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regulatory affairs executive

Kraft Heinz

<div>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 <strong>
  About the Posiion
  <br/>
  <br/>
 </strong>
 Regulatory Affairs Executive ensuring Food Regulatory Compliance and enabling market access for products. Managing product registrations with authority, as well as reviewing, verifying product information and coordinating documentation for regulatory submissions. Supporting regulatory strategies, maintaining strong relationships with local authorities and internal stakeholders to support business growth. Monitoring and analyzing legislative/regulation changes and their impact on our products- brands- and organization. Presenting the organization in various trade associations and industry groups to proactively manage food regulatory advocacy as well as keeping internal stakeholders informed through continuous monitoring of emerging regulations. You&rsquo;ll be directly reporting into Supplier &amp; External Manufacturing Sr Manager - East &amp; dotted-line reporting to Head of Legal T&uuml;rkiye.
 <br/>
 <br/>
 <strong>
  Key Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Check the compliance of the products&rsquo; labels in Turkey against the relevant legislations- government guidelines and company policies. All brands the company produces and imports.
  </li>
  <li>
   Check the compliance of the health and nutritional and other claims against the relevant legislation.
  </li>
  <li>
   Support the Marketing team in providing and approving legislation of the products&rsquo; information relating to product functional - health - nutritional claims including ads and online marketing.
  </li>
  <li>
   Provide information and advice on legislation for product formulation- packaging- and labelling issues.
  </li>
  <li>
   Prepare product registration files with claim substantiation docs and follow up till registration is done.
  </li>
  <li>
   Be in direct contact with distributors or get support from 3rd party companies (for export destinations) to support and understand any new regulatory updates/ requirements.
  </li>
  <li>
   Support the business with regulatory information relating to products produced and sold in other regions.
  </li>
  <li>
   Work with cross country teams to ensure regulatory compliance of export and import products including filling necessary applications.
  </li>
  <li>
   Horizon scanning possible regulatory related changes within your region. Build and maintain relationships with the relevant authorities to maintain awareness of new food legislation and government guidance.
  </li>
  <li>
   Track- monitor and report completion of necessary changes that need to be done due to new regulations in order to prevent any penalties from authority.
  </li>
  <li>
   Ensure that ingredients- formulas- labeling- and packaging are in full compliance with the local laws and regulations where the products are sold; and provide training to the organization on relevant regulatory topics
  </li>
  <li>
   Monitor and provide advice/analysis on best practices from the market for the categories we play in &amp; share it consistently with other RA teams across the company
  </li>
  <li>
   Build presence in the local trade associations and industry groups as a forum to discuss upcoming or existing regulatory changes; and proactively monitor regulatory activities in our markets to address and influence proposed regulations to preserve the organization&rsquo;s freedom to operate
  </li>
  <li>
   Provide proposals for the amendment of existing or new regulations to support the interests of the organization
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications &amp; Experience
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bacherlor&rsquo;s degree in Food Technology/ Pharmacy or related disciplines. Master degree is an advantage
  </li>
  <li>
   Minimum 3 years&rsquo; working experience in the field of regulatory affairs, preferably within an international environment.
  </li>
  <li>
   Familiar with Turkey food registration procedures and regulatory aspects.
  </li>
  <li>
   Good understanding of the commercial drivers of F&amp;B industry and an associated ability to provide advice/guidance that takes these into consideration
  </li>
  <li>
   Analytical skills and attention to detail with the capability to appropriately define issues, questions, and data
  </li>
  <li>
   Skills such as project management, problem solving, ability to present information in easily understood format at internal and external meetings, good time management, negotiation and interpersonal skills
  </li>
  <li>
   Ability to work both independently and as part of a team as required
  </li>
  <li>
   Be able to balance company commercial needs with compliance requirements
  </li>
  <li>
   Ability to think strategically and innovatively for resolution of regulatory issues
  </li>
  <li>
   Commitment to continued improvement in department processes and performance
  </li>
  <li>
   Strong team player, assisting others with workload peaks and the management of challenging situations
  </li>
  <li>
   Fluency in English and Turkish
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 This position can be based in either Susurlul factory or &Idot;stanbul Headquarter.
 <br/>
 <br/>
 <strong>
  About Us
  <br/>
  <br/>
 </strong>
 The Kraft Heinz Company is one of the largest food and beverage companies in the world, with eight $1 billion+ brands and global sales of approximately $25 billion. We&rsquo;re a globally trusted producer of high-quality, great-tasting, and nutritious foods for over 150 years. Our brands are truly global, with products produced and marketed in over 40 countries. These beloved products include condiments and sauces, cheese and dairy, meals, meats, refreshment beverages, coffee, infant and nutrition products, and numerous other grocery products in a portfolio of more than 200 legacy and emerging brands.
 <br/>
 <br/>
 No matter the brand, we&rsquo;re united under one vision To sustainably grow by delighting more consumers globally. Bringing this vision to life is our team of 39,000+ food lovers, creative thinkers, and high performers worldwide. Together, we help provide meals to those in need through our global partnership with Rise Against Hunger. We also stand committed to responsible, sustainable practices that extend to every facet of our business, our consumers, and our communities. Every day, we&rsquo;re transforming the food industry with bold thinking and unprecedented results. If you share our passion &ndash; and are ready to create the future, build a legacy, and lead as a global citizen &ndash; there&rsquo;s only one thing to do join our table and let&rsquo;s make life delicious!
 <br/>
 <br/>
 <strong>
  Our Culture of Ownership, Meritocracy and Collaboration
  <br/>
  <br/>
 </strong>
 We're not afraid to think differently. Embrace new ideas. Dream big. We empower our people at every level &ndash; from entry-level intern to senior leader &ndash; to own their work. We share a responsibility to think like Owners &ndash; to be mindful of the collective and sustained success of Kraft Heinz &ndash; which we apply to every situation, every day.
 <br/>
 <br/>
 As part of Kraft Heinz, you're supported to grow and achieve. You&rsquo;re expected to bring your authentic self to work every day, to lead with humility, and drive outstanding performance at every level &ndash; and you&rsquo;ll be rewarded. You&rsquo;re given opportunities to leave a mark and build a legacy. But you won&rsquo;t do it alone. You&rsquo;re supported by passionate teammates along the way, and our collective, collaborative spirit fuels our incredible progress.
 <br/>
 <br/>
 We are proud to be a Great Place to Work certified company. Click to view our certificate https //www.greatplacetowork.com.tr/sertifikasyon/sertifikali-sirketler/kraft-heinz-turkiye/
 <br/>
 <br/>
 Employee Candidate Privacy Notice https //www.heinz.eu/turkey-candidate-privacy-policy
 <br/>
 <br/>
 Location(s)
 <br/>
 <br/>
 Istanbul Branch
 <br/>
 <br/>
 <strong>
  Kraft Heinz is an Equal Opportunity Employer &ndash; Underrepresented Ethnic Minority Groups/Women/Veterans/Individuals with Disabilities/Sexual Orientation/Gender Identity and other protected classes
 </strong>
 <strong>
  .
 </strong>
</div>


