regulatory manager regional projects cmc

<div>
 
 Site Name:
 
 Poznan Grunwaldzka, Bangalore, Egypt - Cairo
 
 
 
 Posted Date:
 
 Dec 12 2025
 
 
 
 Regulatory Project Manager , Regional Projects Team, CMC Excellence
 
 
 
 
 Within the CMC RA group, the Regional Projects team bring together the operation and execution aspects for key regulatory deliverables for new Directives and Guidelines issued in Regions such as the implementation of eCTD Baselining, general Baselining, Localisation initiatives, and Re- Registrations. The Regional Projects team provide regulatory support across the Regions to deliver Submissions as stipulated in the new HA Directives for pharmaceutical, biopharm and vaccines products.
 
 
 
 As Regulatory Manager, Regional Projects CMC you will have managerial responsibility for a direct reports as well as accountability and lead for the completion of assigned projects in the CMC Rx and Vx regulatory area. You will work with Head and Manager of Regional Projects as well as with Establish Products Teams to deliver Team&rsquo;s objectives.
 
 
 
 
 This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following&hellip;
 
 
 
 
 
 <ul>
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 Managing people aspects of a team of direct reports to create and sustain an efficient and motivating working environment
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 Take accountability for tracking, analyzing and reporting of team performance against departmental KPIs
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 Ensure proper escalation for resource or quality considerations
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 Independently assess, manage, and/or drive the CMC strategy, coordinate, timely preparation, and author multiple complex CMC technical regulatory documents to support applications for marketing authorisation, lifecycle activities and maintenance of registered products across Rx, Bx and Vx portfolios in accordance with the applicable regulatory and scientific standards, taking into account the Regional Directives and evolving regulatory requirements.
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 Understand internal and external Regulatory environment with the ability to participate in corporate evaluation and provide CMC regulatory support and advice to Localisation projects, and provide guidance to R&amp;D teams, Quality Control, GSC, QA and LOC.
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 Ensure adequate interaction and partnership with Senior Stakeholders (Leadership Team) in order to define proper regulatory CMC filing strategy demonstrating flexible thinking and continuous improvement while maintaining customer focus.
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 Ensure adequate contribution during interactions with Worldwide Regulatory Authorities.  Authors responses to Regulatory Agency questions.
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 Identify risks associated with submission data and information packages and can influence people, systems, processes, and formulate alternative approaches.
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 Contribute to, and lead (as required) the creation, maintenance and continuous improvement of CMC Regulatory processes, work instructions, policies and systems.
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 Ensure information submitted in marketing applications meets CMC and regional requirements and escalates to line manager, as applicable, risk or issues that have business impact.
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 Independently manage the completion of data assessment, ensure all appropriate CMC regulatory aspects, serve as dossier approver, identify improvement opportunities, and confidently execute a dossier that is fit for purpose per agreed dossier strategy and timelines.
 
 
 
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 </ul>
 
 
 Why you?
 
 
 
 
 
 
 Basic Qualifications:
 
 
 
 
 
 <ul>
 <li>
 Master&rsquo;s degree or higher in a relevant scientific discipline.
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 Experience in an international regulatory environment or working with multiple markets.
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 Sound understanding of pharmaceutical industry and regulatory processes with expertise in CMC area
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 Project Management experience
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 Capability to build and maintain a team
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 Fluent English
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 Strong interpersonal and communication skills
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 Ability to perform multiple tasks, set the right priorities to deliver objectives on time
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 Adapting to changing circumstances through priorities reassessment and a disciplined, logical work style.
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 Exceptional flexibility and growth mindset
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 Change management and strong learning agility
 
 
 
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 </ul>
 
 
 Preferred Qualifications:
 
 
 
 
 
 <ul>
 <li>
 Well-developed leadership skills,
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 Negotiation and problem solving skills,
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 Practical knowledge of risk management,
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 Veeva Vault knowledge would be an asset
 
 
 
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 </ul>
 
 What we offer:
 
 
 
 
 <ul>
 <li>
 Performance with Choice &ndash; flexibility in working mode (hybrid working model 2/3 days per week in the office), flexible working hours.
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 Established job in an international, well-known pharmaceutical company.
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 Opportunity to work in professional team playing crucial role in maintaining GSK portfolio on the markets.
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 Opportunity to work within GSK standards and documentation applied globally.
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 Wide range of benefits (Medical Plan, Life Insurance, Employee Retirement Program, Sport and recreation cards, Recreation allowance, annual bonus).
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 Supportive &amp; friendly working environment.
 
