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regulatory affairs specialist

Perrigo

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

Regulatory Affairs, Associate Specialist

Orcawise

<p><b>Legal Fellows &ndash; Responsible AI (RAIMS RAG Content Development)</b></p><p><b>Location:</b> Remote (Global)</p><p><b>Start Date:</b> Rolling</p><p><b>Commitment:</b> Part-time or Project-Based (Flexible)</p><p><b>Program:</b> Orcawise Innovation Program (OIP)</p><p><b>About the Opportunity</b></p><p>Are you a legally-minded innovator who&rsquo;s passionate about <b>Responsible AI</b>?</p><p>Join us at OIP <b>Orcawise Innovation Program</b>, a 100-day research-based work experience program helping graduates and experienced legal professionals transition to a career in AI.</p><p>Orcawise is building the world&rsquo;s first <b>RAIMS&trade; (Responsible AI Management System)</b> aligned with <b>ISO 42001</b>, the <b>EU AI Act</b>, and emerging governance standards.</p><p>We&rsquo;re seeking talented legal minds to help us shape the knowledge engine that powers <b>RAIMS RAG</b>&mdash;a retrieval-augmented system that makes complex AI laws, policies, and standards accessible to real-world teams.</p><p><b>What You&rsquo;ll Do</b></p><ul><li>Translate laws and policies (EU AI Act, ISO 42001, NIST AI RMF, etc.) into <b>structured, explainable Q&amp;A content</b></li><li>Build modular legal knowledge chunks for <b>RAG (retrieval-augmented generation)</b> pipelines</li><li>Draft plain-language answers to prompts like:</li><li>&ldquo;What are our Article 29 obligations for high-risk AI?&rdquo;</li><li>&ldquo;How do we show human oversight under ISO Clause 8?&rdquo;</li><li>Label and tag content by <b>risk tier, audience, regulation, and governance role</b></li><li>Collaborate with legal engineers, prompt writers, and compliance leads</li></ul><p><b>Ideal Profile</b></p><ul><li>Background in <b>Law, Policy, Regulatory Affairs, or Compliance</b></li><li>Familiarity with at least one of the following:</li><li><b>EU AI Act</b>, <b>GDPR</b>, <b>ISO 42001</b>, <b>ISO 23894</b>, <b>NIST AI RMF</b></li><li>Ability to write <b>plain-language, high-precision</b> summaries of legal text</li><li>Interest in <b>AI, LLMs, and Responsible Tech</b></li><li>Bonus: experience with AI policy research, AI audits, or prompt engineering</li></ul><p><b>Who This Is For</b></p><p>This role is perfect for:</p><ul><li>Legal analysts or compliance professionals exploring <b>AI governance</b></li><li><b>JD / LLM / PhD students</b> in tech law, data protection, or regulatory science</li><li>Legal content writers or editors with policy-to-practice experience</li><li>Professionals seeking portfolio experience in <b>AI + Law</b></li></ul><p><b>Why Join?</b></p><ul><li>Help shape the <b>first regulatory-grade AI governance system</b> (RAIMS&trade;)</li><li>Work with global AI standards and policy experts</li><li>Get credited on a real-world RAG system used by enterprises</li><li>Access potential long-term roles or consulting opportunities with the Orcawise vast ecosystem of employers and 30+ responsible Ai community.</li></ul><p><b>How to Apply</b></p><p>Send us:</p><ul><li>A short note on why this excites you and confirmation that you can commit the time to this work experience program.</li><li>A very brief writing sample (legal explainer, article summary, or policy brief)</li></ul><p>Job Types: Part-time, Temporary</p><p>Application Question(s):</p><ul><li>Can you commit the time for a 100-day volunteer work experience program?</li><li>Can you attend AI training sessions, team briefings and on-demand courses as part of this work experience program? </li><li>Are you fluent in English language? </li></ul><p>Education:</p><ul><li>Master's (Preferred)</li></ul><p>Language:</p><ul><li>English (Required)</li></ul>

