marketing manager

account manager

human resources manager

manager, audit

medical manager

regulatory affairs manager

Manpower Türkiye

<div>
 <p>
  We are seeking a
  <strong>
   Regulatory Affairs and Commercial Operations Specialist
  </strong>
  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.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Responsibilities
  </strong>
 </p>
 <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>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications
  </strong>
 </p>
 <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>
 <p>
 </p>
</div>


Regulatory Affairs 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

Kerry

<div>
 Requisition ID: 60794
 <br/>
 <br/>
 Position Type: FT Permanent
 <br/>
 <br/>
 <strong>
  <strong>
   About Kerry
   <br/>
   <br/>
  </strong>
 </strong>
 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.
 <br/>
 <br/>
 <strong>
  About The Role
  <br/>
  <br/>
 </strong>
 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.
 <br/>
 <br/>
 <strong>
  <strong>
   Key responsibilities
   <br/>
   <br/>
  </strong>
 </strong>
 <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.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications And Skills
  <br/>
  <br/>
 </strong>
 <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
   <br/>
   <br/>
  </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.
 <br/>
 <br/>
 <strong>
  Recruiter
  <br/>
  <br/>
 </strong>
 <strong>
  Posting Type:
 </strong>
 LI
 <br/>
 <br/>
</div>


Regulatory Scientist Turkey & CIS

<div><p><b>Requisition ID: 60794</b><br>
<b>Position Type: FT Permanent</b><br>
<b>Workplace Arrangement: #LI-Onsite</b></p>
<div><div><div><h2 class="jobSectionHeader"><b>
About Kerry</b></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"><b>
About the role</b></h2>
</div><div><p>
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.</p></div></div><p></p><div><div><h2 class="jobSectionHeader"><b><br>
Key responsibilities</b></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><p></p><div><div><h2 class="jobSectionHeader"><b><br>
Qualifications and skills</b></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><p>
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.</p>
<p><b>Recruiter:</b> #LI-RG1<br>
<b>Posting Type:</b> LI</p></div>

Kedrion Biopharma

<div>
 <p>
  Kedrion Biopharma is a biopharmaceutical company specializing in the development, production and distribution of plasma-derived products. Kedrion has been producing plasma products for over 40 years and has a market presence in about 100 countries. Our employees are committed to the highest standards and therapies for the patients and clinicians in haematology, immunology, neurology, and transfusion medicine.
 </p>
 <p>
  <br/>
 </p>
 <p>
  We're looking for a
  <strong>
   Scientific Services Manager,
  </strong>
  to join our team in Istanbul or Ankara.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Role Purpose:
  </strong>
 </p>
 <p>
  Scientific Service is the Responsible Person in charge of information on medicines which the Company puts on the market. Serves as technical and scientific reference, providing accurate, timely, fair-balanced medical information internally within Company and to external customers.
 </p>
 <p>
  He/She is responsible for fulfilling requirements for the Scientific Service role, according to the EU Directive 2001/83/EC in general and the local laws.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Main Responsibilities:
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Compiling and collating all information received from any source concerning the medicines that the Company puts on the market.
  </li>
  <li>
   Ensuring that product advertisements correspond to the content of the current effective marketing authorization/registration and comply with Turkey legal requirements for advertising and promotion, as well as Company procedures and policies.
  </li>
  <li>
   Ensuring that regulations on advertising &amp; promotion, external communication and interaction with healthcare professionals by the Company sales representatives are promptly implemented.
  </li>
  <li>
   Manages unsolicited requests for medical information from external customers (including product requests for unlicensed products in Turkey), in alignment with international best practices and Company policies and procedures.
  </li>
  <li>
   Reviews and approves evidence-based, balanced Medical Response Documents (MRDs) such as Standard Response Letters (SLRs) and Frequently Asked Questions (FAQs) dedicated to Turkey, ensuring compliance with local regulations.
  </li>
  <li>
   Reviews and approves Summary of Products Characteristics (SmPC) for products commercialized in the Country.
  </li>
  <li>
   Ensures records of medical inquiries, advertising &amp; promotion review/approval process, sales representatives training, in compliance with applicable regulations, Company policies and procedures.
  </li>
  <li>
   Maintains global interactions, mainly with Italy, relating to compliance with regulations for advertising &amp; promotion, therapeutic and medical information, and reporting activities.
  </li>
  <li>
   Responsible for setting up local procedures for the management of medical and scientific activities (Medical Inquiries Management, Promotional Material review, Scientific Training Management, etc.).
  </li>
  <li>
   Responsible for providing information and assistance to Regulatory Authorities, and for ensuring the decisions taken by the authorities or bodies responsible for monitoring advertising of medicinal products are immediately and fully complied with.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Requirements:
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Professional experience in related fields of at least two years.
  </li>
  <li>
   Professional experience in quality management in pharmaceutical industry.
  </li>
  <li>
   Written and spoken fluency in Turkish and English.
  </li>
  <li>
   Education: university studies degree in the field of pharmacy
  </li>
  <li>
   Place of residence: Turkey
  </li>
 </ul>
</div>


