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legal & compliance manager Jobs in Istanbul

legal & compliance manager

medical science liaison

regulatory affairs specialist

Perrigo Company plc

<div>
 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
 </em>
</div>


Regulatory Affairs, Associate Specialist

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>

Danone

<div>About the job
<p><b>
Danone T&uuml;rkiye</b> is looking for a talented colleague for the <b>&quot;Regulatory Affairs Manager </b>&quot; position. Take this opportunity to GROW together!</p><br>
<p></p>
<p>
As a Regulatory Affairs Manager, you will be an <i>individual contributor</i> in this role and reporting to the <i>Head of Regulatory Affairs.</i></p><br>
<p></p>
<p><b><i>
In this role you will;</i></b><i>
 </i></p><p><i>Ensure sufficient compliance governance to meet regulatory obligations of the dairy business unit
</i></p><ul><li><i>Ensure full compliance of recipes, products, labeling and any kind of product communication (press, TV, online, etc.)
</i></li></ul><ul><li><i>Provide regulatory assessments for innovation projects to give direction by exploiting opportunities where possible and avoiding regulatory hurdles
</i></li></ul><ul><li><i>Lead and manage product approval and licensing process related to products
</i></li></ul><ul><li><i>Propose &amp; implement action plans in response to regulatory changes in the market</i></li></ul>
<ul><li><i>Anticipate the development of new regulations and effectively communicate company position in relevant external environment
</i></li></ul><ul><li><i>Advocacy and lobby on new regulation development via trade associations and by establishing effective relationship with authorities
</i></li></ul><p><i>&bull; Educate all relevant functions on regulatory compliance to ensure consistent implementation of regulatory requirements &bull; Identify and predict issues that could impact the business and communicate them to relevant business partners; assist them to implement agreed actions
</i></p>About you
<ul><li>Have at least 5 years of related experience in Food, Beverage sector in Regulatory Affairs department</li></ul>
<ul><li>University degree in Food Engineer, Chemical Engineer, or relevant disciplines</li></ul>
<ul><li>Have in knowledge of food and beverages&rsquo; regulations and related EU regulations (preferably)</li></ul>
<p>
&bull; Excellent command of written and spoken English &bull; Attention to details, very-well organized, and logical/systematic thinking</p>
<ul><li>Capable to pro-actively engage and liaise with internal/external stakeholders (good communication skills)</li></ul>
About us
<p><b>
Being a Danoner means that you create your own working experience.</b></p><br>
<ul>
<li>You could design your own way of working with our hybrid working model.</li>
<li>Our head office is in Ata&#351;ehir.</li>
<li>You could decide your daily 8-hours of working period within our flexible-working hours practice.</li>
<li>We know that you will have home expenses during home office days. So, Danone supports you for your expenses with an allowance as well!</li>
<li>Summers are flexible here! You could work fully remote for 4 weeks during July and August.</li>
<li>We also enjoy Fridays during summer period between July and August by finishing our works by 1500 and enjoy the rest of the day and starting the weekend earlier.</li>
Danone offers various types of leave days to support Danoners&rsquo; work-life balance and well-being. We have a wide variety of leave types, such as in your first year 5 days of &quot;Im New in Danone Leave&quot;; 1 day of &quot;My Future is Good Leave&quot; for our social responsibility activities. These options cater to different aspects of employees' lives and needs, reflecting the company's commitment to not only professional growth but also personal and social responsibilities.<br>
<li>
<br>
<br>
</li></ul><p>We are proud to promote diversity and equal opportunity within our teams. We believe that our differences will make a difference, and that an inclusive work environment will drive our growth as a company, as a team, and as individuals. We will therefore consider all implementations* by fostering an inclusive work culture where everyone can feel at home.<br>
<br>
All nominations will be considered regardless of origin, background, religion, sex, sexual orientation, age, gender identity, disability.<br>
<br>
<b>Working with us</b> is about being able to do things your way. The way you work, the way you develop, the way you progress,<b> i</b><b>t&rsquo;s all up to you.</b><br>
<br>
Working here, you&rsquo;ll need to enjoy a fast-paced environment, a little complexity and challenging tasks but it is packed with opportunities. You will work for some of the best-known brands in the world, such as Activia, Danone, Danino, Danette, Aptamil, Bebelac, Hayat, and S&#305;rma, and we absolutely guarantee that you can just be yourself.<br>
<br>
<b>Be innovative and entrepreneurial and the impact you could make might just amaze you</b>. Join our movement for a healthier world. <b>One Planet One Health BY YOU.</b><br>
<br>
At Danone T&uuml;rkiye, inspired by our <b>B Corp</b> journey, we continuously challenge ourselves to improve and measure our social and environmental impact. This journey inspires us to constantly challenge ourselves, measure what truly matters, and create long-term value &mdash; not just for our business, but for our people, partners, communities, and future generations. <b>If you&rsquo;re looking to grow your career with purpose, you&rsquo;re in the right place.</b></p><br>
<p></p>
<p><b>
What&rsquo;s next?</b><br>
<br>
Visit our website www.danone.com to discover more about us and to find out how you could be part of it all!</p></div>

