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Manpower Türkiye

<div>
 
 We are seeking a
 
 Regulatory Affairs and Commercial Operations Specialist
 
 for our client in the cosmetics and personal care industry. This role focuses on managing product registration, licensing, and compliance processes, ensuring all products meet legal and industry standards. The ideal candidate has strong experience in regulatory affairs, excellent coordination with official authorities, and the ability to integrate regulatory activities with commercial operations.
 
 
 
 
 
 
 Responsibilities
 
 
 <ul>
 <li>
 Manage licensing processes related to the Ministry of Health and the Turkish Medicines and Medical Devices Agency (T&Idot;TCK), including production, import, and product registration licenses.
 </li>
 <li>
 Prepare, collect, and archive all necessary documentation for license applications and renewals.
 </li>
 <li>
 Ensure that supply and import processes comply with the regulations of relevant health authorities.
 </li>
 <li>
 Conduct correspondence and maintain communication with domestic and international regulatory bodies.
 </li>
 <li>
 Prepare and submit reports requested by health authorities in a timely manner.
 </li>
 <li>
 Manage procurement processes with domestic and international suppliers for raw materials and packaging components, ensuring favorable pricing and delivery conditions.
 </li>
 <li>
 Coordinate logistics and transportation activities related to imports.
 </li>
 <li>
 Monitor raw material inventory and collaborate with warehouse teams to prevent overstock or shortages.
 </li>
 <li>
 Handle and follow up on all customs procedures for imported raw materials and packaging components.
 </li>
 <li>
 Prepare and review customs documentation, including invoices, packing lists, and permits.
 </li>
 <li>
 Collaborate with shipping agents and customs brokers to ensure smooth operations.
 </li>
 <li>
 Stay up to date with customs regulations and ensure accurate implementation.
 </li>
 </ul>
 
 
 
 
 
 Qualifications
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in Pharmacy, Chemistry, Biology, Food Engineering, Business Administration, or a related field.
 </li>
 <li>
 Experience in regulatory affairs or commercial operations within the pharmaceutical, cosmetics, or personal care industry.
 </li>
 <li>
 Strong knowledge of requirements and procedures of health authorities, particularly T&Idot;TCK.
 </li>
 <li>
 Proven experience in international procurement, customs, and import operations.
 </li>
 <li>
 Proficiency in MS Office applications, especially Excel and Word.
 </li>
 <li>
 Fluency in both written and spoken Turkish and English.
 </li>
 <li>
 Detail-oriented, well-organized, and a strong team player.
 </li>
 </ul>
 
 
</div>

Regulatory Affairs Specialist

Bayer

<div>
 
 
 Bayer is a life science company and a global leader in health care and nutrition.
 
 
 
 
 
 
 Our innovative products support efforts to overcome the major challenges presented by a growing and aging global population.
 
 
 
 
 
 We carry out all our work in line with our mission
 
 &ldquo;Health for All, Hunger for None&rdquo;
 
 and we offer innovative solutions in the fields of
 
 health and agriculture
 
 .&rdquo;
 
 
 
 
 
 
 YOUR TASKS AND RESPONSIBILITIES
 
 
 
 
 
 
 
 
 
 While our strong preference is for candidates based in Istanbul, we are also open to those located in Ankara.
 
 
 
 
 
 
 
 <ul>
 <li>
 Support the preparation, submission, tracking and archiving of regulatory applications accordingly to the agreed project plans under the supervision of Regulatory team by organizing the required documentation and ensuring legal compliance. Assist in keeping track of and maintaining the existing registrations.
 </li>
 <li>
 Help ensure the completeness and accuracy of the information at relevant portfolio databases in a timely manner.
 </li>
 <li>
 Contribute to regulatory compliance throughout the life cycle of Bayer&rsquo;s products by assisting in stewardship activities as needed
 </li>
 <li>
 Assist in preparing authorized label text for the products
 </li>
 <li>
 Provide support in monitoring and replying to regulatory questions concerning the registration application during the (re)evaluation processes and after approval of the products in order to meet the conditions for prolonging and maintaining the registration of Turkey portfolio.
 </li>
 </ul>
 
 
 
 
 
