Qureos Mentor

<div><div><div><div><div><div><b>Entity:</b> CSL Behring</div>
<div><b>Job Category:</b> Research Development &amp; Sciences</div>
<div><b>Job Family:</b> Global &amp; Regional Regulatory Affairs</div>
<div><b>Job Type:</b> Full Time</div>
<div><b>Location</b><b>:</b> Riyadh, Riyadh, Saudi Arabia</div>
<div><b>Employer Reference:</b> R-266747</div>
</div></div><div></div><h2 class="jobSectionHeader"><b>Job Description</b></h2>
<div><div><div><b>Main Responsibilities and Accountabilities</b></div><div><b>
1. Strategic Focus</b></div><ul><div><div>
Lead the development and execution of regulatory strategies for complex projects across KSA and MEA partner markets:</div></div><div><ul><div><div>
Assess regulatory pathways and identify optimal submission strategies to accelerate approvals while ensuring compliance with local and global requirements.</div></div><div><div>
Anticipate regulatory challenges and proactively design mitigation plans to minimize risks and delays.</div></div><div><div>
Align regulatory strategies with business objectives, product lifecycle plans, and commercial priorities to support timely market access.</div></div><div><div>
Collaborate with cross-functional teams (clinical, quality, manufacturing, commercial) to integrate regulatory considerations into project planning and decision-making.</div></div><div><div>
Drive innovative approaches to meet evolving regulatory requirements and leverage regional insights to influence global strategy.</div></div></ul></div></ul><div></div><ul><div><div><br>
Ensure oversight on key processes and frameworks to manage third-party activities end-to-end, ensuring compliance with regulations and company standards; perform due diligence, monitor partner performance, and address deviations promptly.</div></div></ul><div></div><div><b><br>
2. Technical Regulatory Responsibilities for KSA (in Coordination with Scientific Office Manager)</b></div><ul><div><div>
Responsible for technical regulatory activities in KSA, while coordinating all actions with the Scientific Office Manager for the TSO in Saudi, including:</div></div></ul><ul><div><ul><div><div>
Performing regulatory assessments for new products and variations.</div></div><div><div>
Preparing and compiling complete regulatory dossiers in alignment with SFDA requirements.</div></div><div><div>
Managing electronic submissions through the SDR portal via the Scientific Office in KSA.</div></div><div><div>
Responding to SFDA queries and deficiency letters promptly and effectively.</div></div><div><div>
Ensuring compliance with all local regulatory standards and timelines for approvals.</div></div><div><div>
Maintaining proactive communication with SFDA to facilitate smooth review processes.</div></div></ul></div></ul><div></div><ul><div><div><br>
Also responsible for interaction with distributors and local partners for local manufacturing projects in KSA to ensure all regulatory activities are on track and aligned with compliance requirements.</div></div></ul><div><b>
3. Regulatory Oversight for Partner Markets in MEA (Assigned Markets)</b></div><ul><div><div>
Manage distributors and partners in assigned Partner Business markets.</div></div><div><div>
Prepare regulatory dossiers and provide regulatory assessments for these markets, ensuring compliance with local requirements and company standards.</div></div><div><div>
Ensure distributors submit dossiers to Health Authorities on time and in full compliance with regulatory requirements.</div></div><div><div>
Conduct audits and assessments to ensure compliance with local requirements and quality standards; implement corrective actions and risk mitigation strategies.</div></div><div><div>
Act as RA representative in audits/inspections and ensure readiness and timely CAPA closure.</div></div><div><div>
Serve as escalation point for partner-related issues and align closely with GRA for contract management.</div></div></ul><div><b>
4. Regulatory Intelligence &amp; Authority Interaction</b></div><ul><div><div>
Stay updated on regulatory requirements, guidelines, and industry trends; communicate changes to GRA and local teams.</div></div><div><div>
Communicate with Health Authorities, specifically SFDA, for all regulatory activities as needed, while ensuring coordination with the Scientific Office Manager.</div></div></ul><div><b>
5. Submission Management</b></div><ul><div><div>
Support regional regulatory teams in planning and submission preparation according to local requirements.</div></div><div><div>
Perform preparation and submission of regulatory dossiers, including variations, labeling, and NDAs, ensuring compliance with local regulations.</div></div><div><div>
Demonstrate strong knowledge of eCTD structure and requirements, including publishing tools (e.g., DocuBridge), eCTD compilation, and technical validation.</div></div><div><div>
Ensure familiarity with electronic submission processes through SDR in in Saudi Arabia ; maintain awareness of all technical aspects related to electronic submissions.</div></div></ul><div><b>
6. Systems &amp; Data Integrity</b></div><ul><div><div>
Maintain accurate and timely updates in regulatory systems and databases such as Veeva Vault RIM.</div></div><div><div>
