regulatory affairs senior associate

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>
 <li>
 
 Access
 
 &ndash; Providing high quality trusted medicines regardless of geography or circumstance.
 </li>
 <li>
 
 Leadership
 
 &ndash; Advancing sustainable operations and innovative solutions to improve patient health; and
 </li>
 <li>
 
 Partnership
 
 &ndash; Leveraging our collective expertise to connect people to products and services.
 </li>
 </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.
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 <li>
 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.
 </li>
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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.
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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>
 <li>
 Demonstrate regulatory experience with a pharmaceutical company with proven examples of contribution.
 </li>
 <li>
 Proven ability to manage Regulatory issues and consistently deliver to time, cost and quality standards.
 </li>
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 Demonstrate experience of effective delivery in a matrix environment.
 </li>
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 Technically competent to understand CMC submissions, interpret and communicate requirements, and identify potential risks.
 </li>
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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.
 </li>
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 Act independently with less supervision.
 </li>
 <li>
 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

PwC Middle East

<div>
 
 Line of Service
 
 
 
 Tax
 
 
 
 Industry/Sector
 
 
 
 Not Applicable
 
 
 
 Specialism
 
 
 
 General Tax Consulting
 
 
 
 Management Level
 
 
 
 Associate
 
 
 
 Job Description &amp; Summary
 
 
 
 A career in our Tax Accounting practice, within Tax services, will provide you with the opportunity to help our clients meet and manage their tax obligations across unique but ever changing tax specialties. You&rsquo;ll advise clients on their local and overseas tax affairs, while acting as a strategic consultant related to business analysis, managing indirect taxes, dispute resolution, and global enterprise tax solutions.
 
 
 Our team provides our clients with customised tax solutions and tax accounting advice based on their niche and business need. You&rsquo;ll support the team with deferred tax validation projects, remediation and restatement, tax basis balance sheets and financial statement carve out preparation.
 
 
 To really stand out and make us fit for the future in a constantly changing world, each and every one of us at PwC needs to be a purpose-led and values-driven leader at every level. To help us achieve this we have the PwC Professional; our global leadership development framework. It gives us a single set of expectations across our lines, geographies and career paths, and provides transparency on the skills we need as individuals to be successful and progress in our careers, now and in the future.
 
 
 
 Responsibilities
 
 
 
 As an Associate, you'll work as part of a team of problem solvers, helping to solve complex business issues from strategy to execution. PwC Professional skills and responsibilities for this management level include but are not limited to:
 
 
 <ul>
 <li>
 Invite and give in the moment feedback in a constructive manner.
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 Share and collaborate effectively with others.
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 Identify and make suggestions for improvements when problems and/or opportunities arise.
 </li>
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 Handle, manipulate and analyse data and information responsibly.
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 Follow risk management and compliance procedures.
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 Keep up-to-date with developments in area of specialism.
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 Communicate confidently in a clear, concise and articulate manner - verbally and in the materials I produce.
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 Build and maintain an internal and external network.
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 Seek opportunities to learn about how PwC works as a global network of firms.
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 Uphold the firm's code of ethics and business conduct.
 
 
 </li>
 </ul>
 
 Education
 
 
 (if blank, degree and/or field of study not specified)
 
 
 
 
 Degrees/Field Of Study Required
 
 
 
 Degrees/Field of Study preferred:
 
 
 
 Certifications
 
 
 (if blank, certifications not specified)
 
 
 
 
 Required Skills
 
 
 
 
 Optional Skills
 
 
 
 
 Desired Languages
 
 
 (If blank, desired languages not specified)
 
 
 
 
 Travel Requirements
 
 
 
 Not Specified
 
 
 
 Available for Work Visa Sponsorship?
 
 
 
 No
 
 
 
 Government Clearance Required?
 
 
 
 Yes
 
 
 
 Job Posting End Date
 
</div>

Tax & Legal Services - Accounting and Payroll - Associate - Cairo

EVA pharma

<div>
 
 Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for&nbsp;Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are committed to fostering a supportive and innovative environment for&nbsp;our team members.
 
