avukat

legal counsel

INTEC Energy Solutions

<div>
 <p>
  INTEC Energy Solutions delivers best-in-class services in Engineering, Procurement, Construction (EPC), Battery Energy Storage Systems (BESS), Development, Consultancy, and Operation &amp; Maintenance, along with New Energy Solutions.
 </p>
 <p>
  <br/>
 </p>
 <p>
  With a globally experienced team, INTEC has managed over 190 projects and achieved an impressive installed and secured capacity of 3.9 GWp. Headquartered in the United Kingdom, INTEC also operates offices in Germany, T&uuml;rkiye, Australia, New Zealand, Azerbaijan, Romania, and Mauritius, with plans for further expansion.
 </p>
 <p>
  <br/>
 </p>
 <p>
  As an international company, we are looking for a
  <strong>
   Legal Counsel
  </strong>
  based in
  <strong>
   Ankara.
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Responsibilities:
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Draft, review, and negotiate a wide range of contracts, including EPC agreements, supply and subcontractor agreements, NDAs, and service contracts.
  </li>
  <li>
   Provide contractual input during tender preparation and risk assessment stages.
  </li>
  <li>
   Ensure all contractual obligations are understood, tracked, and fulfilled by both internal teams and external parties.
  </li>
  <li>
   Collaborate closely with engineering, procurement, legal, project management, and finance teams to ensure consistency and compliance.
  </li>
  <li>
   Identify and mitigate contractual and commercial risks throughout the project lifecycle.
  </li>
  <li>
   Support in claims management, dispute resolution, and the preparation of notices and responses.
  </li>
  <li>
   Maintain organized records of all contracts and amendments, ensuring clear documentation and version control.
  </li>
  <li>
   Contribute to the development and continuous improvement of internal contract templates, policies, and procedures.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications &amp; Experience:
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   University degree in
   <strong>
    Law.
   </strong>
  </li>
  <li>
   <strong>
    2&ndash;5 years of relevant experience
   </strong>
   in contract negotiation and contract management, particularly related to
   <strong>
    EPC projects
   </strong>
   .
  </li>
  <li>
   Experience may be gained from a
   <strong>
    law firm
   </strong>
   ,
   <strong>
    consultancy
   </strong>
   , or an
   <strong>
    engineering/construction/energy company
   </strong>
   .
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Competencies:
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Familiarity with
   <strong>
    EPC contract structures
   </strong>
   ; knowledge of
   <strong>
    FIDIC contracts
   </strong>
   is a strong plus.
  </li>
  <li>
   Ability to
   <strong>
    review, revise, and draft EPC contracts
   </strong>
   and related subcontract and supply agreements.
  </li>
  <li>
   Comfortable
   <strong>
    participating in and managing contract negotiations
   </strong>
   with international clients, partners, and subcontractors.
  </li>
  <li>
   Strong
   <strong>
    communication and coordination skills
   </strong>
   , especially when working with internal stakeholders across legal, engineering, procurement, and commercial teams.
  </li>
  <li>
   <strong>
    Excellent written and spoken English
   </strong>
   is essential for effective communication and contract work in our international projects.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   What We Offer:
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   The opportunity to work on meaningful renewable energy projects in a fast-growing global industry.
  </li>
  <li>
   A collaborative, innovative, and mission-driven work environment.
  </li>
  <li>
   Competitive salary and benefits.
  </li>
  <li>
   Professional growth and learning opportunities.
  </li>
 </ul>
 <p>
 </p>
</div>