Regulatory Affairs Manager (Temporary)

Roche

<div><p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><p></p><div>
The Position</div><p><b>
Key Responsibilities:</b></p><ul><li><p>
Develop innovative regulatory strategies for Roche&rsquo;s new products and indications to enable fast market access.</p></li><li><p>
Define regulatory submission and approval timelines, and plan launch dates accordingly.</p></li><li><p>
Manage GMP, prioritization, and registration submissions for innovative products.</p></li><li><p>
Adapt global product dossiers to meet local regulatory requirements; gather and prepare additional documentation as needed.</p></li><li><p>
Design and implement policy initiatives to shape the Turkish regulatory environment in alignment with Roche&rsquo;s strategy.</p></li><li><p>
Ensure inspection-readiness for GMP and regulatory audits; manage related processes within relevant systems.</p></li><li><p>
Collaborate closely with cross-functional teams for the launch planning of new products or indications.</p></li><li><p>
Engage in effective advocacy activities with health authorities, industry associations, and key stakeholders.</p></li><li><p>
Conduct the necessary correspondence for all registered/non-registered products and follow up with the Ministry processes</p></li></ul><p></p><p><b>
Who You Are:</b></p><ul><li><p>
Bachelor&rsquo;s degree in Pharmacy, Chemical Engineering, Chemistry, or a related field</p></li><li><p>
Minimum 5 years of experience in regulatory affairs, ideally working in cross-functional settings</p></li><li><p>
Hands-on knowledge and solid understanding of regulatory processes and requirements</p></li><li><p>
Preferably, some experience in coordinating or supporting project activities within a team environment</p></li><li><p>
A collaborative mindset with the ability to motivate colleagues and contribute to team development</p></li><li><p>
Willingness and capability to share knowledge, provide support, and offer guidance within the team when needed</p></li><li><p>
Strong communication skills and a team-oriented approach</p></li><li><p>
High ethical standards and a basic understanding of relevant compliance regulations</p></li><li><p>
Proficiency in both written and spoken Turkish and English</p></li><li><p>
Comfortable working in a dynamic, agile environment; open to change, self-motivated, responsible, and eager to learn</p></li></ul><p></p><div>
Who we are</div><p>
A healthier future drives us to innovate. Together, more than 100&rsquo;000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p><br>
Let&rsquo;s build a healthier future, together.</p><p></p><p><b>
Roche is an Equal Opportunity Employer.</b></p></div>

Regulatory Affairs Partner

Calik Holding

<div>
 <p>
  <strong>
   Qualifications
  </strong>
 </p>
 <ul>
  <li>
   Bachelor's degree in Law,
  </li>
  <li>
   3+ years of experience in compliance, legal, or regulatory roles,
  </li>
  <li>
   Strong understanding of national and international compliance standards,
  </li>
  <li>
   Excellent communication and analytical skills,
  </li>
  <li>
   Fluency in English; additional languages are plus.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Responsibilities
  </strong>
 </p>
 <ul>
  <li>
   Having interest and experience in regulatory and compliance matters,
  </li>
  <li>
   Possessing knowledge in analyzing and assessing compliance risks or sanctions,
  </li>
  <li>
   Conducting comprehensive work on the Compliance Program and preparing related procedures and policy documents,
  </li>
  <li>
   Providing training and awareness sessions to employees on ethics and compliance topics,
  </li>
  <li>
   Managing and monitoring the process of the Personal Data Protection Law, including handling VERBIS registrations and reporting,
  </li>
  <li>
   Working on ethical principles, ethics hotline, and compliance policy documents,
  </li>
  <li>
   Tracking legislative changes and informing companies accordingly,
  </li>
  <li>
   Supporting departments in preparing internal documents such as contracts, procedures, and policy texts,
  </li>
  <li>
   Responding to Due Diligence (DD) questionnaires and preparing company documentation.
  </li>
 </ul>
 <p>
 </p>
</div>


