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regulatory affairs, associate specialist Jobs in Istanbul

regulatory affairs, associate specialist

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administrative affairs manager

financial reporting analyst Jobs in Istanbul

financial reporting analyst

regulatory consultant

regulatory affairs analyst

Ferring Pharmaceuticals, Inc.

<div><div>Job Description:</div><div>
Regulatory Affairs Associate</div><div></div><div>
At Ferring Pharmaceuticals, we help people around the world build families and live better lives. We are entrepreneurial and innovative, with a global team focused on scientific advances in the areas of reproductive and women&rsquo;s health, gastroenterology and urology. Ferring + You is all about working together and sharing ideas, so that we can bring science to life for patients around the world.</div><div>
Joining our Regulatory team, you will be part of an empowering and collaborative culture where your work plays a key role in ensuring patient safety, regulatory compliance and sustainable access to medicines. By working closely with cross-functional teams and external stakeholders, you will support regulatory excellence, life-cycle management and the consistent maintenance of our portfolio. Your contribution helps ensure that high-quality therapies remain available, compliant and trusted throughout their entire life cycle.</div><div></div><div>
Ferring+You</div><div></div><div>
We are looking for a Regulatory Affairs Associate to join our team and take a key role in regulatory compliance, quality assurance, document governance, and cross-functional business support in line with local regulations and global procedures, reporting directly to the Regulatory Affairs Manager.</div><div></div><div>
Your day at Ferring</div><ul><li><div>
Act as Document Accountable Person (DAP) and Document Controller (DC), ensuring document lifecycle management, consistency, and compliance</div></li><li><div>
Serve as the main local regulatory contact and manage regulatory compliance activities</div></li><li><div>
Coordinate new drug approvals, including dossier preparation, submissions, and follow-up with local Health Authorities</div></li><li><div>
Manage regulatory submissions, variations, renewals, and product lifecycle activities</div></li><li><div>
Support and coordinate regulatory inspections and maintain validity of licenses and certificates</div></li><li><div>
Monitor regulatory intelligence, assess impact, and proactively communicate regulatory changes</div></li><li><div>
Ensure timely and accurate updates in global and local regulatory systems (e-CTD, Veeva Vault, Track Wise, etc.)</div></li><li><div>
Prepare, review, and approve artworks and labeling to support submissions and product launches</div></li><li><div>
Review promotional and non-promotional materials in line with local regulations and global procedures</div></li><li><div>
Support Quality Management System (QMS) implementation and sustainability, including local market release</div></li><li><div>
Support regulatory and pricing applications, including document coordination and pricing data monitoring</div></li></ul><div></div><div>
Behind our collaboration&hellip;There&rsquo;s you</div><ul><li><div>
University degree in Pharmacy</div></li><li><div>
Min. 2-3 years of practical experience in regulatory and quality assurance</div></li><li><div>
Know-how of interactions with regulatory authorities</div></li><li><div>
Experience with e-CTD, Veeva Vault, Track Wise, and pricing is a plus</div></li><li><div>
Eager to learn personality, team player approach, attention to details</div></li><li><div>
Fluent in English language (written and verbal)</div></li></ul><div></div><div>
People come first at Ferring</div><div></div><ul><li><div>
Get inspired from our commitment to advocate for everyone&rsquo;s right to build a family, no matter who you are, where you live or who you love</div></li><li><div>
Our inclusive support package &ndash; &ldquo;Building Families at Ferring&rdquo; provides equal and accessible policies for all employees who wish to start their family journey, ensuring a global standard, irrespective of location and role</div></li><li><div>
Parental leave for both birthing and non-birthing parents</div></li><li><div>
Extended support on family building journey</div></li></ul><div></div><div>
Making a difference in the life of millions of people means we succeed by working together. Our diverse backgrounds, experiences, expertise, and perspectives enable us to find solutions to even the most challenging problems, and our success is tied to each team member&rsquo;s contributions. Imagine the power of your career when it&rsquo;s Ferring + You.</div><div></div><div>
Behind our purpose&hellip; There&rsquo;s you</div><div>
If our mission and your vision are aligned, please apply.</div><div>
We strive to build and maintain an inclusive and diverse workplace with equal opportunities and mutual respect for all employees regardless of their backgrounds and socioeconomic status.</div><div></div><div>
Location:</div>
Ferring Turkey</div>

Regulatory Affairs Associate

Perrigo France

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 <br/>
 <br/>
 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
</div>


Regulatory Affairs, Associate 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>


