This document contains the resume of Anan Othman, outlining his personal and professional experience. He is currently a Senior Production Supervisor at JOSWE Medical with over 15 years of experience in production and quality management roles. Previous positions include Production Manager at United Veterinary Drugs Industrial Company from 2009 to 2015, Quality Control Department Manager from 2008 to 2009, and Production Department Manager from 2004 to 2008 at the same company. He holds a B.Sc. in Chemical Industries Engineering and is proficient in English, Arabic, and various computer programs.
SAI Global Webinar: Tips for Effective Internal AuditingSwitzerland09
Tips and Techniques for Managing an Effective Audit Program
A key source of information for the leadership of any organization is the internal audit process. A well-managed and comprehensive internal audit program is invaluable to the leadership as it provides them with a clear photograph of the current state of the enterprise. Implemented properly the internal audit process can not only focus attention on nonconforming processes, it should also be a driver for best practice sharing and identification of continual improvement opportunities. The success or failure of an internal auditing program starts with leadership support. Too often however, leadership does not fully appreciate or understand the value the audit process can provide to an organization. It is simply viewed as another in a series of requirements to be completed.
Join Carmine Liuzzi, Industry Leader and Management Systems Consultant with SAI Global for a free 1-hour webinar to discover tips on how organizations can gain the maximum business benefits from an effective internal audit program.
Agenda:
• Why We Audit?
• The Ideal Audit Process – Items for Consideration
• How to Gain Leadership Support for Audits - Value-Added Nonconformity Statements
• Q&A
Duties & Responsibilities of Quality Assurance Managerssagarusms14
Quality assurance managers play an important role in business by ensuring that products meet certain thresholds of acceptableness. They plan direct or coordinate quality assurance programs and formulate quality control policies. They also work to enhance an organization's efficiency and profitableness by reducing waste. If you're conscientious, inquisitive and committed to excellence, you'll realize it gratifying to work in this quality compliance occupation.
SAI Global Webinar: Tips for Effective Internal AuditingSwitzerland09
Tips and Techniques for Managing an Effective Audit Program
A key source of information for the leadership of any organization is the internal audit process. A well-managed and comprehensive internal audit program is invaluable to the leadership as it provides them with a clear photograph of the current state of the enterprise. Implemented properly the internal audit process can not only focus attention on nonconforming processes, it should also be a driver for best practice sharing and identification of continual improvement opportunities. The success or failure of an internal auditing program starts with leadership support. Too often however, leadership does not fully appreciate or understand the value the audit process can provide to an organization. It is simply viewed as another in a series of requirements to be completed.
Join Carmine Liuzzi, Industry Leader and Management Systems Consultant with SAI Global for a free 1-hour webinar to discover tips on how organizations can gain the maximum business benefits from an effective internal audit program.
Agenda:
• Why We Audit?
• The Ideal Audit Process – Items for Consideration
• How to Gain Leadership Support for Audits - Value-Added Nonconformity Statements
• Q&A
Duties & Responsibilities of Quality Assurance Managerssagarusms14
Quality assurance managers play an important role in business by ensuring that products meet certain thresholds of acceptableness. They plan direct or coordinate quality assurance programs and formulate quality control policies. They also work to enhance an organization's efficiency and profitableness by reducing waste. If you're conscientious, inquisitive and committed to excellence, you'll realize it gratifying to work in this quality compliance occupation.
Campden BRI and Alchemy in partnership with BRC, SGS, SQF and TSI have released the results of the fourth annual global survey of food safety training. The survey questioned food and drink manufacturers and processors worldwide to identify the needs, effectiveness and challenges of food safety training in the industry.
The results reveal some interesting trends:
Improving food safety culture was the top training goal for almost 80% of those surveyed
Many companies are not exploiting the specialist expertise available in their HR departments
Traditional training methods are still favored over online methods
Presented By :- Raghav Sharma
Class :- M.Pharm, 1st sem.
Department :- Pharmaceutics
Institute :- Parul Institute of Pharmacy
Content :-
Current good manufacturing Practices
Equipment and their maintenance
Production Management
Conclusion
References
Good Manufacturing Practices (GMP) is a system that ensures that the goods produced by various
manufacturing facilities are consistently produced and controlled according to specified quality
standards. There are GMP systems for everything from cosmetics to pharmaceutical products
and of course, food.
GMP looks at every aspect of the manufacturing process to guard against potential risks that can
prove detrimental to its products. Cross-contamination, mislabeling, and adulteration are just a
few of the things GMP aims to prevent. Thus it aims to make customers happy and satisfied by
delivering them safe food.
Campden BRI and Alchemy in partnership with BRC, SGS, SQF and TSI have released the results of the fourth annual global survey of food safety training. The survey questioned food and drink manufacturers and processors worldwide to identify the needs, effectiveness and challenges of food safety training in the industry.
The results reveal some interesting trends:
Improving food safety culture was the top training goal for almost 80% of those surveyed
Many companies are not exploiting the specialist expertise available in their HR departments
Traditional training methods are still favored over online methods
Presented By :- Raghav Sharma
Class :- M.Pharm, 1st sem.
Department :- Pharmaceutics
Institute :- Parul Institute of Pharmacy
Content :-
Current good manufacturing Practices
Equipment and their maintenance
Production Management
Conclusion
References
Good Manufacturing Practices (GMP) is a system that ensures that the goods produced by various
manufacturing facilities are consistently produced and controlled according to specified quality
standards. There are GMP systems for everything from cosmetics to pharmaceutical products
and of course, food.
GMP looks at every aspect of the manufacturing process to guard against potential risks that can
prove detrimental to its products. Cross-contamination, mislabeling, and adulteration are just a
few of the things GMP aims to prevent. Thus it aims to make customers happy and satisfied by
delivering them safe food.
I'm Looking forward to a challenging work opportunity in your esteemed organization, where my experiences can be utilized and enriched and I can share in achieving the organization mission and strategic goals.
certificates link:
https://www.slideshare.net/AhmedShehta12/ss-250260913
To obtain a position within the Biotech arena that will enable me to use my strong organizational skills, educational background and ability to work well with people.
2-Quality-assurance-6th-Sem Quality control and GMP
CV Anan Othman
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.