Compliance Lawyer

<div><p>&#304;&#351; Tan&#305;m&#305;</p><br>
<ul><li>TSE, TAREKS, BTK, TPS vb. i&#351;lemlerle ilgili ba&#351;vurular&#305;n yap&#305;lmas&#305; ve ekibin ba&#351;vurular&#305;n&#305;n kontrol edilip takip edilmesi</li>
<li>G&uuml;ncel Deklarasyon &amp; CE beyan&#305; vb. konularla ilgili test raporu ve/veya di&#287;er belgelerin kontrol edilmesi ve ekibin bu y&ouml;nde geli&#351;tirilmesi</li>
<li>TSE, TAREKS, BTK, TPS vb. mevzuat g&uuml;ncellemelerinin takip edilmesi ve bu g&uuml;ncellemelerin i&ccedil; ve d&#305;&#351; m&uuml;&#351;terilere bildirilmesi</li>
<li>TSE, TAREKS, BTK, TPS vb. uygulamalar i&ccedil;in proaktif dok&uuml;mantasyon ve bilgi kontrollerinin yap&#305;lmas&#305; ve bunlar&#305;n i&ccedil; ve d&#305;&#351; m&uuml;&#351;terilere bildirilmesi</li>
<li>Gerekti&#287;inde GSM ama&ccedil;l&#305; cihazlar i&ccedil;in IMEI/TAC kayd&#305; ba&#351;vurusunun yap&#305;lmas&#305; ve ekibin ba&#351;vurular&#305;n&#305;n kontrol edilip takip edilmesi</li>
<li>&#304;&#351; takip kontrollerinin yap&#305;lmas&#305; ve s&uuml;re&ccedil; raporlar&#305;n&#305;n d&uuml;zenlenmesi (Ba&#351;vuru sistemi ve Evrim program&#305; &uuml;zerinden)</li>
<li>Gerekti&#287;inde &Uuml;r&uuml;n G&uuml;venli&#287;i Birimi, TSE Birimi, BTK vb. birimlerle ileti&#351;ime ge&ccedil;ilmesi ve ziyaret edilmesi</li>
<li>Gerekti&#287;inde i&ccedil; ve d&#305;&#351; m&uuml;&#351;teri toplant&#305;lar&#305;na kat&#305;l&#305;m sa&#287;lanmas&#305;</li>
<li>Gerekti&#287;inde konuyla ilgili projelere liderlik edilmesi</li></ul><br>
<p>Yetkinlikler</p><br>
<ul><li>TSE, TAREKS, BTK, TPS, vb. konular&#305;nda en az 7 y&#305;l deneyimli</li>
<li>Ekip liderli&#287;i/y&ouml;neticili&#287;i pozisyonunda en az 2 y&#305;l deneyimli</li>
<li>G&uuml;ncel Deklarasyon &amp; Test Raporu uygulamalar&#305; ve mevzuatlar&#305; konusunda y&uuml;ksek deneyim sahib&#304;</li>
<li>Genel d&uuml;zeyde G&uuml;mr&uuml;k Yaz&#305;l&#305;m&#305; (Evrim program&#305;) ve MS Office uygulamalar&#305; bilgisi</li>
<li>Tercihen &#304;ngilizce bilen</li>
<li>G&uuml;&ccedil;l&uuml; ileti&#351;im becerileri, tak&#305;m &ccedil;al&#305;&#351;mas&#305; ve m&uuml;&#351;teri odakl&#305; yakla&#351;&#305;m</li>
<li>B S&#305;n&#305;f&#305; ehliyet sahibi ve aktif olarak ara&ccedil; kullanabilen</li>
<li>Askerlik g&ouml;revinin tamamlanm&#305;&#351; ya da muaf (erkek adaylar i&ccedil;in)</li>
</ul><div>#LI-TUR</div></div>

