وظائف GSK في مصر

The Regulatory Submission Specialist is responsible for supporting regulatory submission activities including authoring reviewing providing Regulatory registration requirements and compiling dossiers for assigned deliverables in compliance with health authority regulations and GS ...

The candidate will lead the development and enforcement of a chemical management and exposure control program aligned with local regulations. The role involves supervising contractors and site activities to ensure safe execution of EHS operations while driving continuous improvem ...

We are seeking professionals with the following required skills and qualifications to help us achieve our goals: · - Bachelor's degree in Pharmaceutical Sciences, Chemistry, Biology or a related science field. · - 0 to 3 years of practical laboratory experience in analytical test ...

This role will provide YOU the opportunity to lead key activities to progress YOUR career. · Managing multiple project assignments simultaneously, including CMC variations, source transfers, and handling Health Authority Questions (HAQs) for Finished Products, Intermediates, and ...

We manufacture and supply reliable high-quality medicines and vaccines to meet patients needs and drive our performance.Our network of medicines manufacturing sites delivered billion packs of medicines in help make a positive impact on health of millions people. · ...

We are seeking Regulatory Project Manager (Delivery Lead) to join our GRA Vx Mature CMC team. · The CMC Mature Vx Delivery Lead plays a critical role in supporting registered vaccines products by managing complex CMC submissions (such as CMC Post-approval variations, Health Autho ...

We manufacture and supply reliable high-quality medicines vaccines to meet patients needs drive our performance.Our network of 37 medicines vaccines manufacturing sites delivered 1.7 billion packs of medicines vaccine doses in Cairo Egypt help make a positive impact on health of ...

We manufacture reliable high-quality medicines vaccines meet patients needs drive performance.Our network 37 medicines vaccines manufacturing sites delivered 1.7 billion packs medicines 409 million vaccine doses in help make positive impact health millions people. · Technology tr ...

We are looking for professionals with required skills to achieve our goals: Bachelor's Degree or MSc Degree in Occupational Health Sciences, Industrial Hygiene, Chemical Engineering, Physician or other science related field. · Bachelor's Degree or MSc Degree in Occupational Healt ...

You will help maintain the quality and availability of our medicines by leading Chemistry, Manufacturing and Controls (CMC) renewals.This role offers growth, visible impact on patient access, · and alignment with GSK's mission of uniting science, technology and talent to get ahea ...

+Job Summary · A Reg Submission Specialist at GSK will support regulatory submission activities like authoring and reviewing submissions in compliance with health authority regulations. · +ResponsibilitiesDeliver assigned submissions within agreed timelines. · Follow up on multip ...

The Regulatory Project Manager will lead regulatory projects for Vaccines portfolio that support product lifecycle activities across markets., · ,,Independently assesses manages drives CMC strategy coordinates timely prepares authors multiple complex CMC technical regulatory docu ...

We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients. · ...

We need a Microbiology Section Head in Egypt who will lead our microbiology section at our site. · Lead daily microbiology laboratory activities. · Ensure microbiological monitoring and investigations meet regulatory standards. · ...

We are looking for a Hematology Medical Affairs Manager with medical doctor degree and experience in launching products within highly specialized therapeutic areas. · ...

The Regulatory Project Manager will lead key activities to progress their career in the CMC RA group. The role involves assessing and managing submission deliverables, coordinating multiple complex technical regulatory documents and providing regulatory support across Rx, Bx and ...

The Senior Regulatory Specialist is responsible for ensuring timely delivery of regulatory activities across multiple projects and dosage forms. · Acting as the New Registration CMC representative on Regulatory Networks and Matrix Teams. · Provides regulatory guidance to Global S ...

This role will provide YOU the opportunity to lead key activities to progress YOUR career. · ...

The New Registration CMC team bring together the operation and execution aspects for key regulatory deliverables such as new chemical entity product expansion dossiers and CTA submissions.This role will provide YOU the opportunity to lead key activities to progress YOUR career. · ...

We are seeking Regulatory Project Manager (Delivery Lead) to join our GRA Vx Mature CMC team. · Take ownership for multiple complex CMC regulatory submissions · ...