regulatory law specialist

<div><p><b>About the role</b></p><p></p><p><b>
7+ years of major law firm or in-house experience in the insurance industry.</b></p><p>
This job provides the prospective candidate the opportunity to work with various teams throughout AIG including Underwriting (multiple lines of business), Comptrollers, Investments, Regulatory Reporting, Tax, and Litigation, as well as regulators.</p><p></p><p>
This is a dynamic and client-facing position for a self-starting, intellectually curious lawyer who is willing to dive in to a number of challenging projects while at the same time tending to ordinary course matters needed to support the day-to-day responsibilities. The job requires an individual who can multi-task, manage and prioritize work flows. In this challenging and dynamic role, you will have the opportunity to demonstrate and expand your legal expertise by being responsible for various aspects within AIG&rsquo;s regulatory team.</p><p></p><p>
This position is primarily dedicated to providing insurance regulatory support for operations of AIG&rsquo;s Property Casualty business. Areas of responsibility will include support of underwriting, comptrollers and other groups that need assistance in addressing particular aspects of state insurance law or federal law, as applicable. This will include drafting of filings with applicable regulators. The position will also require legal research, general policy review, and counsel of business partners.</p><p></p><p><b>
Specific Responsibilities</b></p><ul><li><p>
Support issues related to insurance policy rate and form filings.</p></li><li><p>
Support issues related to market conduct and financial exams.</p></li><li><p>
Prepare regulatory filings (e.g., Holding Company, and company licensing).</p></li><li><p>
Partner and interact with state regulators.</p></li><li><p>
Support issues related to consumer complaints, and information requests.</p></li><li><p>
Provide guidance concerning financial statement disclosures.</p></li><li><p>
Oversee monitoring of insurance laws and insurance department actions.</p></li><li><p>
Effectively work in a team environment, closely collaborate and provide team support with peers across Legal, Compliance and other control functions.</p></li></ul><p></p><p><b>
Education/Experience</b></p><ul><li><p>
7+ years of major law firm or in-house experience in the insurance industry.</p></li><li><p>
Must have experience with Property &amp; Casualty insurance</p></li><li><p>
Experience handling insurance regulatory matters and demonstrable experience in one or more of the areas of responsibility.</p></li><li><p>
Problem-solving skills that demonstrate ability to critically evaluate and analyze issues and recommend well thought-out and/or creative solutions.</p></li><li><p>
Experience with drafting, mark-ups and negotiation of agreements.</p></li><li><p>
Demonstrated ability to work in a fast paced environment and to find creative solutions on diverse matters requiring complex legal and strategic analysis.</p></li><li><p>
Excellent written and oral communications skills.</p></li><li><p>
Strong organizational, time management and project management skills.</p></li><li><p>
Capable of working independently and/or as part of a team.</p></li><li><p>
Knowledgeable about regulatory and risk management functions.</p></li><li><p>
Good judgment and ability to provide timely legal advice.</p></li><li><p>
Ability to identify and develop solutions to legal and business risks.</p></li><li><p>
JD required.</p></li><li><p>
Admittance to at least one state.</p></li></ul><p></p><p>
For positions based in NYC, the base salary range is $150,000 -$172,000. For positions based in NJ, the base salary range is $145,000 - $168,000. For positions based in Illinois, the base salary range is $142,000 - $168,000. The position is eligible for a bonus in accordance with the terms of the applicable incentive plan. In addition, we&rsquo;re proud to offer a range of competitive benefits, a summary of which can be viewed here: AIG Benefits Overview</p><p></p><p>
#LI-'CY1</p><p></p><p>
At AIG, we value in-person collaboration as a vital part of our culture, which is why we ask our team members to be primarily in the office. This approach helps us work together effectively and create a supportive, connected environment for our team and clients alike.</p><p></p><p><b>
Enjoy benefits that take care of what matters</b></p><p>
At AIG, our people are our greatest asset. We know how important it is to protect and invest in what&rsquo;s most important to you. That is why we created our Total Rewards Program, a comprehensive benefits package that extends beyond time spent at work to offer benefits focused on your health, wellbeing and financial security&mdash;as well as your professional development&mdash;to bring peace of mind to you and your family.</p><p></p><p><b>
Reimagining insurance to make a bigger difference to the world</b></p><p>
American International Group, Inc. (AIG) is a global leader in commercial and personal insurance solutions; we are one of the world&rsquo;s most far-reaching property casualty networks. It is an exciting time to join us &mdash; across our operations, we are thinking in new and innovative ways to deliver ever-better solutions to our customers. At AIG, you can go further to support individuals, businesses, and communities, helping them to manage risk, respond to times of uncertainty and discover new potential. We invest in our largest asset, our people, through continuous learning and development, in a culture that celebrates everyone for who they are and what they want to become.</p><p></p><p><b>
Welcome to a culture of </b><b>inclusion</b></p><p>
We&rsquo;re committed to creating a culture that truly respects and celebrates each other&rsquo;s talents, backgrounds, cultures, opinions and goals. We foster a culture of inclusion and belonging through learning, cultural awareness activities and Employee Resource Groups (ERGs). With global chapters, ERGs are a cornerstone for our culture of inclusion. The talent of our people is one of AIG&rsquo;s greatest assets, and we are honored that our drive for positive change has been recognized by numerous recent awards and accreditations.</p><p></p><p><i>
AIG provides equal opportunity to all qualified individuals regardless of race, color, religion, age, gender, gender expression, national origin, veteran status, disability or any other legally protected categories.</i></p><p></p><p>
AIG is committed to working with and providing reasonable accommodations to job applicants and employees with disabilities. If you believe you need a reasonable accommodation, please send an email to candidatecare@aig.com.</p><p></p>
AIG reserves the right to conduct a criminal background check, tailored to the requirements of a job, after a conditional employment offer is made. Unless otherwise required by law, AIG does not automatically exclude any applicant with a criminal conviction for a job or class or jobs. For more information about Philadelphia law specifically, copy and paste the following link within your browser: http://www.phila.gov/HumanRelations/PDF/BTB%20POSTER%20FINAL_3-9-16.pdf<p></p><div><div><div><div><div><div><div><p>
Functional Area:</p></div></div></div></div></div></div></div>
LG - Legal, Regulatory &amp; Gov't Affairs<p></p>
AIG PC Global Services, Inc.</div><p></p>