Legal Counsel

Migros Ticaret

<div>
 <p>
  <strong>
   <em>
    <u>
     Migros&rsquo;ta &Idot;yi Gelece&gbreve;i Birlikte Tasarlayal&inodot;m!
    </u>
   </em>
  </strong>
  🧡
 </p>
 <p>
  <br/>
 </p>
 <p>
  Hayat bir al&inodot;&scedil;veri&scedil; bizim i&ccedil;in, mutluluk al&inodot;p, mutluluk verdi&gbreve;imiz... Raflar&inodot;m&inodot;z &ouml;d&uuml;l ve ba&scedil;ar&inodot;larla dolu&hellip; 20 y&inodot;ld&inodot;r &ldquo;T&uuml;rkiye&rsquo;nin En Be&gbreve;enilen Perakende &Scedil;irketi&rdquo; se&ccedil;ilmek, T&uuml;rkiye&rsquo;nin ilk sadakat program&inodot;n&inodot; yaratmak, T&uuml;rk perakende m&uuml;&scedil;terisini kasiyersiz kasa ile tan&inodot;&scedil;t&inodot;rmak, Perakende sekt&ouml;r&uuml;nde ilk AR-GE merkezini kurmak ba&scedil;ar&inodot;lar&inodot;m&inodot;zdan sadece birka&ccedil; tanesidir.
 </p>
 <p>
  Migroslular olarak biz, Perakendenin ge&ccedil;mi&scedil;ine ve gelece&gbreve;ine &ccedil;ok merakl&inodot;y&inodot;z!
 </p>
 <p>
  T&uuml;rkiye&rsquo;de modern perakende sekt&ouml;r&uuml;n&uuml;n &ouml;nc&uuml;s&uuml; olarak, 1954&rsquo;ten bu yana bizim i&scedil;imiz, iyi gelece&gbreve;i tasarlamakt&inodot;r! Her Migroslu&rsquo;nun kendi kariyer hikayesini yaratmas&inodot;na f&inodot;rsat sa&gbreve;lad&inodot;&gbreve;&inodot;m&inodot;z &ldquo;&Idot;yi Gelecek Yolculu&gbreve;umuzun&rdquo; bir par&ccedil;as&inodot; olmak isterseniz, ba&scedil;vurunuzu bekliyoruz!
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <em>
    <u>
     Migros&rsquo;ta Bizler;
    </u>
   </em>
  </strong>
 </p>
 <p>
  😊 Yapt&inodot;&gbreve;&inodot;m&inodot;z her i&scedil;te mutluluk yarat&inodot;r&inodot;z.
 </p>
 <p>
  🤝 Kendimize g&uuml;venir, Kar&scedil;&inodot;m&inodot;zdakine g&uuml;ven verir ve g&uuml;ven duyar&inodot;z.
 </p>
 <p>
  🌿👫 Hassas noktam&inodot;z do&gbreve;a ve insand&inodot;r.
 </p>
 <p>
  🌟 &Idot;yi gelece&gbreve;e &ouml;nc&uuml;l&uuml;k ederiz.
 </p>
 <p>
  🏆 Potansiyeli a&scedil;ar&inodot;z b&uuml;y&uuml;k ba&scedil;ar&inodot;lar ya&scedil;ar&inodot;z.
 </p>
 <p>
  🚀 &Idot;yi fikirler geli&scedil;tirir "yok art&inodot;k" denilen fikirlere "var art&inodot;k" deriz.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Sizde Arad&inodot;&gbreve;&inodot;m&inodot;z &Ouml;zellikler Neler?
   </u>
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   &Uuml;niversitelerin Hukuk fak&uuml;ltelerinden mezun,
  </li>
  <li>
   En az 5 y&inodot;l &scedil;irketlerin hukuk departmanlar&inodot;nda g&ouml;rev alm&inodot;&scedil; ve/veya d&inodot;&scedil;ar&inodot;dan &scedil;irketlere hukuki dan&inodot;&scedil;manl&inodot;k sunmu&scedil; olan,
  </li>
  <li>
   Tercihen Perakende sekt&ouml;r&uuml;nden &ccedil;al&inodot;&scedil;m&inodot;&scedil; olan,
  </li>
  <li>