Demonstrate advanced experience in Veeva, including:</div></div></ul><ul><div><ul><div><div>
Managing end-to-end regulatory workflows within Veeva Vault RIM.</div></div><div><div>
Uploading, organizing, and maintaining submission documents in compliance with global and local standards.</div></div><div><div>
Ensuring data integrity and version control for all regulatory records.</div></div><div><div>
Generating reports and dashboards to track submission status and compliance KPIs.</div></div><div><div>
Coordinating with global teams to ensure alignment of Veeva processes across regions.</div></div></ul></div></ul><div><b>
7. Labeling Responsibilities</b></div><ul><div><div>
Experience in end-to-end labeling processes, including country-specific labels and multi-country shared labels.</div></div><div><div>
Ensure compliance with local GCC labeling requirements.</div></div><div><div>
Coordinate labeling activities with other team members for MEA shared labels to ensure timely updates and consistency.</div></div><div><div>
Demonstrate knowledge of GLAMS labeling process and maintain accurate labeling records in the system.</div></div></ul><div><b>
8. Local Manufacturing Projects</b></div><ul><div><div>
Manage local manufacturing partners in KSA to ensure they are updated with the latest technical dossier of the product.</div></div><div><div>
Ensure partners perform regulatory activities on time, including variations, labeling updates, and registration renewals.</div></div><div><div>
Be actively involved in any new initiatives for local manufacturing in KSA and other MEA markets, providing regulatory guidance and support from planning through execution.</div></div></ul><div><b>
9. Stakeholder Management &amp; Training</b></div><ul><div><div>
Act as primary interface with local partners in assigned markets, representing the company&rsquo;s regulatory interests and fostering strong relationships.</div></div><div><div>
Align with commercial in Partner Business Markets to ensure timely and standardized delivery of partner-specific activities.</div></div><div><div>
Monitor training effectiveness and compliance; ensure proper training programs are developed and implemented.</div></div><div><div>
Lead and deliver complex regional strategies across CSL products, ensuring alignment with company and commercial objectives.</div></div><div><div>
Provide guidance for regulatory activities across MEA countries, adapting strategies to local requirements.</div></div></ul><div>
-</div><div><b>
Position Qualifications and Experience Requirements</b></div><div></div><div><b>
Education</b></div><ul><div><div>
Bachelor&rsquo;s degree in pharmacy, life sciences, or related field.</div></div><div><div>
Certifications in quality or vendor management (e.g., CQA, CMQ, CSQP) desirable.</div></div></ul><div></div><div><b><br>
Experience</b></div><ul><div><div>
Minimum 10+ years in regulatory affairs within pharmaceutical, biotechnology, or healthcare industry.</div></div><div><div>
Proven ability to develop and execute regulatory strategies for complex projects.</div></div><div><div>
Strong experience in communication and negotiation with Health Authorities, specifically SFDA.</div></div><div><div>
Hands-on experience in regulatory dossier preparation (variations, labeling, NDAs).</div></div><div><div>
Proficiency in regulatory systems and databases such as Veeva Vault RIM.</div></div><div><div>
Expertise in eCTD structure, publishing tools (e.g., DocuBridge), and electronic submission processes.</div></div><div><div>
Experience managing local manufacturing projects, particularly in KSA.</div></div><div><div>
Regional regulatory experience across multiple MEA countries.</div></div><div><div>
Demonstrated ability to work in a highly matrixed organization and establish successful cross-functional relationships.</div></div><div><div>
Experience in Pharmacovigilance is desirable.</div></div></ul><div></div><div><b><br>
Competencies</b></div><ul><div><div>
Fluent in Arabic and English (oral and written).</div></div><div><div>
Advanced MS Office skills.</div></div><div><div>
Strong organizational, time management, and interpersonal skills in a global environment.</div></div><div><div>
Ability to work independently and collaboratively, with strong problem-solving and decision-making skills.</div></div></ul></div>
</div><h2 class="jobSectionHeader"><b>About CSL Behring</b></h2>
<div>
<div>CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients' needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.</div>
<div>CSL Behring operates one of the world's largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.</div>
<div>To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/.</div>
</div>
<h2 class="jobSectionHeader"><b>Our Benefits</b></h2>
<div>
<div>For more information on CSL benefits visit How CSL Supports Your Well-being | CSL.</div>
</div>
<h2 class="jobSectionHeader"><b>You Belong at CSL</b></h2>
<div>
<div>At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.</div>
<div>To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging</div>
</div>
<h2 class="jobSectionHeader"><b>Equal Opportunity Employer</b></h2>
<div>
<div>CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement.</div></div></div></div></div><div></div>

