Mohammed Tarawneh

• Responsible for all technical operations & departments and ensuring that they are performed
according to the GMP requirements inside departments (QA, QC, Production, Warehouse, and R&D).
• Improving and leading production processes and continuous quality systems processes to facilitate
future production processes.
• Effective communication, finding appropriate solutions for the work environment, and sharing
information appropriately with all team members and individuals.
• approved and verified the results and tests of laboratories, the research and development
department, and the results of the stability study, and prepared the required files for registration.
• Preparing daily, weekly, and monthly production plans in cooperation with warehouses to ensure
timely completion of orders.
• Monitoring and following up production processes and schedules to ensure the production plan is
achieved at the right time.
• Maintaining a safe and healthy work environment by adhering to regulations, laws, and public safety.
• Follow up on subordinates and employees to do their work to the fullest extent, improve their
performance, and train them properly.
• Monitors product quality standards and implements quality assurance and compliance programs.
• To ensure that customer requirements are effectively transcribed in the technical documentation and
database.
• To highlight any issues in the preparation of technical documents and databases and offer solutions
when necessary.
• Support Project Management, Regulatory and QC, and Customers requiring technical documentation
support.
• Leads and actively participates in the investigation of issues related to the technical documentation
and database.
• Responsible for ensuring that required technical documents are available to ensure that products
manufactured meet the requirements and specifications.
• Updates the technical database ensuring availability of the technical documents within the agreed
time frame.
• To ensure that only effective documents are used in the operations.
• To adhere to the GMP & GLP norms.
• To check for new and revisions to existing technical documents from customers and other sources to
ensure updating of the technical database and documents.
• To file required records following relevant instructions in order to provide and report whenever
necessary.
• Review current work practices to improve quality standards.
• To update and capture results of validation studies and incorporate them in the technical database
and documents.

QC and R&D Manager :
• Create new products (new formulas).
• Develop new and old products.
• Follow up stability products.
• Find solutions for several problems on products or in production plant.
• Choosing best raw materials that compatible with our materials specification and give approval to purchase the materials before purchase order.
• Cooperation with Business Development Manager to find and select the correct and the best new product as required by marketing demand.
• Preparing registration files for local and global market.
• Control all factory process by applying GMP in (production, Packaging and warehouse) by distribution the missions between our QC team.
• Take samples of raw materials and packaging for testing
• Give Raw/Packaging materials release to start weighing, preparing and packaging products after do the needful test from QC ( Physio - chemical test) and microbiology labs.
• Preparing first three batches for new products in production.
• Give training and follow up the new employee or trainee.
• Preparing Batch record for production, regarding to production facilities.
• Preparing SOPs for QC, Micro and Research & Development departments.
• Performed initial client assessment and analysis to begin research process.
• Analyzed departmental documents for appropriate distribution and filing.
• Obtained documents, clearances, certificates and approvals from local, state and federal agencies.

Administrator for technology transfer, stability, scaling up, validation batches, production supervisor for cephalosporin plant

as a senior formulator in R&D

Formulator, scaling up batches, stability, validation process

Production supervisor