human resources specialist Jobs in Istanbul

human resources specialist

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junior human resources specialist

legal support specialist Jobs in Istanbul

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regulatory affairs specialist Jobs in Istanbul

regulatory affairs specialist

regulatory specialist

<div><h1 class="jobSectionHeader"><b>Job Description Summary</b></h1>
An exciting opportunity for a Regulatory Affairs Specialist, the role will be based in Istanbul, Turkey.<p></p><h1 class="jobSectionHeader"><b>
Job Description</b></h1><p><b>
We are the makers of possible</b></p><p></p><p>
BD is one of the largest global medical technology companies in the world. Advancing the world of health&trade; is our Purpose, and it&rsquo;s no small feat. It takes the imagination and passion of all of us&mdash;from design and engineering to the manufacturing and marketing of our billions of MedTech products per year&mdash;to look at the impossible and find transformative solutions that turn dreams into possibilities.</p><p></p><p><b>
Why Join Us?</b></p><p></p><p>
A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.</p><p></p><p>
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you&rsquo;ll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place.</p><p></p><p>
Become a <b>maker of possible </b>with us!</p><p></p><p><b>
About the role</b></p><p>
The Regulatory Specialist is responsible for supporting and driving regulatory activities across multiple projects and product lines. You will be responsible for launching of Medical Device &amp; In-Vitro Diagnostic products in the Turkish market in addition to ensuring the absence of any regulatory issue in alignment with company standards and country regulations. This role ensures compliance with industry standards and regulatory requirements by reviewing and approving advertising and promotional materials, leading regulatory and product-related documentation, along with providing local regulatory support.</p><h2 class="jobSectionHeader"><b>
Main responsibilities will include</b><b> </b><b>:-</b></h2><ul><li>
Responsible for all regulatory activities including but not limited to pre-registration, registration and re-registration steps in accordance with local regulations and business strategies.</li><li>
Develop and maintain communication system with local stakeholders and regional partners</li><li>
Updating regulatory knowledge due to procedures and changes in local directives.</li><li>
Ensuring all products meet regulatory requirements by supporting all assigned regulatory aspects of product approval and post market compliance.</li><li>
Scheduling and prioritizing projects and planning submissions with the corresponding partners.</li><li>
Perform and manage Ad Prom local activities</li><li>
Maintain the reimbursement prosses of Social Security Institute (SSI) on determined periods, collaboratively work with local teams, follow up on the approvals and inform business teams.</li><li>
Keep the local business communication alive regarding registrations and reimbursement updates</li><li>
Participating in relevant organizations representing the company.</li></ul><p></p><p><b>
About You :-</b></p><ul><li>
Bachelor&rsquo;s degree in science, engineering or equivalent.</li><li>
Proficiency in Microsoft Office programs (Word, Excel, PowerPoint)</li><li>
Good command of English both written and verbally</li><li>
Self-motivated and self-confident</li><li>
Effective communicator with strong organizational and problem-solving skills</li><li>
Detail oriented and ability to work independently</li><li>
Medical Device registration employee certification is a nice to have.</li></ul><h2 class="jobSectionHeader"><b>
Click on apply if this sounds like you!</b></h2><p>
At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.</p><p></p><p>
Becton, Dickinson and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics.</p><h2 class="jobSectionHeader"><b>
To learn more about BD visit: </b><b>https://bd.com/careers</b></h2><p></p><p>
Required Skills</p><p>
Optional Skills</p><p></p><p>
.</p><h1 class="jobSectionHeader"><b>
Primary Work Location</b></h1>
TUR Istanbul - R&uuml;zgarl&#305;bah&ccedil;e Mah<p></p><h1 class="jobSectionHeader"><b>
Additional Locations</b></h1><p></p><h1 class="jobSectionHeader"><b>
Work Shift</b></h1></div>

