public relations specialist Jobs in Istanbul

public relations specialist

regulatory scientist turkey & cis Jobs in Istanbul

regulatory scientist turkey & cis

accounting and administrative affairs specialist Jobs in Istanbul

accounting and administrative affairs specialist

administrative affairs specialist/senior specialist Jobs in Istanbul

administrative affairs specialist/senior specialist

administrative assistant Jobs in Istanbul

administrative assistant

regulatory affairs coordinator

Mars

<div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p><b>Job Description:</b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div><p>
Drive engagement and lead the Regulatory Affairs function for Eurasia Cluster in the following duties:</p><ul><li>
Ensure compliance in the cluster markets for the product-related regulation, including but not limited to: Ingredients, labelling, claims, product registration, packaging, cross border sanitary conditions</li><li>
Maximize opportunity &amp; minimize risk by guiding business decisions at cluster level based on regulatory insight and provide appropriate governance structure</li><li>
Manage horizon scan for all markets in the cluster, capturing risk &amp; opportunity to inform business stakeholders and influence regulators</li><li>
Develop stakeholder mapping and engagement plan to build long-term relationship &amp; develop the network &amp; influence within the trade associations and regulators for each cluster markets</li><li>
Provide technical/product/nutritional presentations to key internal and external stakeholders to disseminate information regarding Royal Canin products and pet nutrition</li><li>
Other regulatory tasks, enabling Royal Canin products to cross-borders and be commercialized in Eurasia markets, may be included in the scope of responsibility for this role, provided their complexity is in line with the job level of the role</li></ul><p></p><p>
This role report to the Eurasia, India, South Africa RA Sr Team Manager and part of the Royal Canin Regulatory Affairs Team. As part of the EA Cluster RA Manager, this role plays a key role in the collaboration and coordination of cluster-wide regulatory activities. The job requires a solid understanding of regulatory frameworks in different markets, as well as strong communication skills to manage cross-country regulatory operations and to negotiate effectively both internally and externally at different levels. Main scope of responsibilities (but not limited) is as below:</p><p><b>
Regulatory Innovation &amp; Compliance</b></p><ul><li>
Follow global and local regulatory trends to anticipate risks and opportunities for our products.</li><li>
Monitor new and upcoming regulations and assess their impact on our ingredients, product formulations, and innovation plans.</li><li>
Lead regulatory change management where needed to ensure product compliance.</li><li>
Evaluate and validate product claims (on-pack/off-pack), ensuring they are compliant, scientifically supported, and aligned with company policies.</li></ul><p></p><p><b>
Regulatory Advocacy &amp; Issue Management</b></p><ul><li>
Identify opportunities for regulatory alignment and simplification across countries to support business growth.</li><li>
Support regulatory advocacy efforts by coordinating local actions, providing data, and engaging with authorities or trade associations.</li><li>
Help prepare technical documents and responses to regulatory or competitive challenges (e.g., claims, labelling).</li><li>
Contribute to regulatory strategies for new ingredients, packaging, or products by collecting data and coordinating with internal and external stakeholders.</li><li>
Act as a point of contact for regulatory or quality related PRIMPS, ensuring proper documentation and expert support.</li></ul><p></p><p><b>
Regulatory Trade Compliance &amp; Product Registration</b></p><ul><li>
Monitor sanitary regulations (e.g., disease outbreaks, health certificate changes) that may impact import/export and inform teams to manage risks.</li><li>
Prepare and submit product registration files, as well as any other need to ensure it (e.g. samples etc), including new products, changes, or variations, and manage follow-up with authorities.</li><li>
Ensure valid and up-to-date licenses and permits for product imports and site approvals where required.</li></ul><p></p><p><b>
Education &amp; Professional Qualifications</b></p><ul><li>
M.S. or equivalent in a technical area, such as veterinary medicine, food science, food safety, chemistry, toxicology, nutrition, other biological science,</li><li>
Minimum of five (5) years of experience in Regulatory Affairs, Public Policy, or Trade Association related field for multiple markets</li><li>
Solid knowledge of the small animal health industry &amp;/ nutrition and science</li><li>
Experience of communicating with, and influencing trade, and professional organizations</li></ul><p></p><p><b>
Knowledge / Experience</b></p><ul><li>
Excellent understanding and working knowledge of nutrition and, ideally, pet food/feed law and/or pharmaceuticals and regulatory frameworks.</li><li>
Minimum of five (5) years of experience in Regulatory Affairs, Public Policy, or Trade Association related field for multiple markets</li><li>
Excellent communication skills, fluent in both spoken and written English and Ukraine is mandatory.</li><li>
Veterinary/Scientific knowledge important</li><li>
Experience of communicating with consultants / contractors</li><li>
Microsoft Office proficiency required</li><li>
Ability to connect with diverse culture and adopt to changes</li></ul><p></p><p><b>
Key Supporting Competencies</b></p><ul><li>
Business Acumen</li><li>
Dealing with Ambiguity</li><li>
Organizational Agility</li><li>
Perspective</li><li>
Functional/technical skills</li><li>
Integrity &amp; Trust</li></ul><p></p><p><b>
Key Functional Competencies &amp; Technical Skills</b></p><ul><li>
Excellent project management / organizational skills combined with the ability to handle many tasks simultaneously working under pressure and delivering within tight deadlines. Veterinary &amp; Scientific knowledge</li><li>
Excellence in creating and maintaining internal networks within markets teams, as well as creating and maintaining external networks with trade associations, and local authorities.</li><li>
Be viewed as a trusted partner by internal and external experts, trade associations and local authorities Excellent interpersonal, communication (verbal and written) and problem-solving skills.</li><li>
Ability to manage Regulatory Monitoring and Horizon Scanning for the cluster</li><li>
Ability to inform assess and manage the Risks and Opportunities, as well as informing the business on time.</li><li>
Internal and External influence and collaboration</li></ul></div><p></p>

