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regulatory affairs specialist

Envista Holdings

<div><p>Operating Company: DEXIS<br>
Location: Istanbul,Istanbul,TR<br>
Date Posted: November 11, 2025<br>
Req Number: R5024578</p></div><div></div>
<br><div><p><b>Job Description:</b></p> <p>Interprets federal/state/international regulations as they apply to our products, processes and/or procedures advises on impact of regulations, devises strategies for compliance, and liaison with regulatory bodies. Investigates and resolves compliance problems, questions and complaints. Audits and evaluates current policies, procedures, and documentation for compliance with regulations and statutes. Determine the need for and prepare regulatory submissions, negotiate the resolution of agency questions, and secure market clearance and/or approval and appropriate country licenses and certificates for new products and/or changes to existing products. Executes appropriately on product recalls. Respond to regulatory agency inquiries. Support the manufacturing lines when nonconformance exists to ensure appropriate regulatory assessments and requirements.</p><p> </p><p><b>Job Requirements:</b></p> <p><b>Reports to Role</b>: Head of RA Regions &amp; Registrations</p><p></p> <p><b>Location</b> (HQ or Region, Country, Site):</p> <p>Istanbul, Turkey, EH TURKEY SA&#286;LIK &Uuml;R&Uuml;NLER&#304; VE H&#304;ZMETLER&#304; L&#304;M&#304;TED &#350;&#304;RKET&#304;. Fully remote</p><p></p> <p><b><i>PURPOSE </i></b><i>&ndash; in a few sentences, briefly describe the overall purpose of the role, i.e. why the role exists</i></p> <p>The Regulatory Affairs Specialist supports regulatory affairs activities for international product registration by providing regulatory documentation and stakeholder support to ensure the timely regulatory approvals and maintenance of products in compliance with local regulatory requirements.</p><p></p> <p>The Regulatory Affairs Specialist is accountable for timely execution of regulatory strategies to support launch activities and maintain compliance status for international product registration.</p> <p><b><i>ACCOUNTABILITIES </i></b><i>&ndash; describe role accountabilities/responsibilities, i.e. what the role does. Should cover the following:</i></p> <p>The Regulatory Affairs Specialist is accountable for compliance and delivery for all assigned countries and registrations in Regions.</p> <p><b>Regions &amp; Registrations</b></p><ul> <li>Contribute to development and execution of regulatory strategies for respective department projects, compliance projects as well as lifecycle management activities.</li> <li>Contribute to execution of International RA support projects for market access to REGIONS and ensure all RA related elements &amp; requirements implemented.</li> <li>Align with local distributors and with local RA, understand requirements, and assists with the deliverables/ files related to preparing ROW submissions; uploads deliverables/ files into repository. Consults with others on these efforts as required.</li> <li>Prepare, order, and maintain oversight of all Free Sales Certificates, Certificates of Foreign Government and Country of Origin certificates requested for international regulatory approvals</li> <li>Prepare core documentation &quot;regulatory submission packages&quot; for new product registrations in international markets</li> <li>Prepare country specific documents for international regulatory approvals including, but not limited to manufacturer statements, Letters of Authorization and Power of Attorney</li> <li>Review submission documents prepared by local RA to be used in country registrations</li> <li>Support provision of regulatory guidance for Nobel Biocare IFU and labeling processes</li> <li>Conduct regulatory release and delisting of products using specialized regulatory software</li> <li>Is aware of procedures and only makes decisions in line with procedure on simple topics</li> <li>Plan out workload to deliver on time, able to make adjustments when required and prioritizing work together with manager</li> <li>Prepare, and follow-up on International regulatory assessments for product changes</li> <li>Closely monitoring together with local country representatives guidelines, regulations, changes in the marketplace and regulator positions for the assigned markets to ensure new requirements are caught, impact assessed and escalated if required</li> <li>Close gaps created due to changed or new local country requirements by initatin projects and/or incorporating into global processes.</li></ul><ul> <li>Support the provision of regulatory guidance to project teams in assigned projects and markets, in terms of requirements and related submission to support optimal timelines and required compliance levels.</li></ul><ul> <li>Support the assembly of documents and the submission to authorities in countries of responsibility</li> <li>Supports the monitoring of the regulatory environment and maintenance of the information resources</li> <li>Support internal and external audits in the audit preparation and audit back office</li> <li>Contributes and participates in the review of change requests to ensure compliance and the potential for regulatory submissions</li> <li>May assist with reviews of promotional materials.