 
 
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 </ul>
 We&rsquo;re looking for someone who thrives in a collaborative environment, is passionate about delivering results, and is eager to make a difference. If this sounds like you, we&rsquo;d love to hear from you!
 
 
 As an Inclusive employer, we encourage you to reach out if you need any adjustments during the recruitment process. Please contact our Recruitment Team at pl.recruitment-adjustments@gsk.com to discuss your needs.
 
 
 As an Inclusive employer, we encourage you to reach out if you need any adjustments during the recruitment process. Please contact our Recruitment Team at pl.recruitment-adjustments@gsk.com to discuss your needs.
 
 
 
 Why GSK?
 
 
 
 
 Uniting science, technology and talent to get ahead of disease together.
 
 
 
 GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases &ndash; to impact health at scale.
 
 
 People and patients around the world count on the medicines and vaccines we make, so we&rsquo;re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
 
 
 GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.
 
 
 
 Important notice to Employment businesses/ Agencies
 
 
 
 GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
 
 
 Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK&rsquo;s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/
 
 
</div>

Regulatory Manager Regional Projects CMC

Viatris

<div>
 
 At VIATRIS&trade;, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.
 
 
 
 
 
 Viatris empowers people worldwide to live healthier at every stage of life.
 
 
 
 
 
 We do so via:
 
 
 
 
 <ul>
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 Access
 
 &ndash; Providing high quality trusted medicines regardless of geography or circumstance.
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 <li>
 
 Leadership
 
 &ndash; Advancing sustainable operations and innovative solutions to improve patient health; and
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 Partnership
 
 &ndash; Leveraging our collective expertise to connect people to products and services.
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 </ul>
 
 
 
 
 Every day, we rise to the challenge to make a difference and here&rsquo;s how the (Regulatory Affairs Senior Associate) role will make an impact:
 
 
 
 
 
 
 Key responsibilities for this role include:
 
 
 <ul>
 <li>
 Support the local regulatory team in the development of regulatory strategies to support the registration of new products, line extensions, major variations, and lifecycle management.
 </li>
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 Develop strong partnerships with in-country and above country teams to facilitate the development and implementation of registration strategies to expedite the registration of new products, line extensions and life-cycle optimization.
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 Responsible for enhancing relationships with key external agencies (Egyptian Drug authority EDA). Manage the EDA interface throughout the development and lifecycle of a product.
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 Maintain licenses (e.g. Marketing Authorizations) in compliance with local regulations by ensuring that corporate regulatory processes, SOP&rsquo;s and systems are followed.
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 Ensure a submission planning and forecasting tool is utilized to update timelines, when necessary, communicate changes to relevant partners.
 </li>
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 Capable of authoring some local submission components in relevant databases.
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 Ensure submission packages are reviewed against local CMC requirements for consistency and completeness.
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 Liaise with the manufacturing sites for obtaining supporting documents as needed.
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 Participate in local and regional regulatory initiatives promoting a culture aligned with Viatris values and which supports compliance, innovation and talent development and retention.
 </li>
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 Maintain compliance with the regulatory systems, processes and procedures.
 </li>
 </ul>
 
 
 
 
 
 The minimum qualifications for this role are:
 
 
 <ul>
 <li>
 2-3 years of experience in regulatory affairs, preferably in human medicines.
 </li>
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 Demonstrate regulatory experience with a pharmaceutical company with proven examples of contribution.
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 Proven ability to manage Regulatory issues and consistently deliver to time, cost and quality standards.
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 Demonstrate experience of effective delivery in a matrix environment.
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 Technically competent to understand CMC submissions, interpret and communicate requirements, and identify potential risks.
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 Knowledge of drug development, regulations, and guidelines.
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 Knowledge and understanding of quality systems and processes.
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 Ability to influence peers in the organization.
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 Team player.
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 Act independently with less supervision.
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 Analytical thinking.
 </li>
 </ul>
 
 
 
 
 At Viatris, we offer competitive salaries, benefits, and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others.
 
