Supervisor
Al- Taqaddom Pharmaceuticals Industries.
E-mail abd_lm@yahoo.com
If given a chance to work in your organization I assure best of my services to the Organization
and up to the expectations of my superiors.