Scientific & Regulatory Affairs

Perrigo

<p></p><div><p>At Perrigo, we are driven by our mission to <b><i>Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All</i></b>. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing <b><i>The Best Self-Care for Everyone</i></b>, we are the people behind the brands you trust. We are Opill&reg;, Compeed&reg;, Solpadeine&reg;, NiQuitin&reg;, ACO&reg;, and many more. <b>We Are Perrigo</b>. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.</p><p></p><p><br>
Join us on our One Perrigo journey as we evolve to win in self-care.</p><p></p><div><div><div><h2 class="jobSectionHeader"><b><br>
Description Overview</b></h2></div><div><p>
In this role you will be responsible for the hands on regulatory activities required to maintain existing commercial products, and support in making correct and timely new product applications of Perrigo products on the Turkish market. You will support to ensure compliance with the existing legislation for Medicines, Medical Devices, Biocides and Cosmetics. Another key aspect of the role will be supporting in the achievement of the overall Regulatory, Quality &amp; Safety objectives and timely realization of operational activities. In this position you collaborate closely with the Corporate Regulatory and Turkish Commercial colleagues to strive to help the customer the best.</p></div></div><div><div><h2 class="jobSectionHeader"><b>
Scope of the Role</b></h2></div><div><ul><li>
Support in the management of change by preparing applications and technical files in support of existing commercial product regulatory maintenance;</li><li>
Support in the regulatory activities on new product development (NPD), including artwork approvals, label claims and associated supporting documentation;</li><li>
Develop and approve label specifications (master text and local artwork text) in compliance with SOPs, as well as promotional materials from a regulatory perspective;</li><li>
Maintain regulatory files and data systems in compliance with SOPs;</li><li>
Represent regulatory affairs in project meetings with both Perrigo staff and external contacts;</li><li>
Follow up on changes in (inter)national regulations and legislations, and support in the interpretation, communication and implementation;</li><li>
Liaise with Corporate Regulatory, responding to regulatory queries and providing and review of registration documents as necessary for the Turkish and/or European territory;</li><li>
Support in the communication with local regulatory authorities regarding license applications and notice of change.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Experience Required</b></h2></div><div><ul><li>
University Degree in a Scientific Subject;</li><li>
Minimum of 2 years work experience within Regulatory Affairs required, within at least one of the following categories Medical Devices, Biocides, Cosmetics and Medicines;</li><li>
Excellent communicator in Turkish and English;</li><li>
Proficient computer skills esp. Microsoft (word, excel, powerpoint); experience with Veeva, TVT, Trackwise is an asset;</li><li>
Eye for detail, punctual, well organized;</li><li>
Being flexible and adaptable to change;</li><li>
Ability to support several concurrent projects/products simultaneously;</li></ul></div></div></div><p><b>
Benefits</b><br>
We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.</p><p>
Find out more about <b>Total Rewards</b> at Perrigo.</p><p></p><p><b><br>
Hybrid Working Approach</b><br>
We love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.</p><p></p><p><br>
We are proud to be included in the Forbes list of &quot;America's Best Employers by State 2024&quot;. Find out more <b>here</b></p><p></p><p><b><br>
Applicants please note:</b> To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) Thank you.</p><p></p><p><i><br>
We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law. #weareperrigo</i></p></div>