Regulatory Affairs Senior Manager, GRA, RPR MEA

<div><div><div><div><div><div><b>Entity:</b> CSL Behring</div>
<div><b>Job Category:</b> Commercial</div>
<div><b>Job Family:</b> Sales</div>
<div><b>Job Type:</b> Full Time</div>
<div><b>Location</b><b>:</b> Istanbul, Turkey</div>
<div><b>Employer Reference:</b> R-265675</div>
</div></div><div></div><h2 class="jobSectionHeader"><b>Job Description</b></h2>
<div><div><div><b>Position Purpose:
</b></div><div></div><ul><div><div>To promote CSL Behring&rsquo;s products as defined by the company to HCPs in allocated clinics within the territory.</div></div><div><div>
To deliver medical, financial and share goals of the business</div></div><div><div>
To increase awareness towards the selected disease areas and the identification rates of the relevant diseases in defined geographical areas</div></div></ul><div></div><div><b>
Reporting Relationships:
</b></div><div>Role this position reports to: National Sales Manager</div><div></div><div><b>
Main Responsibilities and Accountabilities:
</b></div><div></div><div>1-Responsible for achieving CSL Behring sales targets and effective management of defined regional accounts</div><div></div><div>
2-Closely coordinates with National Sales Manager and Commercial Operation departments and serves as the primary interface between customers in the region and the company.</div><div></div><div>
3-<b>The position has responsibility for:</b></div><ul><div><div>
Identifying and visiting the hospitals &amp; treating centers to find the patients with relevant diseases.</div></div><div><div>
Raising awareness and interest for the related diseases in order to motivate patient screening in the visited centers.</div></div><div><div>
Promoting the products during daily visits and at medical events</div></div><div><div>
Developing and managing the relations with the Key Opinion Leaders in the territory.</div></div><div><div>
Initiating and organizing medical training activities to increase knowledge levels on the diseases and products.</div></div><div><div>
Providing support for the activities like clinical trials, patient surveys. etc.</div></div><div><div>
Periodical review of progress against objectives and strategic plan.</div></div><div><div>
Managing tender administration (bidding process, fulfilment) in close collaboration with the responsible functions (National Sales)</div></div><div><div>
Evaluation of customer needs and facilitation of issues between the customer and other departments within CSL Behring</div></div><div><div>
Creating, implementing and updating a CRM based visit plan to main customers as well as a detailed reporting of customer contacts, visits and meetings via Veeva</div></div></ul><div></div><div><b>
Position Qualifications and Experience Requirements:
</b></div><ul><div><div>Bachelor&rsquo;s degree in life sciences, MD is a plus</div></div><div><div>
Turkish &ndash; native, English &ndash; a plus</div></div><div><div>
A min of 2-5 years RAM experience in innovative pharmaceutical or biotech pharmaceutical companies preferably in Biotech &amp; Rare Disease area</div></div></ul><div></div><div><b><br>
additional Comments:</b></div><div>
Travel within the region (60% of time)</div><div>
This Position will work Izmir Region</div></div><div></div>
</div><h2 class="jobSectionHeader"><b>About CSL Behring</b></h2>
<div>
<div>CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients' needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.</div>
<div>CSL Behring operates one of the world's largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.</div>
<div>To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/.</div>
</div>
<h2 class="jobSectionHeader"><b>Our Benefits</b></h2>
<div>
<div>For more information on CSL benefits visit How CSL Supports Your Well-being | CSL.</div>
</div>
<h2 class="jobSectionHeader"><b>You Belong at CSL</b></h2>
<div>
<div>At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.</div>
<div>To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging</div>
</div>
<h2 class="jobSectionHeader"><b>Equal Opportunity Employer</b></h2>
<div>
<div>CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement.</div>
</div>
<h2 class="jobSectionHeader"><b>Location</b></h2>
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Regional Account Manager - Izmir

