1. Anan Othman
Personal Data
Gender : Male
Nationality : Jordanian
Date of Birth : November 8th
, 1975
Marital Status : Married
Work Experience
August 2015- Current
Production Senior Supervisor
JOSWE Medical
 Responsible for the liquids Production Department.
 Plan, organize, supervise and implement manufacturing procedures in
accordance with Quality Assurance methods, new process
technologies, organizational strategies and quarterly/annual budgets.
 Implementation of good manufacturing practice “GMP”
 oversee the production process, drawing up a production schedule
 monitor the production processes and adjust schedules as needed;
 liaise among different departments, e.g. suppliers, managers;
 ensure that the production is cost effective;
 decide what resources are required;
 draft a timescale for the job;
 Set the quality standards;
 monitor product standards and implement quality-control programs;
 work with managers to implement the company's policies and goals;
 ensure that health and safety guidelines are followed;
 supervise and motivate a team of workers;
 review worker performance;
 identify training needs.
January 1st
,2009 – Feb,2015
Production Manager
United Veterinary Drugs Industrial Company (UVEDCO)
Primary Duties:
 Responsible for the production Department, Maintenance
Department , and inventory Departments
 Implementation of good manufacturing practice GMP
Duties activities
Production Departments:
• Planned, organized, supervised and implemented manufacturing procedures
in accordance with Quality Assurance methods, new process technologies,
organizational strategies and quarterly/annual budgets.
Mobile: +962-79-0169234
Fax: +962-6-5561282
Email: a.mahmoud75@hotmail.com
P.O. Box 1504,
Amman 11910 - Jordan

2. Main Contributions:
 Knowledge of manufacturing principles, standard production procedures and
stocking protocols
 Managed comprehensive planning activities
 Assist to monitor all department budgets and manage all inventories on
quarterly basis and assist all team members to manage all production
schedules
 Managed all work flow for projects and maintain control on same and
managed an efficient inventory level of all safety stock and review all volume
requirements for all production materials.
 Supervised and administered staff and equipment/machines throughout
production process.
 Analyzed and prepared production budgets and timelines required to
complete production projects.
 Ensured timely stocking of material
 Ensured that all safety and quality measures were adhered to during
production process, from beginning to end.
 Enabled proper utilization of resources, reducing wastage
 Exceptional leadership skills with proven ability to hire, lead, motivate and
develop personnel
Maintenance Department
 Supervising with department staff all production machines and laboratory
apparatus.
 Ensure availability of spare parts by communicating with primary vendors
and suppliers for faulted machines and ensure availability of spare parts to
use on demand.
 Follow up maintenance reports and repair reports.
Inventory Department – Raw Material
 Ensure availability of all necessary raw material required for production
according to monthly and quarterly plan.
 Coordination between raw material inventory and Quality control
Department to deliver the raw materials that comply with the quality
standards (B.P. and U.S.P.)
Inventory Department – Finished Products
 Organise dispatch of finished products in terms of orders and production
date
January 1st
,2008 – January 1st
,2009
Quality Control Department Manager
United Veterinary Drugs Industrial Company (UVEDCO)
• Supervising quality control procedures and ensure Total Quality
Management TQM.
March 1st
,2004 – January 1st
,2008
Production Department Manager
United Veterinary Drugs Industrial Company (UVEDCO)
• Supervising all production line and capacity for products that UVEDCO
produce.
• Responsible to produce veterinary drugs in powder, liquid, injectable dosage
forms and feed additives.
• Responsible for reporting on the performance of the quality system to

3. UVEDCO management for review and as basis for improvement of the
quality system. Supervising all production line and capacity for products that
UVEDCO produce.
• Coordinating between Production, QC, Material and maintenance
departments to ensure that the finished product is produced with highest
quality
May 1st
, 2002 – February 24th
2004
Research and Development Department (R&D), Chemical Analyst
United Pharmaceuticals Company
Tasks Executed during work:
• Analytical method validation.
• Physical and Chemical Analysis.
• Implementing GMP regulations in lab system
All Analysis were carried out by using the following instruments:
 Physical Instruments (Hardness, disintegration, dissolution and memotitrator
tester).
 UV spectrophotometer
 High performance liquid chromatography (HPLC)
 Gas chromatography
Training Course
December 19th
, 2011 – January 16th
, 2012
Project Management Training and Certification Program (PMP) – 52hours
The course was held at Engineers Training Centre (ETC)/JEA.
Presented by Eng. Muneer D. Al-Sabbagh
July 1st
, 2000 – August 1st
, 2000
The Arab Pharmaceutical Manufacturing Co.LTD. (APM).
The course was held to obtain the following aspects and skills: -
 Preparing product for chemical analysis and tests.
 Using laboratory analysing instruments as IR and UV spectra, HPLC and
Gas chromatography.
 Training on various types of pharmaceutical manufacturing machines.
Education
B.Sc. Chemical Industries Engineering/Oran University of Science and Technology
USTO/Algeria, 2001.
Sweilleh Secondary High School, Scientific Stream.
Languages
Arabic: Native Speaker
English: good in both written & Spoken B.Sc. Chemical Industries
Computer
Literacy
Good command of Microsoft Office programmes and the implementation and use of
a variety of planning software.
Other I own a car and have a valid driving license.