Regulatory Affairs, Associate Specialist

Viatris

<div>Viatris &#304;la&ccedil;lar&#305; Ltd. &#350;ti<div></div><div>
At VIATRIS, 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.<br>
<br>
Viatris empowers people worldwide to live healthier at every stage of life.<br>
<br>
We do so via:<br>
<br>
Access &ndash; Providing high quality trusted medicines regardless of geography or circumstance;<br>
Leadership &ndash; Advancing sustainable operations and innovative solutions to improve patient health; and<br>
Partnership &ndash; Leveraging our collective expertise to connect people to products and services.</div><div><br>
Every day, we rise to the challenge to make a difference, and here&rsquo;s how the Regulatory Affairs Portfolio Executive role will make an impact:</div><div></div><div>
The objective of this job is to contribute to the strategic business decisions regarding the licensing of a product in Turkey, within the framework of the the local laws, regulations, guidance and company procedures/policies.</div><div></div><div>
To make the applications regarding the licensing processes for new products and regarding the maintaining/improving of the current license status for existing licensed products, in the area of responsibility in accordance with the licensing legislation and company procedures, to follow-up the processes, and to fulfil the approval requirements. Carrying out the works defined as &quot;Key Responsibilities&quot; below, along with all transactions related to compliance with legislation of regulatory.</div><div></div><div>
To be responsible for the coordination of preparation/updating of SOPs, reports, presentations, launch tables, budgets and databases and for monitoring the regulations, and to provide support to the department head on strategic issues.</div><div></div><div>
Key responsibilities for this role include:</div><ul><li><div>
To contribute to the strategic business decisions regarding the licensing of a product in Turkey.</div></li><li><div>
To carry out all relevant activities in the matters related to prioritization, GMP and registration in accordance with the launch plan for new products</div></li><li><div>
To carry out the organization of GMP audits, to accompany the audits, and then to ensure the acquisition of the GMP certificate by ensuring that all the associated requirements are met.</div></li><li><div>
License and GMP renewal for currently licensed/approved products, Type I and II variations, artwork change applications, SmPC-PIL update applications, sales permission applications, and the meeting of official authorities&rsquo; requests; to provide, review and control the dossier and documents, determine and provide the deficiencies, follow-up the internal approvals if available, prepare the application letters and files, make the applications in accordance with local regulation/guidance/announcements, follow-up the process and ensure the approvals.</div></li><li><div>
To take actions to prevent the regulatory related stock-out risk for the registered products in the market.</div></li><li><div>
To fulfill the registration/approval process requirements for all portfolio.</div></li><li><div>
To follow the legislations, to implement the updates in business and transactions, to determine the impacts of the updates for the products and to take the necessary actions, if any to file/to ensure to be filed.</div></li><li><div>
To ensure the required information within the scope of legislation and provide technical and operational support in the matters relating to production and quality if needed.</div></li><li><div>
Artwork responsibility</div></li></ul><div></div><div>
The minimum qualifications for this role are:</div><ul><li><div>
Bachelor&rsquo;s degree related field.</div></li><li><div>
More than 5 years of industry experience</div></li><li><div>
Advanced Turkish and English in writing and speaking.</div></li><li><div>
Male candidates must have completed their military service.</div></li><li><div>
Ability to use Microsoft Office programs effectively.</div></li></ul><div></div><div>
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><div></div><div>
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><div></div><div>
Viatris is an Equal Opportunity Employer.</div></div><div></div>