Regulatory Affairs Executive

<p></p><div><div><div><div><div><div><div><div><div><ul><div><b>All Posting Locations:</b> Besiktas, Istanbul, TR
</div><div><b>Job Functions:</b> Quality</div>
<div><b>Date Published:</b> December 19, 2025</div>
<div><b>Ref#:</b> R-97518</div></ul><div></div><div><br>
</div></div></div></div></div></div></div></div></div><p></p><div><div><div><div><div><div>ABOUT THE ROLE</div></div><div><div>
Job Description</div>
<p><b>About the Posiion</b></p>
<p>Regulatory Affairs Executive ensuring Food Regulatory Compliance and enabling market access for products. Managing product registrations with authority, as well as reviewing, verifying product information and coordinating documentation for regulatory submissions. Supporting regulatory strategies, maintaining strong relationships with local authorities and internal stakeholders to support business growth. Monitoring and analyzing legislative/regulation changes and their impact on our products- brands- and organization. Presenting the organization in various trade associations and industry groups to proactively manage food regulatory advocacy as well as keeping internal stakeholders informed through continuous monitoring of emerging regulations. You&rsquo;ll be directly reporting into Supplier &amp; External Manufacturing Sr Manager &ndash; East &amp; dotted-line reporting to Head of Legal T&uuml;rkiye.</p>
<p><b>Key Responsibilities</b></p>
<ul><li><p>Check the compliance of the products&rsquo; labels in Turkey against the relevant legislations- government guidelines and company policies. All brands the company produces and imports.</p>
</li><li><p>Check the compliance of the health and nutritional and other claims against the relevant legislation.</p>
</li><li><p>Support the Marketing team in providing and approving legislation of the products&rsquo; information relating to product functional &ndash; health &ndash; nutritional claims including ads and online marketing.</p>
</li><li><p>Provide information and advice on legislation for product formulation- packaging- and labelling issues.</p>
</li><li><p>Prepare product registration files with claim substantiation docs and follow up till registration is done.</p>
</li><li><p>Be in direct contact with distributors or get support from 3rd party companies (for export destinations) to support and understand any new regulatory updates/ requirements.</p>
</li><li><p>Support the business with regulatory information relating to products produced and sold in other regions.</p>
</li><li><p>Work with cross country teams to ensure regulatory compliance of export and import products including filling necessary applications.</p>
</li><li><p>Horizon scanning possible regulatory related changes within your region. Build and maintain relationships with the relevant authorities to maintain awareness of new food legislation and government guidance.</p>
</li><li><p>Track- monitor and report completion of necessary changes that need to be done due to new regulations in order to prevent any penalties from authority.</p>
</li><li><p>Ensure that ingredients- formulas- labeling- and packaging are in full compliance with the local laws and regulations where the products are sold; and provide training to the organization on relevant regulatory topics</p>
</li><li><p>Monitor and provide advice/analysis on best practices from the market for the categories we play in &amp; share it consistently with other RA teams across the company</p>
</li><li><p>Build presence in the local trade associations and industry groups as a forum to discuss upcoming or existing regulatory changes; and proactively monitor regulatory activities in our markets to address and influence proposed regulations to preserve the organization&rsquo;s freedom to operate</p>
</li><li><p>Provide proposals for the amendment of existing or new regulations to support the interests of the organization</p>
</li></ul><p><b>Qualifications &amp; Experience</b></p>
<ul><li><p>Bacherlor&rsquo;s degree in Food Technology/ Pharmacy or related disciplines. Master degree is an advantage</p>
</li><li><p>Minimum 3 years&rsquo; working experience in the field of regulatory affairs, preferably within an international environment.</p>
