RSO Specialist (Project based end of 2025)

RSO Specialist (Project based end of 2025) page is loaded

RSO Specialist (Project based end of 2025)

locationsCairo time typeVollzeit posted onHeute ausgeschrieben job requisition idR2710415

Job Purpose:

Co-ordinate between the M&S departments and DRA team in regulatory aspects of Chemistry, manufacturing and control for pharmaceutical products.
Manage the regulatory activities with the Egyptian Drug Authority Inspection department.

KEY RESPONSIBILITIES AND DUTIES:

Preparing the registration files in coordination with DRA department during new registration or re-registration:-
Preparation of IA part of regulatory files (Products Renewal)
Reviewing of IA part of regulatory files (New Products)
Regulatory compliance checking (Gap analysis)
Review & Approval of updated method of analysis from QC
Revising stability data, gathering raw material specifications, printed packaging materials.
Send updated data to DRA with samples of finished products, with their certificates.
Managing of submission of variations to DRA to be submitted to EDA to close any identified regulatory GAPs found.
Initiate the CTD file for local and exported products.

Managing regulatory activities with the EDA inspector

Receiving of all the new EDA decisions & informing the concerned departments for implementation.
Managing the release of certain products with the EDA inspector.
Following Raw materials & finished products sampling with the EDA inspector on weekly basis

HSE Responsibilities:

Ensures HSE approval on any SOP that requires certain HSE precautions.
Ensures HSE approval on any change.
Follow the laboratory safety procedures
Commitment to the appropriate PPE use.
Follow the approved HSE policy and requirements.
Following the statutory legislation concerning Health, Safety and environmental law.
Hydrocarbons/ hazardous substance & waste segregation in accordance with approved waste management system.

Others:

Perform other duties as assigned.
Respect of company’s values, code of ethics and social charter.
Respect of personal data protection charter.
Responsible for applying the HSE related requirements for the company in all related working procedures.
JOB-HOLDER’s ENTRY REQUIREMENTS:*
Education:
Bachelor of Pharmacy.
Related Experience:
3-5 years experience
Regulatory activities experience is preferred.
Special Knowledge/Skills:
Communication & Presentation skills
Computer skills
Sense of urgency & Follow up skills
Time management skills, High organization & planning skills
Good Command of English Language
Attention to Details
Hard Worker and Team Worker
competencies:
Stretch to go beyond the level we have operated at up until now
Take actions instead of waiting to be told what to do
Act in the interest of our patients and customers
Put the interests of the organization ahead of my own or those of our team
Act for Change, Strive for results, Cooperate Transversally, Commit to Customer
Think Strategically, Lead Teams, Develop People, Make Decisions.
Diversity und Inklusion sind in den Grundwerten von Sanofi verankert und spiegeln sich in unserer Arbeitsweise wider. Wir respektieren die Vielfalt unserer Belegschaft in Hinsicht auf ihre Herkunft, Erfahrungen und Lebensweisen. Wir erkennen die Bereicherung, die diese Vielfalt birgt, und fördern Inklusion sowie eine Arbeitsumgebung, in der diese Unterschiede sich weiter entwickeln können, zur Stärkung des Lebens unserer Mitarbeiter, Patienten und Kunden.