</li> <li>Has a yearly training program in place specified by manager.</li> <li>Support the creation and maintenance of regulatory procedures and templates.</li> <li>Can revise or create Technical Files.</li> <li>Support the review of labels and IFUs</li> <li>Support provision of regulatory guidance for Nobel Biocare IFU and labeling processes</li> <li>Tracks and maintains files on current status of licenses, registrations and product information as per agreed formats in the different systems in use by the organization</li> <li>Can collect the regulatory compliance status of main countries, contribute to regulatory status of other regions of devices affected by HHE/Deviation/CAPA/Recall.</li> <li>Provide internal trainings on requirements for area under their responsibility.</li> <li>Knows and understands the EBS philosophy and employs it in daily RA activities and standard work.</li> <li>Able to provide input in terms of activities required to be added to a DM or VPM.</li> <li>Trained on PSP procedures to solve standard problems; analyzes information and standard practices to make judgments.</li></ul> <p><b><i>KNOWLEDGE, SKILLS &amp; EXPERIENCE </i></b><i>&ndash; </i><i>Functional/technical competencies specific to the role and required to perform the role</i></p> <p><b>Critical Knowledge and Qualifications: </b><i>(what the role holder must know; including any required general or professional qualifications/education)</i></p><ul> <li>A minimum of a Bachelor&rsquo;s degree from accredited college or university is required.</li> <li>Basic knowledge of medical device quality management systems such as 21 CFR Part 820 and ISO 13485.</li> <li>Basic knowledge of international legislation in some countries.</li> <li>Knowledge of main general documents required as FSC &amp; legalization process</li></ul> <p><b>Critical Skills/technical know-how: </b><i>(what the role holder must be able to do)</i></p><ul> <li>Fluency in English a must. Further languages is an advantage.</li> <li>Able to communicate effectively with team members, project team members, manager and other stakeholders; this includes: able to listen and grasp key information, able to clearly convey straightforward information, able to read non-verbal communication, such as reading body language and able to give short presentations to RA team on straightforward information</li> <li>Demonstrates and advocates for working together in the spirit of openness, honesty and transparency that encourages engagement, collaboration, respectful interactions and trust.</li> <li>Seeks out diverse ideas, opinions and insights, and applies them in workplace.</li> <li>Works closely with direct team and project teams and starts building up network of colleagues, stakeholders, SMEs and customers.</li> <li>Is aware of procedures and regulations and is able to assess situation on simple topics</li> <li>Creates clarity and direction amid complexity and develops solutions</li> <li>Never compromises on patient safety.</li> <li>Have a positive attitude and 'can do' spirit</li> <li>Ability to be flexible and adaptable. Maintain a professional demeanor under pressure.</li> <li>Demonstrate a commitment to getting the job done right and on time and prioritizing work together with manager.</li> <li>Be able to manage several projects, tasks products and/or countries work load and takes ownership.</li> <li>Have attention to detail to task in hand but also start seeing bigger picture / wider process.</li> <li>Know when to ask questions.</li></ul><p></p> <p><b>Critical Experience:</b></p><ul> <li>Minimum 2 years' experience in regulatory affairs or associated field within medical device industry.</li></ul> <h2 class="jobSectionHeader"><b>COMPETENCIES &ndash; Essential for the role</b></h2> <p><i>Determine max. 6 competencies, refer to List and Definition of Competencies</i></p><ul> <li>Continuous Improvement</li> <li>Planning and Organizing</li> <li>Strategy execution</li> <li>Driving Execution</li> <li>Learning Orientation</li> <li>Actively contribute to successful team</li></ul><p> </p><p><b>Operating Company:</b></p> <p>DEXIS</p> <p>Envista and its family of companies (Envista) will not accept unsolicited resumes from any source other than directly from a candidate. Envista will consider unsolicited referrals and/or resumes submitted by vendors such as search firms, staffing agencies, professional recruiters, fee-based referral services and recruiting agencies (Agency) to have been referred by the Agency free of charge and Envista will not pay a fee for any placement resulting from the receipt such unsolicited resumes. An Agency must obtain advance written approval from Envista's internal Talent Acquisition or Human Resources team to submit resumes, and then only in conjunction with a valid fully-executed contract approved by the Global Talent Acquisition leader and in response to a specific job opening. Envista will not pay a fee to any Agency that does not have such agreement and written approval in place.</p></div>