TSE TAREKS TAKIM LİDERİ

Pfizer

<div><div>POSITION PURPOSE</div><div></div><ul><li>
The Sr. Director, Turkey Country Medical provides leadership to the in-country Medical Affairs (MA) Team he/she is leading aligned with the Category strategies, business goals and customer needs;</li><li>
Represents the company to external bodies for medical issues;</li><li>
Represents Pfizer through relationships with medical associations, societies, academic medical centers and industry associations;</li><li>
Represents Pfizer in high-level interactions with regulatory authorities as required;</li><li>
Takes accountability together with the respective Category medical leads and medical function leads for the compliance of medical operations, including medical communication and promotional material with applicable guidelines;</li><li>
In partnership with the responsible functions supports and facilitates in-country adherence of MQG, pharmacovigilance, product quality, regulatory, medical information and clinical activities and processes to relevant regulations and Pfizer SOPs, and;</li><li>
Has oversight of the medical functions within all categories in relation to compliance and talent development.</li></ul><div></div><div>
PRIMARY RESPONSIBILITIES</div><div>
Development, Implementation and Communication of Medical Affairs Strategies and the in-country Medical Affairs Function</div><ul><li>
Participates in Strategic Planning Process to provide insight, expertise and medical support to the business;</li><li>
Ensures processes and procedures within medical are continuously reviewed and updated to meet current and future business needs;</li><li>
Aligns / influences medical teams with global and regional brand functions, where appropriate;</li><li>
Establishes vision, direction and role purpose for the team;</li><li>
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;</li><li>
Devises country medical plans on scientifically sound principles that will bring benefits to the patients, working in close collaboration and in alignment with the Global and Emerging Market teams and in accordance with the overall brand and portfolio strategy;</li><li>
Allocates financial and FTE resources as per the operating plan provisions;</li><li>
Implements medical strategies according to the medical plans, across the category portfolio of medicines, with emphasis on the data generating and the data communication activities;</li><li>
Ensures in-country implementation and execution of product-specific non-routine risk minimization measures;</li><li>
Provides medical support and guidance to Country President to ensure that the commercial objectives of each medicine are realized through adherence to the highest ethical, legal, regulatory standards;</li><li>
Provides scientific input to the Market Access strategies and tactics in Turkey;</li><li>
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 president);</li><li>
Communicates the value of the MA function to external stakeholders, aligning with customer needs, enhancing reputation and bringing medical insights into the organisation.</li></ul><div></div><div>
Build Organizational Capability and Management of People</div><ul><li>
Leads, motivates and enhances the performance of the Medical Affairs Team and in-country solid line reports through coaching and by direct example;</li><li>
Supports talent management within the all category medical functions, ensuring that Pfizer colleagues within the Category Medical Teams and partner lines management are aware of opportunities.</li></ul><div></div><div>
&rsquo;One Pfizer&rsquo;</div><ul><li>
Represents the immediate point of reference to the Country President for medical issues, advises the Country president on medical issues and assures appropriate resolution;</li><li>
Chairs the Country Medical Committee with the purpose of maintaining compliance and information flow as well as to facilitate the resolution of issues that arise within the broader Category medical teams and partner functions;</li><li>
Represents the Category medical and partner functions in the Country Leadership Team (CLT), and ensures direct representation in the CLT, when appropriate;</li><li>
Partners with the responsible functions with respect to responses to Regulatory, Safety, and/or Clinical issues with potential impact on public health, or a potential impact on the organization's reputation;</li><li>
Represents Pfizer in industry bodies and associations;</li><li>
Coordinates and is responsible for the &lsquo;one medical voice of Pfizer&rsquo; when interacting with important external customers including professional societies, medical schools, media, government and payers.</li></ul><div></div><div>
In-Country Compliance</div><ul><li>
Ensures consistent application of local regulations and standards on promotional material, medical and scientific relations, transparency of grant payments and FCPA across the Categories in-country.</li><li>
Supports local inspections as defined by the local inspection action plan(s).</li><li>
Sponsors audits/inspections under Medical Division accountability.</li><li>
Provides support for audits on Platform Lines as required.</li><li>
Ensures appropriate oversight and successful implementation of the Country Medical Quality Plan.</li></ul><div></div><div>
Memberships</div><ul><li>
Regular Member of the CLT;</li><li>
Regular Member and Chairperson of the in-country Medical Leadership Team;</li><li>
Chairperson of the Country Medical Committee.</li></ul><div></div><div>
Resources Managed (budget and FTEs)</div><ul><li>
Solid line reports: In-country Medical Affairs Category Leads, Medical Affairs Enablement Lead</li><li>
Dotted Line: In-country Medical Quality Governance (MQG) function; Medical Information</li><li>
Budget responsibility for the in-country medical affairs organization</li></ul><div></div><div>
REQUIRED SKILL SET</div><div></div><div>
Qualifications (i.e., preferred education, experience, attributes)</div><ul><li>
Medical Doctor (Must) with solid education and experience;</li><li>
At a minimum 5 years of experience in the pharmaceutical industry, especially Medical Affairs and / or Clinical Research;</li><li>
Comprehensive understanding of the international health environment;</li><li>
Deep understanding of the country health environment including its structure, policy, key members and scientific societies;</li><li>
Profound knowledge of relevant international Codes of Practice, guidelines and regulations as well as applicable Pfizer SOPs;</li><li>
Comprehensive knowledge of pharmacovigilance and regulatory legislation and the drug development process and how these aspects impact the product portfolio;</li><li>
Line management experience and general business management experience.</li></ul><div></div><div>
Core Competencies</div><ul><li>
Holds people accountable;</li><li>
Strategic and innovative thinking;</li><li>
Commits to &ldquo;One Pfizer&rdquo;;</li><li>
Anticipates customer and market needs.</li></ul><div></div><div>
Technical/Functional Competencies</div><ul><li>
Fluency in business English;</li><li>
Ability to analyze, define and convey complex concepts and strategies and to communicate these to demanding external and internal customers;</li><li>
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.</li></ul><div>
This is a GJL 110 role.</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>

Sr. Director, Turkey Country Medical

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Sr. Director, Turkey Country Medical