Regulatory Affairs Portfolio Executive

Kerry

<div>
 Requisition ID: 60794
 <br/>
 <br/>
 Position Type: FT Permanent
 <br/>
 <br/>
 <strong>
  <strong>
   About Kerry
   <br/>
   <br/>
  </strong>
 </strong>
 Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment.
 <br/>
 <br/>
 <strong>
  About The Role
  <br/>
  <br/>
 </strong>
 In this role, you be an individual contributor responsible for strategic and proactively influencing, leading and communicating on regulatory matters within Kerry and externally. Concurrently you will ensure all Kerry Products are compliant for sale within MENAT (Middle East, North Africa, and Turkey) &amp; CIS.
 <br/>
 <br/>
 <strong>
  <strong>
   Key responsibilities
   <br/>
   <br/>
  </strong>
 </strong>
 <ul>
  <li>
   Ensure timely registration on new products/SKUs in Turkey and CIS markets by working closely and lesioning with the relevant competent authorities.
  </li>
  <li>
   Support border clearance of import/export consignments by working closely with customs and relevant authorities.
  </li>
  <li>
   Maintenance and implementation of the Regulatory management system (Optiva, MDM and etc).
  </li>
  <li>
   Monitor changes in the food regulations and pro&hyphen;actively liaise with relevant RD&amp;A representatives and/or local competent authorities to minimize any impact to the business.
  </li>
  <li>
   Ensure continuous regulatory intelligence and knowledge sharing across the organization.
  </li>
  <li>
   Assess the impact of upcoming regulatory changes and advise on impact to supply chain/distribution processes
  </li>
  <li>
   Support New Product Development through participation at product brief and artwork development stages.
  </li>
  <li>
   Provide expertise and direction on product classification and product claims during the NPD Process.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications And Skills
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Liaise &amp; communicate with Corporate Legal and Finance team on strategic and operational regulatory issues
  </li>
  <li>
   Create and drive the global regulatory organization goals &amp; objectives in line with the Kerry global regulatory strategy
  </li>
  <li>
   Bachelor&rsquo;s Degree in Food Science or similar field, with minimum 2 years&rsquo; experience in Regulatory for a Global Food Business industry.
  </li>
  <li>
   Experience in working with the government (Turkey &amp; CIS Food Authorities)
  </li>
  <li>
   Expert observation, analysis and judgement (i.e., analytical and objective mind-set)
  </li>
  <li>
   Strong background in Food Science &amp; Regulatory standards of Turkey &amp; CIS
  </li>
  <li>
   Ability to work with cross-functional teams within the organization at all levels
  </li>
  <li>
   Must be able to speak and write in Russian &amp; English
   <br/>
   <br/>
  </li>
 </ul>
 Beware of scams online or from individuals claiming to represent us. A Kerry employee will not solicit candidates through a non-Kerry email address or phone number. In addition, Kerry does not currently utilise video chat rooms (e.g., Google Hangouts) to conduct interviews. Refuse any request that asks you to provide payment to participate in the hiring process (e.g., purchasing a &ldquo;starter kit,&rdquo; investing in training, or something similar). Kerry will not ask you to pay any money at any point in the hiring process with the exception of reimbursable travel expenses. In addition, any payments made by Kerry will be from official firm accounts bearing the Kerry name.
 <br/>
 <br/>
 <strong>
  Recruiter
  <br/>
  <br/>
 </strong>
 <strong>
  Posting Type:
 </strong>
 LI
 <br/>
 <br/>
</div>