Legal Fellows - Responsible AI

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>

Medtronic

<div><p>At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You&rsquo;ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
</p><p></p><h1 class="jobSectionHeader"><b>A Day in the Life
</b></h1>In partnership with the business, we lead a world class ethics and compliance program that mitigates risk, while fostering and championing a culture of ethics and compliance. We help the business deliver results in the right way, every day. As Senior Compliance Specialist, you will be the primary point of contact for the countries and operating units you will support. You will partner with Centers of Expertise and Legal Business Partners to ensure the business can achieve its strategic objectives while mitigating risks. We believe that when people from different cultures, genders, and points of view come together, innovation is the result &mdash;and everyone wins. Medtronic walks the walk, creating an inclusive culture where you can thrive.
<br>
<br>
Bring your talents to an industry leader in medical technology and healthcare solutions &ndash; we&rsquo;re a market leader and growing every day. You can be proud to be a part of technologies that are rooted in our long history of mission-driven innovation. You will be empowered to shape your own career. We support your growth with the training, mentorship, coaching and guidance you need to own your future success. Together, we can transform healthcare. This position will reside in Istanbul, Turkey and supports Turkey and Middle East countries.
<p></p><p><b>Responsibilities may include the following and other duties may be assigned:
</b></p><ul><li>Implement and manage development, implementation, administration of compliance policies, procedures, and practices to ensure alignment with legal and ethical standards of the organization
</li><li>Drive employee communication and training programs to support the elements of the companywide compliance program.
</li><li>Maintain current knowledge of laws for finance, advertising and marketing reporting, regulations, and industry guidance that impact the company's compliance program. Understand and collaborate on a wide range of competing business priorities, market challenges, and tailor risk-based compliance solutions accordingly.
</li><li>Foster strategic partnerships with multiple key internal and external high-level stakeholders, including executive leadership, to ensure local and regional compliance program deliverables are met. Demonstrate ability to identify key risks and the related controls with operating unit processes and design control test steps to address key risks.
</li><li>Being a member of local trade associations
</li><li>Implementing a channel compliance program for distributors and agents including due diligence, onsite monitoring, training and education.
</li><li>Create and manage effective action plans in response to audit discoveries and compliance violations.
</li><li>Participate in creation of periodic metrics, dashboards, and reporting of monitoring results as needed.
</li><li>Implement and manage development of channel compliance program in the territory based on global channel compliance program, ensure transparency requirements are met
</li></ul><p></p><p><b>Required Knowledge and Experience:
</b></p><ul><li>5 years of experience in compliance
</li><li>Bachelor degree
</li><li>Ability to work independently, prioritize tasks, and manage multiple projects or tasks simultaneously
</li><li>Good communication skills and proactive attitude towards stakeholders
</li><li>Fluent in Turkish and English
</li><li>High analytical skills
</li><li>Good knowledge of legal requirements and procedures.
</li><li>Proficiency in Microsoft Office and other relevant software.
</li><li>Good knowledge of compliance requirements and procedures.
</li></ul><p></p><p><b>Physical Job Requirements
</b><br>
<br>
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
</p><p></p><h1 class="jobSectionHeader"><b>Benefits &amp; Compensation
</b></h1><p><b>Medtronic offers a competitive Salary and flexible Benefits Package
</b><br>
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.<br>
<br>
</p><p></p><h1 class="jobSectionHeader"><b>About Medtronic
</b></h1><p>We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
<br>
Our Mission &mdash; to alleviate pain, restore health, and extend life &mdash; unites a global team of 95,000+ passionate people.
<br>
We are engineers at heart&mdash; putting ambitious ideas to work to generate real solutions for real people. From the R&amp;D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.</p></div><p></p>