<div><div><div><div><div><div><b>Entity:</b> CSL Behring</div>
<div><b>Job Category:</b> Commercial</div>
<div><b>Job Family:</b> Marketing</div>
<div><b>Job Type:</b> Full Time</div>
<div><b>Location</b><b>:</b> Riyadh, Riyadh, Saudi Arabia</div>
<div><b>Employer Reference:</b> R-265682</div>
</div></div><div></div><h2 class="jobSectionHeader"><b>Job Description</b></h2>
<div><div><div><b>Role Summary</b></div><div>
The Iron &amp; Hemophilia Brand Manager will be responsible for leading the development, execution, and performance of the iron deficiency and hemophilia portfolio across Saudi Arabia and the UAE. This role will drive brand strategy, launch excellence, market shaping activities, and cross-functional collaboration to achieve strong market growth in line with the company&rsquo;s objectives. The ideal candidate brings proven experience in the Saudi pharmaceutical market, strong strategic and operational marketing capabilities, and a deep understanding of specialty care, rare diseases, or hematology.</div><div></div><div><b>
Key Responsibilities</b></div><div>
1. Brand Strategy &amp; Planning</div><ul><div><div>
Develop and implement the annual brand plan for the iron and hemophilia portfolio in KSA and UAE.</div></div><div><div>
Conduct market analysis, competitive intelligence, and strategic forecasting to identify growth opportunities.</div></div><div><div>
Adapt global/ regional strategies to local market needs while ensuring alignment with corporate direction.</div></div></ul><div></div><div>
2. Launch Excellence</div><ul><div><div>
Lead the preparation, execution, and post-launch performance tracking for new product launches.</div></div><div><div>
Build and execute launch readiness plans, including positioning, messaging, promotional materials, and KPIs.</div></div><div><div>
Coordinate cross-functional launch teams (medical, market access, regulatory, sales).</div></div></ul><div></div><div>
3. Marketing Execution</div><ul><div><div>
Plan and deliver promotional campaigns, digital and omnichannel marketing initiatives, and stakeholder engagement plans.</div></div><div><div>
Drive development of scientific and promotional content, ensuring compliance with company and regulatory standards.</div></div><div><div>
Support planning and execution of medical events, advisory boards, and educational initiatives in collaboration with medical affairs.</div></div></ul><div></div><div>
4. Cross-Functional Collaboration</div><ul><div><div>
Work closely with medical, commercial, regulatory, supply chain, and market access teams to ensure smooth execution of brand activities.</div></div><div><div>
Partner with sales teams to drive implementation of marketing initiatives and monitor field performance.</div></div></ul><div></div><div>
5. Market &amp; Stakeholder Engagement</div><ul><div><div>
Build strong relationships with key opinion leaders (KOLs), hematologists, nephrologists, and relevant stakeholders.</div></div><div><div>
Identify unmet needs in the iron and hemophilia therapeutic areas and drive market development programs.</div></div></ul><div></div><div>
6. Business &amp; Performance Management</div><ul><div><div>
Monitor brand performance, market share, KPIs, and budget utilization.</div></div><div><div>
Provide accurate forecasting in coordination with supply and commercial planning teams.</div></div><div><div>
Recommend strategic adjustments based on performance insights and market evolution.</div></div></ul><div></div><div><b>
Qualifications</b></div><ul><div><div>
Bachelor&rsquo;s degree in Pharmacy or Medicine &mdash; mandatory.</div></div><div><div>
Master&rsquo;s degree or additional qualifications in Marketing or Business Administration &mdash; preferred.</div></div></ul><div></div><div><b>
Experience Requirements</b></div><ul><div><div>
Minimum 3 years of experience as a Senior Brand/ Marketing Manager in a multinational pharmaceutical company &mdash; must.</div></div><div><div>
Solid track record of leading portfolio of products</div></div><div><div>
Saudi Arabia pharmaceutical market experience &mdash; must.</div></div><div><div>
Proven launch experience of specialty or biologic products &mdash; must.</div></div><div><div>
Experience in rare diseases, hematology, or gene therapy &mdash; strong plus.</div></div><div><div>
Experience with the UAE market &mdash; plus.</div></div></ul></div>
</div><h2 class="jobSectionHeader"><b>About CSL Behring</b></h2>
<div>
<div>CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients' needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.</div>
<div>CSL Behring operates one of the world's largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.</div>
<div>To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/.</div>
</div>
<h2 class="jobSectionHeader"><b>Our Benefits</b></h2>
<div>
<div>For more information on CSL benefits visit How CSL Supports Your Well-being | CSL.</div>
</div>
<h2 class="jobSectionHeader"><b>You Belong at CSL</b></h2>
<div>
<div>At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.</div>
<div>To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging</div>
</div>
<h2 class="jobSectionHeader"><b>Equal Opportunity Employer</b></h2>
<div>
<div>CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement.</div></div></div></div></div><div></div>