Regulatory Scientist Turkey & CIS

Kerry Dairy Ireland

<div>
 Requisition ID: 60794
 <br/>
 <br/>
 Position Type: FT Permanent
 <br/>
 <br/>
 <strong>
  Workplace Arrangement
  <br/>
  <br/>
 </strong>
 <strong>
  About Kerry
  <br/>
  <br/>
 </strong>
 Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment.
 <br/>
 <br/>
 <strong>
  About The Role
  <br/>
  <br/>
 </strong>
 In this role, you be an individual contributor responsible for strategic and proactively influencing, leading and communicating on regulatory matters within Kerry and externally. Concurrently you will ensure all Kerry Products are compliant for sale within MENAT (Middle East, North Africa, and Turkey) &amp; CIS.
 <br/>
 <br/>
 <strong>
  Key Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Ensure timely registration on new products/SKUs in Turkey and CIS markets by working closely and lesioning with the relevant competent authorities.
  </li>
  <li>
   Support border clearance of import/export consignments by working closely with customs and relevant authorities.
  </li>
  <li>
   Maintenance and implementation of the Regulatory management system (Optiva, MDM and etc).
  </li>
  <li>
   Monitor changes in the food regulations and pro&hyphen;actively liaise with relevant RD&amp;A representatives and/or local competent authorities to minimize any impact to the business.
  </li>
  <li>
   Ensure continuous regulatory intelligence and knowledge sharing across the organization.
  </li>
  <li>
   Assess the impact of upcoming regulatory changes and advise on impact to supply chain/distribution processes
  </li>
  <li>
   Support New Product Development through participation at product brief and artwork development stages.
  </li>
  <li>
   Provide expertise and direction on product classification and product claims during the NPD Process.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications And Skills
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Liaise &amp; communicate with Corporate Legal and Finance team on strategic and operational regulatory issues
  </li>
  <li>
   Create and drive the global regulatory organization goals &amp; objectives in line with the Kerry global regulatory strategy
  </li>
  <li>
   Bachelor&rsquo;s Degree in Food Science or similar field, with minimum 2 years&rsquo; experience in Regulatory for a Global Food Business industry.
  </li>
  <li>
   Experience in working with the government (Turkey &amp; CIS Food Authorities)
  </li>
  <li>
   Expert observation, analysis and judgement (i.e., analytical and objective mind-set)
  </li>
  <li>
   Strong background in Food Science &amp; Regulatory standards of Turkey &amp; CIS
  </li>
  <li>
   Ability to work with cross-functional teams within the organization at all levels
  </li>
  <li>
   Must be able to speak and write in Russian &amp; English
   <br/>
   <br/>
  </li>
 </ul>
 Beware of scams online or from individuals claiming to represent us. A Kerry employee will not solicit candidates through a non-Kerry email address or phone number. In addition, Kerry does not currently utilise video chat rooms (e.g., Google Hangouts) to conduct interviews. Refuse any request that asks you to provide payment to participate in the hiring process (e.g., purchasing a &ldquo;starter kit,&rdquo; investing in training, or something similar). Kerry will not ask you to pay any money at any point in the hiring process with the exception of reimbursable travel expenses. In addition, any payments made by Kerry will be from official firm accounts bearing the Kerry name.
 <br/>
 <br/>
 <strong>
  Recruiter
  <br/>
  <br/>
 </strong>
 <strong>
  Posting Type:
 </strong>
 LI
 <br/>
 <br/>
</div>


Xiaomi Technology

<div>
 <p>
  1. Import/Export HS code management: Professional for Turkey import/export customs HS code policy especially for phone, pad, TV, fridge and AIOT products, choose correct HS code for cost saving and compliance follow government policy.
 </p>
 <p>
  2. AEO Certification: well known the AEO certification application process and policy, better to have AEO application experience.
 </p>
 <p>
  3. Regulatory Policy Research: Proficient in the regulations and policies of various Turkey ports involved in import/export business. Responsible for monitoring changes in customs regulatory policies from customs and other relevant regulatory authorities. Combining the company's business model and current situation, this position allows for rapid and thorough interpretation, development of solutions, and implementation to ensure the healthy and compliant development of the company's business.
 </p>
 <p>
  <br/>
 </p>
 <p>
  4. Customs Relationship Maintenance: Develop, establish, and maintain strong relationships with customs and other regulatory authorities. Maintain close ties with local government departments to secure customized support policies and promote mutually beneficial government-enterprise partnerships.
 </p>
 <p>
  <br/>
 </p>
 <p>
  5. Import/Export Customs Operations: Gain a deep understanding of the platform's core customs clearance ports and declaration terminal business processes and characteristics, and be responsible for the quality of port operations. Based on the platform's business model, this position involves regular management of service providers, and ongoing assessment and optimization efforts, especially for increase the Import efficiency.
 </p>
 <p>
  6. Import/Export Customs Abnormality Management: Monitor the company's Import/ export declaration processes at ports, identifying, monitoring, and resolving Import/export customs risks.
 </p>
 <p>
  7. Utilize digital and visual operational tools to improve operational efficiency and quality.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <br/>
 </p>
 <p>
  1. Proficient in spoken and written English and Turkish
 </p>
 <p>
  2. Bachelor's degree or above in a related field, such as international customs affairs, logistics management, or logistics and customs clearance supervision. Familiarity with Turkey Customs' Import/export business models. Experience with customs affairs in the cross-border electronics industry is preferred.
 </p>
 <p>
  3. Proficiency in Turkey customs affairs, including import and export clearance and commodity classification, with proficiency in relevant electronics products customs skills (classification, import and export controls, valuation, origin, etc.).
 </p>
 <p>
  4. Excellent interpersonal and communication skills, strong verbal and written communication skills, and demonstrated resource integration and business innovation capabilities.
 </p>
 <p>
  5. Demonstrated ability to work effectively as a team, independently handle tasks, and collaborate on cross-departmental projects. Strong sense of responsibility, ability to withstand work pressure.
 </p>
 <p>
 </p>
</div>