Regulatory Counsel

Legal Route - Global Legal Recruitment

<p>This global health care group is seeking a talented and dynamic counsel to join and lead the Data Protection legal team for this arm of their business. The role involves advising across the business on various legal risks and obligations under data protection and regulatory laws across the MENA region and beyond. The role is a great opportunity for any candidate who is keen to tackle some of today's toughest and important legal challenges in this cutting-edge area of law. You must have flexibility to adapt to changing priorities and organizational needs. In addition, you must have the ability to operate independently in a small but growing international legal team, working on issues in a vibrant, fast-paced environment. This role will provide strategic and tactical legal counseling to internal legal, product, operations and business teams on a range of privacy, data protection, and security related legal and compliance initiatives and disputes for the group of companies. This role will also be responsible for developing and maintaining relationships with data protection regulators throughout both the Middle East and globally. This is a full-time position based in Abu Dhabi.</p> Responsibilities <ul> <li>Assist healthcare product lawyers in evaluating the impact of privacy laws, regulatory guidance and enforcement actions, and other related guidelines on product features</li> <li>Support members of the legal, business, and policy teams on privacy and security-related legal matters, including areas related to partnerships, acquisitions, integrations, and other business development opportunities</li> <li>Develop regulatory strategy in connection with new product features and initiatives, and coordinate responses to inquiries from data protection regulators in those regions</li> <li>Drive high-profile and high-impact projects involving privacy analysis and compliance with stakeholders across the business, policy, legal, communications, security, and other departments</li> <li>Work with the wider legal team on regulatory and data protection matters</li> <li>Help draft and oversee the development and management of the business(and its affiliates') terms and data policies across the full range of the healthcare providers different products</li> <li>Help develop and conduct general and role-specific data protection trainings across the business</li> </ul> Minimum Qualifications <ul> <li>8+ years of legal experience, including at a law firm and/or prior in-house experience with internet or technology companies (applicable regulatory, or product counseling will be considered)</li> <li>Experience with global privacy laws, regulations, and industry guidelines, especially including those relevant for the healthcare environment</li> <li>Lawyer qualified to practice law in at least one jurisdiction in the Middle East. (UK/US/Australia/Canada and Ireland etc)</li> <li>Ability to prioritize work and provide advice under deadlines</li> <li>Business judgment and client counseling experience</li> </ul> Preferred Qualifications <ul> <li>In-depth knowledge of legal issues in the area of healthcard/medical devices/laboratories including an excellent understanding of regional or country specific data protection laws in Middle East and/or globally</li> <li>Industry or government experience working directly with data protection authorities in the Middle East and/or Africa</li> <li>Experience in driving and managing large-scale data protection projects across multiple jurisdictions is a plus</li> <li>Excellent problem-solving, written and oral communication and interpersonal skills</li> </ul><img src="https://www.jobg8.com/Tracking.aspx?KHgzDCyz%2b4z4ZjdUFkG5Plpt0hTKLDKQt" width="0" height="0" />

Data Protectio/ Regulatory Lawyer - Health Care Group - Abu Dhabi

University of Vermont

<div><div><div><div>Position Details
</div><p></p><div><div><div><div><b>Advertising/Posting Title</b></div> <div>Regulatory Specialist</div>
</div><br>
<div><div><b>Posting Summary</b></div>
<div>Provide support for the regulatory aspects of clinical trial participation at the University of Vermont Cancer Center. Prepare and track regulatory documentation. Provide guidance and subject matter expertise to other members of the research team for regulatory and compliance aspects of conducting clinical research. Maintain documentation in compliance with federal and local regulations, and distribute materials to local and affiliate sites.</div>
</div><br>
<div><div><b>Minimum Qualifications (or equivalent combination of education and experience)</b></div>
<div>Bachelor&rsquo;s degree and one to three years related experience with or demonstrated ability to learn federal regulations and guidelines required. Ability to make independent decisions in a fast-paced, regulated environment required. Ability to work collaboratively with investigators, staff, and regulators required. Effective written and verbal communication skills and editorial skills required.</div>
</div><br>
<div><div><b>Desirable Qualifications</b></div>
<div>Experience at an academic research organization, research certification (e.g., CCRP, RAC), familiarity with Click software, and experience related to oncology clinical trials desirable.</div>
</div><br>
<div><div><b>Anticipated Pay Range</b></div> <div>$24.50-$27.00/hr</div>
</div><br>
<div><div><b>Other Information</b></div>
</div><br>
<div></div><div><div><b>Special Conditions</b></div> <div>Bargaining unit position, External candidates must complete a 4-month probationary period, A probationary period may be required for current UVM employees, This position is eligible for a hybrid schedule with an option to split time between campus and elsewhere, in accordance with the university telecommuting policy, Background Check required for this position, A probationary period may be required</div>
</div><br>
<div><div><b>FLSA</b></div> <div>Non-Exempt</div>
</div><br>
<div><div><b>Union Position</b></div> <div>Yes, UVMSU</div>
</div><br>
</div></div></div><div><div>Posting Details
<p>Position will be posted for a minimum of one week, after which it is subject to removal without notice.</p>
</div><div><div><div><div><b>Job Location</b></div> <div>Burlington, Vermont, United States</div>
</div><br>
<div><div><b>Job Open Date</b></div> <div>10/06/2025</div>
</div><br>
<div><div><b>Job Close Date (Jobs close at 11:59 PM EST.)</b></div>
</div><br>
<div></div><div><div><b>Open Until Filled</b></div> <div>No</div>
</div><br>
</div></div></div><div><div>Our Common Ground Statement
<p>The University of Vermont is a welcoming, educationally purposeful community committed to creating an inclusive environment that embraces intellectual diversity and global perspectives. We seek to prepare students to be accountable leaders who will bring to their work a grasp of complexity, effective problem-solving and communication skills, and an enduring commitment to learning and ethical conduct. Members of the University of Vermont community embrace and advance the values of Our Common Ground: Respect, Integrity, Innovation, Openness, Justice, and Responsibility. Staff play a critical role in this effort and the successful candidate will demonstrate a strong commitment to UVM&rsquo;s mission and advancing Our Common Ground values through the execution of their job duties.</p>
</div></div><div></div><div><div>Position Information
</div><p></p><div><div><div><div><b>Position Title</b></div> <div>Research Data Analysis OC2 N</div>
</div><br>
<div><div><b>Posting Number</b></div> <div>S5771PO</div>
</div><br>
<div><div><b>Department</b></div> <div>Vermont Cancer Center/55060</div>
</div><br>
<div><div><b>Position Number </b></div><div>012279</div>
</div><br>
<div><div><b>Percent of Full-Time</b></div> <div>1.0</div>
</div><br>
<div><div><b>Standard Hours at 1.0 FTE</b></div> <div>37.5</div>
</div><br>
<div><div><b>Term (months per year)</b></div> <div>12</div></div></div></div></div></div></div><p></p>