</li><li><p>Familiar with Turkey food registration procedures and regulatory aspects.</p>
</li><li><p>Good understanding of the commercial drivers of F&amp;B industry and an associated ability to provide advice/guidance that takes these into consideration</p>
</li><li><p>Analytical skills and attention to detail with the capability to appropriately define issues, questions, and data</p>
</li><li><p>Skills such as project management, problem solving, ability to present information in easily understood format at internal and external meetings, good time management, negotiation and interpersonal skills</p>
</li><li><p>Ability to work both independently and as part of a team as required</p>
</li><li><p>Be able to balance company commercial needs with compliance requirements</p>
</li><li><p>Ability to think strategically and innovatively for resolution of regulatory issues</p>
</li><li><p>Commitment to continued improvement in department processes and performance</p>
</li><li><p>Strong team player, assisting others with workload peaks and the management of challenging situations</p>
</li><li><p>Fluency in English and Turkish</p>
</li></ul><p>This position can be based in either Susurlul factory or İstanbul Headquarter.</p>
<p><b>About Us</b><br>
The Kraft Heinz Company is one of the largest food and beverage companies in the world, with eight $1 billion+ brands and global sales of approximately $25 billion. We&rsquo;re a globally trusted producer of high-quality, great-tasting, and nutritious foods for over 150 years. Our brands are truly global, with products produced and marketed in over 40 countries. These beloved products include condiments and sauces, cheese and dairy, meals, meats, refreshment beverages, coffee, infant and nutrition products, and numerous other grocery products in a portfolio of more than 200 legacy and emerging brands.</p>
<p>No matter the brand, we&rsquo;re united under one vision To sustainably grow by delighting more consumers globally. Bringing this vision to life is our team of 39,000+ food lovers, creative thinkers, and high performers worldwide. Together, we help provide meals to those in need through our global partnership with Rise Against Hunger. We also stand committed to responsible, sustainable practices that extend to every facet of our business, our consumers, and our communities. Every day, we&rsquo;re transforming the food industry with bold thinking and unprecedented results. If you share our passion &ndash; and are ready to create the future, build a legacy, and lead as a global citizen &ndash; there&rsquo;s only one thing to do join our table and let&rsquo;s make life delicious!</p>
<p><b>Our Culture of Ownership, Meritocracy and Collaboration</b></p>
<p>We're not afraid to think differently. Embrace new ideas. Dream big. We empower our people at every level &ndash; from entry-level intern to senior leader &ndash; to own their work. We share a responsibility to think like Owners &ndash; to be mindful of the collective and sustained success of Kraft Heinz &ndash; which we apply to every situation, every day.</p>
<p>As part of Kraft Heinz, you're supported to grow and achieve. You&rsquo;re expected to bring your authentic self to work every day, to lead with humility, and drive outstanding performance at every level &ndash; and you&rsquo;ll be rewarded. You&rsquo;re given opportunities to leave a mark and build a legacy. But you won&rsquo;t do it alone. You&rsquo;re supported by passionate teammates along the way, and our collective, collaborative spirit fuels our incredible progress.</p><br>
<p>We are proud to be a Great Place to Work certified company. Click to view our certificate: https://www.greatplacetowork.com.tr/sertifikasyon/sertifikali-sirketler/kraft-heinz-turkiye/</p>
<p>Employee Candidate Privacy Notice https //www.heinz.eu/turkey-candidate-privacy-policy</p>
<div>Location(s)</div>
<p>Istanbul Branch</p><p><br>
</p><p><b>Kraft Heinz is an Equal Opportunity Employer &ndash; Underrepresented Ethnic Minority Groups/Women/Veterans/Individuals with Disabilities/Sexual Orientation/Gender Identity and other protected classes</b><b>.</b></p></div></div></div></div></div></div>