Marketing lead Iron & Hemophilia

<div><div><div><div><div><div><b>Entity:</b> CSL Behring</div>
<div><b>Job Category:</b> Commercial</div>
<div><b>Job Family:</b> Sales</div>
<div><b>Job Type:</b> Full Time</div>
<div><b>Location</b><b>:</b> Riyadh, Riyadh, Saudi Arabia</div>
<div><b>Employer Reference:</b> R-266150</div>
</div></div><div></div><h2 class="jobSectionHeader"><b>Job Description</b></h2>
<div><div><div><b>Responsibilities:</b></div><ul><div><div>
Responsible for sales and effective management of key accounts within assigned region</div></div><div><div>
Works with regional management to establish strategy and tactical initiatives that align closely with those of key CSL brands</div></div><div><div>
Develops strategic account and sales plans to increase penetration of CSL products</div></div><div><div>
Builds and maintains relationships with key customers to enable sustainable business growth</div></div><div><div>
Collaborates with business teams, marketing and medical affairs to ensure alignment and full utilization of resources</div></div></ul><div><b><br>
Qualifications:</b></div><ul><div><div>
Robust knowledge of pharmaceutical market dynamics, regulations and key stakeholders in KSA</div></div><div><div>
Experience with managing distributors including strategy execution, performance management and supply chain</div></div><div><div>
Preferably to have experience with pharmaceutical <b>plasma</b> producs</div></div></ul></div><br>
<div></div>
</div><h2 class="jobSectionHeader"><b>About CSL Behring</b></h2>
<div>
<div>CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients' needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.</div>
<div>CSL Behring operates one of the world's largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.</div>
<div>To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/.</div>
</div>
<h2 class="jobSectionHeader"><b>Our Benefits</b></h2>
<div>
<div>For more information on CSL benefits visit How CSL Supports Your Well-being | CSL.</div>
</div>
<h2 class="jobSectionHeader"><b>You Belong at CSL</b></h2>
<div>
<div>At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.</div>
<div>To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging</div>
</div>
<h2 class="jobSectionHeader"><b>Equal Opportunity Employer</b></h2>
<div>
<div>CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement.</div>
</div>
<h2 class="jobSectionHeader"><b>Location</b></h2>
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Sorry, we have no imagery here.</p></div><div><p>
Sorry, we have no imagery here.</p></div><div><p>
Sorry, we have no imagery here.</p></div><div><p>
Sorry, we have no imagery here.</p></div><div><p>
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Map data &copy;2025 Google</div></div></div><div></div><div><div>
Terms</div></div></div></div></div></div></div></div></div></div>

Commercial Lead

Join CSL and explore 4   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

CSL

ABOUT_COMPANY

Regulatory Affairs Senior Manager, GRA, RPR MEA

Regional Account Manager - Izmir

Marketing lead Iron & Hemophilia

Commercial Lead