   &Ouml;zellikle i&scedil; hukuku, idare ve vergi hukuku, t&uuml;ketici hukuku ve perakende mevzuat&inodot;na hakim alan&inodot;nda tecr&uuml;beli,
  </li>
  <li>
   MS Office uygulamalar&inodot;na h&acirc;kim, sunum tecr&uuml;besi olan,
  </li>
  <li>
   &Idot;ngilizce bilen,
  </li>
  <li>
   &Ccedil;&ouml;z&uuml;m odakl&inodot;, planl&inodot;, tak&inodot;m &ccedil;al&inodot;&scedil;mas&inodot; ve zaman y&ouml;netimi konular&inodot;nda yetkin,
  </li>
  <li>
   Takip ve organizasyon yetene&gbreve;ine sahip.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Aram&inodot;za Kat&inodot;ld&inodot;&gbreve;&inodot;n&inodot;zda Neler Yapacaks&inodot;n&inodot;z?
   </u>
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  Hukuk departman&inodot;m&inodot;zda Mevzuat Uyum ve Ma&gbreve;aza Problemleri biriminde &Idot;&ccedil; Anadolu B&ouml;lgesinde g&ouml;rev alacakt&inodot;r.
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Ma&gbreve;azalara hukuki destek verilmesi,
  </li>
  <li>
   Hukuki dava ve &Idot;cra takibi,
  </li>
  <li>
   Arabuluculuk s&uuml;re&ccedil;lerinin takibi,
  </li>
  <li>
   &Idot;dari mercilerle g&ouml;r&uuml;&scedil;me ve itiraz s&uuml;re&ccedil;lerinin takibi,
  </li>
  <li>
   Mevzuat&inodot;n takibi ve hukuki inceleme ve g&ouml;r&uuml;&scedil; verilmesi.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Yetenek Kazan&inodot;m&inodot; S&uuml;recimiz Nas&inodot;l &Idot;lerleyecek?
   </u>
  </strong>
 </p>
 <ul>
  <li>
   &Ouml;zge&ccedil;mi&scedil; &Ouml;n De&gbreve;erlendirme S&uuml;reci
  </li>
  <li>
   &Idot;nsan Kaynaklar&inodot; G&ouml;r&uuml;&scedil;mesi
  </li>
  <li>
   De&gbreve;erlendirme Testleri
  </li>
  <li>
   Birim G&ouml;r&uuml;&scedil;mesi
  </li>
  <li>
   Referans Ara&scedil;t&inodot;rmas&inodot;
  </li>
  <li>
   Teklif S&uuml;reci 🤞🏻
  </li>
 </ul>
 <p>
  <em>
   *G&ouml;r&uuml;&scedil;&uuml;len pozisyonun niteli&gbreve;ine g&ouml;re s&uuml;re&ccedil; ad&inodot;mlar&inodot;nda de&gbreve;i&scedil;iklik ger&ccedil;ekle&scedil;ebilir.
  </em>
 </p>
 <p>
  <br/>
 </p>
 <p>
  📲Sosyal Medya kanallar&inodot;nda i&scedil; f&inodot;rsatlar&inodot;m&inodot;z&inodot; takip etmeye devam edebilirsiniz.
 </p>
 <p>
  <strong>
   #Migros #&Idot;yi&Idot;&scedil;&Idot;yiGelecek
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <em>
   *S&uuml;rd&uuml;r&uuml;lebilir b&uuml;y&uuml;me, e&scedil;it imkanlar ve farkl&inodot; bak&inodot;&scedil; a&ccedil;&inodot;lar&inodot;yla m&uuml;mk&uuml;nd&uuml;r. Lead Network Europe (NPO)&rsquo;nun Gold Partneri olarak; &Idot;nsan Haklar&inodot; ve F&inodot;rsat E&scedil;itli&gbreve;i politikam&inodot;z do&gbreve;rultusunda, Migros&rsquo;ta herkesin &scedil;effaf, adil ve e&scedil;it haklara sahip olmas&inodot; gerekti&gbreve;ine inan&inodot;yor ve &ccedil;al&inodot;&scedil;&inodot;yoruz.
  </em>
 </p>
 <p>
 </p>
</div>