Regulatory Specialist

Education Above All Foundation

<div>
 <p>
  At Education Above All (EAA), policy and advocacy power our mission to protect and promote the right to education worldwide. The Law and Policy Specialist will play a key role in advancing PEIC&rsquo;s thought leadership and legal advocacy by conducting research, collaborating with strategic partners, and disseminating findings through publications and events. This position offers the opportunity to engage with international partners, contribute to global education and development initiatives, and strengthen EAA&rsquo;s ability to deliver sustainable and impactful results, ensuring that the right to education remains protected in contexts of conflict and insecurity.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Activities
  </strong>
 </p>
 <p>
  The successful candidate will contribute to PEIC&rsquo;s research, advocacy, and policy work through the following key responsibilities:
 </p>
 <ul>
  <li>
   Conduct research on law, policy, and global governance to inform PEIC&rsquo;s advocacy and thought leadership.
  </li>
  <li>
   Contribute to the development and publication of briefings and policy engagements that advance PEIC&rsquo;s legal advocacy to protect education during conflict and insecurity.
  </li>
  <li>
   Track and interpret developments in international law and policy related to PEIC&rsquo;s mandate and share insights within the organization.
  </li>
  <li>
   Contribute to PEIC&rsquo;s thought leadership, publications, and legal advocacy strategies, ensuring alignment with EAA&rsquo;s goals.
  </li>
  <li>
   Represent PEIC in international, regional, and national forums, conferences, and workshops.
  </li>
  <li>
   Build and maintain partnerships with universities, legal research centers, human rights organizations, and private sector partners to advance PEIC&rsquo;s mission.
  </li>
  <li>
   Collaborate with the EAA External Relations team to support outreach and partnerships with Qatari and international stakeholders.
  </li>
  <li>
   Strengthen internal policies and practices to enhance the reach and visibility of PEIC&rsquo;s thought leadership across EAA.
  </li>
  <li>
   Collaborate with internal departments on fundraising, communication, and knowledge-sharing initiatives.
  </li>
  <li>
   Liaise with external consultants and contractors to support the effective delivery of program activities.
  </li>
  <li>
   Monitor implementation progress to ensure timely and quality completion of work plans.
  </li>
  <li>
   Prepare and maintain program documentation such as concept notes, proposals, meeting minutes, and reports, ensuring results are tracked and evaluated.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Education
  </strong>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree in International Law, Human Rights Law, Humanitarian Law, Public Policy, Political Science, International Relations, or a related field.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Experience
  </strong>
 </p>
 <ul>
  <li>
   3&ndash;5 years of relevant professional experience in legal research, policy analysis, political science, international relations, public policy, or legal advocacy.
  </li>
  <li>
   Candidates with fewer years of experience may also be considered if they demonstrate a strong understanding of the field and a genuine passion for advocacy and advancing the right to education.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Knowledge and Skills
  </strong>
 </p>
 <ul>
  <li>
   Solid understanding of law, policy, and global governance, with a focus on international law and education-related issues.
  </li>
  <li>
   Strong intellectual curiosity and ability to conduct policy-oriented research and analysis.
  </li>
  <li>
   Proven technical knowledge of legal and policy frameworks relevant to education in contexts of conflict and insecurity.
  </li>
  <li>
   Excellent written and verbal communication skills in English, with the ability to produce clear and impactful publications and briefs.
  </li>
  <li>
   Strong ability to build and maintain effective stakeholder relationships across diverse institutions and sectors.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   What We Offer
  </strong>
 </p>
 <p>
  More than a job, an opportunity to grow your career while making a meaningful global impact.
 </p>
 <ul>
  <li>
   Career growth and professional development through continuous learning, mentoring, and exposure to diverse projects.
  </li>
  <li>
   International collaboration with leading NGOs, UN agencies, governments, and global institutions shaping the future of education and human rights.
  </li>
  <li>
   A mission-driven culture built on purpose, innovation, and impact, empowering children, communities, and nations through the transformative power of education.
  </li>
  <li>
   An inclusive and multicultural environment that values diversity, integrity, and shared commitment to sustainable change.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   How to Apply
  </strong>
 </p>
 <p>
  <u>
   This role is open to
  </u>
  <strong>
   <u>
    Qatari Nationals only
   </u>
  </strong>
  <u>
   .
  </u>
 </p>
 <p>
  Interested candidates should send their CV to
  <strong>
   career@eaa.org.qa
  </strong>
  with the subject line:
  <strong>
   Law &amp; Policy Specialist &ndash; [Your Name]
  </strong>
 </p>
 <p>
  Only shortlisted candidates will be contacted. If you do not hear from us, we regret that your application has not been successful.
 </p>
 <p>
  <br/>
 </p>
 <p>
  We wish you the best of luck.
 </p>
 <p>
  EAA Recruitment Team
 </p>
 <p>
 </p>
</div>


