marketing manager

account manager

assistant legal manager

legal & compliance manager Jobs in Istanbul

legal & compliance manager

hr manager

regulatory affairs manager

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)

<div>Site Name: Turkey - Istanbul 
Posted Date: Nov 4 2025 
At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&amp;D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people&rsquo;s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients&rsquo; needs and have the highest probability of success. We&rsquo;re uniting science, technology, and talent to get out of disease together. Find out more:
Our approach to R&amp;D
Regulatory Lead 
Are you ready to make a meaningful impact in regulatory affairs while advancing your career? In this role, you will play a key part in ensuring compliance with health authority regulations and supporting the delivery of regulatory submissions. You&rsquo;ll collaborate with cross-functional teams, contribute to process improvements, and help maintain the lifecycle of products. We value candidates who are detail-oriented, proactive, and passionate about driving results. Join us to grow your skills, work on impactful projects, and help us achieve our mission of uniting science, technology, and talent to get ahead of disease together.
Responsibilites:
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:<div><ul><li> 
Develop and implement regulatory strategies to ensure timely submissions and approvals.</li></ul></div><ul><li> 
Preparation and completion of regulatory submissions and approvals of NCEs (new chemical entities) within the defined timelines</li><li>Execution of maintenance activities of the registered products including post-approval submissions (renewals, technical variations, new indication, label updates) and conduct effective cross-functional interactions to preserve business continuity</li><li>Execution and follow up regulatory processes for both locally manufactured and imported products.</li><li>Follow up CMC activities of locally manufactured products in collaboration with External Supply &amp; Quality teams</li><li>Follow up on the MoH correspondences.</li><li>Participation to brand teams and giving input for regulatory activities and action plans.</li><li>Execution of GMP related tasks including inspection submissions which require close follow up with internal and external stakeholders</li><li>Monitor changes in local and global regulations and assess their impact on product registrations.</li><li>Collaborate with cross-functional teams to ensure alignment and execution of regulatory plans.</li><li>Build and maintain strong relationships with health authorities and external stakeholders.</li><li>Identify risks and propose solutions to ensure business continuity and compliance.</li></ul>
Why you?
Basic Qualifications
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:<div><ul><li> 
Bachelor&rsquo;s degree in pharmacy, chemistry, or a related scientific field.</li><li>Minimum of 5 years of experience in regulatory affairs within the pharmaceutical industry.</li><li>Strong knowledge of local regulatory requirements and processes.</li><li>Proficiency in English (written and verbal).</li></ul></div><ul><li>Good knowledge of MS Office tools</li><li>Excellent organizational skills and attention to detail.</li><li>Ability to work collaboratively in a team environment and adapt to dynamic situations.</li></ul>
Preferred Qualifications
If you have the following characteristics, it would be a plus:<div><ul><li> 
Master&rsquo;s degree in regulatory affairs, pharmacy, or a related field.</li><li>Experience working in a matrixed, international environment.</li><li>Familiarity with regulatory systems and tools, such as Veeva Vault or similar platforms.</li><li>Knowledge of global regulatory requirements, including EU and US markets.</li><li>Strong interpersonal skills and ability to engage with senior stakeholders effectively.</li><li>Demonstrated ability to identify process improvement opportunities and implement solutions.</li></ul></div>
This role is hybrid, requiring two days per week in the office. 
 
If you&rsquo;re ready to take the next step in your career and contribute to impactful work, we encourage you to apply today!
GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.
Why GSK? 
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases &ndash; to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we&rsquo;re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
Contact information: 
You may apply for this position online by selecting the Apply now button.
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</div>

Regulatory Lead

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

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>

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>

Danone

<div>About the job

We are seeking a highly motivated and experienced Legal &amp; Compliance Manager to join our dynamic team. This role is pivotal in ensuring legal integrity and regulatory compliance across multiple business units and categories, including Dairy, Plant-Based, SN, EDP, Export, and E-Commerce. Plus, the position offers a unique opportunity to work transversally across functions such as HR, Finance, IT/Data, Marketing, and Operations, while also contributing to global reporting and governance initiatives. 


Key Responsibilities:
<ul>
<li>Provide legal guidance on competition law, sanctions, integrity, and personal data privacy (DPO scope).</li>
<li>Support compliance programs including ethics line, policy implementation, risk mapping, and internal/external audits.</li>
<li>Contribute to legal and compliance excellence and operations, including training and internal control compliance.</li>
</ul>About you
<ul><li>Law degree with strong academic credentials; additional certifications/education in economics, finance, compliance, competition or data privacy are a plus.</li>
<li>Min. 5 years of legal and/or compliance experience, preferably in FMCG, retailer or multinational environments. Proven expertise in Turkish commercial law, regulatory frameworks, and compliance operations.</li>
<li>Strong communication skills in Turkish and English.</li>
<li>High ethical standards, strategic thinking, and ability to work in a matrix organization.</li>
</ul>About us

We are proud to promote diversity and equal opportunity within our teams. We believe that our differences will make a difference, and that an inclusive work environment will drive our growth as a company, as a team, and as individuals. We will therefore consider all implementations* by fostering an inclusive work culture where everyone can feel at home.