Avukat (İç Anadolu)

PSI CRO

<div>
 <strong>
  Company Description
  <br/>
  <br/>
 </strong>
 We are the company that cares &ndash; for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
 <br/>
 <br/>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 We are in search of an experienced professional dedicated to developing strategic relationships with clinical research sites, with the aim of optimizing and advancing the progress of clinical trials.
 <br/>
 <br/>
 <strong>
  General Responsibilities:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Maintain and refine internal site databases in cooperation with Study Startup, Clinical Operations and Process Improvement
  </li>
  <li>
   Participate in the development of improvement strategies for the site identification process, implementation thereof, as well as related training activities
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Project Responsibilities:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Define the main study objectives and the optimal site profile
  </li>
  <li>
   Create initial list of potential sites
  </li>
  <li>
   Communicate with project teams on project/ regional level to fine-tune strategy and methodology of initial and follow-up site contacts depending on indication, regional specifics, and technologies in use
  </li>
  <li>
   In cooperation with the project team, maintain a study site identification tracker for further site evaluation and selection activities
  </li>
  <li>
   Liaise with project teams to evaluate status and progress of site identification, to identify and highlight any potential risks or issues to timelines or objectives
  </li>
  <li>
   In cooperation with Legal, perform due diligence check of regulatory and legal limitations applicable to the recommended investigators or clinical sites
  </li>
  <li>
   Support the project team throughout study startup and further on, whenever additional rounds of site identification are necessary, and/or additional information on the site/investigator is needed
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   University/college degree (Life Sciences/Pharmacy/Healthcare field is a plus), or an equivalent combination of education, training and experience
  </li>
  <li>
   Minimum 3 years of proven prior experience in on-site monitoring activities
  </li>
  <li>
   Full professional working proficiency in Turkish and English
  </li>
  <li>
   Understanding of Good Clinical Practice, local laws and applicable regulations in Turkey
  </li>
  <li>
   Communication and collaboration skills
  </li>
  <li>
   Demonstrated ability to work in a dynamic environment, under compressed deadlines across several projects, each with unique requirements
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Additional Information
  <br/>
  <br/>
 </strong>
 <strong>
  <strong>
   We offer:
   <br/>
   <br/>
  </strong>
 </strong>
 <ul>
  <li>
   Excellent, flexible working conditions
  </li>
  <li>
   Extensive training and supportive team
  </li>
  <li>
   Competitive salary and benefits package
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 Take your career to a whole new level. Join a company committed to prioritizing its employees and dedicated to investing in their ongoing professional growth and success.
</div>


Site Identification Specialist (Feasibility)

Kedrion Betaphar

<div><div>Kedrion Biopharma is a biopharmaceutical company specializing in the development, production and distribution of plasma-derived products. Kedrion has been producing plasma products for over 40 years and has a market presence in about 100 countries. Our employees are committed to the highest standards and therapies for the patients and clinicians in haematology, immunology, neurology, and transfusion medicine.</div><div></div><div><br>
We're looking for a <b>Scientific Service Manager,</b> to join our team in Turkey.</div><div></div><div><b><br>
Role Purpose:</b></div><div>
Scientific Service is the Responsible Person in charge of information on medicines which the Company puts on the market. Serves as technical and scientific reference, providing accurate, timely, fair-balanced medical information internally within Company and to external customers.</div><div>
He/She is responsible for fulfilling requirements for the Scientific Service role, according to the EU Directive 2001/83/EC in general and the local laws.</div><div></div><div><b><br>
Main Responsibilities:</b></div><br>
<div></div><ul><li>
Compiling and collating all information received from any source concerning the medicines that the Company puts on the market.</li><li>
Ensuring that product advertisements correspond to the content of the current effective marketing authorization/registration and comply with Turkey legal requirements for advertising and promotion, as well as Company procedures and policies.</li><li>
Ensuring that regulations on advertising &amp; promotion, external communication and interaction with healthcare professionals by the Company sales representatives are promptly implemented.</li><li>
Manages unsolicited requests for medical information from external customers (including product requests for unlicensed products in Turkey), in alignment with international best practices and Company policies and procedures.</li><li>
Reviews and approves evidence-based, balanced Medical Response Documents (MRDs) such as Standard Response Letters (SLRs) and Frequently Asked Questions (FAQs) dedicated to Turkey, ensuring compliance with local regulations.</li><li>
Reviews and approves Summary of Products Characteristics (SmPC) for products commercialized in the Country.</li><li>
Ensures records of medical inquiries, advertising &amp; promotion review/approval process, sales representatives training, in compliance with applicable regulations, Company policies and procedures.</li></ul><ul><li>
Maintains global interactions, mainly with Italy, relating to compliance with regulations for advertising &amp; promotion, therapeutic and medical information, and reporting activities.</li><li>
Responsible for setting up local procedures for the management of medical and scientific activities (Medical Inquiries Management, Promotional Material review, Scientific Training Management, etc.).</li><li>
Responsible for providing information and assistance to Regulatory Authorities, and for ensuring the decisions taken by the authorities or bodies responsible for monitoring advertising of medicinal products are immediately and fully complied with.</li></ul><div></div><div><b><br>
Requirements:</b></div><br>
<div></div><ul><li>
Professional experience in related fields of at least two years.</li><li>
Professional experience in quality management in pharmaceutical industry.</li></ul><ul><li>
Written and spoken fluency in Turkish and English.</li><li>
Education: university studies degree in the field of pharmacy</li><li>
Place of residence: Turkey
</li></ul><div><div><div><h2 class="jobSectionHeader"><b>Job Description</b></h2></div></div></div></div><div></div>