</div>

Regulatory Affairs Senior Associate

York Press

<div>
 
 
 
 Project Manager &ndash; Education Assessment Projects (Cairo-based)
 
 
 
 
 
 
 
 We are seeking a
 
 dynamic Project Manager
 
 with a solid background in the education sector to join our team and support the delivery of national and regional assessment projects. The ideal candidate will bring up to
 
 5 years of experience
 
 in education&mdash;
 
 preferably in student assessment or curriculum projects
 
 &mdash;along with strong coordination, reporting, and stakeholder management skills.
 
 
 
 
 
 
 Key Requirements:
 
 
 <ul>
 <li>
 
 Prince2 Certified
 
 Project Manager.
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 Up to
 
 5 years of experience
 
 in the education field.
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 <li>
 Demonstrated experience in managing assessment-related initiatives is highly desirable.
 </li>
 <li>
 
 Excellent communication and reporting skills
 
 &mdash;must be confident in liaising with ministries, officials, and third-party vendors.
 </li>
 <li>
 
 Based in Cairo
 
 and able to attend meetings or coordination sessions in person as needed.
 </li>
 <li>
 Highly
 
 organized, proactive, and adaptable
 
 , with the ability to work under pressure and meet deadlines.
 </li>
 </ul>
 
 
</div>

Project Manager

Amarox KSA

<div>
 
 
 Company Description
 
 
 
 Amarox is one of the fastest-growing pharmaceutical companies in Saudi Arabia, with a rapidly expanding presence across the Middle East and Africa.
 
 
 Through our marketing team, we drive strategic growth, healthcare innovation, and measurable impact across Saudi Arabia&rsquo;s healthcare sector.
 
 
 At Amarox, we empower our teams to lead healthcare transformations, drive innovation, and create meaningful regional impact.
 
 
 
 
 
 
 Role Description
 
 
 
 We are seeking a Cairo-based Product Manager to lead and grow Saudi portfolios in Cardio-Metabolic, GIT &amp; OTC categories, operating closely with Amarox KSA&rsquo;s leadership.
 
 
 
 
 
 
 Responsibilities
 
 
 
 &bull;	Develop and execute strategic brand plans aligned with the Saudi healthcare market and Amarox&rsquo;s growth objectives.
 
 
 &bull;	Lead full product lifecycle management&mdash;including segmentation, positioning, launch excellence, optimization, and maturity management.
 
 
 &bull;	Drive cross-functional coordination with Sales, Medical, Access, and Regulatory teams to enable flawless execution.
 
 
 &bull;	Analyze IQVIA datasets, market trends, competition, and commercial performance to shape strategy and maximize portfolio impact.
 
 
 &bull;	Design and implement CRM-driven campaigns, digital initiatives, and multichannel programs that enhance HCP reach and engagement.
 
 
 &bull;	Ensure compliance with SFDA, MOH, and internal policies across all brand activities.
 
 
 &bull;	Support forecasting, budgeting, and launch readiness of priority brands.
 
 
 &bull;	Contribute to organizational learning by identifying best practices and performance.
 
 
 
 
 
 
 Requirements
 
 
 
 &bull;	Bachelor&rsquo;s Degree in Pharmacy (Mandatory).
 
 
 &bull;	Minimum 5 years of pharmaceutical Product Management experience.
 
 
 &bull;	Proven track record within CardioMetabolic, GIT, or OTC therapeutic areas.
 
 
 &bull;	Prior experience with multinational or leading regional pharmaceutical companies.
 
 
 &bull;	Strong command of Saudi healthcare dynamics, private market, and tender sector.
 
 
 &bull;	High proficiency with IQVIA tools, CRM platforms, brand analytics, and digital KPIs.
 
</div>

Product Manager (Cardio-Metabolic, GIT & OTC)

Majid Al Futtaim

<div>
 
 
 JOB TITLE
 
 
 
 Associate Manager - Quality and Hygiene private label | MAF Retail | Head Office Egypt
 
 
 
 
 
 
 ROLE SUMMARY
 
 
 
 The Associate Manager - Quality and Hygiene is responsible for supporting activities to ensure the highest quality of hygiene and food safety in all areas of operations within the store.
 