Law & Policy Specialist

Amerikan Hastanesi

<div>
 <p>
  Stembio (
  <strong>
   Ko&ccedil; Holding/Ko&ccedil; Healthcare
  </strong>
  i&scedil;tiraki),
  <strong>
   Mezenkimal K&ouml;k H&uuml;creler (MSC), Eksozomlar, &Idot;mm&uuml;noterapi &Uuml;r&uuml;nleri, Kordon Kan&inodot; Bankalama ve Doku Greftleri
  </strong>
  &uuml;retimi ve haz&inodot;rlanmas&inodot; konusunda uzmanla&scedil;m&inodot;&scedil;, ileri teknolojiye sahip bir
  <strong>
   cGMP laboratuvar&inodot;d&inodot;r
  </strong>
  . Kalite kontrol ve validasyon s&uuml;re&ccedil;lerine b&uuml;y&uuml;k &ouml;nem vererek,
  <strong>
   y&uuml;ksek kaliteli ve reg&uuml;lasyonlara uygun
  </strong>
  h&uuml;cresel tedavi &uuml;r&uuml;nleri sunmay&inodot; taahh&uuml;t ediyoruz.
 </p>
 <p>
  <br/>
 </p>
 <p>
  Yenilik&ccedil;i &uuml;r&uuml;n portf&ouml;y&uuml;m&uuml;zde &mdash; ATMP&rsquo;ler, t&inodot;bbi cihazlar ve kozmetik s&inodot;n&inodot;f biyolojik &uuml;r&uuml;nler dahil &mdash; reg&uuml;lasyon stratejilerini y&uuml;r&uuml;tecek ve destekleyecek, erken geli&scedil;tirme a&scedil;amas&inodot;ndan klinik &ccedil;al&inodot;&scedil;ma izinlerine ve &uuml;r&uuml;n ticarile&scedil;tirmeye kadar t&uuml;m s&uuml;re&ccedil;lerde T&Idot;TCK, ard&inodot;ndan EMA (Avrupa) ve FDA (ABD) &ccedil;er&ccedil;evelerine uygun reg&uuml;lasyon uyumlulu&gbreve;unu sa&gbreve;lamaktan sorumlu
  <strong>
   Stembio
  </strong>
  'da g&ouml;revlendirilmek &uuml;zere bir
  <strong>
   Reg&uuml;lasyon Uzman&inodot;
  </strong>
  aray&inodot;&scedil;&inodot;nday&inodot;z.
 </p>
 <p>
  <br/>
 </p>
 <p>
  E&gbreve;er Ar-Ge, Kalite ve &Uuml;retim ekipleriyle yak&inodot;n i&scedil; birli&gbreve;i i&ccedil;inde &ccedil;al&inodot;&scedil;arak Stembio &uuml;r&uuml;nlerinin uluslararas&inodot; standartlara uygun ve hem yerel hem k&uuml;resel pazarlara haz&inodot;r hale getirilmesi konusunda yetkin oldu&gbreve;unuzu d&uuml;&scedil;&uuml;n&uuml;yorsan&inodot;z, ba&scedil;vurunuzu bekliyoruz!
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Genel Nitelikler
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Biyolojik Bilimler, Biyoteknoloji, Eczac&inodot;l&inodot;k, Biyomedikal M&uuml;hendisli&gbreve;i, Kimya veya ilgili bir alanda lisans veya &uuml;zeri derece.
  </li>
  <li>
   Tercihen biyoteknoloji, ila&ccedil; veya t&inodot;bbi cihaz sekt&ouml;rlerinde en az 5 y&inodot;l Reg&uuml;lasyon alan&inodot;nda deneyim.
  </li>
  <li>
   ATMP, GMP, CE i&scedil;areti, MDR/IVDR ve klinik &ccedil;al&inodot;&scedil;ma d&uuml;zenlemeleri hakk&inodot;nda sa&gbreve;lam bilgi.
  </li>
  <li>
   K&uuml;resel reg&uuml;lasyon &ccedil;er&ccedil;evelerine h&acirc;kimiyet:
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   T&uuml;rkiye:
  </strong>
  T&Idot;TCK (ATMP ve cihaz kay&inodot;tlar&inodot;, klinik &ccedil;al&inodot;&scedil;ma izinleri
 </p>
 <p>
  <strong>
   Avrupa:
  </strong>
  EMA (CAT, EudraCT, EudraVigilance)
 </p>
 <p>
  <strong>
   K&uuml;resel:
  </strong>
  FDA (CBER), ICH k&inodot;lavuzlar&inodot;, ISO standartlar&inodot;
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   &Uuml;r&uuml;n kay&inodot;t dosyalar&inodot;, teknik belgeler ve klinik dok&uuml;mantasyon haz&inodot;rlama deneyimi.
  </li>
  <li>
   T&uuml;rk&ccedil;e ve &Idot;ngilizce yaz&inodot;l&inodot;/s&ouml;zl&uuml; ileti&scedil;im becerileri g&uuml;&ccedil;l&uuml;.
  </li>
  <li>
   &Ccedil;ok disiplinli ekiplerle &ccedil;al&inodot;&scedil;abilen, &ouml;ncelik y&ouml;netimi kuvvetli, dinamik ortamlarda etkin &ccedil;al&inodot;&scedil;abilen.
  </li>
  <li>
   Etik de&gbreve;erlere sahip, d&uuml;zenli, detaylara &ouml;nem veren ve reg&uuml;lasyon bilimi ile yenili&gbreve;e tutkulu.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Rol ve Sorumluluklar
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Reg&uuml;lasyon Stratejisi ve &Uuml;r&uuml;n Geli&scedil;tirme
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Stembio&rsquo;nun &uuml;r&uuml;n portf&ouml;y&uuml; i&ccedil;in reg&uuml;lasyon stratejilerini geli&scedil;tirmek ve uygulamak.
  </li>
  <li>
   Klinik &ccedil;al&inodot;&scedil;ma onaylar&inodot;, GMP sertifikasyonlar&inodot; ve ruhsat ba&scedil;vurular&inodot;n&inodot; (T&Idot;TCK, EMA, FDA) planlamak ve y&ouml;netmek.
  </li>
  <li>
   Ba&scedil;vuru ve onay takvimlerini belirleyerek, i&ccedil; ekiplerle koordinasyon i&ccedil;inde hedeflenen lansman tarihlerine ula&scedil;&inodot;lmas&inodot;n&inodot; sa&gbreve;lamak.
  </li>
  <li>
   K&uuml;resel &uuml;r&uuml;n dosyalar&inodot;n&inodot; yerel reg&uuml;lasyon formatlar&inodot;na uyarlamak ve gerekli ek dok&uuml;mantasyonu haz&inodot;rlamak.
  </li>
  <li>
   Yeni endikasyonlar, teknoloji transferleri ve i&scedil; birlikleri i&ccedil;in reg&uuml;lasyon due diligence &ccedil;al&inodot;&scedil;malar&inodot;na destek vermek.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Reg&uuml;lasyon Uyumu ve Kurumsal &Idot;leti&scedil;im
