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regulatory affairs manager

Medtronic

<div><p>At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You&rsquo;ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
</p><p></p><h1 class="jobSectionHeader"><b>A Day in the Life
</b></h1>Come and join our regional Regulatory Affairs Team as Regulatory Affairs Manager to oversee both pre-market and post-market regulatory activities in Levant, Gulf and Pakistan countries (Cyprus, Iran, Iraq, Jordan, Lebanon, Syria, Bahrain, Kuwait, Oman, Qatar, Yemen, UAE, Pakistan and Afghanistan) and work with a talented team.
<br>
<br>
The role is crucial to enable timely product launches and business continuity in the said regions by sustaining strong relations with distributors, authorities as well as internal stakeholders including country leaders. The role will report into Sr. Regulatory Affairs Manager responsible for Turkiye, West Asia, Levant and Gulf.
<p></p><p><b>Responsibilities may include the following and other duties may be assigned:
</b></p><ul><li>Drives an effective product planning &amp; submission process across region with proactive alignment with relevant stakeholders
</li><li>Leads to compile all materials required in submissions, license renewal and annual registrations
</li><li>Recommends changes for labelling, manufacturing, marketing for regulatory compliance
</li><li>Ensure audit readiness in organization and continue meeting our Quality KPIs
</li><li>Ensures effective monitoring, communication and collaboration on new &amp; changing regulations and required actions
</li><li>Executes a comprehensive Q/RA advocacy strategy and may direct interaction with regulatory agencies on defined matters. Active participation in related Trade Associations
</li><li>Recommends strategies for earliest possible approvals of product dossiers in specified regions and drive optimization and foster innovation in regulatory processes
</li><li>Foster and contribute to the culture of Engagement, Inclusion and Innovation as a people manager.
</li></ul><p></p><p><b>Required Knowledge and Experience:
</b></p><ul><li>Bachelor&rsquo;s degree or equivalent
</li><li>Minimum 5 years of experience in the regulatory affairs
</li><li>Strong leadership skills including proven minimum 1 year of people management
</li><li>Ability to influence to authorities and stakeholders &amp; strong presentation skills
</li><li>Strong communication skills
</li><li>Proven success stories in Regulatory Affairs &amp; Quality Assurance
</li><li>Medical device experience and knowledge in those countries are preferred
</li><li>Strong adoption skills and ability of multi-tasking
</li><li>Strong follow-up skills with being result-oriented
</li><li>Excellent fluency in English both written and verbal.
</li></ul><p></p><p><b>Physical Job Requirements
</b><br>
<br>
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
</p><p></p><h1 class="jobSectionHeader"><b>Benefits &amp; Compensation
</b></h1><p><b>Medtronic offers a competitive Salary and flexible Benefits Package
</b><br>
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.<br>
<br>
</p><p></p><h1 class="jobSectionHeader"><b>About Medtronic
</b></h1><p>We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
<br>
Our Mission &mdash; to alleviate pain, restore health, and extend life &mdash; unites a global team of 95,000+ passionate people.
<br>
We are engineers at heart&mdash; putting ambitious ideas to work to generate real solutions for real people. From the R&amp;D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.</p></div><p></p>