Scientific Services Manager

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

Takeda Pharmaceuticals

<div><p>By clicking the &ldquo;Apply&rdquo; button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda&rsquo;s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.</p><p></p><h2 class="jobSectionHeader"><b>
Job Description</b></h2><p></p><p><b>
Job Purpose</b></p><p></p><p><br>
Act as a trusted scientific partner in the field by engaging healthcare professionals in peer-to-peer scientific exchange, driving insights collection, and supporting local evidence generation, under the strategic guidance of the Medical Manager and in alignment with the Medical Affairs plan.</p><p></p><p><b>
Role Core Responsibilities &amp; Accountabilities</b></p><p></p><ul><li>
Establish and maintain peer-to-peer relationships with HCPs, acting as a scientific resource and trusted partner in assigned territory.</li><li>
Plan and execute territory-level KOL engagement aligned with the local medical plan, brand strategy, and scientific priorities.</li><li>
Facilitate timely, accurate, fair-balanced scientific exchange and medical education aligned with compliance standards.</li><li>
Gather, analyze, and share actionable medical insights from HCPs to inform cross-functional planning and R&amp;D alignment.</li><li>
Represent Takeda at scientific meetings and congresses, providing internal summaries and follow-up insights.</li><li>
Deliver training on disease area, clinical data, and product information to commercial, access, regulatory, and patient services colleagues.</li><li>
Provide scientific support for company-sponsored clinical trials and investigator-initiated research, including feasibility, site interaction, and education.</li><li>
Maintain updated knowledge of therapeutic area and treatment landscape, contributing to internal medical intelligence.</li><li>
Accurately document field activities and HCP interactions using CRM tools, ensuring alignment with SOPs and compliance policies.</li><li>
Collaborate with cross-functional teams to support local initiatives such as advisory boards, speaker training, and patient-focused projects.</li></ul><p></p><p><b>
Role Mandatory Responsibilities</b></p><p></p><ul><li>
To act in-line with Takeda&rsquo;s &ldquo;Information Security Policy&rdquo; and &ldquo;Acceptable Use of Technology Policy&rdquo;.</li><li>
Being a Quality and Safety Ambassador by identifying and promptly communicating product quality and pharmacovigilance issues to appropriate internal teams.</li><li>
Excels in ethical behavior by consistently acting with integrity and serving as a role model for Takeda-ism values and ethical decision-making.</li><li>
Training &amp; Compliance: Ensure full and timely completion of all mandatory Takeda training requirements and compliance with global, regional, and local procedures and SOPs.</li><li>
Speak-up for Integrity: Encourage a culture of openness by raising any concerns in good faith via the Ethics Line, to line management or directly to Ethics &amp; Compliance.</li></ul><p></p><p>
Job Dimension</p><ul><li>
OPEX responsibility: YES</li><li>
Financial Responsibility: YES</li><li>
Volume Impact: No</li><li>
Revenue Impact: No</li></ul><p></p><p>
Role required Qualifications &amp; Capabilities</p><ul><li>
University degree in Medicine or Pharmacy, advanced scientific degree preferred.</li><li>
Demonstrated ability to effectively engage and communicate with KOLs and external medical stakeholders.</li><li>
Highly qualified presentation skills</li><li>
Strong verbal and written communication skills in English and local language.</li><li>
Understanding of relevant therapeutic area, clinical data interpretation, and real-world evidence.</li><li>
Excellent planning, time management, and prioritization skills in a remote/field-based setup.</li><li>
Digital literacy in CRM systems, Microsoft Office, and virtual communication tools.</li><li>
Strong ethical standards and compliance-driven mindset.</li><li>
Minimum 2 years of experience in Medical Affairs or relevant clinical/research environment in the pharmaceutical industry is preferred.</li></ul><p></p><h2 class="jobSectionHeader"><b>
Locations</b></h2>
Istanbul, TurkeyAnkara, Turkey<p></p><h2 class="jobSectionHeader"><b>
Worker Type</b></h2>
Employee<p></p><h2 class="jobSectionHeader"><b>
Worker Sub-Type</b></h2>
Regular<p></p><h2 class="jobSectionHeader"><b>
Time Type</b></h2>
Full time</div>

Medical Science Liaison (HAE)

Explore 486+ Regulatory affairs manager in Istanbul this September. Find roles across top companies and apply now to boost your career.

486 regulatory affairs manager jobs IN Istanbul

Regulatory Affairs Specialist

Regulatory Affairs Portfolio Executive

Regulatory Scientist Turkey & CIS

Regulatory Scientist Turkey & CIS

Scientific Services Manager

Head of Legal

Medical Science Liaison (HAE)