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   T&uuml;rkiye, Avrupa Birli&gbreve;i ve ABD&rsquo;deki ATMP, t&inodot;bbi cihaz ve kozmetik mevzuatlar&inodot;ndaki geli&scedil;meleri takip etmek ve yorumlamak.
  </li>
  <li>
   Reg&uuml;lasyon kurumlar&inodot;yla (T&Idot;TCK, EMA, FDA, Onaylanm&inodot;&scedil; Kurulu&scedil;lar) aktif ileti&scedil;im y&uuml;r&uuml;tmek, denetimlerde ve incelemelerde Stembio&rsquo;yu temsil etmek.
  </li>
  <li>
   GMP ve reg&uuml;lasyon denetimlerine y&ouml;nelik haz&inodot;r olma durumunu sa&gbreve;lamak, denetim cevaplar&inodot;n&inodot; ve CAPA s&uuml;re&ccedil;lerini y&ouml;netmek.
  </li>
  <li>
   T&uuml;rkiye ve AB&rsquo;de ATMP alan&inodot;ndaki reg&uuml;lasyon &ccedil;er&ccedil;evesini &scedil;ekillendiren sekt&ouml;r giri&scedil;imlerinde aktif rol almak.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Standartlar, Sertifikasyon ve Dok&uuml;mantasyon
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Ge&ccedil;erli uluslararas&inodot; standartlara (ISO 13485, ISO 10993, EN, IEC, ICH Q serisi) ve y&ouml;netmeliklere (CE i&scedil;areti, MDSAP, MDR, IVDR) uygunlu&gbreve;u sa&gbreve;lamak.
  </li>
  <li>
   &Uuml;r&uuml;n kay&inodot;t dosyalar&inodot;, teknik dok&uuml;mantasyon, etiketleme ve kullan&inodot;m k&inodot;lavuzlar&inodot;n&inodot; haz&inodot;rlamak, g&ouml;zden ge&ccedil;irmek ve g&uuml;ncel tutmak.
  </li>
  <li>
   Sertifikasyon s&uuml;re&ccedil;lerini (&ouml;r. CE, TSE, Eurovent, PED) koordine etmek; akredite test laboratuvarlar&inodot; ve sertifikasyon kurulu&scedil;lar&inodot;yla ileti&scedil;imi y&uuml;r&uuml;tmek.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Klinik &Ccedil;al&inodot;&scedil;malar ve Pazar Sonras&inodot; Faaliyetler
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Klinik &ccedil;al&inodot;&scedil;ma ba&scedil;vurular&inodot;, tadilatlar&inodot; ve yenilemelerini T&Idot;TCK ve EMA &ccedil;er&ccedil;evelerinde desteklemek.
  </li>
  <li>
   ATMP&rsquo;lere y&ouml;nelik k&uuml;resel klinik ara&scedil;t&inodot;rma ortam&inodot;n&inodot; takip etmek ve Klinik &Ccedil;al&inodot;&scedil;ma Yetkilendirmesi (CTA) dosyalar&inodot;n&inodot;n haz&inodot;rlanmas&inodot;na katk&inodot; sa&gbreve;lamak.
  </li>
  <li>
   Onayl&inodot; &uuml;r&uuml;nler i&ccedil;in pazar sonras&inodot; g&ouml;zetim, g&uuml;venlilik raporlamas&inodot; ve s&uuml;rekli emniyet g&uuml;ncellemelerini y&uuml;r&uuml;tmek.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   &Idot;&ccedil; Kalite ve S&uuml;re&ccedil; Entegrasyonu
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Reg&uuml;lasyon ve GMP standartlar&inodot;na uygunlu&gbreve;u sa&gbreve;lamak &uuml;zere i&ccedil; denetimler ger&ccedil;ekle&scedil;tirmek.
  </li>
  <li>
   Kalite G&uuml;vence, Ar-Ge, &Uuml;retim ve Hukuk ekipleriyle i&scedil; birli&gbreve;i i&ccedil;inde &uuml;r&uuml;n ya&scedil;am d&ouml;ng&uuml;s&uuml;n&uuml;n her a&scedil;amas&inodot;nda reg&uuml;lasyon entegrasyonunu sa&gbreve;lamak.
  </li>
  <li>
   Uyumsuzluk risklerini tespit etmek ve proaktif &ouml;nleme stratejileri geli&scedil;tirmek.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <u>
   Ki&scedil;isel verileriniz, i&scedil; ba&scedil;vurunuzun al&inodot;nmas&inodot; ve de&gbreve;erlendirmesi amac&inodot;yla i&scedil;lenmektedir. &Idot;&scedil;lenen ki&scedil;isel verilerinize ve haklar&inodot;n&inodot;za ili&scedil;kin detayl&inodot; bilgilere websitemizin &ldquo;&Idot;nsan Kaynaklar&inodot;&rdquo; ba&scedil;l&inodot;&gbreve;&inodot; i&ccedil;erisinde yer alan&ldquo;&Ccedil;al&inodot;&scedil;an Aday&inodot; Ayd&inodot;nlatma Metni&rsquo;nden ula&scedil;abilirsiniz.
  </u>
 </p>
 <p>
  <br/>
 </p>
 <p>
  -------------------------------------------------------------------------------------------------------------
 </p>
 <p>
  <br/>
 </p>
 <p>
  Stembio (a Koc Holding/Koc Healthcare company) is a cutting-edge cGMP laboratory specializing in the production and preparation of Mesenchymal Stem Cells (MSCs), Exosomes, Immunotherapy Products, Cord Blood Banking, and Tissue Grafts. We are committed to delivering high-quality, regulatory-compliant cell therapy products through rigorous quality control and validation processes.
 </p>
 <p>
  <br/>
 </p>
 <p>
  We are seeking for a qualified and experienced
  <strong>
   Regulatory Affairs Specialist
  </strong>
  <strong>
   for Stembio,
  </strong>
  who
  <strong>
  </strong>
  will be responsible for ensuring regulatory compliance from early development to clinical trial authorization and product commercialization, initially under Turkish Medicines and Medical Devices Agency (T&Idot;TCK), and subsequently through EMA (Europe) and FDA (U.S.) frameworks,
  <strong>
  </strong>
  to lead and support regulatory strategies across Stembio&rsquo;s innovative product lines &mdash; including ATMPs, medical devices, and cosmetic-grade biologics.
 </p>
 <p>
  <br/>
 </p>
 <p>