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

Gilead Sciences

<div><div>At Gilead, we&rsquo;re creating a healthier world for all people. For more than 35 years, we&rsquo;ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer &ndash; working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world&rsquo;s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.</div><div><br>
Every member of Gilead&rsquo;s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we&rsquo;re looking for the next wave of passionate and ambitious people ready to make a direct impact.</div><div><br>
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.<br>
<br>
Job Description</div><div><br>
Regulatory Affairs Manager Turkiye; is responsible from managing RA submissions &amp; supporting Clinical Trials applications and will serve as a core member of the affiliate Regulatory Team interacting with local Regulatory Authorities and other stakeholders to ensure that the company complies with country&rsquo;s applicable legislations.</div><div></div><div>
Knowledge &amp; Details:</div><ul><li><div>
Manage regulatory submissions to local HA submissions inc. but not limited to Pre-MAA related activities (GMP &amp; prioritization applications), marketing Authorisation (MA) applications &amp; variations and other MA maintenance applications, in line with local HA expectations, Gilead SOPs and business objectives for assigned product(s) or projects.</div></li><li><div>
Stay up to date with local and global regulatory requirements (including ICH), internal policies and support the organization in adapting to legislative changes.</div></li><li><div>
Responsible from ensuring the updates to commercial product packaging and labelling in line with product licenses.</div></li><li><div>
Manage clinical trial applications, amendments, and notifications. Collaborate with Clinical Operations and the CT Hub to complete CT submissions to MOH timely and interacts with cross-functional teams internally and externally to ensure submission package fulfils the MoH requirements on time.</div></li><li><div>
Ensure ongoing clinical trials comply with local legislation and oversee investigational product packaging and labelling approvals.</div></li><li><div>
Plan regulatory and clinical timelines and strategies under the guidance of the Regulatory Affairs Director.</div></li><li><div>
Ensure good and strong relationships with functional areas of the local organization (Medical Affairs, Commercial, Market Access, Legal, etc.) and with Gilead Sciences Global/Regional RA in order to ensure the success of local and international business results from the regulatory point of view.</div></li><li><div>
Build and maintain networks with regulatory stakeholders, including decision-makers and influencers.</div></li><li><div>
Develop and implement regulatory and clinical trial strategies, and manage negotiations with health authorities.</div></li><li><div>
Actively contribute to local and global initiatives that improve regulatory processes.</div></li></ul><div></div><div>
Professional Experience / Key Skills</div><ul><li><div>
Solid experience in total in Regulatory Affairs &amp; Clinical Trials (if possible) related experience in the Pharmaceutical / Biotech Industry. An advanced degree is desirable.</div></li><li><div>
Degree in Pharmaceutical Sciences or equivalent discipline is preferred.</div></li></ul><ul><li><div>
Proven ability to prioritize, conduct, and manage time to meet project deadlines.</div></li><li><div>
Good influencing and negotiating skills. Must be capable of developing and implementing regulatory initiatives and managing negotiations with Regulatory Authorities.</div></li><li><div>
Demonstrates leadership skills with a sphere of influence externally, cross-functionally and within the RA and the affiliate.</div></li><li><div>
Strong focus on achievement of goals and continuous improvement</div></li><li><div>
Solution-oriented and innovative; can identify creative options for resolving issues that respond to multiple stakeholder interests and needs.</div></li><li><div>
Having excellence in multiple project management, good communication and interpersonal skills.</div></li><li><div>
Be an analytical thinker, problem solver, proactive, initiative taker, creative personality</div></li><li><div>
Team player who actively contributes to the team in order to complete tasks, meet goals or manage projects, actively listen others, respect ideas and aim to improve the process.</div></li><li><div>
Fluency in spoken and written English.</div></li><li><div>
Good decision-making skills are important.</div></li><li><div>
Excellent verbal, written, organization skills and interpersonal communication skills required.</div></li></ul><div></div><div><br>
Equal Employment Opportunity (EEO)</div><div>
It is the policy of Gilead Sciences, Inc. and its subsidiaries and affiliates (collectively &quot;Gilead&quot; or the &quot;Company&quot;) to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law, all employment actions relating to issues such as compensation, benefits, transfers, layoffs, returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds, which may include an individual&rsquo;s gender, race, color, national origin, ancestry, religion, creed, physical or mental disability, marital status, sexual orientation, medical condition, veteran status, and age, unless such protection is prohibited by federal, state, municipal, provincial, local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws.</div><div></div><div><br>
For Current Gilead Employees and Contractors:</div><div>
Please apply via the Internal Career Opportunities portal in Workday.</div></div>