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>

OBSS

<div>
 <p>
  <strong>
   Company Description
  </strong>
 </p>
 <p>
  OBSS is Turkey&rsquo;s largest technology consultancy, pioneering product development and technology consulting for an AI-native future. With more than 20 years of experience and offices in Istanbul, Ankara, London, Amsterdam, and Baku, we empower leading companies in banking and finance, insurance, e-commerce, retail, and the start-up ecosystem. Our team of over 1000 talented professionals thrives on collaboration, innovation, and continuous learning.
 </p>
 <p>
  OBSS is looking for a
  <strong>
   Team Lead
  </strong>
  to join our dynamic team and contribute to delivering high-impact, data-driven solutions. You will work on cutting-edge projects, collaborating with cross-functional teams to build advanced models, generate insights, and design scalable solutions that drive real business outcomes.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Main Responsibilities
  </strong>
 </p>
 <ul>
  <li>
   Leading and mentoring a team of Data Analysts and Data Engineers within the regulatory reporting domain.
  </li>
  <li>
   Coordinating the review and maintenance of existing regulatory reports
  </li>
  <li>
   Driving the automation of manual and semi-manual reporting processes.
  </li>
  <li>
   Overseeing the preparation and delivery of regulatory reports (BDDK, MASAK, TCMB, etc.) accurately and on time.
  </li>
  <li>
   Supporting ad hoc reporting needs from business units as well as regulatory authorities.
  </li>
  <li>
   Ensuring the monitoring and reliability of daily ETL processes on MSSQL.
  </li>
  <li>
   Guiding data engineers in enhancing datamart structures for new reporting requirements.
  </li>
  <li>
   Establishing and enforcing documentation standards, reporting guidelines, and data quality procedures.
  </li>
  <li>
   Acting as the main point of contact between technical teams and business stakeholders for regulatory reporting needs.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  This role requires
  <strong>
   hands-on regulatory reporting experience
  </strong>
  , strong
  <strong>
   SQL expertise
  </strong>
  , and proven
  <strong>
   leadership capabilities
  </strong>
  within the banking sector.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications / Technical Skills
  </strong>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s or Master&rsquo;s degree in Computer Science, Information Systems, Statistics or a related field.
  </li>
  <li>
   Minimum
   <strong>
    8-10 years of experience
   </strong>
   in regulatory reporting within the banking sector, with at least
   <strong>
    2 years in a leadership or coordination role
   </strong>
   .
  </li>
  <li>
   Strong knowledge of MSSQL and reporting processes.
  </li>
  <li>
   Demonstrated ability to manage and mentor teams, set priorities, and deliver results under strict deadlines.
  </li>
  <li>
   Solid SQL skills (queries, joins, views, stored procedures).
  </li>
  <li>
   PL&amp;SQL is a plus
  </li>
  <li>
   Hands-on experience with Excel/Power BI or similar reporting tools.
  </li>
  <li>
   Experience in data validation, data quality checks, and control processes.
  </li>
  <li>
   Strong communication, collaboration, and stakeholder management skills.
  </li>
  <li>
   Ability to prepare and enforce documentation such as data standards, procedures, and reporting guidelines.
  </li>
  <li>
   Detail-oriented, highly organized, and able to coordinate multiple priorities simultaneously.
  </li>
  <li>
   Experience in hybrid/agile environments is a plus.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Additional Information
  </strong>
 </p>
 <p>
  <strong>
   Professional Growth &amp; Learning
  </strong>
 </p>
 <p>
  As a tech company, we focus on reskilling and upskilling to support career growth. We offer a personalized Individual Growth Program (IGP), where employees set clear goals for each half of the year. These goals may include trainings, certifications, and personal development milestones, creating a structured roadmap for continuous improvement. The IGP helps employees strengthen both technical and soft skills, ensuring steady professional advancement.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Company Culture and Values
  </strong>
 </p>
 <p>
  We celebrate diversity, inclusion, and equal opportunity, fostering a collaborative environment where innovation can flourish. Our culture emphasizes mentorship, knowledge sharing, and active participation in tech communities, workshops, and team events. This vibrant atmosphere empowers employees to contribute their best while feeling supported and valued.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Benefits and Perks
  </strong>
 </p>
 <p>
  We provide competitive salaries, flexible and hybrid working arrangements, and a wide range of opportunities for growth through training programs, certifications, and workshops. In addition, we offer initiatives designed to build a supportive and engaging workplace where curiosity and collaboration are encouraged. These benefits ensure that employees feel motivated, empowered, and equipped to reach their full potential.
 </p>
 <p>
 </p>
</div>


Team Lead – Regulatory Reporting (Data Analyst Background)

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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Specialty Care Category Medical Director, Türkiye

Primary Care Category Medical Director, Türkiye