  If you are passionate about creating close collaboration with R&amp;D, Quality, and Production teams to ensure Stembio&rsquo;s products meet international standards and are launch-ready for both local and global markets, we encourage you to apply!
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s or higher degree in Biological Sciences, Biotechnology, Pharmacy, Biomedical Engineering, Chemistry, or a related discipline.
  </li>
  <li>
   Minimum 5 years of experience in Regulatory Affairs, ideally within the biotechnology, pharmaceutical, or medical device sectors.
  </li>
  <li>
   Solid understanding of ATMP, GMP, CE marking, MDR/IVDR, and clinical trial regulations.
  </li>
  <li>
   Familiarity with global regulatory frameworks:
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   T&uuml;rkiye:
  </strong>
  T&Idot;TCK (ATMP and Device Registration, Clinical Trial Authorization)
 </p>
 <p>
  <strong>
   Europe:
  </strong>
  EMA (CAT, EudraCT, EudraVigilance)
 </p>
 <p>
  <strong>
   Global:
  </strong>
  FDA (CBER), ICH guidelines, ISO standards
 </p>
 <ul>
  <li>
   Experience in preparing and maintaining product registration files, technical documentation, and clinical dossiers.
  </li>
  <li>
   Strong communication skills in Turkish and English (both written and spoken).
  </li>
  <li>
   Ability to work effectively in cross-functional teams and manage multiple priorities in a dynamic environment.
  </li>
  <li>
   Ethical, organized, and detail-oriented mindset with a passion for regulatory science and innovation.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Responsibilities
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Regulatory Strategy &amp; Product Development
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Develop and execute regulatory strategies for Stembio&rsquo;s Product Pipeline.
  </li>
  <li>
   Plan and manage regulatory submissions for clinical trial approvals, GMP certifications, and marketing authorizations under T&Idot;TCK, EMA, and FDA.
  </li>
  <li>
   Define submission and approval timelines, coordinating with internal teams to meet launch targets.
  </li>
  <li>
   Adapt global product dossiers to local regulatory formats and gather supplementary documentation as needed.
  </li>
  <li>
   Support regulatory due diligence for new indications, technology transfers, and collaborations.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Regulatory Compliance &amp; Institutional Liaison
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Monitor and interpret evolving legislation on ATMPs, medical devices, and cosmetics across T&uuml;rkiye, EU, and the U.S.
  </li>
  <li>
   Maintain active communication with regulatory bodies (T&Idot;TCK, EMA, FDA, Notified Bodies) and represent Stembio during inspections and audits.
  </li>
  <li>
   Ensure inspection-readiness for GMP and regulatory audits; manage audit responses and CAPAs.
  </li>
  <li>
   Engage with industry associations to support advocacy initiatives shaping the Turkish and EU ATMP landscape.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Standards, Certification &amp; Documentation
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Ensure compliance with applicable international standards (ISO 13485, ISO 10993, EN, IEC, ICH Q-series) and directives (CE marking, MDSAP, MDR, IVDR).
  </li>
  <li>
   Prepare, review, and maintain technical documentation, including product registration files, device master records, labeling, and instructions for use.
  </li>
  <li>
   Coordinate certification processes (e.g., CE, TSE, Eurovent, PED) and liaise with accredited test laboratories and certification bodies.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Clinical Trials &amp; Post-Market Activities
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Support clinical trial submissions, amendments, and renewals under T&Idot;TCK and EMA frameworks.
  </li>
  <li>
   Track the global clinical trial landscape for ATMPs and contribute to dossier compilation for Clinical Trial Authorization (CTA).
  </li>
  <li>
   Oversee post-market surveillance, vigilance reporting, and continuous safety updates for approved products.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Internal Quality &amp; Process Integration
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Conduct internal audits to ensure adherence to regulatory and GMP standards.
  </li>
  <li>
   Collaborate with Quality Assurance, R&amp;D, Production, and Legal teams to ensure full regulatory integration across the product lifecycle.
  </li>
  <li>
   Identify compliance risks and develop proactive mitigation strategies.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <u>
   Your personal data is processed for the purpose of receiving and evaluating your job application. You can find detailed information about your processed personal data and rights from the "Employee Candidate Clarification Text" under the "Human Resources" heading of our website.
  </u>
 </p>
</div>