 WHO YOU ARE
 
 
 
 
 
 <ul>
 <li>
 BS or MS in science or engineering (biology, chemistry, agronomy or related subjects)
 </li>
 <li>
 Basic understanding of relevant regulations and requirements for submission process of registration applications and other regulatory dossiers.
 </li>
 <li>
 General awareness and understanding in agronomic industry business and competitive landscape.
 </li>
 <li>
 Willingness to learn and take initiative with the ability to follow guidance and complete assigned tasks.
 </li>
 <li>
 Well-organized, able to work to deadlines
 </li>
 <li>
 Eye for detail and for the big picture
 </li>
 <li>
 Very Good English language (speaking, reading and writing)
 </li>
 <li>
 Strong IT (data management) skills
 </li>
 <li>
 Eagerness to build professional relationships with internal teams and external stakeholders
 </li>
 </ul>
 
 
 
 
 
 WHAT WE OFFER
 
 
 
 
 
 <ul>
 <li>
 Fair and respectful workplace
 </li>
 <li>
 Speak up culture
 </li>
 <li>
 Global &amp; collaborative work environment
 </li>
 <li>
 Diverse, equal &amp; inclusive culture
 </li>
 <li>
 Competitive and fair pay
 </li>
 <li>
 Attractive and meaningful benefit programs
 </li>
 <li>
 Promotion of individual health and well-being
 </li>
 <li>
 Promotion of work-life balance
 </li>
 <li>
 Hybrid working &amp; flexible working for relevant positions
 </li>
 <li>
 Local and global career opportunities
 </li>
 <li>
 Learning &amp; Development Opportunities for both personal and professional growth
 </li>
 </ul>
 
 
 
 
 
 
 
 
 
 
 
 Bayer T&uuml;rk Kimya Sanayi Ltd &Scedil;ti 'ye yapaca&gbreve;&inodot;n&inodot;z ba&scedil;vurular arac&inodot;l&inodot;&gbreve;&inodot; ile toplanacak ki&scedil;isel verileriniz, veri sorumlusu Bayer T&uuml;rk Kimya Sanayi Ltd &Scedil;ti. taraf&inodot;ndan 6698 say&inodot;l&inodot; Ki&scedil;isel Verilerin Korunmas&inodot; Kanunu (KVKK) ile ilgili mevzuat kapsam&inodot;nda i&scedil; ba&scedil;vuru s&uuml;re&ccedil;lerinin y&uuml;r&uuml;t&uuml;lmesi amac&inodot;yla i&scedil;lenecektir. Ayd&inodot;nlatma metnimize
 
 https://www.bayer.com.tr/tr/gizlilik-politikasi
 
 linkinden ula&scedil;abilirsiniz.
 
 
</div>

Regulatory Science Specialist-Crop Science (Project-based)

IQVIA

<div><ul><li>Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites,</li><li>
Ensure adherence to Standard Operation Procedures (SOPs), work instructions (WIs), quality of designated deliverables and project timelines.</li><li>
Perform Regulatory Start-up and Maintenance activities according to applicable regulations, SOPs and WIs.</li><li>
Distribute completed documents to sites and internal project team members.</li><li>
Prepare site regulatory documents, reviewing for completeness and accuracy.</li><li>
Review, prepare and negotiate site contracts and budgets with sites.</li><li>
Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.</li><li>
Review and provide feedback to management on site performance metrics.</li><li>
Review, establish and agree on project planning and project timelines. Ensure monitoring measures are in place and implement contingency plan as needed.</li><li>
Inform team members of completion of regulatory and contractual documents for individual sites.</li><li>
Review, track and follow up the progress, the approval and execution of documents, including contracts, regulatory, ethics, ICF and IP release documents in line with project timelines.</li><li>
Provide local expertise to RSU leads and Project team during initial and on-going project timelines planning.</li><li>
Perform quality control documents provided by sites.</li><li>
May have direct contact with Sponsor on specific initiatives.</li><li>
May perform Site Selection Visits if a trained monitor.</li><li>
May participate in feasibility and/or site identification activities.</li></ul>
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com</div>

Sr. Site Activation Specialist

Kerry

<div>
 Requisition ID: 60794
 
 
 Position Type: FT Permanent
 
 
 
 
 About Kerry
 
 
 
 
 Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment.
 