 
 
 
 Job Summary
 
 
 
 We are seeking a passionate and talented
 
 Product Manager
 
 to join our dynamic team.
 
 
 The ideal candidate will contribute to our mission of enhancing human health and well-being,&nbsp;ensuring that we meet the highest standards of excellence in our industry.
 
 
 
 
 Key Responsibilities:
 
 
 <ul>
 <li>
 Develop and execute a comprehensive product strategy aligned with market needs and company goals
 </li>
 </ul>
 <ul>
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 Conduct market research and competitive analysis to identify opportunities and inform positioning
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 Collaborate closely with marketing, sales, medical affairs, and supply chain teams to optimize promotional strategies, support educational initiatives, and maintain product availability
 </li>
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 Manage relationships with key stakeholders such as healthcare professionals, regulatory bodies, and distributors to gather insights, address concerns, and support product adoption
 </li>
 <li>
 Lead product lifecycle management initiatives by identifying areas for product enhancement, planning line extensions, or preparing for potential phase-outs based on market and competitive dynamics
 </li>
 
 
 </ul>
 
 Requirements
 
 
 
 <ul>
 <li>
 Bachelor's in pharmacy, Medicine, or relevant life sciences; MBA is a plus
 </li>
 <li>
 2-4 years of experience as Brand/Assistant Brand Manager in the pharmaceutical industry, preferably with injectables, diabetes, metabolic, or obesity products
 </li>
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 Strong expertise in consumer (DTC) and HCP integrated campaigns, with proven marketing excellence
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 <li>
 Proficient in English &amp; Arabic (written and verbal) with strong strategic, digital, and innovation focus
 </li>
 <li>
 Demonstrated success in launch readiness, brand building, and consumer marketing capability
 </li>
 </ul>
</div>

Product Manager

GE HealthCare

<div>
 
 Job Description Summary
 
 
 
 Engineering associated with the manufacturing process. Impacts departmental operations and responsible for planning/execution. The role has some autonomy but is focused on execution of activities within an operating discipline covered by standard functional practices and procedures. Some judgment may be required but this is typically with guidance.
 
 
 
 Job Description
 
 
 
 
 This Job is responsible for:
 
 
 
 
 Design Transfer
 
 
 
 <ul>
 <li>
 Lead the design transfer activities of product specifications to manufacturing by working with global design owners and local partners.
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 Review the design specifications feasibility in terms of assembly and test, make sure that production constrains are respected.
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 Define and validate production and test processes including production instructions and reports.
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 Coordination of manufacturing releases
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 Lead the manufacturing documentation development and release
 
 
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 </ul>
 
 Manufacturing Process Set Up, Validation And Continuous Improvement
 
 
 
 <ul>
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 Drive improved product quality by identifying manufacturing issues, developing cost-effective solutions, and overseeing successful implementation into production.
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 Work with contract manufacturing supplier&rsquo;s production associates to resolve manufacturing and quality problems related to methods, processes, tooling, equipment and product design.
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 Monitor and optimize contract manufacturing supplier&rsquo;s workstations designs and manufacturing cycle time
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 Actively support lean, continuous improvement and design for manufacturing initiatives.
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 Monitor and improve productivity, while ensuring all customer commitments are met in a timely, quality and cost-conscious manner
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 Maintain (calibration and verification support) and troubleshoot production equipment
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 Define, validate and control production process including tooling and equipment. Work with local and global suppliers to purchase and maintain them.
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 Validate design specifications and shop floor application of new product, tools, or equipment.
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 Specify and expedite planned maintenance routines on all production equipment and systems.
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 Work closely with regulatory affairs department to support the compliance with all local regulations.
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 Define and support local parts purchases and validation process according to GE HealthCare quality procedures.
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 Design the production layout and assure the conformity to EHS policy and to local regulations.
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 Act as a materials change coordinator or/and manufacturing process leader: be the contact point for design or process change communications and lead the implementation of changes in cooperation with supplier quality engineer (SQE)
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 Provide guidance and expertise to manufacturing engineer
 