Stembio - Regülasyon Uzmanı / Regulatory Affairs Specialist

Southern Company

<div><p><b>Senior Counsel &ndash; Regulatory</b></p>
<p><b>Please Note: You will be required to be in the office at 241 Ralph McGill Blvd, Atlanta, GA a minimum of four (4) days per week and/or as additionally required.</b></p>
<p><b>Relocation assistance may be provided if needed and if you qualify.</b></p>
<p><b>JOB SUMMARY</b></p>
<p>This position will serve as a senior-level attorney in the Company&rsquo;s regulatory practice group and will be responsible for providing legal counsel and strategic guidance on a wide variety of matters. This position will work closely with the Company&rsquo;s business units, members of senior leadership, and outside counsel to develop and implement the Company&rsquo;s legal strategy related to key regulatory matters.</p>
<p><b>JOB RESPONSBILITIES</b></p>
<ul><li>Provide legal counsel on a wide variety of complex regulatory and external affairs matters.</li>
<li>Support key regulatory litigation and compliance efforts related to core aspects of the Company&rsquo;s business, such as integrated resource planning, rate making, and other proceedings.</li>
<li>Develop and support the Company&rsquo;s regulatory-litigation strategies and participate in all aspects of the regulatory-litigation process, including developing and responding to pleadings, drafting motions, briefs, and proposed orders, drafting written testimony, responding to discovery requests, supporting witness preparation, and drafting and negotiating settlement agreements.</li>
<li>Provide accurate and timely legal support focused on the needs of the business, ensuring compliance with applicable laws.</li>
<li>Establish and maintain constructive working relationships with internal business partners, outside counsel, and external stakeholders.</li>
<li>Oversee and collaborate with outside counsel representing the Company.</li>
<li>Assist with management of the legal department budget, including oversight and approval of outside counsel spend.</li>
</ul><p><b>QUALIFICATIONS</b></p>
<ul><li><b>Graduate of an American Bar Association accredited law school with a J.D. degree and strong academic credentials.</b>
</li><li><b>Licensed to practice law in one or more states in which the company or its subsidiaries operate.</b>
</li><li><b>At least 6 years of experience, including law firm experience, practicing in complex business and/or regulatory litigation.</b>
</li><li>Examples of relevant experience include developing litigation strategies in complex cases, developing and responding to pleadings, drafting and responding to motions and legal briefs, developing and responding to discovery, working extensively with witnesses in preparing for hearings, appearing before courts or regulatory bodies, conducting direct and cross examination of witnesses, and negotiating settlement agreements with opposing counsel.
</li><li>Demonstrated ability to manage multiple complex matters with competing deadlines.
</li><li>Excellent interpersonal, written, and verbal communication skills.
</li><li>Strong focus on inclusion, innovative thinking, practical solutions, and providing excellent client service.</li>
<li>Knowledge of relevant utility statutes and rules and regulations is a plus but not required.
</li><li>High ethical standards and behaviors.</li>
<li>Ability to engage frequently with senior company leadership.</li>
<li>Extensive analytical and problem-solving skills and the ability to translate complex legal concepts into easily understood and concise messaging.
</li><li>Able to work autonomously and in a team environment as appropriate.
</li><li><b>Occasional travel is required. (Perhaps up to 25%)</b>
</li></ul><p><b>Georgia Power</b> is the largest electric subsidiary of Southern Company (NYSE: SO), America's premier energy company. Value, Reliability, Customer Service and Stewardship are the cornerstones of the Company's promise to 2.6 million customers in all but four of Georgia's 159 counties. Committed to delivering clean, safe, reliable, and affordable energy at rates below the national average, Georgia Power maintains a diverse, innovative generation mix that includes nuclear, coal and natural gas, as well as renewables such as solar, hydroelectric and wind. Georgia Power focuses on delivering world-class service to its customers every day and the Company is recognized by J.D. Power and Associates as an industry leader in customer satisfaction. For more information, visit www.GeogiaPower.com and connect with the Company on Facebook (Facebook.com/GeorgiaPower), Twitter (Twitter.com/GeorgiaPower) and Instagram (Instagram.com/ga_power).</p>
<p>Southern Company (NYSE: SO ) is a leading energy provider serving 9 million customers across the Southeast and beyond through its family of companies. Providing clean, safe, reliable and affordable energy with excellent service is our mission. The company has electric operating companies in three states, natural gas distribution companies in four states, a competitive generation company, a leading distributed energy solutions provider with national capabilities, a fiber optics network and telecommunications services. Through an industry-leading commitment to innovation, resilience and sustainability, we are taking action to meet customers' and communities' needs while advancing our goal of net-zero greenhouse gas emissions by 2050. Our uncompromising values ensure we put the needs of those we serve at the center of everything we do and are the key to our sustained success. We are transforming energy into economic, environmental and social progress for tomorrow. Our corporate culture has been recognized by a variety of organizations, earning the company awards and recognitions that reflect Our Values and dedication to service. To learn more, visit www.southerncompany.com .</p>
<p>Southern Company invests in the well-being of its employees and their families through a comprehensive total rewards strategy that includes competitive base salary, annual incentive awards for eligible employees and health, welfare and retirement benefits designed to support physical, financial, and emotional/social well-being. This position may also be eligible for additional compensation, such as an incentive program, with the amount of any bonus/awards subject to the terms and conditions of the applicable incentive plan(s). A summary of the benefits offered for this position can be found here https://seo.nlx.org/southernco/pdf/SOCO-Benefits.pdf . Additional and specific details about total compensation and bene&#64257;ts will also be provided during the hiring process.</p>
<p>Southern Company is an equal opportunity employer where an applicant's qualifications are considered without regard to race, color, religion, sex, national origin, age, disability, veteran status, genetic information, sexual orientation, gender identity or expression, or any other basis prohibited by law.</p>
<p>Job Identification: 15352</p>
<p>Job Category: Legal &amp; Compliance</p>
<p>Job Schedule: Full time</p>
<p>Company: Georgia Power</p></div><p></p>

