MOHANNED JALLAD

Duties and responsibilities:
 Leading Project Development in EU registration
 Lead the development of robust, stable and effective formulations to be used for in-house manufacturing and also at 3rd party manufacturers, when provided the amount of medicinal ingredients in the dosage form for new product development.
 Make Quality by Design as EU regulation.
 Patent Evaluation and make non-infringing formula
 Supervise and support formulation researchers through their jobs.
 Evaluation and setting specifications of the materials to be used in the development according to EU.
 Support the analytical methods development.
 Training of formulators on departmental procedures and SOP’s.
 Follow up the development progress with formulators.
 Technical evaluation of the products to be handled.
 Participate in products trouble shooting when applicable.
 Participate in the issuance of raw material, packaging and finished products specifications.
 Contact relevant departments for preparation for scale up batches.
 Follow up the manufacturing of scale up batches.
 Follow up the generation of product development reports.
 Participation in technology transfer between Chanelle Labs and manufacturing areas in Ireland.
 Lead & Follow up with the RA personnel the deficiency letters during registrations
 Prepare manufacturing trial documentation for pilot / small production runs and scale-up operations.
 Lead technology transfer and scale-up operations to manufacture products in-house.
 Participate in investigations into product failure including quality, potency, visual characteristics and other.
 Ensure involvement in all trouble-shooting activities.
 Develop/review Raw Material and Finished Product Specifications, in
 Make Evaluation for New Material DMF according to EMA requirements.
 Skills:
-Develop robust formulation
-Design and Execute Quality by Design
-Technology Transfer
-Preparation of product development report
-Smart in response for Deficiency letter related to EMA assessor.

*Duties and responsibilities:
-Drug formulation and formula design
- In pilot manufacturing of solids and liquid forms.
-Make troubleshooting for Formula and process
- Following up and evaluating the dissolution results for solids.
-Make process validation in production plant
- Make literature survey and Pre-formulation study for new projects
-Suggestion the formula for new projects and make optimization.
-DRUG master formula construction
- Batch manufacturing record build up and checking
- Ordering the required materials for pilot drug manufacturing
- Intra-department coordination and planning
-Requesting and handling R&D raw materials
 Skills:
-Excellent command of table ting and granulation procedures.
-Excellent command of tableting and granulation procedures in
production scale batches
-Vast knowledge of the production scale machines

* Duties & responsibilities
-checking & evaluation for APIs DMF
-Drug formulation and formula design (Solution for infusion bag-
Liquid Vial-Lyophilized powder vial).
- In pilot manufacturing of sterile product
-Make troubleshooting for Formula and process
- Following up and evaluating the results of stability.
-Make process validation in production plant
- Make literature survey and Pre-formulation study for new
projects -Suggestion the formula for new projects and make
optimization. -DRUG master formula construction
- Batch manufacturing record build up and checking
- Ordering the required materials for pilot drug manufacturing
- Intra-department coordination and planning
- Preparing finished product sample for registration, classifications and
tenders purpose
-Preparing designs using CorelDraw & Adobe Illustrator CS5for for registration
, classifications and tenders samples
-Requesting and handling R&D raw materials

*Duties and responsibilities:
-Establishment of R&D department and quality system in company
-upgrading the available company system in order to meet SFDA Pharma requirements
-Reviewing and follow-up for SFDA regulations
-Drug formulation and formula design - In pilot manufacturing of semi-solids and liquid forms. -Make troubleshooting for Formula and process
- Following up and evaluating the results of stability.
-Make process validation in production plant
- Make literature survey and Pre-formulation study for new projects
-Suggestion the formula for new projects and make optimization.
-DRUG master formula construction - Batch manufacturing record build up and checking - Ordering the required materials for pilot drug manufacturing - Intra-department coordination and planning
-Preparing registration file and CTD files
- Preparing finished product sample for registration, classifications and tenders purpose
-Preparing designs using CorelDraw & Adobe Illustrator CS5for for registration, classifications and tenders samples
-Requesting and handling R&D raw materials

*Duties and responsibilities:
-Drug formulation and formula design - In pilot manufacturing of solids, semi-solids and liquid forms. -Make troubleshooting for Formula and process
- Following up and evaluating the dissolution results for solids.
-Make process validation in production plant
- Make literature survey and Pre-formulation study for new projects
-Suggestion the formula for new projects and make optimization.
-DRUG master formula construction - Batch manufacturing record build up and checking - Ordering the required materials for pilot drug manufacturing - Intra-department coordination and planning
-Preparing registration file and CTD files
- Preparing finished product sample for registration, classifications and tenders purpose
-Preparing designs using CorelDraw & Adobe Illustrator CS5for for registration, classifications and tenders samples
-Requesting and handling R&D raw materials

Duties and responsibilities:
-Drug formulation and formula design
- In pilot manufacturing of semi-solids and liquid forms.
-Make troubleshooting for Formula and process
- Make process validation in production plant
- Make literature survey and Pre-formulation study for new projects
-Suggestion the formula for new projects and make optimization.
-Drug master formula construction
- Batch manufacturing record build up and checking
- Ordering the required materials for pilot drug manufacturing
- Intra-department coordination and planning
-Preparing registration file
- Preparing finished product sample for registration, classifications and tenders purpose
-Preparing designs using CorelDraw & Adobe Illustrator CS5for for registration, classifications and tenders samples
- Make calibration and verification for Balances and thermometers
-Requesting and handling R&D raw materials