Novo Nordisk, Inc.

<div><div><div><div><div><p>Regulatory Affairs Product Lead, T&uuml;rkiye (Fixed-Term Contract)
</p></div></div></div></div><div><div><div><div><b>Category: </b>Reg Affairs &amp; Safety Pharmacovigilance
</div></div></div></div><div><div><div><div><b>Location:
</b>İstanbul, Marmara Region, TR<br>
</div></div></div></div><div></div><div><div><div><div><div>This is the opportunity that have a unique combination of scientific insight and the ability to navigate many agendas and stakeholders as our new Regulatory Affairs Product Lead in Novo Nordisk T&uuml;rkiye. This position is a fixed term for 12 months (maternity cover), based in Istanbul, and reports to the Head of Regulatory Affairs and Pharmacovigilance.</div><div><br>
<b>
Your new position</b></div>
<div>
As the Regulatory Affairs Product Lead, you will be responsible for developing the regulatory strategy for innovative products, managing new registration files, technical variations, labelling and safety updates of product registration files and GMP files, in a timely manner and responding effectively to all product registration modifications requested by the HQ/local health authority. You will always act in alignment with our Novo Nordisk Way and demonstrate knowledge of the health care system in Turkey.</div><div><br>
You will be also responsible for
</div><ul><li>Conducting the translation, compilation, submission and follow-up related to all NN registration processes</li>
<li>Holding the responsibility for ensuring that the regulatory tasks are completed in compliance with the NN Corporate Quality Procedures, local regulations and business needs. Accompanying GMP inspection with inspector and conducting all GMP process and communication with stakeholders for assigned manufacturing sites.
</li><li>Being a coherent business partner for the business units, initiate effective cross-functional collaborations for fast regulatory approvals, creating and keeping competitive labels. In addition, you will represent Regulatory Affairs in internal brand teams by providing input on strategy and actions.</li>
<li>Monitoring competitive intelligence on relevant therapeutic areas and local environment for developments in regulations and providing relevant information to key internal and external stakeholders and advising on necessary actions about changing regulations.</li></ul><br>
<div><br>
<b>Your new department</b></div>
<div>
The Clinical, Medical, Regulatory (CMR) department provides timely, accurate, and updated services to support Novo Nordisk in all therapeutic areas. The Clinical, Medical, Regulatory Department is a team of skilled and committed specialists within medical, clinical, regulatory, and safety areas. Regulatory Affairs Unit is responsible for local strategies to obtain and maintain marketing authorisations for Novo Nordisk&rsquo;s new products and life cycle management activities such as new indications and GMP processes. We aim to be the best Regulatory Affairs unit in the global pharma industry, being true business partners and continuously improving our performance while offering our people a great place to work.</div><br>
<div></div>
<div><b>
Your skills &amp; qualifications</b></div>
<div>
You are expected to hold a university degree in Pharmacy, Chemical Engineering, Chemistry, Biology or Medical. You have minimum 3 years of proven experience in regulatory affairs in pharma industry and you should have advanced level of written and spoken English and Turkish. Further sought-after skills are</div><br>
<div></div>
<ul>
<li>You have the ability to manage multiple projects and submissions simultaneously and prioritize workload to meet business deadlines</li>
<li>You have an excellent communication and stakeholder management abilities and effective time management skills, can do mindset</li>
<li>You have good analytical capability and strategical thinking mindset and eagerness to learn influence the organization to move forward</li></ul><br>
<div></div>
<div><b>
Working at Novo Nordisk</b></div>
<div>
At Novo Nordisk, we don&rsquo;t wait for change. We drive it. We&rsquo;re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales &ndash; we&rsquo;re all working to move the needle on patient care.</div><br>
<div></div>
<div><b>
What We Offer</b></div>
<div>
There is, of course, more on offer here than the uniqueness of our culture and the extraordinary results we produce. Being part of a global healthcare company means opportunities to learn and develop are all around us, while our benefits are designed with your career and life stage in mind.</div><br>
<div></div>
<div><b>
D</b><b>eadline</b></div>
<div>
Apply before 31st December 2025. Applications are reviewed on an ongoing basis</div><div></div><div><br>
<i>
Novo Nordisk is currently in the process of adjusting job titles globally. Please note that the job title listed in this advertisement may be subject to change. More detailed information will be provided during the recruitment process.</i></div><div></div><div><br>
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.</div><br>
<div></div>
<div>
We&rsquo;re not your typical healthcare company. In a modern world of quick fixes, we focus on solutions to defeat serious chronic diseases and promote long-term health. Our unordinary mindset is at the heart of everything we do. We seek out new ideas and put people first as we push the boundaries of science, make healthcare more accessible, and treat, prevent, and even cure diseases that affect millions of lives. Because it takes an unordinary approach to drive real, lasting change in health.</div></div></div></div></div></div>