 
 
 
 
 
 ROLE PROFILE
 
 
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 Support the analysis of quality and food safety standards and implement continuous improvements.
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 Implement and monitor HACCP, ISO 22000 and local regulatory standards (e.g., NFSA, EOS).
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 Maintain all documents related to hygiene procedures to ensure quality.
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 Lead internal/external audits and corrective actions
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 Monitor the storage of fresh food according to the set standards and procedures.
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 Monitor and report on the segregation, storage and timely removal of all waste.
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 Implement training for all food and waste handling staff.
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 Implement the hygiene and food safety awareness/climate in the stores to ensure highest quality
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 </ul>
 
 
 
 
 
 REQUIREMENTS
 
 
 <ul>
 <li>
 Bachelor&rsquo;s in Veterinary, Food Science, Microbiology, or related field.
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 5+ years in related food quality control, 3+ years within the retail working with food is preferable.
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 Bachelor&rsquo;s in Veterinary, Food Science, Microbiology, or related field.
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 Lab testing, cold chain logistics.
 </li>
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 Analytical, leadership, crisis management.
 </li>
 </ul>
 
 
 
 
 
 WHAT WE OFFER
 
 
 <ul>
 <li>
 At Majid Al Futtaim, we&rsquo;re on a mission to create great moments, to spread happiness, to build, experiences that stay in our memories for a lifetime. We&rsquo;re proud to say that over the past 27 years, we have built a reputation as a regional market leader in what we do. Join us!
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 Work in a friendly environment, where everyone shares positive vibes and excited about our future.
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 Work with over 45,000 diverse and talented colleagues, all guided by our Leadership Model.
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 </ul>
 
 
</div>

Associate Manager - Quality and Hygiene- Private Label

Tamara

<div>
 
 
 About Us
 
 
 
 Tamara is the leading fintech platform in Saudi Arabia and the wider GCC region with a mission to help people make their dreams come true by building the most customer-centric financial super-app on earth. The company serves millions of users in KSA, UAE and Kuwait, and partners with leading global and regional brands such as SHEIN, Jarir, noon, Amazon, IKEA, eXtra and Farfetch as well as small and medium businesses.
 
 
 Tamara is Saudi&rsquo;s first fintech unicorn and is backed by Sanabil Investments, SNB Capital, Checkout.com, amongst others, operating out of its headquarters in Riyadh, Saudi Arabia with other regional and global support offices.
 
 
 
 
 
 
 Your role
 
 
 
 We're seeking a Facilities Coordinator for our Facilities Management team. As Facilities Coordinator, you will be crucial in managing daily office operations, maintenance, and security. Overseeing staff, contractors, and projects. Ensuring regulatory and safety compliance.
 
 
 Drawing on your proficiency in guaranteeing smooth operations with efficient maintenance practices, you will be responsible for cultivating strong partnerships with service providers and collaborating with building management to ensure seamless daily operations and efficient problem-solving for building-related concerns to create unique experiences only Tamara can provide.
 
 
 
 
 
 With a proven track record of expertise in facilities management software and security systems to optimize operations and ensure a safe environment, highly organized and detail-oriented, and ultimately revolutionize the way millions of users shop, pay, and bank.
 
 
 You are a driven, determined, curious team player, knowing that collective strength means we all win. With a positive outlook, you are solution-oriented&ndash;persevering regardless of circumstances, always finding a way through, no matter the challenges.
 
 
 You will effectively find a way to work with everyone through empathy and respect. You will be driven and comfortable with responding quickly with urgency, with the ability to change course without losing momentum and energy, resulting in great success.
 
 
 
 
 
 
 Your responsibilities
 
 
 
 Maintenance Supervision:
 
 <ul>
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 Oversee troubleshooting, preventive, and predictive maintenance for electrical, mechanical, and plumbing systems.
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 Ensure timely and effective maintenance activities.
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 </ul>
 
 Contractor Management:
 
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 Manage hard and soft services contractors, ensuring quality and timely delivery of services.
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 Maintain good relationships with service providers.
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 </ul>
 
 Project Leadership:
 
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 Lead adhoc and retrofit projects, ensuring they are completed on time and within budget.
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 Coordinate project timelines and resources effectively.
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 </ul>
 
 Ticketing System Management:
 
