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regulatory affairs specialist

<div><h1 class="jobSectionHeader">Job Description Summary</h1>
An exciting opportunity for a Regulatory Affairs Specialist, the role will be based in Istanbul, Turkey.<h1 class="jobSectionHeader">
Job Description</h1>
We are the makers of possible
BD is one of the largest global medical technology companies in the world. Advancing the world of health&trade; is our Purpose, and it&rsquo;s no small feat. It takes the imagination and passion of all of us&mdash;from design and engineering to the manufacturing and marketing of our billions of MedTech products per year&mdash;to look at the impossible and find transformative solutions that turn dreams into possibilities.
Why Join Us?
A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you&rsquo;ll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place.
Become a maker of possible with us!
About the role
The Regulatory Specialist is responsible for supporting and driving regulatory activities across multiple projects and product lines. You will be responsible for launching of Medical Device &amp; In-Vitro Diagnostic products in the Turkish market in addition to ensuring the absence of any regulatory issue in alignment with company standards and country regulations. This role ensures compliance with industry standards and regulatory requirements by reviewing and approving advertising and promotional materials, leading regulatory and product-related documentation, along with providing local regulatory support.<h2 class="jobSectionHeader">
Main responsibilities will include :-</h2><ul><li>
Responsible for all regulatory activities including but not limited to pre-registration, registration and re-registration steps in accordance with local regulations and business strategies.</li><li>
Develop and maintain communication system with local stakeholders and regional partners</li><li>
Updating regulatory knowledge due to procedures and changes in local directives.</li><li>
Ensuring all products meet regulatory requirements by supporting all assigned regulatory aspects of product approval and post market compliance.</li><li>
Scheduling and prioritizing projects and planning submissions with the corresponding partners.</li><li>
Perform and manage Ad Prom local activities</li><li>
Maintain the reimbursement prosses of Social Security Institute (SSI) on determined periods, collaboratively work with local teams, follow up on the approvals and inform business teams.</li><li>
Keep the local business communication alive regarding registrations and reimbursement updates</li><li>
Participating in relevant organizations representing the company.</li></ul>
About You :-<ul><li>
Bachelor&rsquo;s degree in science, engineering or equivalent.</li><li>
Proficiency in Microsoft Office programs (Word, Excel, PowerPoint)</li><li>
Good command of English both written and verbally</li><li>
Self-motivated and self-confident</li><li>
Effective communicator with strong organizational and problem-solving skills</li><li>
Detail oriented and ability to work independently</li><li>
Medical Device registration employee certification is a nice to have.</li></ul><h2 class="jobSectionHeader">
Click on apply if this sounds like you!</h2>
At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.
Becton, Dickinson and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics.<h2 class="jobSectionHeader">
To learn more about BD visit: https://bd.com/careers</h2>
Required Skills
Optional Skills
.<h1 class="jobSectionHeader">
Primary Work Location</h1>
TUR Istanbul - R&uuml;zgarl&#305;bah&ccedil;e Mah<h1 class="jobSectionHeader">
Additional Locations</h1><h1 class="jobSectionHeader">
Work Shift</h1></div>

Regulatory Affairs Specialist

Kraft Heinz

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

Perrigo

<div>At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. 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 The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill&reg;, Compeed&reg;, Solpadeine&reg;, NiQuitin&reg;, ACO&reg;, and many more. We Are Perrigo. 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. 
Join us on our One Perrigo journey as we evolve to win in self-care.<div><div><div><h2 class="jobSectionHeader"> 
Description Overview</h2></div><div>
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.</div></div><div><div><h2 class="jobSectionHeader">
Scope of the Role</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">
Experience Required</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>
Benefits 
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.
Find out more about Total Rewards at Perrigo. 
Hybrid Working Approach 
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. 
We are proud to be included in the Forbes list of &quot;America's Best Employers by State 2024&quot;. Find out more here 
Applicants please note: 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. 
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</div>

Regulatory Affairs, Associate Specialist

BioMarin Pharmaceutical Inc.

<div>
 Who We Are
 
 
 BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health.
 
 
 Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities.
 
 
 Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best &ndash; people with the right technical expertise and a relentless drive to solve real problems &ndash; and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we&rsquo;ve produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options.
 
 
 
 About Worldwide Research And Development
 
 
 
 From research and discovery to post-market clinical development, our WWRD engine involves all bench and clinical research and the associated groups that support those endeavors. Our teams work on developing first-in-class and best-in-class therapeutics that provide meaningful advances to patients who live with genetic diseases.
 