Regulatory Affairs Manager

Mondelēz International

<p></p><div><div><p>Job Description</p><p></p><p><b>
Are You Ready to Make It Happen at Mondel&#275;z International?</b></p><p></p><p><b>
Join our Mission to Lead the Future of Snacking. Make It With Pride.</b></p><p></p><p>
You execute the regulatory affairs strategy for your respective category or categories and geographical area using your technical and regulatory knowledge. You ensure our policies, regulatory programs and requirements of our portfolio carried out.</p><p></p><p><b>
How you will contribute</b></p><p></p><p>
You will deliver on the regulatory affairs strategy and compliance agenda and work with cross-functional stakeholders to assess regulatory business risks and opportunities. You will provide regulatory affairs expertise for technical regulatory developments and help in responses to challenges and crisis management. In this role, you will ensure that ingredients, product composition, claims and labelling compliance are within applicable regulations and company policies. In addition, you will provide guidance to stakeholders on developments in regulatory affairs, support regulatory impact assessments and change management, help develop regulatory affairs tools, and further develop your knowledge of regulatory, science and nutrition risks and opportunities in your market.</p><p></p><p><b>
What you will bring</b></p><p></p><p>
A desire to drive your future and purpose, accelerate your career and the following experience and knowledge:</p><ul><li><p>
Bachelor's Degree, preferably, in Food /Nutrition/Chemistry fields,</p></li><li><p>
Good organizational and communication skills,</p></li><li><p>
An open-minded attitude on problem solving and solution seeking,</p></li><li><p>
Experience in food regulatory field will be treated as an asset,</p></li><li><p>
Fluency in English &amp; Turkish,</p></li><li><p>
Networking and communication skills,</p></li><li><p>
Reliability and accuracy and an efficient work style,</p></li><li><p>
Meeting deadlines,</p></li><li><p>
Attending to detail,</p></li><li><p>
Project management,</p></li><li><p>
Regulatory affairs in an international and multi-functional environment.</p></li></ul><p><b>
More about this role</b></p><p></p><p><b>
What you need to know about this position:</b></p><p></p><p><b>
What extra ingredients you will bring:</b></p><p></p><p><b>
Education / Certifications:</b></p><p></p><p><b>
Job specific requirements:</b></p><p></p><p><b>
Travel requirements:</b></p><p></p><p><b>
Work schedule:</b></p><p></p><p>
Relocation Support Available?
</p><p></p>No Relocation support available<p></p><p>
Business Unit Summary</p><p></p><div>
We value our talented employees, and whenever possible strive to help one of our associates grow professionally before recruiting new talent to our open positions. If you think the open position you see is right for you, we encourage you to apply!</div><div></div><div><i>
Our people make all the difference in our succes</i></div><p></p><p>
Mondel&#275;z International is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law.</p><p></p><p>
Excited to grow your career?</p><p></p><p>
We value our talented employees, and whenever possible strive to help one of our associates grow professionally before recruiting new talent to our open positions. If you think the open position you see is right for you, we encourage you to apply!</p><p></p><p>
IF YOU REQUIRE SUPPORT TO COMPLETE YOUR APPLICATION OR DURING THE INTERVIEW PROCESS, PLEASE CONTACT THE RECRUITER</p><p></p><p>
Job Type</p><p></p>
Regular<p></p>
Scientific Affairs &amp; Regulatory Affairs<p></p>
Product Quality, Safety and Compliance</div></div><p></p>

Regulatory Affairs Scientist I

Mars

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

Scientific & Regulatory Affairs

Perrigo

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

Regulatory Affairs, Associate Specialist

Viatris

<div>Viatris &#304;la&ccedil;lar&#305; Ltd. &#350;ti<div></div><div>
At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.<br>
<br>
Viatris empowers people worldwide to live healthier at every stage of life.<br>
<br>
We do so via:<br>
<br>
Access &ndash; Providing high quality trusted medicines regardless of geography or circumstance;<br>
Leadership &ndash; Advancing sustainable operations and innovative solutions to improve patient health; and<br>
Partnership &ndash; Leveraging our collective expertise to connect people to products and services.</div><div><br>
Every day, we rise to the challenge to make a difference, and here&rsquo;s how the Regulatory Affairs Portfolio Executive role will make an impact:</div><div></div><div>
The objective of this job is to contribute to the strategic business decisions regarding the licensing of a product in Turkey, within the framework of the the local laws, regulations, guidance and company procedures/policies.</div><div></div><div>
To make the applications regarding the licensing processes for new products and regarding the maintaining/improving of the current license status for existing licensed products, in the area of responsibility in accordance with the licensing legislation and company procedures, to follow-up the processes, and to fulfil the approval requirements. Carrying out the works defined as &quot;Key Responsibilities&quot; below, along with all transactions related to compliance with legislation of regulatory.</div><div></div><div>
To be responsible for the coordination of preparation/updating of SOPs, reports, presentations, launch tables, budgets and databases and for monitoring the regulations, and to provide support to the department head on strategic issues.</div><div></div><div>
Key responsibilities for this role include:</div><ul><li><div>
To contribute to the strategic business decisions regarding the licensing of a product in Turkey.</div></li><li><div>
To carry out all relevant activities in the matters related to prioritization, GMP and registration in accordance with the launch plan for new products</div></li><li><div>
To carry out the organization of GMP audits, to accompany the audits, and then to ensure the acquisition of the GMP certificate by ensuring that all the associated requirements are met.</div></li><li><div>
License and GMP renewal for currently licensed/approved products, Type I and II variations, artwork change applications, SmPC-PIL update applications, sales permission applications, and the meeting of official authorities&rsquo; requests; to provide, review and control the dossier and documents, determine and provide the deficiencies, follow-up the internal approvals if available, prepare the application letters and files, make the applications in accordance with local regulation/guidance/announcements, follow-up the process and ensure the approvals.</div></li><li><div>
To take actions to prevent the regulatory related stock-out risk for the registered products in the market.</div></li><li><div>
To fulfill the registration/approval process requirements for all portfolio.</div></li><li><div>
To follow the legislations, to implement the updates in business and transactions, to determine the impacts of the updates for the products and to take the necessary actions, if any to file/to ensure to be filed.</div></li><li><div>
To ensure the required information within the scope of legislation and provide technical and operational support in the matters relating to production and quality if needed.</div></li><li><div>
Artwork responsibility</div></li></ul><div></div><div>
The minimum qualifications for this role are:</div><ul><li><div>
Bachelor&rsquo;s degree related field.</div></li><li><div>
More than 5 years of industry experience</div></li><li><div>
Advanced Turkish and English in writing and speaking.</div></li><li><div>
Male candidates must have completed their military service.</div></li><li><div>
Ability to use Microsoft Office programs effectively.</div></li></ul><div></div><div>
At Viatris, we offer competitive salaries, benefits, and an inclusive environment where you can use your experiences, perspectives, and skills to help make an impact on the lives of others.</div><div></div><div>
At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others.</div><div></div><div>
Viatris is an Equal Opportunity Employer.</div></div><div></div>