 
 </li>
 </ul>
 
 Quality Control
 
 
 
 <ul>
 <li>
 Responsible for determining processes requiring validation, development of plans and analysis criteria, execution and final analysis.
 </li>
 <li>
 Ensuring regulatory compliance through Validation &amp; Verification.
 </li>
 <li>
 Lead quality metrics follow up and control in production and drives process quality improvements and simplification
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 Assure that corrective action is taken to resolve observed safety concerns in all areas.
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 Support and follow up contract manufacturing supplier&rsquo;s CAPA cases management.
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 Support SQE &amp; follow up for contract manufacturing supplier&rsquo;s SCAR&rsquo;s
 </li>
 <li>
 Ensure compliance to GE HealthCare quality procedures and local regulations.
 
 
 </li>
 </ul>
 
 Minimum Requirements
 
 
 
 <ul>
 <li>
 B.S. Degree in Mechanical, Electrical, Industrial Engineering or related technical degree
 </li>
 <li>
 7 years of experience in production, engineering
 </li>
 <li>
 Good analytical and planning skills
 </li>
 <li>
 Excellent English (Writing &amp; Communicating)
 
 
 </li>
 </ul>
 
 
 
 Additional Information
 
 
 
 
 
 
 Relocation Assistance Provided:
 
 Yes
 
 
</div>

Manufacturing Engineer

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
 
 
 <ul>
 <li>
 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.
 </li>
 <li>
 Implement the hygiene and food safety awareness/climate in the stores to ensure highest quality
 </li>
 </ul>
 
 
 
 
 
 REQUIREMENTS
 
 
 <ul>
 <li>
 Bachelor&rsquo;s in Veterinary, Food Science, Microbiology, or related field.
 </li>
 <li>
 5+ years in related food quality control, 3+ years within the retail working with food is preferable.
 </li>
 <li>
 Bachelor&rsquo;s in Veterinary, Food Science, Microbiology, or related field.
 </li>
 <li>
 Lab testing, cold chain logistics.
 </li>
 <li>
 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!
 </li>
 <li>
 Work in a friendly environment, where everyone shares positive vibes and excited about our future.
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 <li>
 Work with over 45,000 diverse and talented colleagues, all guided by our Leadership Model.
 </li>
 </ul>
 
 
</div>

Associate Manager - Quality and Hygiene- Private Label

dopay

<div>
 
 About Dopay
 
 
 
 dopay is building the infrastructure that helps businesses move away from cash payroll and gives employees reliable access to digital financial services. We operate at the intersection of payments, regulation, and real-world operations, with a strong focus on scale, trust, and financial inclusion.
 
 
 As part of our next phase, dopay is preparing to obtain a Payment Service Provider (PSP) license from the Central Bank of Egypt, a foundational milestone for the company's long-term growth.
 
 
 
 The Role
 
 
 
 We are hiring a Program Manager to lead dopay through the PSP licensing process and to help design how the company operates as a licensed entity.
 
 
 This is not a narrow compliance role. It is a senior cross-functional role that sits between regulation, business operations, product, and technology. You will own the licensing program end-to-end while ensuring the business is genuinely ready to operate as a licensed PSP on Day 1 &mdash; operationally, commercially, and organizationally.
 
 
 Once the PSP license is granted, this role evolves into owning critical, cross-functional initiatives across the company to support our growth objectives.
 
 
 
 What You'll Do
 
 
 
 You will translate PSP regulatory requirements into a clear execution plan and drive it across legal, finance, risk, operations, product, and engineering. You'll coordinate internal teams and external advisors, keep timelines tight, surface risks early, and support structured engagement with the Central Bank of Egypt and our bank partners.
 
 
 In parallel, you'll help design dopay's licensed-state operating model &mdash; defining how regulated processes actually work day-to-day, from onboarding and transaction monitoring to incident management, outsourcing oversight, and regulatory reporting. Your focus will be on embedding regulatory requirements into real workflows.
 