Regulatory Affairs Manager

Binance

<div><div>Binance is a leading global blockchain ecosystem behind the world&rsquo;s largest cryptocurrency exchange by trading volume and registered users. We are trusted by over 280 million people in 100+ countries for our industry-leading security, user fund transparency, trading engine speed, deep liquidity, and an unmatched portfolio of digital-asset products. Binance offerings range from trading and finance to education, research, payments, institutional services, Web3 features, and more. We leverage the power of digital assets and blockchain to build an inclusive financial ecosystem to advance the freedom of money and improve financial access for people around the world.</div><div></div><div><br>
As a Regulatory Counsel for Turkey, you will assist with a broad range of legal and regulatory matters related to financial products and services in the FinTech, crypto, and blockchain sectors within Turkey. You will provide expert legal and regulatory support to local and global business teams, ensuring compliance with Turkish laws and regulations, and help drive the company&rsquo;s strategic initiatives in this rapidly evolving market.</div>
<h3 class="jobSectionHeader"><b>Key Responsibilities:</b></h3><ul><li>
Advise on regulatory perimeter assessments, licensing and registration applications, product compliance, regulatory investigations, advertising, and consumer protection matters specific to Turkey&rsquo;s financial and crypto regulatory framework.</li><li>
Support local and global business teams on product launches, marketing campaigns, and promotional activities by providing legal/regulatory guidance, drafting product terms, and ensuring compliance with Turkish regulatory requirements.</li><li>
Maintain strong working relationships with internal stakeholders through effective contract management, budget oversight, and timely legal advice.</li><li>
Keep abreast of the latest developments in Turkish laws and regulations affecting crypto, FinTech, and blockchain industries, providing strategic, forward-looking advice to foster compliance and mitigate risks.</li><li>
Proactively identify legal and regulatory challenges and propose practical solutions to support business objectives.</li><li>
Collaborate closely with legal teams across different time zones to provide seamless, around-the-clock legal support.</li><li>
Manage relationships with external counsel and regulatory authorities in Turkey.</li><li>
Represent the company in legal proceedings or regulatory matters in Turkey when required, safeguarding the company&rsquo;s interests.</li></ul><h3 class="jobSectionHeader"><b>
Requirements:</b></h3><ul><li>
Qualified to practice law in Turkey.</li><li>
5-10 years of post-qualification experience, preferably with a focus on financial services, FinTech, crypto, or blockchain sectors.</li><li>
Law degree from a reputable university; advanced degrees (e.g., Master&rsquo;s in Financial or Technology Law) are a plus.</li><li>
Experience working in a top-tier law firm or in-house legal team with exposure to Turkish financial regulatory authorities.</li><li>
Strong knowledge of Turkish financial, crypto, and consumer protection regulations.</li><li>
Proven ability to work independently and pragmatically in a fast-paced, global environment.</li><li>
Excellent project management skills and ability to coordinate with cross-functional teams across multiple locations and cultures.</li><li>
Strong time management skills to handle multiple priorities and meet tight deadlines.</li><li>
Passionate about FinTech innovation and cryptocurrency adoption in Turkey.</li></ul><div><b>
Why Binance</b></div><ul><li>Shape the future with the world&rsquo;s leading blockchain ecosystem</li><li>Collaborate with world-class talent in a user-centric global organization with a flat structure</li><li>Tackle unique, fast-paced projects with autonomy in an innovative environment</li><li>Thrive in a results-driven workplace with opportunities for career growth and continuous learning</li><li>Competitive salary and company benefits</li><li>Work-from-home arrangement (the arrangement may vary depending on the work nature of the business team)</li></ul><div></div><div><br>
Binance is committed to being an equal opportunity employer. We believe that having a diverse workforce is fundamental to our success.</div><div><i>
By submitting a job application, you confirm that you have read and agree to our </i><b><i>Candidate Privacy Notice</i></b><i>.</i></div>
<p>
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.</p></div>