Regulatory Affairs Specialist

Kraft Heinz

<div>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 <strong>
  About the Posiion
  <br/>
  <br/>
 </strong>
 Regulatory Affairs Specialist ensuring Food Regulatory Compliance and enabling market access for products. Managing product registrations with authority, as well as reviewing, verifying product information and coordinating documentation for regulatory submissions. Supporting regulatory strategies, maintaining strong relationships with local authorities and internal stakeholders to support business growth. Monitoring and analyzing legislative/regulation changes and their impact on our products- brands- and organization. Presenting the organization in various trade associations and industry groups to proactively manage food regulatory advocacy as well as keeping internal stakeholders informed through continuous monitoring of emerging regulations. You&rsquo;ll be directly reporting into Supplier &amp; External Manufacturing Sr Manager - East &amp; dotted-line reporting to Head of Legal T&uuml;rkiye.
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 <br/>
 <strong>
  Key Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Check the compliance of the products&rsquo; labels in Turkey against the relevant legislations- government guidelines and company policies. All brands the company produces and imports.
  </li>
  <li>
   Check the compliance of the health and nutritional and other claims against the relevant legislation.
  </li>
  <li>
   Support the Marketing team in providing and approving legislation of the products&rsquo; information relating to product functional - health - nutritional claims including ads and online marketing.
  </li>
  <li>
   Provide information and advice on legislation for product formulation- packaging- and labelling issues.
  </li>
  <li>
   Prepare product registration files with claim substantiation docs and follow up till registration is done.
  </li>
  <li>
   Be in direct contact with distributors or get support from 3rd party companies (for export destinations) to support and understand any new regulatory updates/ requirements.
  </li>
  <li>
   Support the business with regulatory information relating to products produced and sold in other regions.
  </li>
  <li>
   Work with cross country teams to ensure regulatory compliance of export and import products including filling necessary applications.
  </li>
  <li>
   Horizon scanning possible regulatory related changes within your region. Build and maintain relationships with the relevant authorities to maintain awareness of new food legislation and government guidance.
  </li>
  <li>
   Track- monitor and report completion of necessary changes that need to be done due to new regulations in order to prevent any penalties from authority.
  </li>
  <li>
   Ensure that ingredients- formulas- labeling- and packaging are in full compliance with the local laws and regulations where the products are sold; and provide training to the organization on relevant regulatory topics
  </li>
  <li>
   Monitor and provide advice/analysis on best practices from the market for the categories we play in &amp; share it consistently with other RA teams across the company
  </li>
  <li>
   Build presence in the local trade associations and industry groups as a forum to discuss upcoming or existing regulatory changes; and proactively monitor regulatory activities in our markets to address and influence proposed regulations to preserve the organization&rsquo;s freedom to operate
  </li>
  <li>
   Provide proposals for the amendment of existing or new regulations to support the interests of the organization
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications &amp; Experience
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bacherlor&rsquo;s degree in Food Technology/ Pharmacy or related disciplines. Master degree is an advantage
  </li>
  <li>
   Minimum 3 years&rsquo; working experience in the field of regulatory affairs, preferably within an international environment.
  </li>
  <li>