 
 Regulatory Affairs Associate - Turkey
 
 
 <ul>
 <li>
 Fixed Term Temporary position for up to 7 months (Maternity Leave Cover)
 </li>
 <li>
 Bachelors degree in Pharmacy, Chemical Engineering, Chemistry.
 </li>
 <li>
 Minimum 1 years of Regulatory Affairs experience in a pharmaceutical company,
 </li>
 <li>
 Excellent command of English (both written and spoken),
 </li>
 <li>
 Strong commitment to compatibility, scientific quality and integrity
 </li>
 <li>
 Analytical thinking
 </li>
 <li>
 Good communication and teamwork collaboration
 </li>
 <li>
 Good detail-capturing skills while working in a fast-moving environment
 </li>
 <li>
 Role is based in Turkey
 
 
 </li>
 </ul>
 
 Job Description
 
 
 
 <ul>
 <li>
 Submission of Health Authority applications for registered and non-registered products and follow approval process. (GMP applications, new Marketing Authorization (MA) application, renewal submissions, lifecycle activities etc.)
 </li>
 <li>
 Compile all required documents received from Global Headquarters and prepare submission dossiers according to local requirements and make timely applications.
 </li>
 <li>
 Conduct the correspondences for all registered/non-registered products and follow up the Health Authority processes.
 </li>
 <li>
 Assist in managing global/local projects.
 </li>
 <li>
 Ensure the databases are updated on a timely basis.
 </li>
 <li>
 Evaluate local regulations/guidance for impact to any complex submission (e.g., MA, GMP) while ensuring that elements, quality, accuracy and format of regulatory submissions comply with applicable laws and regulatory standards.
 
 
 </li>
 </ul>
 Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.
 
 
 Equal Opportunity Employer/Veterans/Disabled
 
 
 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, or protected veteran status and will not be discriminated against on the basis of disability.
</div>

Regulatory Affairs Associate - (Fixed Term Maternity Cover)

Calik Holding

<div>
 
 
 Qualifications
 
 
 <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>
 
 
 
 
 
 Key Responsibilities
 
 
 <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>
 
 
</div>

Compliance Lawyer

Türkiye Ödeme ve Elektronik Para Kuruluşları Birliği

<div>
 
 
 &nbsp;Genel Nitelikler
 
 :
 
 
 &middot; &Ouml;deme ve elektronik para veya bankac&inodot;l&inodot;k sekt&ouml;r&uuml;nde en az 3 y&inodot;l deneyimli olmak,
 
 
 &middot; Hukuk fak&uuml;ltesi mezunu olmak (Lisans),
 
 
 .
 
 Bankac&inodot;l&inodot;k veya &ouml;deme ve elektronik para mevzuat&inodot;na h&acirc;kim olmak,
 
 
 
 .
 
 Resmi yaz&inodot;&scedil;ma ve mevzuat diline hakim olmak,
 
 
 
 &middot; Erkek adaylar i&ccedil;in askerlik hizmetini tamamlam&inodot;&scedil; ya da en az 2 y&inodot;l tecilli olmak,
 
 
 &middot; Yaz&inodot;l&inodot; ve s&ouml;zl&uuml; ileti&scedil;im becerileri g&uuml;&ccedil;l&uuml; olmak,
 
 
 &middot; Tak&inodot;m &ccedil;al&inodot;&scedil;mas&inodot;na yatk&inodot;n, sorumluluk sahibi olmak,
 
 
 &middot; MS Office programlar&inodot;n&inodot; etkin kullanabilmek,
 
 
 &middot; Tercihen &Idot;ngilizce bilmek.
 
 
 
 
 
 
 &Idot;&scedil; Tan&inodot;m&inodot;:
 
 
 
 &middot;Birlik ad&inodot;na yap&inodot;lacak resmi yaz&inodot;&scedil;malar&inodot;n haz&inodot;rlanmas&inodot;, kontrol edilmesi ve yaz&inodot;&scedil;ma s&uuml;re&ccedil;lerinin takibinin sa&gbreve;lanmas&inodot;,
 
 
 &middot;Mevzuat de&gbreve;i&scedil;iklikleri ve sekt&ouml;rel geli&scedil;melere ili&scedil;kin d&uuml;zenli mevzuat takibi yap&inodot;lmas&inodot;, &ouml;zetlenmesi ve Birlik y&ouml;netimine/&uuml;yelere raporlanmas&inodot;,
 
 
 &middot;Birlik g&ouml;r&uuml;&scedil;&uuml; olu&scedil;turulurken Birlik &uuml;yelerinden gelen geri bildirimlerin sistemli &scedil;ekilde toplanmas&inodot;, analiz edilmesi ve kar&scedil;&inodot;la&scedil;t&inodot;rmal&inodot; de&gbreve;erlendirme yap&inodot;lmas&inodot;
 
 
 &middot;Kamu kurumlar&inodot; (TCMB, MASAK, BDDK, G&Idot;B vb.) ile y&uuml;r&uuml;t&uuml;len mevzuat isti&scedil;are, g&ouml;r&uuml;&scedil; ve de&gbreve;erlendirme s&uuml;re&ccedil;lerinin koordinasyonu ve g&ouml;r&uuml;&scedil; dok&uuml;manlar&inodot;n&inodot;n haz&inodot;rlanmas&inodot;na katk&inodot; verilmesi,
 