Regulatory Counsel - Türkiye

Boehringer Ingelheim

<p></p><div><p><b>&#305;:
</b></p><ul><li>Veteriner a&#351;&#305;/ila&ccedil;/yem katk&#305; &uuml;r&uuml;nlerimizim ruhsatland&#305;rma s&uuml;re&ccedil;lerinin y&uuml;r&uuml;t&uuml;lmesi ve takibi
</li><li>Ruhsat ba&#351;vurular&#305; i&ccedil;in gerekli dok&uuml;mantasyonun haz&#305;rlanmas&#305; ve ilgili otoritelerle ileti&#351;imin ve takibinin sa&#287;lanmas&#305;
</li><li>Mevzuat de&#287;i&#351;ikliklerinin takip edilerek s&uuml;re&ccedil;lere entegre edilmesi
</li><li>Dosya g&uuml;ncellemeleri, varyasyon ba&#351;vurular&#305; ve ruhsat yenileme i&#351;lemlerinin ger&ccedil;ekle&#351;tirilmesi
</li><li>&#304;&ccedil; ve d&#305;&#351; payda&#351;larla etkin ileti&#351;im ve koordinasyonun sa&#287;lanmas&#305;
</li>GMP Denetim ve incelemelerde ruhsatland&#305;rma s&uuml;re&ccedil;lerine destek verilmesi<br>
<li>
</li></ul><p></p><p><b>Aranan Yetkinlikler:
</b></p><ul><li>&Uuml;niversitelerin tercihen Veteriner veya Eczac&#305;l&#305;k, Kimya, Biyoloji ya da ilgili b&ouml;l&uuml;mlerinden mezun
</li><li>Tercihen ila&ccedil; sekt&ouml;r&uuml;nde ruhsatland&#305;rma alan&#305;nda en az 1-2 y&#305;l deneyimli
</li><li>T&uuml;rkiye ve uluslararas&#305; ruhsatland&#305;rma mevzuat&#305;na hakim
</li><li>&#304;yi derecede &#304;ngilizce bilen
</li><li>MS Office programlar&#305;n&#305; etkin kullanabilen
</li><li>Analitik d&uuml;&#351;&uuml;nme ve problem &ccedil;&ouml;zme becerisine sahip
</li><li>Tak&#305;m &ccedil;al&#305;&#351;mas&#305;na yatk&#305;n, ileti&#351;im becerileri g&uuml;&ccedil;l&uuml;
</li><li>Planlama ve organizasyon yetene&#287;i geli&#351;mi&#351;
</li><li>Sorumluluk sahibi, dikkatli ve detay odakl&#305;</li></ul></div>

Regulatory Affairs Executive

Mars Athletic Club

<div>
 <p>
  As Turkey&rsquo;s largest fitness community with our brands
  <strong>
   MAC/One, MACFit, MAC Studio, and NuSpa
  </strong>
  , we are looking for a
  <strong>
   Compensation and Benefits Specialist
  </strong>
  to join our
  <strong>
   People &amp; Culture team
  </strong>
  at our
  <strong>
   headquarters in Ortak&ouml;y
  </strong>
  .
 </p>
 <p>
  Being part of
  <strong>
   MAC
  </strong>
  means joining a community that is constantly evolving, improving, and moving toward a better life.
 </p>
 <p>
  Here, ideas are valued, team spirit is supported, and feeling good is just as important as working efficiently.
 </p>
 <p>
  If you want to be part of our well-being community, we look forward to your application.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications and Skills
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s or Master&rsquo;s degree graduate,
  </li>
  <li>
   Minimum
   <strong>
    5 years of experience
   </strong>
   in payroll and compensation processes within Human Resources,
  </li>
  <li>
   Knowledge of
   <strong>
    Labor Law
   </strong>
   ,
   <strong>
    Social Security
   </strong>
   ,
   <strong>
    incentive programs
   </strong>
   , and
   <strong>
    &Idot;&Scedil;KUR procedures and regulations
   </strong>
   ,
  </li>
  <li>
   Experienced in
   <strong>
    Social Security incentive calculations
   </strong>
   ,
  </li>
  <li>
   Proficient in
   <strong>
    personnel affairs
   </strong>
   and
   <strong>
    timekeeping (attendance) processes
   </strong>
   ,
  </li>
  <li>
   Strong
   <strong>
    follow-up
   </strong>
   and
   <strong>
    attention to detail
   </strong>
   ,
  </li>
  <li>
   Preferably experienced in the
   <strong>
    retail sector
   </strong>
   ,
  </li>
  <li>
   Strong
   <strong>
    interpersonal
   </strong>
   and
   <strong>
    teamwork skills
   </strong>
   ,
  </li>
  <li>
   Analytical thinking and problem-solving ability,
  </li>
  <li>
   Proficient in
   <strong>
    MS Office programs
   </strong>
   ,
  </li>
  <li>
   Preferably experienced with
   <strong>
    Logo payroll software
   </strong>
   ,
  </li>
  <li>
   Knowledge of
   <strong>
    disciplinary procedures
   </strong>
   (such as written warnings, defense requests, and termination processes),
  </li>
  <li>
   Strong
   <strong>
    planning, tracking, and reporting
   </strong>
   skills.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   What Awaits You in This Role
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   End-to-end management of
   <strong>
    payroll processes
   </strong>
   ,
  </li>
  <li>
   Tracking and execution of
   <strong>
    government incentive processes
   </strong>
   ,
  </li>
  <li>
   Managing
   <strong>
    Labor Law
   </strong>
   ,
   <strong>
    Social Security
   </strong>
   , and
   <strong>
    &Idot;&Scedil;KUR
   </strong>
   processes,
  </li>
  <li>
   Ensuring all
   <strong>
    personnel affairs, payroll, and legal processes
   </strong>
   of our employees are executed in line with relevant regulations,
  </li>
  <li>
   Conducting and following up on
   <strong>
    official correspondence
   </strong>
   ,
  </li>
  <li>
   Maintaining
   <strong>
    personnel files
   </strong>
   in an accurate, complete, and up-to-date manner and ensuring
   <strong>
    system entries
   </strong>
   ,
  </li>
  <li>
   Following up on
   <strong>
    new hires
   </strong>
   and
   <strong>
    termination processes
   </strong>
   ,
  </li>
  <li>
   Taking an active role in
   <strong>
    salary payments
   </strong>
   and
   <strong>
    employee benefits processes
   </strong>
   ,
  </li>
  <li>
   Preparing
   <strong>
    reports
   </strong>
   related to area of responsibility,
  </li>
  <li>
   Tracking and controlling
   <strong>
    employee leave processes
   </strong>
   .
  </li>
 </ul>
 <p>
 </p>
</div>