 
 
 About The Role
 
 
 
 In this role, you be an individual contributor responsible for strategic and proactively influencing, leading and communicating on regulatory matters within Kerry and externally. Concurrently you will ensure all Kerry Products are compliant for sale within MENAT (Middle East, North Africa, and Turkey) &amp; CIS.
 
 
 
 
 Key responsibilities
 
 
 
 
 <ul>
 <li>
 Ensure timely registration on new products/SKUs in Turkey and CIS markets by working closely and lesioning with the relevant competent authorities.
 </li>
 <li>
 Support border clearance of import/export consignments by working closely with customs and relevant authorities.
 </li>
 <li>
 Maintenance and implementation of the Regulatory management system (Optiva, MDM and etc).
 </li>
 <li>
 Monitor changes in the food regulations and pro&hyphen;actively liaise with relevant RD&amp;A representatives and/or local competent authorities to minimize any impact to the business.
 </li>
 <li>
 Ensure continuous regulatory intelligence and knowledge sharing across the organization.
 </li>
 <li>
 Assess the impact of upcoming regulatory changes and advise on impact to supply chain/distribution processes
 </li>
 <li>
 Support New Product Development through participation at product brief and artwork development stages.
 </li>
 <li>
 Provide expertise and direction on product classification and product claims during the NPD Process.
 
 
 </li>
 </ul>
 
 Qualifications And Skills
 
 
 
 <ul>
 <li>
 Liaise &amp; communicate with Corporate Legal and Finance team on strategic and operational regulatory issues
 </li>
 <li>
 Create and drive the global regulatory organization goals &amp; objectives in line with the Kerry global regulatory strategy
 </li>
 <li>
 Bachelor&rsquo;s Degree in Food Science or similar field, with minimum 2 years&rsquo; experience in Regulatory for a Global Food Business industry.
 </li>
 <li>
 Experience in working with the government (Turkey &amp; CIS Food Authorities)
 </li>
 <li>
 Expert observation, analysis and judgement (i.e., analytical and objective mind-set)
 </li>
 <li>
 Strong background in Food Science &amp; Regulatory standards of Turkey &amp; CIS
 </li>
 <li>
 Ability to work with cross-functional teams within the organization at all levels
 </li>
 <li>
 Must be able to speak and write in Russian &amp; English
 
 
 </li>
 </ul>
 Beware of scams online or from individuals claiming to represent us. A Kerry employee will not solicit candidates through a non-Kerry email address or phone number. In addition, Kerry does not currently utilise video chat rooms (e.g., Google Hangouts) to conduct interviews. Refuse any request that asks you to provide payment to participate in the hiring process (e.g., purchasing a &ldquo;starter kit,&rdquo; investing in training, or something similar). Kerry will not ask you to pay any money at any point in the hiring process with the exception of reimbursable travel expenses. In addition, any payments made by Kerry will be from official firm accounts bearing the Kerry name.
 
 
 
 Recruiter
 
 
 
 
 Posting Type:
 