Senior Compliance Specialist

<div>
 At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You&rsquo;ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
 <br/>
 <br/>
 <strong>
  A Day in the Life
  <br/>
  <br/>
 </strong>
 In partnership with the business, we lead a world class ethics and compliance program that mitigates risk, while fostering and championing a culture of ethics and compliance. We help the business deliver results in the right way, every day. As Senior Compliance Specialist, you will be the primary point of contact for the countries and operating units you will support. You will partner with Centers of Expertise and Legal Business Partners to ensure the business can achieve its strategic objectives while mitigating risks. We believe that when people from different cultures, genders, and points of view come together, innovation is the result &mdash;and everyone wins. Medtronic walks the walk, creating an inclusive culture where you can thrive.
 <br/>
 <br/>
 Bring your talents to an industry leader in medical technology and healthcare solutions &ndash; we&rsquo;re a market leader and growing every day. You can be proud to be a part of technologies that are rooted in our long history of mission-driven innovation. You will be empowered to shape your own career. We support your growth with the training, mentorship, coaching and guidance you need to own your future success. Together, we can transform healthcare. This position will reside in Istanbul, Turkey and supports Turkey and Middle East countries.
 <br/>
 <br/>
 <strong>
  Responsibilities may include the following and other duties may be assigned:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Implement and manage development, implementation, administration of compliance policies, procedures, and practices to ensure alignment with legal and ethical standards of the organization
  </li>
  <li>
   Drive employee communication and training programs to support the elements of the companywide compliance program.
  </li>
  <li>
   Maintain current knowledge of laws for finance, advertising and marketing reporting, regulations, and industry guidance that impact the company's compliance program. Understand and collaborate on a wide range of competing business priorities, market challenges, and tailor risk-based compliance solutions accordingly.
  </li>
  <li>
   Foster strategic partnerships with multiple key internal and external high-level stakeholders, including executive leadership, to ensure local and regional compliance program deliverables are met. Demonstrate ability to identify key risks and the related controls with operating unit processes and design control test steps to address key risks.
  </li>
  <li>
   Being a member of local trade associations
  </li>
  <li>
   Implementing a channel compliance program for distributors and agents including due diligence, onsite monitoring, training and education.
  </li>
  <li>
   Create and manage effective action plans in response to audit discoveries and compliance violations.
  </li>
  <li>
   Participate in creation of periodic metrics, dashboards, and reporting of monitoring results as needed.
  </li>
  <li>
   Implement and manage development of channel compliance program in the territory based on global channel compliance program, ensure transparency requirements are met
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Required Knowledge and Experience:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   5 years of experience in compliance
  </li>
  <li>
   Bachelor degree
  </li>
  <li>
   Ability to work independently, prioritize tasks, and manage multiple projects or tasks simultaneously
  </li>
  <li>
   Good communication skills and proactive attitude towards stakeholders
  </li>
  <li>
   Fluent in Turkish and English
  </li>
  <li>
   High analytical skills
  </li>
  <li>
   Good knowledge of legal requirements and procedures.
  </li>
  <li>
   Proficiency in Microsoft Office and other relevant software.
  </li>
  <li>
   Good knowledge of compliance requirements and procedures.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Physical Job Requirements
  <br/>
  <br/>
 </strong>
 The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
 <br/>
 <br/>
 <strong>
  Benefits &amp; Compensation
  <br/>
  <br/>
 </strong>
 <strong>
  Medtronic offers a competitive Salary and flexible Benefits Package
  <br/>
  <br/>
 </strong>
 A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
 <br/>
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  About Medtronic
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 We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
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 Our Mission &mdash; to alleviate pain, restore health, and extend life &mdash; unites a global team of 95,000+ passionate people.
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 We are engineers at heart&mdash; putting ambitious ideas to work to generate real solutions for real people. From the R&amp;D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
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 Learn more about our business, mission, and our commitment to diversity here
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Explore 247+ Regulatory affairs specialist in Istanbul this September. Find roles across top companies and apply now to boost your career.

247 regulatory affairs specialist jobs IN Istanbul

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Senior Compliance Specialist