Associate Partner and Projects Director
Agon Consult
Total years of experience :24 years, 5 Months
Agon Consult.
Duration Involved January 2010 till present
Role Associate Partner and Projects Director
Responsibilities
- Senior consultant of Industrial companies for the compliance diagnosis and system establishment, the systems include but not limited to:
1. cGMP and GLP requirements
2. GSDP requirements.
3. Service Quality and Excellence
4. Leadership
5. ISO Systems
6. Six Sigma
- Trainer in the following subjects: 1. GMP Compliance Overview
2. Process Control
3. Quality Control
4. Process Optimization
5. Good Documentation Practices
6. Good Storage and Distribution Practices
7. Validation and Qualification: a. Equipment Qualification
b. Water System Qualification
c. HVAC Qualification
d. Process Validation
8. Statistics in Quality
- Initiation and design of business scenarios for the clients to fulfil their requirements and design a tailor-made Consultancy solutions, programs and Training.
Naratech Pharmaceutical Consultancy
Duration Involved January 2008 till 2010
Role GCC Project manger
Responsibilities
- Project management of pharmaceutical manufacturer's compliance diagnosis and system establishment according to cGMP and GLP requirements, to enable companies to register in EU and the GCC countries.
- Project Management of drug stores and cold products store diagnosis and system establishment according to GSDP requirements.
- Follow up the projects from initiation and marketing phases through the conceptual design phase, kick off meeting, carrying out the diagnosis study, task plans initiation and implementation, follow ups and coordination with contractors, suppliers and client, supervise the implementation process up to the inspection phase and project close up.
- Initiation and design of the training department strategy every year, from the suggesting of the workshops and conferences, initiation of the courses, securing the sponsorship (if needed) till the successful delivery of the workshop and conference.
- Initiation and design of business scenarios for the clients to fulfil their requirements and design a tailor-made programs and solutions.
Pro Leads Research Company
Duration Involved January 2007 till January 2008
Role Part Time Researcher
Responsibilities
I took the role of a part time researcher due to my re location to Dubai - UAE where I was working as a researcher who is responsible for following up the Oil and Gas projects in the GCC and report the milestones of these projects into the Pro Leads website and publish these updates through their magazine.
Free Lancer - Self Employed
Duration Involved October 2005 till August 2006
Role Project manger
Responsibilities
- Project management of pharmaceutical manufacturer's compliance diagnosis and system establishment according to cGMP and GLP requirements, to enable companies to register in EU and GCC countries.
- Establish and follow up the Quality system for major pharmaceutical and veterinary drug manufacturers to ensure their compliance to the EU regulations.
- Help under establishment companies by reviewing the conceptual designs, process flow, personnel and material flow diagrams, procurement of utilities and machinery and establishing the quality system.
- Initiation and design of business scenarios for the client's needs to fulfil their requirements and design a tailor-made programs and solutions.
Total Innovative Solutions
Duration Involved March 2005 till October 2005
Role Project manger
Responsibilities
- Project management of pharmaceutical manufacturer's compliance diagnosis and system establishment according to cGMP and GLP requirements, to enable companies to register in EU and GCC countries.
- Establish and follow up the Quality system for major pharmaceutical and veterinary drug manufacturers to secure their compliance to the EU regulations.
- Help under establishment companies by reviewing the conceptual designs, process flow, personnel and material flow diagrams, procurement of utilities and machinery and establishing the quality system.
- Initiation and design of business scenarios for the client's needs to fulfil their requirements and design a tailor-made programs and solutions.
Advanced Pharmaceutical Industries (HIKMA at later stage)
Duration Involved May 2002 till March 2005
Role Quality and Validation Engineer
Responsibilities
- Also I was involved in developing quality control methodologies and tests related to in process testing and finished product testing, and I was also involved in raw material sourcing process.
- As the firm was preparing to be registered in the European Union, I
performed as part of the registration steering committee which guided all the other departments toward a comprehensive quality system, and also I performed as a part of the validation steering team, I designed, supervised, wrote and executed validation protocols in the following areas: * Building and facility, water treatment unit, HVAC unit, Utilities, Labs equipments, Production equipments, Process validation, Cleaning validation,
- As part of the quality assurance section I designed and performed Internal Quality Audits that covered all the departments and all the quality requirements.
- Researched for, developed and performed a statistical treatment of the data out of the process validation, analysis data results treatment, Sampling plans design.
Chemical and Mining Co.
Duration Involved Sep 1999 till May 2002
Role Quality Engineer
Responsibilities
- Monitoring and controlling of lines and process for slurry explosives according to the quality and safety requirements.
B.Sc IN CHEMICAL ENGINEERING 1994-1999 Al-Balqa University-Amman College for Technical Engineering Amman-Jordan