 LI
 
 
</div>

Regulatory Scientist Turkey & CIS

<div>Requisition ID: 60794 
Position Type: FT Permanent 
Workplace Arrangement: #LI-Onsite
<div><div><div><h2 class="jobSectionHeader">
About Kerry</h2>
</div><div>Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment.</div></div><div><div><h2 class="jobSectionHeader">
About the role</h2>
</div><div>
In this role, you be an individual contributor responsible for strategic and proactively influencing, leading and communicating on regulatory matters within Kerry and externally. Concurrently you will ensure all Kerry Products are compliant for sale within MENAT (Middle East, North Africa, and Turkey) &amp; CIS.</div></div><div><div><h2 class="jobSectionHeader"> 
Key responsibilities</h2>
</div><div><ul><li>Ensure timely registration on new products/SKUs in Turkey and CIS markets by working closely and lesioning with the relevant competent authorities.</li>
<li>Support border clearance of import/export consignments by working closely with customs and relevant authorities.</li>
<li>Maintenance and implementation of the Regulatory management system (Optiva, MDM and etc).</li>
<li>Monitor changes in the food regulations and pro&#8208;actively liaise with relevant RD&amp;A representatives and/or local competent authorities to minimize any impact to the business.</li>
<li>Ensure continuous regulatory intelligence and knowledge sharing across the organization.</li>
<li>Assess the impact of upcoming regulatory changes and advise on impact to supply chain/distribution processes</li>
<li>Support New Product Development through participation at product brief and artwork development stages.</li>
<li>Provide expertise and direction on product classification and product claims during the NPD Process.</li></ul></div></div><div><div><h2 class="jobSectionHeader"> 
Qualifications and skills</h2>
</div><div><ul><li>Liaise &amp; communicate with Corporate Legal and Finance team on strategic and operational regulatory issues</li>
<li>Create and drive the global regulatory organization goals &amp; objectives in line with the Kerry global regulatory strategy</li>
<li>Bachelor&rsquo;s Degree in Food Science or similar field, with minimum 2 years&rsquo; experience in Regulatory for a Global Food Business industry.</li>
<li>Experience in working with the government (Turkey &amp; CIS Food Authorities)</li>
<li>Expert observation, analysis and judgement (i.e., analytical and objective mind-set)</li>
<li>Strong background in Food Science &amp; Regulatory standards of Turkey &amp; CIS</li>
<li>Ability to work with cross-functional teams within the organization at all levels</li>
<li>Must be able to speak and write in Russian &amp; English</li>
</ul></div></div></div>
Beware of scams online or from individuals claiming to represent us. A Kerry employee will not solicit candidates through a non-Kerry email address or phone number. In addition, Kerry does not currently utilise video chat rooms (e.g., Google Hangouts) to conduct interviews. Refuse any request that asks you to provide payment to participate in the hiring process (e.g., purchasing a &ldquo;starter kit,&rdquo; investing in training, or something similar). Kerry will not ask you to pay any money at any point in the hiring process with the exception of reimbursable travel expenses. In addition, any payments made by Kerry will be from official firm accounts bearing the Kerry name.
Recruiter: #LI-RG1 
Posting Type: LI</div>

Freedom Finance MENAT

<div>
 
 We are seeking a highly skilled
 
 Corporate Finance Specialist
 
 with expertise in capital markets, M&amp;A, and corporate advisory. The successful candidate will lead the origination and execution of equity capital markets transactions, including IPOs, follow-ons, and private placements, while providing strategic guidance on capital raising, investor relations, and corporate restructuring. This role requires advanced financial modeling capabilities, deep knowledge of equity and debt markets, and a strong understanding of regulatory frameworks such as SPK guidelines.
 
 
 
 
 
 
 Responsibilities:
 
 
 
 
 
 <ul>
 <li>
 Lead the origination and execution of equity capital markets (ECM) transactions, including IPOs, follow-ons, and private placements.
 </li>
 <li>
 Build and maintain advanced financial models and valuation frameworks tailored for public market readiness and investor presentations.
 </li>
 <li>
 Coordinate with issuers, legal teams, and auditors to prepare IPO prospectuses, valuation reports, and marketing materials in accordance with SPK guidelines.
 </li>
 <li>
 Provide end-to-end advisory on capital-raising processes, investor relations, and corporate restructuring strategies aligned with market trends.
 </li>
 <li>
 Drive internal alignment across compliance, sales, legal, and strategy teams to ensure timely and successful deal execution.
 </li>
 <li>
 Monitor and report on developments in local and international capital markets, creating actionable insights for senior management and clients.
 </li>
 <li>
 Evaluate key financial health indicators, including solvency and coverage ratios, to assess creditworthiness and suitability for debt instrument issuance.
 </li>
 <li>
 Conduct pre-transaction financial due diligence on prospective clients for both equity and debt capital market engagements.
 </li>
 <li>
 Provide end-to-end advisory on buy-side and sell-side M&amp;A opportunities, aligning transaction structures with client strategies while ensuring regulatory and financial compliance.
 </li>
 </ul>
 
 
 
 
 
 Requirements:
 
 
 
 
 