All nominations will be considered regardless of origin, background, religion, sex, sexual orientation, age, gender identity, disability.

Working with us is about being able to do things your way. The way you work, the way you develop, the way you progress, it&rsquo;s all up to you. 
Working here, you&rsquo;ll need to enjoy a fast-paced environment, a little complexity and challenging tasks but it is packed with opportunities. You will work for some of the best-known brands in the world, such as Activia, Danone, Danino, Danette, Aptamil, Bebelac, Hayat, and S&#305;rma, and we absolutely guarantee that you can just be yourself. 

Be innovative and entrepreneurial and the impact you could make might just amaze you. Join our movement for a healthier world. One Planet One Health BY YOU.

At Danone T&uuml;rkiye, inspired by our B Corp journey, we continuously challenge ourselves to improve and measure our social and environmental impact.

This journey inspires us to constantly challenge ourselves, measure what truly matters, and create long-term value &mdash; not just for our business, but for our people, partners, communities, and future generations. 
If you&rsquo;re looking to grow your career with purpose, you&rsquo;re in the right place. 


What we offer

This is a visible position within the company, we offer opportunities where you can grow your expertise and have an end-to-end responsibility to drive &quot;change&quot; &amp; &quot;growth&rdquo;. You will have a chance to experience 360 ways of working with multiple stakeholders. We develop talents and growth potential to enable strong career development for our employees. 


At Danone T&uuml;rkiye, we do not aim to be the best company in the world, but better for the world. 
That&rsquo;s why, inspired by our B Corp journey, we continuously challenge ourselves to improve and measure our social and environmental impact. 
Through this journey, we strive to create long-term value for our employees, partners, communities, and future generations. 


What&rsquo;s next?

Visit our website www.danone.com to discover more about us and to find out how you could be part of it all!

#LI-TU</div>

Legal & Compliance Manager

Dinkal Sigorta

<div>
 
 Dinkal, a subsidiary of Akk&ouml;k Holding, offers comprehensive services across all insurance segments&mdash;including fire, health, accident (including aviation), transportation (including marine), and engineering insurance.
 
 
 With its strong market position, broad coverage options, competitive pricing, and expert consultancy services, Dinkal has earned a well-respected place in the Turkish insurance sector.
 
 
 
 
 
 We are looking for a Financial Affairs Manager to lead our financial strategy and operations.
 
 
 
 
 
 
 Responsibilities:
 
 
 <ul>
 <li>
 Oversee the preparation of financial statements, including balance sheets, P&amp;L, and income statements
 </li>
 <li>
 Lead the preparation and review of IFRS reports
 </li>
 <li>
 Manage statutory books and conduct regular trial balance checks in line with legal standards
 </li>
 <li>
 Prepare annual financial budgets in line with both VUK and IFRS
 </li>
 <li>
 Supervise tax declarations and social security filings in compliance with regulations
 </li>
 <li>
 Keep up with regulatory changes and ensure team alignment
 </li>
 <li>
 Coordinate administrative and legal operations
 </li>
 <li>
 Oversee the fixed asset management, including depreciation and revaluation
 </li>
 <li>
 Handle special insurance processes related to company assets and personnel
 </li>
 <li>
 Monitor bank transactions in collaboration with relevant departments
 </li>
 <li>
 Lead and support the finance team with performance tracking and development
 </li>
 <li>
 Develop and maintain strategic relationships with group companies,
 </li>
 <li>
 Establish effective communication with internal departments to ensure coordination across business processes.
 </li>
 </ul>
 
 
 
 
 
 Qualifications:
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in Economics, Business Administration, Finance or a related field,
 </li>
 <li>
 Minimum 10 years of professional experience in finance.
 </li>
 <li>
 Experience in the insurance sector is a must.
 </li>
 <li>
 Strong command of English, both written and verbal
 </li>
 <li>
 Solid knowledge of TMS, IFRS, Taxation, Insurance, Brokerage, and Social Security regulations, with the ability to follow regulatory updates
 </li>
 <li>
 Proficiency in industry-specific software &mdash; experience with Benta&scedil; Elwin and Ada is a strong plus
 </li>
 <li>
 Strong analytical mindset, effective communicator, and team leader
 </li>
 </ul>
 
 
</div>

Financial Affairs Manager

Explore 604+ Regulatory affairs manager in Istanbul this November. Find roles across top companies and apply now to boost your career.

604 regulatory affairs manager jobs IN Istanbul

Regulatory Affairs Associate - (Fixed Term Maternity Cover)

Regulatory Lead

Regulatory Affairs, Associate Specialist

Regulatory Affairs Specialist

Regulatory Affairs Specialist

Legal & Compliance Manager

Financial Affairs Manager