Waheed Ibrahim Email & Phone Number

Riyadh, Saudi Arabia

Working as a team lead for the external environment shaping as part of the Saudi Diversity, Equity and inclusion (DEICO) committee

Riyadh, Saudi Arabia

Riyadh, Saudi Arabia

Riyadh, Saudi Arabia

Al-Riyadh Governorate, Saudi Arabia

I worked on this function as a part of the human drug section, which is part of the products licensing department, Executive licensing directorate, drug sector. And the following is a brief description of the responsibilities:*Assuring certification payments was received by SFDA.*Assuring all registration/renewal requirements are fulfilled.*Reviewing the product registration information.*Updating products information on SFDA systems, including SDR website (registration, renewal, and variation submissions), SFDA website, registration system.*Issuing registration and renewal certificate.Others:*Training new employees.*Statistical analysis (generating weekly, monthly and yearly reports).*Writing and updating standard operation procedures (SOP’s).*Reviewing and responding to special importation requests (importation and clearance exemption requests with unsubmitted or pending variations).*Reviewing the fundamentals and requirements for registration of pharmaceutical companies and their products, reviewing the law of pharmaceutical establishments and products. *Coordinating and modulating training programs (workshops) made by the SFDA.

Al-Riyadh Governorate, Saudi Arabia

I worked on this function as a part of the human drug section, which is part of the products licensing department, Executive licensing directorate, drug sector. And the following is a brief description of the responsibilities:Importation and clearance exemptions specialist:*reviewing and responding to special importation requests (importation and clearance exemption requests with unsubmitted or pending variations).* Recommending the approval or rejection of the request.Member and rapporteur of registration committee of drug companies and their products. This committee was responsible for approving or rejecting registration of pharmaceutical products and their manufacturers, pricing, products deletion, suspension of pharmaceutical products or manufacturers, deciding the appropriate prescription status for a pharmaceutical product:*Coordinating meetings for the committee.*Presenting topics to the committee during there meetings.*Assuring that the committee follow the roles and regulations of the SFDA.*Voting as a member with the committee.*Writing response and final approval letters to companies based on the committee decision.*Responding to company inquiries (either letters, phones or emails).*Responding to patent protection inquiries.Others:*Responding to Twitter (social media application) inquiries submitted to licensing directorate.*Following up and ensuring the execution of tasks assigned to managers and supervisors within the licensing directorate.*Following up on strategic plans with project managers within the licensing directorate.*Training new employees.*Statistical analysis (generating weekly, monthly and yearly reports).*Writing and updating standard operation procedures (SOP’s).*Coordinating and modulating training programs (workshops) made by the SFDA,

Al-Riyadh Governorate, Saudi Arabia

I worked on this function as a part of the human drug section, which is part of the products licensing department, Executive licensing directorate, drug sector. And the following is a brief description of the responsibilities:Product manager for GCC submissions:*Reception of files from GCC central committee for drug registration.*GCC files validation (for drug registration, variations, and renewals).*Submission to evaluating departments and following up.*Generating evaluation reports.*Updating evaluation reports.*responding to company inquiries (either letters, phones or emails).Member and rapporteur of prepatory committee to evaluate the safety and effectiveness of pharmaceuticals, the committee was responsible for evaluating drug registration, variation and renewal requests specially in relation to safety and efficacy:*Coordinating meetings for the committee.*Presenting topics to the committee during there meetings.*Assuring that the committee follow the roles and regulations of the SFDA.*Voting as a member with the committee.*Writing response and final approval letters to companies based on the committee decision.*Evaluating the committee performance.*responding to company inquiries (either letters, phones or emails).Others:*Responding to Twitter (social media application) inquiries submitted to licensing directorate.*Following up and ensuring the execution of tasks assigned to managers and supervisors within the licensing directorate.*Following up on strategic plans with project managers within the licensing directorate.*Training new employees.*Statistical analysis (generating weekly, monthly and yearly reports).*Writing and updating standard operation procedures (SOP’s). *Inspection of pharmaceutical industries to assure good manufacturing practice (GMP).

Al-Riyadh Governorate, Saudi Arabia

I worked on this function as a part of the human drug section, which is part of the products licensing department, Executive licensing directorate, drug sector. And the following is a brief description of the responsibilities:Variations specialist:*Reception, validation of variations requests.*Submission of variations to evaluating departments and and following up.*Writing responses and final approval letters for variations to pharmaceutical companies.Product manager for GCC submissions:*Reception of files from GCC central committee for drug registration.*GCC files validation (for drug registration, variations, and renewals).*Submission to evaluating departments and following up.*Generating evaluation reports.*Updating evaluation reports.*responding to company inquiries (either letters, phones or emails).Others:*Statistical analysis (generating weekly, monthly and yearly reports).*Writing and updating standard operation procedures (SOP’s).*Developing follow up procedures to assure pharmaceutical companies compliance with the requirements of the SFDA,

Al-Riyadh Governorate, Saudi Arabia

I worked on this function as a part of the human drug section, which is part of the products licensing department, Executive licensing directorate, drug sector. And the following is a brief description of the responsibilities:*Drug registration files validation.*Submission to evaluating departments and following up.*Responding to company inquiries (either letters, phones or emails).Others: *collecting product samples from pharmacies.*Participation with the inspection unit during pilgrimage.*Statistical analysis (generating weekly, monthly and yearly reports).*Writing and updating standard operation procedures (SOP’s).

Riyadh, Saudi Arabia

Worked as a pharmacist OJT in different areas including; main in-patient and out-patient pharmacies, paediatric pharmacy, rehabilitation pharmacy and maternity pharmacy. The work included preparing prescriptions, labelling, reviewing prescription (type of medication, amount prescribed, dosing, and drug interactions), reviewing prescription requests with doctor's when needed to ensure correct medications are provided, dispensing prescription drugs to patients and instructing on their use, talking to a patient about their medications and attending weekly presentations in the pharmacy.

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Master Degree, Pharmacuetics, 4.74 Out Of 5

Graduated with a G.P.A. of 4.74 out of 5 (equivelant to 3.81 out of 4 as per word education services (WES) evaluation). My research.

Bachelor Degree, Pharmaceutical Sciences, 4.33 Out Of 5

Graduated with a G.P.A. of 4.33 out of 5 (equivalent to (3.21 out of 4) as per world education services (WES) evaluation) and a "Very.