Regulatory Affairs Product Lead, Türkiye (Fixed-Term Contract)

Transmed Holding Limited

<div>Overview:
<div>
Transmed Turkiye is a full-service distributor company across 13 countries, managing distribution, sales, and marketing for 35 leading brands. We strongly believe in putting people first &ndash; our customers, our teams, our partners.</div><div></div><div><br>
We are seeking a <b>Regulatory Affairs Officer</b>.</div>
Responsibilities:<div></div><div><b><br>
JOB DESCRIPTION:</b></div><br>
<div></div><ul><li>
Conducting preliminary evaluations of imported and planned-to-be-imported products for compliance with local and international regulations,</li><li>
Managing the regulatory approval processes for food, food supplements, cosmetics, cleaning products, and animal-origin products,</li><li>
Following up on official correspondence with the Ministry of Agriculture and Forestry, Ministry of Health, and Ministry of Environment, Urbanization and Climate Change,</li><li>
Registering and archiving products in the relevant ministry systems (e.g., GGBS, HBS),</li><li>
Continuously monitoring regulatory updates and inform relevant departments in a timely manner,</li><li>
Managing the follow-up and renewal processes of supplier quality certificates,</li><li>
Collaborating with Demand Planning, Category, and Business Development teams during new product launches,</li><li>
Working in cooperation with consultancy firms during permit and approval processes.</li></ul>
Qualifications:<div></div><div><b><br>
*** This position does not offer a hybrid / remote option.</b></div><br>
<div></div><ul><li>
Bachelor&rsquo;s Degree in Food Engineering or in a related field,</li><li>
Minimum 2 years of experience in regulatory affairs for food, non-food, and cosmetic products,</li><li>
Preferably experienced in regulatory processes at consultancy or import companies,</li><li>
Advanced MS Office skills,</li><li>
Proficient in English,</li><li>
Proactive in following regulations, detail and result-oriented,</li><li>
Strong communication skills and a good team player,</li><li>
Completed military service for male candidates.</li></ul></div>