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 Manage the facilities ticketing system, addressing stakeholders' requests promptly.
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 Ensure timely resolution of issues and maintain accurate records.
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 </ul>
 
 Health and Safety:
 
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 Implement and oversee health and safety protocols, including incident management, evacuation, and emergency response plans.
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 Conduct regular staff training sessions on safety procedures as per authorities requirements.
 </li>
 </ul>
 
 Visitor and Security Management:
 
 <ul>
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 Manage visitor and guest protocols, including sign-in processes and issuing visitor badges.
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 Monitor office security systems and maintain a secure environment.
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 </ul>
 
 Building Management:
 
 <ul>
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 Liaise with building management on day-to-day concerns and ensure smooth operations.
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 Address and resolve building-related issues promptly.
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 </ul>
 
 Regulatory Compliance:
 
 <ul>
 <li>
 Ensure all operations comply with local authorities' requirements.
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 Maintain up-to-date knowledge of regulatory requirements and standards.
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 </ul>
 
 Utility Provision:
 
 <ul>
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 Ensure the continuous provision of all utility requirements, including water, electricity, and HVAC systems.
 </li>
 <li>
 Monitor utility usage and identify opportunities for efficiency.
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 </ul>
 
 Asset Management:
 
 <ul>
 <li>
 Ensure all assets are managed within the Asset Management System.
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 Maintain maintenance history records and generate reports as needed.
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 </ul>
 
 Consumables Management:
 
 <ul>
 <li>
 Manage stocks of consumables, including chemicals, pantry supplies, and stationery.
 </li>
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 Ensure safe storage and proper inventory control.
 </li>
 </ul>
 
 Policy Adherence:
 
 <ul>
 <li>
 Ensure adherence to all office policies and guidelines.
 </li>
 <li>
 Promote efficient utilization of facilities and resources.
 </li>
 </ul>
 
 
 
 
 
 Your expertise
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in electrical or mechanical engineering.
 </li>
 <li>
 Proven 1-3 experience in facilities management or a related field.
 </li>
 <li>
 Strong organizational and multitasking skills.
 </li>
 <li>
 Excellent communication and interpersonal skills.
 </li>
 <li>
 Proficiency with facilities management software and security systems.
 </li>
 <li>
 Ability to handle emergencies calmly and efficiently.
 </li>
 </ul>
 
 
</div>

Facilities Coordinator

Red Bull

<div>
 The Sports Events Manager designs and executes an efficient national event program on a highly professional level. He/she is one of the most important drivers of innovation and creativity in our events and athletes&rsquo; projects. Innovation is priority, followed by excellent and efficient execution.
 
 
 In addition, he/she leverages global/international Red Bull content in sport scenes and supports interesting 3rd party projects with an approach aligned with Red Bull.
 
 
 
 All the responsibilities we'll trust you with:
 
 
 
 
 Create National Event Programs
 
 
 
 Create/improve an innovative and outstanding national event program by inventing and executing new sports events and athlete projects. These are highly relevant for regional and national consumer groups, offer personal experiences to participants and spectators, and create unique media content.
 
 
 
 Event Organization
 
 
 
 Organize Red Bull events/projects of all scales with strong focus on participants, spectators and media while assuring top quality and efficiency. Brief and supervise suitable partners (freelancer/event agency/Field Marketing Manager or Student Marketeers and Brand Manager) to follow Red Bull principles and needs and objectives from communications, legal, finance and sales. Budget and brand appearance responsibility for all national event activities according to international benchmarks and guidelines. Assure external partner contribution for defined projects assuring a high level of efficiency.
 
 
 
 Your areas of knowledge and expertise that matter most for this role:
 
 
 
 <ul>
 <li>
 At least 3+ years of experience in events planning &amp; execution.
 </li>
 <li>
 Has a passion for Red Bull and sports.
 </li>
 <li>
 Fit for outdoor work.
 </li>
 <li>
 Ability to plan, design, organize, and execute events and projects of all scales.
 </li>
 <li>
 Ability to lead project teams and follow a 360-degree marketing and organizational approach.
 </li>
 <li>
 Leadership, innovation and teamwork.
 </li>
 <li>
 Creative, innovative, open-minded, sporty, motivated, communicative, and responsible.
 
 
 </li>
 </ul>
 Driving license University enrollment
</div>

Sports Events Manager

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