   Familiar with Turkey food registration procedures and regulatory aspects.
  </li>
  <li>
   Good understanding of the commercial drivers of F&amp;B industry and an associated ability to provide advice/guidance that takes these into consideration
  </li>
  <li>
   Analytical skills and attention to detail with the capability to appropriately define issues, questions, and data
  </li>
  <li>
   Skills such as project management, problem solving, ability to present information in easily understood format at internal and external meetings, good time management, negotiation and interpersonal skills
  </li>
  <li>
   Ability to work both independently and as part of a team as required
  </li>
  <li>
   Be able to balance company commercial needs with compliance requirements
  </li>
  <li>
   Ability to think strategically and innovatively for resolution of regulatory issues
  </li>
  <li>
   Commitment to continued improvement in department processes and performance
  </li>
  <li>
   Strong team player, assisting others with workload peaks and the management of challenging situations
  </li>
  <li>
   Fluency in English and Turkish
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 This position can be based in either Susurlul factory or &Idot;stanbul Headquarter.
 <br/>
 <br/>
 <strong>
  About Us
  <br/>
  <br/>
 </strong>
 The Kraft Heinz Company is one of the largest food and beverage companies in the world, with eight $1 billion+ brands and global sales of approximately $25 billion. We&rsquo;re a globally trusted producer of high-quality, great-tasting, and nutritious foods for over 150 years. Our brands are truly global, with products produced and marketed in over 40 countries. These beloved products include condiments and sauces, cheese and dairy, meals, meats, refreshment beverages, coffee, infant and nutrition products, and numerous other grocery products in a portfolio of more than 200 legacy and emerging brands.
 <br/>
 <br/>
 No matter the brand, we&rsquo;re united under one vision To sustainably grow by delighting more consumers globally. Bringing this vision to life is our team of 39,000+ food lovers, creative thinkers, and high performers worldwide. Together, we help provide meals to those in need through our global partnership with Rise Against Hunger. We also stand committed to responsible, sustainable practices that extend to every facet of our business, our consumers, and our communities. Every day, we&rsquo;re transforming the food industry with bold thinking and unprecedented results. If you share our passion &ndash; and are ready to create the future, build a legacy, and lead as a global citizen &ndash; there&rsquo;s only one thing to do join our table and let&rsquo;s make life delicious!
 <br/>
 <br/>
 <strong>
  Our Culture of Ownership, Meritocracy and Collaboration
  <br/>
  <br/>
 </strong>
 We're not afraid to think differently. Embrace new ideas. Dream big. We empower our people at every level &ndash; from entry-level intern to senior leader &ndash; to own their work. We share a responsibility to think like Owners &ndash; to be mindful of the collective and sustained success of Kraft Heinz &ndash; which we apply to every situation, every day.
 <br/>
 <br/>
 As part of Kraft Heinz, you're supported to grow and achieve. You&rsquo;re expected to bring your authentic self to work every day, to lead with humility, and drive outstanding performance at every level &ndash; and you&rsquo;ll be rewarded. You&rsquo;re given opportunities to leave a mark and build a legacy. But you won&rsquo;t do it alone. You&rsquo;re supported by passionate teammates along the way, and our collective, collaborative spirit fuels our incredible progress.
 <br/>
 <br/>
 Employee Candidate Privacy Notice https //www.heinz.eu/turkey-candidate-privacy-policy
 <br/>
 <br/>
 Location(s)
 <br/>
 <br/>
 Istanbul Branch
 <br/>
 <br/>
 <strong>
  Kraft Heinz is an Equal Opportunity Employer &ndash; Underrepresented Ethnic Minority Groups/Women/Veterans/Individuals with Disabilities/Sexual Orientation/Gender Identity and other protected classes
 </strong>
 <strong>
  .
 </strong>
</div>