Regulatory Affairs Officer

Perrigo France

<div>
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 Regulatory Affairs, Associate Specialist
 <br/>
 <br/>
 Location:
 <br/>
 <br/>
 Istanbul, TR, 34732
 <br/>
 <br/>
 At Perrigo, we are driven by our mission to
 <em>
  <strong>
   Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All
  </strong>
 </em>
 . 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
 <strong>
  <em>
   The Best Self-Care for Everyone
  </em>
 </strong>
 , we are the people behind the brands you trust. We are Opill&reg;, Compeed&reg;, Solpadeine&reg;, NiQuitin&reg;, ACO&reg;, and many more.
 <strong>
  We Are Perrigo
 </strong>
 . 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.
 <br/>
 <br/>
 Join us on our One Perrigo journey as we evolve to win in self-care.
 <br/>
 <br/>
 <strong>
  Description Overview
  <br/>
  <br/>
 </strong>
 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.
 <br/>
 <br/>
 <strong>
  Scope of the Role
  <br/>
  <br/>
 </strong>
 <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.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Experience Required
  <br/>
  <br/>
 </strong>
 <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;
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Benefits
  <br/>
  <br/>
 </strong>
 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.
 <br/>
 <br/>
 Find out more about
 <strong>
  Total Rewards
 </strong>
 at Perrigo.
 <br/>
 <br/>
 <strong>
  Hybrid Working Approach
  <br/>
  <br/>
 </strong>
 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.
 <br/>
 <br/>
 We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more
 <strong>
  here
  <br/>
  <br/>
 </strong>
 <strong>
  Applicants please note:
 </strong>
 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.
 <br/>
 <br/>
 <em>
  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
  <br/>
  <br/>
 </em>
 Apply now &raquo;
 <br/>
 <br/>
 <strong>
  Find Similar Jobs
  <br/>
  <br/>
 </strong>
 Scientific Affairs_UK, Scientific Affairs_GR, Scientific Affairs_FR, Scientific Affairs_DE, Scientific Affairs
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Regulatory Affairs, Associate Specialist