Regulatory Affairs Portfolio Executive

Daiichi Sankyo

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

TR-Market Access Lead

Freedom Finance MENAT

<div>
 <p>
  We are seeking a highly experienced and strategic
  <strong>
   Head of Legal
  </strong>
  to lead our company&rsquo;s legal department in T&uuml;rkiye. The successful candidate will oversee all legal corporate affairs, ensuring compliance with laws and regulations while providing expert legal advice to senior leadership. This role involves managing legal risks, drafting and negotiating key agreements, and supporting business initiatives through sound legal counsel. The Head of Legal will also build strong collaborative relationships across departments and ensure adherence to regulatory requirements such as those set by the Capital Markets Board (CMB).
 </p>
 <p>
  <br/>
 </p>
 <p>
  Responsibilities:
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Lead all legal corporate affairs within the organization, setting strategic direction for legal activities and ensuring effective execution.
  </li>
  <li>
   Oversee and implement key legal processes, including legal drafting, negotiations, and commercial settlement agreements.
  </li>
  <li>
   Manage legal risk across the business, providing expert legal advice and proactive solutions to senior leadership on all matters of law.
  </li>
  <li>
   Identify complex legal issues internally and work towards resolution without routinely engaging external legal services.
  </li>
  <li>
   Ensure reliable and timely execution of the company&rsquo;s daily legal operations, safeguarding organizational interests.
  </li>
  <li>
   Build and sustain collaborative relationships with heads of other departments to align legal strategies and facilitate cross-functional teamwork.
  </li>
  <li>
   Ensure full compliance with regulations set by the Capital Markets Board (CMB) and other relevant regulatory bodies.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  Requirements:
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Outstanding skills in legal negotiation, consistently achieving positive outcomes in complex scenarios.
  </li>
  <li>
   Strongly result-oriented and service-driven, with proven problem-solving abilities and the flexibility to adapt in a fast-paced, dynamic environment.
  </li>
  <li>
   Demonstrated ability to influence cross-functional teams and senior leadership, driving alignment towards unified business objectives.
  </li>
  <li>
   Exceptional communication and interpersonal skills, capable of building credibility with internal stakeholders and external parties.
  </li>
  <li>
   Bachelor&rsquo;s degree in Law (LLB) required; advanced degree or legal certifications a plus.
  </li>
  <li>
   Minimum 10 years&rsquo; experience in corporate legal practice, including significant experience in leading legal teams.
  </li>
  <li>
   In-depth knowledge of corporate law, capital markets regulations, and risk management.
  </li>
 </ul>
 <p>
 </p>
</div>


Head of Legal

Explore 367+ Regulatory affairs manager in Istanbul this September. Find roles across top companies and apply now to boost your career.