Customs Operations Manager(A15586)

Daiichi Sankyo

<p></p><div><h2 class="jobSectionHeader"><b>Passion for Innovation. Compassion for Patients.</b></h2><br>
<p>
</p><p>With over 120 years of experience and approximately 19,000 employees in more than 30 countries/regions, Daiichi Sankyo is dedicated to discovering, developing, and delivering new standards of care that enrich the quality of life around the world.</p>
<p>
In Europe, we focus on two areas: The goal of our Specialty Business is to protect people from cardiovascular disease, the leading cause of death in Europe, and help patients who suffer from it to enjoy every precious moment of life.</p>
<p>
In Oncology, we are driving innovation in solid tumours and blood cancers, founded on breakthrough science from our own labs in Japan. We aspire to create better tomorrows for people living with cancer and their loved ones.</p>
<p>
Our European headquarters are in Munich, Germany, and we have affiliates in 15 European countries and Canada.</p><p></p><p><br>
We're looking for a Market Access Lead who will lead processes for pricing, reimbursement, access, stakeholder engagement processes for Daiichi Sankyo Turkey oncology portfolio. S/he will be working closely with affiliate commercial teams and with regional teams, DSTR brand teams including Pricing, Reimbursement and Access, Regulatory Affairs, marketing and medical affairs. This person will support the Market Access team in Turkey will be reporting to Market Access and Regulatory Affairs Director and will be working in close collaboration with DS International Regulatory Affairs DSE Oncology&amp; DSE Market Access OBU.</p><br>
<p></p>
<p><b>
Responsibilities:</b></p>
<p>
Lead development of pricing, reimbursement, HTA and access activities working cross-functionally/regionally<br>
Enhance information exchange and best practice sharing across MSC and DSE; drive adoption of pricing tools and resources<br>
Ensure price submissions are done accurately and timely manner while working closely with DSE price team for IRP process, tracking reimbursement and pricing lists, stakeholder engagement<br>
Generation of reimbursement dossier in line with local requirements while generating local data and adapting Global CE models<br>
Insight generation and information among DSTR teams regarding competitors and DSTR portfolio pricing, reimbursement and sectoral analysis &amp; closely monitoring developments in healthcare environment<br>
Stakeholder engagement activities for OBU product portfolio stakeholders like KoLs, SSI &amp; MoH and TEB as well as other govermental agencies.<br>
Support alliance processes &amp; BC processes to ensure OBU access processes are managed flawlessly.<br>
Determine proactive price strategies of the products which are licensed or to be licensed and price application to Ministry of Health<br>
Collaborate with Regulatory &amp; Commercial &amp; Sales and Medical teams to generate access strategies.</p><br>
<p></p>
<p><b>
Knowledge and Skills:</b></p>
<p>
2 or more years of hands on experience acquired at pharmaceutical companies,<br>
demonstrated experience with developing pricing, reimbursement and access<br>
Strong strategic mindset &amp; analytical &amp; pro-active approach- ability to work well in a matrix team environment and independently<br>
Excellent communication skills (oral and written)<br>
Strong process/project management skills<br>
Strong business acumen &amp; solution-oriented<br>
Fluency in English<br>
Agile mindset and willing to work in a dynamic environment</p><h2 class="jobSectionHeader"><b>
Why work with us?</b></h2><p><br>
</p>
<p>Working at Daiichi Sankyo is more than just a job &ndash; it is your chance to make a difference and change patients&rsquo; lives for the better. We can only achieve this ambitious goal together. That is why we foster a culture of mutual respect and continuous learning, with a strong commitment to inclusion and diversity. Here, you will have the opportunity to grow, think boldly, and contribute your ideas. If you have a proactive mindset and passion for addressing the needs of patients, we eagerly await your application.</p>
<p>For more information: www.daiichi-sankyo.at</p></div><p></p>

TR-Market Access Lead

Explore 134+ Regulatory affairs coordinator in Istanbul this September. Find roles across top companies and apply now to boost your career.

134 regulatory affairs coordinator jobs IN Istanbul

Scientific & Regulatory Affairs

Regulatory Affairs, Associate Specialist

Regulatory Affairs Portfolio Executive

Regulatory Scientist Turkey & CIS

Regulatory Scientist Turkey & CIS

Customs Operations Manager(A15586)

TR-Market Access Lead