Pfizer

<div><div><div>ROLE SUMMARY:</div></div><div></div><div><div>
Bridging science, strategy and medical innovation, the medical organization will have a lasting impact on patients across diverse European healthcare landscapes.</div></div><div><div>
The Specialty Care Category Director (SCCD) will lead a team of medical affairs scientists dedicated to Pfizer&rsquo;s assets (Inflamation &amp; Immunology, Hospital and Rare Diseases) in T&uuml;rkiye reporting directly to Country Medical Senior Director. This team will ensure the safe and effective use of Pfizer medicines and vaccines.</div></div><div><div>
As part of the Specialty Care Category LT, the SCCD will drive scientific and operational excellence for all Specialty Care Category (SCC) medical processes and will manage Medical Affairs Scientists.</div></div><div></div><div><div>
ROLE RESPONSIBILITIES</div></div><div><ul><li><div>
Accountable for informing and co-developing the SCC medical operating plan and fully accountable for execution while embracing new tools and frameworks for medical excellence and operational efficiency.</div></li><li><div>
Drives a customer and patient centric medical organization that leverages strong scientific and medical expertise to build strong partnerships with HCPs, regulators, and external stakeholders, while providing strategic thought partnership for commercial marketing, regulatory, compliance and access initiatives.</div></li><li><div>
Represents the SCC to external bodies for SCC related issues;</div></li><li><div>
Represents SCC through relationships with medical associations, societies, academic medical centers and industry associations.</div></li></ul></div><div><ul><li><div>
Plans and executes the respective KOL strategy for Turkey on highly ethical and medical professionalism grounds and brings their input into the medical strategies and plans;</div></li><li><div>
Communicates the value of the MA function to internal stakeholders (championing cross functional working, and working with the Global and Emerging Market teams and Country Medical Director);</div></li><li><div>
Along with Category and MQG teams, designs, implements and evaluates systems and processes to ensure full compliance with legal and regulatory requirements.</div></li><li><div>
A caring, compassionate and authentic leader who upholds the highest standards of ethics, probity, integrity and compliance with regulatory, financial and legal requirements and fosters a high-performing medical team culture, supporting growth and talent development.</div></li><li><div>
Leads, manages and coaches in-country Medical Affairs Scientists who will generate, analyse, exchange and act on insights that support the safe and effective development and utilization of Pfizer medicines and vaccines to improve patient outcomes.</div></li><li><div>
Communicates the value of the MA function to external stakeholders, aligning with customer needs, enhancing reputation and bringing medical insights into the organisation.</div></li></ul><div></div><div>
QUALIFICATIONS</div><div><ul><li><div>
A Pharmacy or Medical degree coupled with strong pharmaceutical experience and knowledge. A medical degree (MD) and/or PhD is highly desirable.*</div></li></ul></div><div><ul><li><div>
Minimum of 5 years of experience in medical affairs or transferrable knowledge from related roles is of preference. (Therapeutic area experience is preferred)</div></li></ul></div><div><ul><li><div>
Experience in leading teams through transformation is of preference.</div></li></ul></div><div><ul><li><div>
Ability to lead in a matrixed, cross-functional environment.</div></li></ul></div><div><ul><li><div>
Strong understanding of Turkish healthcare system, regulatory landscapes, and medical governance.</div></li></ul></div><div><ul><li><div>
A full, detailed understanding of regulatory requirements and compliance in the pharmaceutical industry</div></li></ul></div><div><ul><li><div>
Excellent communication, interpersonal and leadership skills.</div></li></ul><div></div><div>
CORE COMPETENCIES</div><div><ul><li><div>
Holds people accountable;</div></li></ul></div><div><ul><li><div>
Strategic and innovative thinking;</div></li></ul></div><div><ul><li><div>
Commits to &ldquo;One Pfizer&rdquo;;</div></li></ul></div><div><ul><li><div>
Anticipates customer and market needs.</div></li></ul><div></div><div>
TECHNICAL/FUNCTIONAL COMPETENCIES</div><div><ul><li><div>
Fluency in business English;</div></li></ul></div><div><ul><li><div>
Ability to analyze, define and convey complex concepts and strategies and to communicate these to demanding external and internal stakeholders;</div></li></ul></div><div><ul><li><div>
Excellent strategic skills including creativity and effectiveness in identifying and addressing major strategic challenges together with the ability to balance short-term needs and long-term vision.</div></li></ul></div><div></div><div><div>
This is a GJL 100 role</div><ul><li>(Exceptional situation for the latter educational requirement does not apply to those colleagues who are Pharmacists only and who already hold a Medical Affairs position internally)</li></ul></div></div></div></div><div></div><div><div>
Purpose</div></div><div><div>
Breakthroughs that change patients' lives... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.</div></div><div></div><div><div><br>
School of Leaders</div><div>
We, as Pfizer Turkey, make a difference with our visionary and pioneering approaches ranging from our concept of raising leaders through rotations, providing international career opportunities to creating a flexible, enjoyable work environment. There are no limits to what we can accomplish to touch lives here!</div></div><div></div><div><div><br>
Flexibility</div><div>
We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let&rsquo;s start the conversation!</div></div><div></div><div><div><br>
Equal Employment Opportunity</div><div>
We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms &ndash; allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.</div></div><div></div>
Medical</div><div></div>