Pfizer

<div><div>The Regulatory Head will lead, manage, and provide strategic direction to the country-based regulatory teams, driving the development and execution of regulatory strategies and plans for the country and, where applicable, the region. This role will represent GRS on the Country Leadership Team (CLT) and local Country Medical Council (or equivalent) to ensure strong collaboration with key stakeholders (e.g., Commercial, Medical) and enable a focused regulatory approach that supports country business objectives.</div><ul><li><div>
Lead and manage the regulatory team in developing and executing regulatory strategies to support the registration of new products, line extensions, major variations, lifecycle management, GMP process and medical devices. Ensure that local regulatory teams provide strategic regulatory input into global regulatory strategies, aligning local regulatory activities with global objectives to achieve optimal business and compliance outcomes</div></li><li><div>
Develop strong partnerships with in-country teams (e.g., Country Managers, Medical, Marketing, Supply Chain) and GRS-EM Therapeutic Area and Regional Teams to enable the development and implementation of registration strategies that expedite the approval of new products, line extensions, and lifecycle optimization initiatives.</div></li><li><div>
Provide strategic contribution to the country leadership teams &ndash; anticipate what GRS-EM needs to contribute to achieve business objectives.</div></li><li><div>
Responsible for building and maintaining strategic relationships with key external agencies (e.g., HAs/BoH, RKOLs) and managing the HA/BoH interface throughout the product development and lifecycle. Foster long-term, positive relationships grounded in integrity, quality, compliance, and leadership, serving as the primary liaison and main contact for local government regulators on all regulatory-related activities.</div></li><li><div>
Define the overall regulatory strategy for the product registration pathway, including:</div></li><li><div>
Regulatory frameworks: Identify applicable global, regional, and local regulations, standards, and classification requirements relevant to the product category.</div></li><li><div>
Evaluation data: Determine the necessary preclinical, clinical, and performance data to support safety, efficacy, and quality claims for submission.</div></li><li><div>
Product lifecycle management: maintain licenses (e.g. Marketing Authorizations) in compliance with local regulations by ensuring that corporate regulatory processes, SOP&rsquo;s and systems (e.g. CMC change control, product labelling, etc.) are in place, and that the regional RA staff (permanent and contract) are properly trained in these systems and procedures.</div></li><li><div>
Monitor and assess local regulatory environment: Stay informed of local regulations and emerging trends, providing impact assessments to key stakeholders. Leverage regulatory intelligence and landscape knowledge to support the development and implementation of regulatory and business strategies, and positively influence local legislative initiatives affecting the business.</div></li><li><div>
Oversee regulatory submissions and approvals: Manage the preparation, submission, and approval of CTA, NDA, and lifecycle (LC) submissions in accordance with established GRS-EM performance metrics.</div></li><li><div>
Ensure regulatory compliance: Ensure that all regulatory activities&mdash;including new product submissions, clinical trial applications, and existing licenses&mdash;fully comply with local regulations, requirements, and practices.</div></li><li><div>
Build and lead a high-performing regulatory function in Turkey, fostering regulatory excellence through:</div></li><li><div>
Strategic leadership: Establish a best-in-class regulatory organization aligned with global standards and local compliance requirements.</div></li><li><div>
Collaboration: Drive strong cross-functional partnerships with R&amp;D, quality, medical, and commercial teams to accelerate approvals and market access.</div></li><li><div>
Continuous improvement: Cultivate a culture of regulatory innovation, leveraging reusable blueprints, knowledge sharing, and rapid iteration to enhance efficiency and consistency across submissions and lifecycle activities.</div></li><li><div>
Develop and enhance the capabilities and capacities of the regulatory teams by identifying training and development needs and implementing targeted programs to strengthen expertise and operational excellence.</div></li></ul><div></div><div>
Qualifications</div><div></div><div>
Experience: Minimum of 15 years in regulatory affairs, including product registration and CMC management, with 7 &ndash;10 years in a people management role.</div><div>
Education: Degree in Pharmaceuticals or Chemistry is a must</div><div>
Regulatory Knowledge: Strong understanding of regional and global regulatory environments and their impact on regulatory strategy and implementation.</div><div>
Technical Expertise: Knowledge of drug development practices, GMP inspection requirements, local regulations and guidelines.</div><div>
Proven Skills: Demonstrated ability to develop and implement regulatory strategies effectively.</div><div>
Leadership &amp; Strategic Thinking:</div><ul><li><div>
Ability to think strategically and align regulatory initiatives with business objectives.</div></li><li><div>
Excellent communication and negotiation skills</div></li><li><div>
Strong problem-solving capabilities</div></li><li><div>
Understanding of the business and financial environment</div></li><li><div>
In-depth knowledge of the pharmaceutical industry</div></li></ul><div></div><div><div>
Purpose</div></div><div><div>
Breakthroughs that change patients' lives... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.</div></div><div></div><div><div><br>
School of Leaders</div><div>
We, as Pfizer Turkey, make a difference with our visionary and pioneering approaches ranging from our concept of raising leaders through rotations, providing international career opportunities to creating a flexible, enjoyable work environment. There are no limits to what we can accomplish to touch lives here!</div></div><div></div><div><div><br>
Flexibility</div><div>
We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let&rsquo;s start the conversation!</div></div><div></div><div><div><br>
Equal Employment Opportunity</div><div>
We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms &ndash; allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.</div></div><div></div>
Regulatory Affairs</div><div></div>