Senior Counsel - Regulatory (In Ofc 4 Days/Wk)

ByteDance

<div>
 <strong>
  Responsibilities
  <br/>
 </strong>
 About the Team:
 <br/>
 Our legal team provides key support for all ByteDance&rsquo;s innovative initiatives, state-of-the-art products, and integrated platforms servicing our global video market. We help our technological and business teams enable their vision by providing integrated legal guidance and support. The ByteDance team is growing fast and is seeking highly experienced, bright and capable legal professionals to join the team. One of the critical challenges is the need for our team to provide exceptional legal support for the Data Privacy and Data Protection matters involving ByteDance. The following describes the responsibilities and requirements for the role.
 <br/>
 <br/>
 Responsibilities:
 <br/>
 - Provide data privacy legal support in the APAC and Emerging Markets (AEM) region with a focus on managing regulatory matters for the entire company and in over 120+ markets. This will include leading on regulatory investigations, litigation, government policy, external communications, et cetera.
 <br/>
 - Monitor privacy across markets to determine trends and issues for the company to address.
 <br/>
 - Coordinate internal communication, projects, and training amongst different teams.
 <br/>
 - Identify areas of common concern, redundancies in operation, and inefficiencies in order to develop standards and policies to improve workflow in the region.
 <br/>
 - Plan any other required activities so international and regional legal teams can meet their objectives and provide actionable deliverables to the company at large.
 <br/>
 - Merge solutions across key jurisdictions and their legal requirements with a focus on AEM but should have a foundational knowledge of other global laws (i.e. GDPR, CCPA, et cetera).
 <br/>
 - Increasingly advise on algorithmic and artificial intelligence-related matters.
 <br/>
 <br/>
 <strong>
  Qualifications
  <br/>
 </strong>
 Minimum Qualifications
 <br/>
 - Qualified to practice law and in good standing in UK, US, or other common law jurisdiction.
 <br/>
 - Significant experience managing privacy legal and regulatory matters
 <br/>
 - Experience working on data privacy efforts globally/regionally for a major multinational corporation or advising agency on data privacy issues.
 <br/>
 - Detail-oriented that can coordinate across multiple teams/countries.
 <br/>
 - Strong sense of problem-solving and proactive work ethic.
 <br/>
 - Determination to face tough challenges in a fast-paced environment while keeping a sense of humor.
 <br/>
 - Fluency in written and spoken English.
 <br/>
 <br/>
 Preferred Qualifications
 <br/>
 - Internationally recognized data privacy certifications or courses would be advantageous.
 <br/>
 - Demonstrated ability to lead / manage data privacy efforts globally / regionally
 <br/>
 - Experience, and more importantly personal interest, in technology, social network, internet, and all things digital is ideal.
 <br/>
 - Experience leading highly contentious and complex regulatory issues
 <br/>
 <br/>
 <strong>
  About Us
  <br/>
 </strong>
 Founded in 2012, ByteDance's mission is to inspire creativity and enrich life. With a suite of more than a dozen products, including TikTok, Lemon8, CapCut and Pico as well as platforms specific to the China market, including Toutiao, Douyin, and Xigua, ByteDance has made it easier and more fun for people to connect with, consume, and create content.&ZeroWidthSpace;
 <br/>
 <br/>
 <br/>
 <strong>
  Why Join ByteDance
  <br/>
 </strong>
 Inspiring creativity is at the core of ByteDance's mission. Our innovative products are built to help people authentically express themselves, discover and connect &ndash; and our global, diverse teams make that possible. Together, we create value for our communities, inspire creativity and enrich life - a mission we work towards every day.&ZeroWidthSpace;
 <br/>
 As ByteDancers, we strive to do great things with great people. We lead with curiosity, humility, and a desire to make impact in a rapidly growing tech company. By constantly iterating and fostering an "Always Day 1" mindset, we achieve meaningful breakthroughs for ourselves, our Company, and our users. When we create and grow together, the possibilities are limitless. Join us.&ZeroWidthSpace;
 <br/>
 Diversity &amp; Inclusion&ZeroWidthSpace;
 <br/>
 ByteDance is committed to creating an inclusive space where employees are valued for their skills, experiences, and unique perspectives. Our platform connects people from across the globe and so does our workplace. At ByteDance, our mission is to inspire creativity and enrich life. To achieve that goal, we are committed to celebrating our diverse voices and to creating an environment that reflects the many communities we reach. We are passionate about this and hope you are too.&ZeroWidthSpace;
</div>


Privacy Counsel (Regulatory), APAC & Emerging Markets

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