Compensation Benefits Specialist

Trispera Pharma Solutions

<div>
 <p>
  <strong>
   Who We Are
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  Trispera is a dynamic medical affairs and pharmaceutical distribution company based in Istanbul, T&uuml;rkiye, with a dedicated focus on rare diseases. As a young and agile start-up, we are committed to ethical business practices and value development-driven collaboration.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Job Description
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  We are seeking a Medical Doctor or Pharmacist with proven experience as a Regional Medical Manager to join our growing team. The successful candidate will play a pivotal role in leading our medical affairs operations in the field of rare diseases.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Responsibilities
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  &bull; Act as the primary point of contact for healthcare professionals (HCPs), ensuring clear, consistent, and effective communication with all external stakeholders. Establish and maintain trusted scientific partnerships through regular, high-quality medical interactions. This is a field-based role, requiring regular on-site interactions with HCPs three days per week.
 </p>
 <p>
  &bull; Provide up-to-date and relevant scientific and product information to key opinion leaders and the broader medical community to foster clinical confidence and understanding.
 </p>
 <p>
  &bull; Map patient journeys, diagnostic practices, and treatment pathways while developing peer-to-peer relationships with relevant HCPs.
 </p>
 <p>
  &bull; Organize and participate in medical meetings, advisory boards, and congress-related engagements.
 </p>
 <p>
  &bull; Develop and implement scientific communication strategies. Support the creation and review of publications in alignment with the company&rsquo;s scientific narrative.
 </p>
 <p>
  &bull; Review medical communication tools, educational resources, and promotional materials for scientific accuracy and regulatory compliance.
 </p>
 <p>
  &bull; Effectively communicate the medical value of the company&rsquo;s products to both internal and external stakeholders.
 </p>
 <p>
  &bull; Identify educational gaps among HCPs and deliver scientific, non-promotional presentations to address those needs.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications and Skills
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  &bull; MD or PharmB degree,
 </p>
 <p>
  &bull; Minimum 5 years of experience in the pharmaceutical industry (preferred),
 </p>
 <p>
  &bull; Minimum 2 years of experience in the field of rare diseases (preferred),
 </p>
 <p>
  &bull; Background in endocrinology, metabolism, oncology, or hematology (preferred),
 </p>
 <p>
  &bull; Experience in start-up environments or adaptability to fast-paced, agile settings,
 </p>
 <p>
  &bull; Excellent command of both written and spoken English and Turkish,
 </p>
 <p>
  &bull; High level of personal discipline, professionalism, and adherence to ethical standards,
 </p>
 <p>
  &bull; Strong interpersonal and communication skills,
 </p>
 <p>
  &bull; Comfortable working within a matrix management model,
 </p>
 <p>
  &bull; Flexibility with working hours,
 </p>
 <p>
  &bull; Based in Istanbul,
 </p>
 <p>
  &bull; For male candidates: Completion of military service (if applicable).
 </p>
</div>


Regional Medical Manager

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