 
 &middot;Sekt&ouml;re ve uygulamalara ili&scedil;kin konularda bilgi notlar&inodot; haz&inodot;rlanmas&inodot; s&uuml;re&ccedil;lerine katk&inodot; verilmesi,
 
 
 &middot;Y&uuml;r&uuml;t&uuml;len t&uuml;m mevzuat ve koordinasyon &ccedil;al&inodot;&scedil;malar&inodot;n&inodot;n d&ouml;nemsellik esas&inodot;na g&ouml;re raporlanmas&inodot;, &ccedil;&inodot;kt&inodot;lar&inodot;n sistematik olarak ar&scedil;ivlenmesi,
 
 
 &middot;Birlik b&uuml;nyesinde haz&inodot;rlanacak meslek&icirc; tanzim kararlar&inodot;, rehberler, y&ouml;nergeler ve di&gbreve;er i&ccedil; d&uuml;zenlemelerin olu&scedil;turulmas&inodot;, g&uuml;ncellenmesi ve uygulanmas&inodot;na y&ouml;nelik s&uuml;re&ccedil;lere aktif katk&inodot; sa&gbreve;lanmas&inodot;,
 
 
 &middot;Komite ve &ccedil;al&inodot;&scedil;ma gruplar&inodot;na ili&scedil;kin t&uuml;m s&uuml;re&ccedil;lerin y&uuml;r&uuml;t&uuml;lmesi, kontrol&uuml;, takibi, raporlanmas&inodot;n&inodot;n yap&inodot;lmas&inodot; ve s&uuml;re&ccedil;lerin etkin ve verimli y&uuml;r&uuml;t&uuml;lmesine y&ouml;nelik gerekli aksiyonlar&inodot;n al&inodot;nmas&inodot;n&inodot;n sa&gbreve;lanmas&inodot;,
 
 
 &middot;Birli&gbreve;e iletilen g&uuml;ndemlerin, g&ouml;r&uuml;&scedil; taleplerinin, &ouml;nerilerin de&gbreve;erlendirilmesi, ilgili komite veya &ccedil;al&inodot;&scedil;ma grubu g&uuml;ndemine al&inodot;nmas&inodot;na y&ouml;nelik s&uuml;re&ccedil;lerin tamamlanmas&inodot;n&inodot;n sa&gbreve;lanmas&inodot;,
 
 
 &middot;Komite ve &ccedil;al&inodot;&scedil;ma grubu toplant&inodot;lar&inodot; ile di&gbreve;er toplant&inodot;lara kat&inodot;l&inodot;m sa&gbreve;lanmas&inodot; ve Birli&gbreve;e y&ouml;nelik konularda bilgi ve g&ouml;r&uuml;&scedil; verilmesi,
 
 
 &middot;Toplant&inodot; tutana&gbreve;&inodot;nda al&inodot;nan kararlar&inodot;n kayda al&inodot;nmas&inodot; ve takibinin yap&inodot;lmas&inodot;,
 
 
 &middot;Toplant&inodot; g&uuml;ndemine ili&scedil;kin i&ccedil;erik, sunum veya dok&uuml;mantasyonun haz&inodot;rlanmas&inodot; veya haz&inodot;rlanmas&inodot;n&inodot;n takibi,
 
 
 &middot;Genel Sekreter ve Genel Sekreter Yard&inodot;mc&inodot;s&inodot; taraf&inodot;ndan verilen yaz&inodot; i&scedil;lerinin ve ara&scedil;t&inodot;rmalar&inodot;n yap&inodot;lmas&inodot;,
 
 
 
 
 
 &middot;T&uuml;m bu i&scedil; ve i&scedil;lemlere ili&scedil;kin Genel Sekretere ve Genel Sekreter Yard&inodot;mc&inodot;s&inodot;na gerekli bilgilendirme ve raporlamalar&inodot;n yap&inodot;lmas&inodot;,
 
 
 
 
 
 &middot;Y&ouml;netim Kurulu Ba&scedil;kan&inodot;, Y&ouml;netim Kurulu, Genel Sekreter ve Genel Sekreter Yard&inodot;mc&inodot;s&inodot; taraf&inodot;ndan verilen di&gbreve;er g&ouml;revlerin yerine getirilmesi
 
</div>

Mevzuat Koordinatörü

Freedom Finance MENAT

<div>
 
 We are seeking a highly experienced and strategic
 
 Head of Legal
 
 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).
 
 
 
 
 
 Responsibilities:
 
 
 
 
 <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>
 
 
 
 
 Requirements:
 
 
 
 
 <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>
 
 
</div>

Head of Legal

Explore 322+ Regulatory affairs specialist in Istanbul this November. Find roles across top companies and apply now to boost your career.

322 regulatory affairs specialist jobs IN Istanbul

Regulatory Affairs Specialist

Regulatory Affairs Specialist

Regulatory Affairs, Associate Specialist

Regulatory Affairs Associate - (Fixed Term Maternity Cover)

Compliance Lawyer

Mevzuat Koordinatörü

Head of Legal