 
 Post-license, you'll lead cross-functional programs related to regulated products, services, and operating models, acting as a bridge between growth, operations, product, platform, and risk to ensure initiatives are scalable, executable, and defensible under regulatory scrutiny.
 
 
 
 What Success Looks Like
 
 
 
 The PSP license is submitted on time and with credibility. dopay is operationally ready to function as a licensed PSP from Day 1. Regulatory requirements are embedded into how teams actually work. After licensing, regulated products and services can scale faster because the foundations were designed correctly.
 
 
 
 Requirements
 
 
 
 
 Who We're Looking For
 
 
 
 You have experience leading complex, cross-functional initiatives in regulated environments such as fintech, banking, payments, or similar sectors. You are comfortable working across business, operations, product, technology, and compliance, and you can turn regulatory ambiguity into structured execution.
 
 
 You are pragmatic, detail-aware without being bureaucratic, and comfortable being accountable in high-stakes situations. Experience working with regulators, auditors, or supervisory bodies is a strong plus. Arabic and English fluency is required.
 
 
 
 Job Requirements
 
 
 
 <ul>
 <li>
 5+ years of experience leading complex, cross-functional initiatives in regulated environments (e.g. fintech, banking, payments, financial services, telecom, or similarly supervised sectors)
 </li>
 <li>
 Proven experience owning program-level outcomes across multiple teams, rather than delivering a single, fixed-scope project
 </li>
 <li>
 Strong understanding of how regulation impacts business models, operating processes, and product design, not just documentation
 </li>
 <li>
 Demonstrated ability to translate regulatory or supervisory requirements into practical execution plans and real operating workflows
 </li>
 <li>
 Experience working with regulators, supervisory bodies, auditors, or external compliance stakeholders is strongly preferred
 </li>
 <li>
 Comfort operating in environments with high ambiguity, evolving requirements, and competing priorities
 </li>
 <li>
 Ability to coordinate and influence senior stakeholders across business, operations, product, technology, risk, and compliance without formal authority
 </li>
 <li>
 Excellent written and verbal communication skills, including the ability to produce clear, regulator-grade documentation
 </li>
 <li>
 Pragmatic, execution-oriented mindset with sound judgment under pressure
 </li>
 <li>
 Experience in high-growth or scaling organizations is a strong plus
 </li>
 <li>
 Fluency in Arabic and English is required
 
 
 </li>
 </ul>
 
 Benefits
 
 
 
 
 Why Join dopay?
 
 
 
 You'll be be part of a fast-growing fintech company revolutionizing payroll disbursement in Egypt and work closely with senior leadership on one of the most important milestones in the company's journey. This role offers long-term ownership beyond licensing and the opportunity to help shape how a fintech operates under regulation at scale.
</div>

Program Manager

<div>
 
 
 Line of Service
 
 
 Advisory
 
 
 
 
 Industry/Sector
 
 
 Not Applicable
 
 
 
 
 Specialism
 
 
 Advisory - Other
 
 
 
 
 Management Level
 
 
 Senior Associate
 
 
 
 
 Job Description &amp; Summary
 
 
 
 
 Required Skills
 
 
 
 
 
 Optional Skills
 
 
 Accepting Feedback, Accepting Feedback, Active Listening, Agile Methodology, Analytical Thinking, Business Case Development, Business Process Modeling, Communication, Competitive Analysis, Creativity, Customer Needs Analysis, Customer Relationship Management, Customer Satisfaction, Digitization, Embracing Change, Emotional Regulation, Empathy, Inclusion, Intellectual Curiosity, Learning Agility, Marketing Management, Market Research, Market Trends, Operationalization, Optimism {+ 17 more}
 
 
 
 
 
 Desired Languages
 
 
 
 
 (If blank, desired languages not specified)
 
 
 
 
 
 
 Travel Requirements
 
 
 Not Specified
 
 
 
 
 Available for Work Visa Sponsorship?
 
 
 No
 
 
 
 
 Government Clearance Required?
 
 
 No
 
 
 
 
 Job Posting End Date
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
</div>

ETIC, Product Designer - Senior Associate

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