Specialty Care Category Medical Director, Türkiye

<div><div><div><div>ROLE SUMMARY:</div></div><div></div><div><div>
Bridging science, strategy and medical innovation, the medical organization will have a lasting impact on patients across diverse European healthcare landscapes.</div></div><div><div>
The Primary Care Category Director (PCD) will lead a team of medical affairs scientists dedicated to Pfizer&rsquo;s Vaccines and Internal Medicine assets in T&uuml;rkiye reporting directly to Country Medical Senior Director. This team will ensure the safe and effective use of Pfizer medicines and vaccines.</div></div><div><div>
As part of the Primary Care Category LT, the Medical Category Director will drive scientific and operational excellence for all Primary Care Category medical processes and will manage Medical Affairs Scientists.</div></div><div></div><div><div><br>
ROLE RESPONSIBILITIES</div></div><div><ul><li><div>
Accountable for informing and co-developing the Primary Care Category (PCC) medical operating plan and fully accountable for execution while embracing new tools and frameworks for medical excellence and operational efficiency.</div></li></ul></div><div><ul><li><div>
Drives a customer and patient centric medical organization that leverages strong scientific and medical expertise to build strong partnerships with HCPs, regulators, and external stakeholders, while providing strategic thought partnership for commercial marketing, regulatory, compliance and access initiatives.</div></li></ul></div><div><ul><li><div>
Represents the PCC to external bodies for Vaccine related issues;</div></li></ul></div><div><ul><li><div>
Represents PCC through relationships with medical associations, societies, academic medical centers and industry associations;</div></li></ul></div><div><ul><li><div>
Plans and executes the respective KOL strategy for Turkey on highly ethical and medical professionalism grounds and brings their input into the medical strategies and plans;</div></li></ul></div><div><ul><li><div>
Communicates the value of the MA function to internal stakeholders (championing cross functional working, and working with the Global and Emerging Market teams and Country Medical Director);</div></li></ul></div><div><ul><li><div>
Along with Category and MQG teams, designs, implements and evaluates systems and processes to ensure full compliance with legal and regulatory requirements.</div></li></ul></div><div><ul><li><div>
A caring, compassionate and authentic leader who upholds the highest standards of ethics, probity, integrity and compliance with regulatory, financial and legal requirements and fosters a high-performing medical team culture, supporting growth and talent development.</div></li></ul></div><div><ul><li><div>
Leads, manages and coaches in-country Medical Affairs Scientists who will generate, analyse, exchange and act on insights that support the safe and effective development and utilization of Pfizer medicines and vaccines to improve patient outcomes.</div></li></ul></div><div><ul><li><div>
Communicates the value of the MA function to external stakeholders, aligning with customer needs, enhancing reputation and bringing medical insights into the organisation.</div></li></ul></div></div><div></div><div><div><div>
QUALIFICATIONS</div></div><div><ul><li><div>
A Pharmacy with PhD or Medical degree coupled with strong pharmaceutical experience and knowledge. A medical degree (MD) and/or PhD is highly desirable.*</div></li></ul></div><div><ul><li><div>
Minimum of 5 years of experience in medical affairs or transferrable knowledge from related roles is of preference. (Vaccines exp. is preferred)</div></li></ul></div><div><ul><li><div>
Experience in leading teams through transformation is of preference.</div></li></ul></div><div><ul><li><div>
Ability to lead in a matrixed, cross-functional environment.</div></li></ul></div><div><ul><li><div>
Strong understanding of Turkish healthcare system, regulatory landscapes, and medical governance.</div></li></ul></div><div><ul><li><div>
A full, detailed understanding of regulatory requirements and compliance in the pharmaceutical industry</div></li></ul></div><div><ul><li><div>
Excellent communication, interpersonal and leadership skills.</div></li></ul></div><div></div><div><div>
CORE COMPETENCIES</div></div><div><ul><li><div>
Holds people accountable;</div></li></ul></div><div><ul><li><div>
Strategic and innovative thinking;</div></li></ul></div><div><ul><li><div>
Commits to &ldquo;One Pfizer&rdquo;;</div></li></ul></div><div><ul><li><div>
Anticipates customer and market needs.</div></li></ul></div><div></div><div><div>
TECHNICAL/FUNCTIONAL COMPETENCIES</div></div><div><ul><li><div>
Fluency in business English;</div></li></ul></div><div><ul><li><div>
Ability to analyze, define and convey complex concepts and strategies and to communicate these to demanding external and internal stakeholders;</div></li></ul></div><div><ul><li><div>
Excellent strategic skills including creativity and effectiveness in identifying and addressing major strategic challenges together with the ability to balance short-term needs and long-term vision.</div></li></ul></div><div><div>
This is a GJL 100 role</div></div><div><ul><li>(Exceptional situation for the latter educational requirement does not apply to those colleagues who are Pharmacists only and who already hold a Medical Affairs position internally)</li></ul></div></div><div></div><div><div>
Purpose</div></div><div><div>
Breakthroughs that change patients' lives... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.</div></div><div></div><div><div><br>
School of Leaders</div><div>
We, as Pfizer Turkey, make a difference with our visionary and pioneering approaches ranging from our concept of raising leaders through rotations, providing international career opportunities to creating a flexible, enjoyable work environment. There are no limits to what we can accomplish to touch lives here!</div></div><div></div><div><div><br>
Flexibility</div><div>
We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let&rsquo;s start the conversation!</div></div><div></div><div><div><br>
Equal Employment Opportunity</div><div>
We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms &ndash; allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.</div></div><div></div>
Medical</div><div></div>

Primary Care Category Medical Director, Türkiye

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