 <ul>
 <li>
 
 CMB Level 3 License
 
 </li>
 <li>
 3&ndash;7 years of relevant experience in Corporate Finance, Project Finance, M&amp;A, or similar fields
 </li>
 <li>
 Bachelor&rsquo;s degree from a reputable university in Finance, Economics, Business Administration, or related fields
 </li>
 <li>
 Highly motivated, with strong interpersonal and communication skills
 </li>
 <li>
 Deep understanding of equity and debt capital markets, regulatory frameworks, and corporate finance principles
 </li>
 <li>
 Proficient in financial modeling, valuation techniques (DCF, Comparable Companies, Precedent Transactions), and capital-raising mechanics
 </li>
 <li>
 Strong analytical thinking, a project ownership mindset, and the ability to manage multiple stakeholder interests
 </li>
 <li>
 Proficiency in English
 </li>
 </ul>
</div>

Corporate Finance Specialist

Roche

<div>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.<div>
The Position</div>
We are looking for an experienced and passionate Legal Specialist to join our Legal team at Roche Diagnostics Turkiye. In this role, you will play a key part in protecting our reputation and supporting strategic decision-making with expert legal guidance.
What will you do?
As a Legal Specialist, you will be a strategic partner for Roche, providing proactive and commercially focused legal services and solutions. You will oversee legal compliance, mitigate risks, support corporate governance, and advise on business operations. Your role includes managing contracts, handling litigation, monitoring regulatory developments, and ensuring company policies align with legal requirements.
Key responsibilities include:<ul><li>
Drafting, reviewing, and negotiating bilingual legal documents such as contracts and agreements.</li><li>
Leading key contract negotiations and maintaining Roche&rsquo;s contract template pool.</li><li>
Keeping company departments updated on changes in laws and recent cases, assessing potential risks, and offering legal solutions.</li><li>
Handling litigation to safeguard Roche&rsquo;s legal rights and interests.</li><li>
Managing corporate maintenance topics, including company registration and corporate filings.</li><li>
Overseeing external legal counsel on various legal matters.</li><li>
Providing legal support for commercial and operational projects.</li><li>
Delivering legal training to employees and third parties, such as distributors and suppliers.</li><li>
Managing legal department reporting responsibilities and documentation.</li></ul>
Who are you?
As a Legal Specialist, you are a proactive and business-minded legal professional with a strong ability to navigate complex regulatory environments. You thrive in a fast-paced and dynamic setting, and you bring the following qualifications and skills:<ul><li>
A Bachelor&rsquo;s Degree in Law (Master&rsquo;s preferred).</li><li>
At least 6-7 years of experience in contract law, commercial law, and tender law.</li><li>
Strong expertise in developing business models and customer solutions that drive superior business results.</li><li>
Excellent verbal and written communication skills in English (additional languages are a plus).</li><li>
High adaptability and eagerness for continuous learning and self-development.</li><li>
Exceptional analytical, investigative, and organizational skills.</li><li>
Experience in the healthcare industry is an advantage.</li></ul>
Why Roche?
At Roche, we believe in fostering a culture of learning, innovation, and collaboration. We offer an environment where you have the freedom to shape your role in a way that aligns with your strengths and ambitions. Diversity and inclusion are at the core of our identity, and we encourage you to bring your authentic self to work every day.
What do we offer?<ul><li>
A dynamic and market-leading company with national and international career opportunities.</li><li>
A chance to make a meaningful impact by improving the lives of patients worldwide.</li><li>
An agile and people-focused work environment, where autonomy and decision-making are valued.</li><li>
Opportunities for personal and professional growth, with Roche investing in your development.</li></ul><div>
Who we are</div>
A healthier future drives us to innovate. Together, more than 100&rsquo;000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. 
Let&rsquo;s build a healthier future, together.
Roche is an Equal Opportunity Employer.</div>

Legal Specialist

Explore 268+ Regulatory specialist in Istanbul this September. Find roles across top companies and apply now to boost your career.

268 regulatory specialist jobs IN Istanbul

Regulatory Affairs Specialist

Regulatory Science Specialist-Crop Science (Project-based)

Sr. Site Activation Specialist

Regulatory Scientist Turkey & CIS

Regulatory Scientist Turkey & CIS

Corporate Finance Specialist

Legal Specialist