Türkiye Regulatory Lead

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

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

Regulatory Lead

Fortrea

<div><p><b>Start-Up Specialist (Contract Negotiator)</b></p><p><br>
 Location: office based, Istambul or home based</p><p></p><p><b>
Join our mission to advance clinical research.</b></p><p><br>
We&rsquo;re seeking a Site-Readiness and <b>Start-Up Specialist </b>to be the go-to expert for site agreements negotiation with sites in Turkey.</p><p></p><p><b>
What You&rsquo;ll Do:</b></p><ul><li>
Perform initial and amended contract and budget negotiations with the sites</li><li>
Serve as the primary contact for investigative sites during start-up and maintenance</li><li>
Prepare and manage essential regulatory documents for submissions</li><li>
Track timelines, flag risks, and support the team with regulatory expertise</li><li>
Act as a knowledge resource to train or mentor junior colleagues, when applicable</li></ul><p></p><p><b>
What You Bring:</b></p><ul><li>
At least 1 year of experience with contract negotiation</li><li>
Good knowledge of local procedures (submissions and communication via site portals)</li><li>
Good knowledge of MOH tariffs and their implementation in the site budgets</li><li>
Degree in life sciences or equivalent experience.</li><li>
Strong organizational skills, attention to detail, and proactive problem-solving</li><li>
Proficient English language skills</li></ul><p></p><p><b>
Nice to Have:</b></p><ul><li>
Experience with Turkish MOH regulatory systems and sites portals</li></ul><p></p><p><b>
Why Join Us?</b></p><p></p><p>
You&rsquo;ll be part of a dedicated, collaborative team driving impactful clinical studies. We offer a flexible work environment, continuous learning, and opportunities to grow within global trials.</p><p></p><p><b>
Apply now</b> to make a real difference in the future of health!</p><p></p><p>
Learn more about our EEO &amp; Accommodations request here.</p></div>

Start-up Specialist - Contract negotiation

CoinTR

<div>
 <p>
  <strong>
   About the Role:
  </strong>
 </p>
 <p>
  At CoinTR, we are committed to building a secure, transparent, and fully compliant digital asset ecosystem. We are seeking a Compliance Specialist to strengthen our regulatory compliance operations and ensure full adherence to both local and international standards.
 </p>
 <p>
  In this role, you will be responsible for implementing and monitoring compliance procedures, supporting internal audits, and ensuring that CoinTR&rsquo;s operations comply with MASAK, SPK, and other relevant regulations.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Responsibilities:
  </strong>
 </p>
 <ul>
  <li>
   Ensure company compliance with MASAK, SPK, and other applicable financial and crypto asset regulations.
  </li>
  <li>
   Oversee and review Know Your Customer (KYC) and Know Your Business (KYB) procedures to ensure compliance with regulatory standards.
  </li>
  <li>
   Contribute to the Suspicious Transaction Reporting (STR) process through data analysis and case evaluation.
  </li>
  <li>
   Review and improve internal procedures, risk assessments, and control mechanisms on a regular basis.
  </li>
  <li>
   Support internal and external audit processes by preparing and maintaining required documentation.
  </li>
  <li>
   Monitor new regulations, assess their impact, and assist in updating company policies accordingly.
  </li>
  <li>
   Promote compliance awareness across teams and support internal compliance training initiatives.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications:
  </strong>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree in Law, Economics, Business Administration, Finance, or a related field.
  </li>
  <li>
   Minimum 2 years of experience in compliance, audit, or risk management within financial services, banking, fintech, or crypto industries.
  </li>
  <li>
   Strong knowledge of AML/CFT, KYC, KYB, and other relevant MASAK regulatory frameworks.
  </li>
  <li>
   Excellent analytical and problem-solving skills with a strong attention to detail.
  </li>
  <li>
   Strong communication and interpersonal abilities.
  </li>
  <li>
   Fluency in English (both written and spoken) is preferred.
  </li>
  <li>
   Team-oriented mindset and ability to adapt to a fast-paced, dynamic environment.
  </li>
 </ul>
</div>


Compliance Officer

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