Scientific Service Manager

RÖNESANS HOLDİNG

<div>
 <p>
  <strong>
   Qualifications and Requirements
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  &ldquo;R&ouml;nesans Holding is among the signatories of the UN Global Compact, which calls on companies to align their strategies and operations with universal human rights, labor, environment and anti-corruption principles and to take care to advance social goals, and the United Nations Global Compact adopts the universally accepted declarations.
 </p>
 <p>
  <br/>
 </p>
 <p>
  R&ouml;nesans Holding is an employer that aims to ensure the implementation of human resources by observing transparent and ethical values &ZeroWidthSpace;without compromising the main principles of honesty, flexibility and development. All applications are made according to equal opportunities regardless of gender, language, religion, race and ethnic origin, and no discrimination is made.&rdquo;
 </p>
 <p>
  <br/>
 </p>
 <p>
  We are seeking a highly qualified
  <strong>
   Health, Safety, and Environmental Manager
  </strong>
  to join our team. This position will be based at our
  <em>
   Ankara Head Office
  </em>
  and will play a key role in overseeing the company's HSE operations on a local scale.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications and Requirements
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree in Engineering, Occupational Health and Safety, or a closely related field. (Preference for postgraduate qualifications in HSE or a related field.)
  </li>
  <li>
   Minimum of 10 years of relevant OHS experience, ideally in civil construction industry.
  </li>
  <li>
   Holding internationally recognized certifications/diploma such as NEBOSH, OSHA, or equivalent (A Grade OHS certification is highly preferred; B Grade acceptable depending on experience.)
  </li>
  <li>
   Solid understanding of ISO 45001 systems is required. Candidates holding an ISO 45001 Internal or Lead Auditor certification will be given preference.
  </li>
  <li>
   Strong knowledge and practical understanding of equipment and machinery management processes, including procurement, mobilization, operation, and maintenance phases, with particular emphasis on health and safety requirements.
  </li>
  <li>
   Fluency in English (both written and spoken) is essential;
  </li>
  <li>
   Ability and willingness to travel internationally and domestically on short notice. The candidate is expected to provide on-site support, audits, and consultancy to project teams across all company sites in T&uuml;rkiye, as required.
  </li>
  <li>
   Proficiency in conducting comprehensive incident investigations and leading root cause analysis initiatives.
  </li>
  <li>
   Strong organizational, research, and project management skills.
  </li>
  <li>
   Completion of military service is mandatory for male candidates.
  </li>
  <li>
   Advanced proficiency in Microsoft Office (Excel, Word, PowerPoint) and HSE-specific software.
  </li>
  <li>
   Ability to foster collaboration and teamwork while effectively leading teams across multiple locations.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   JOB DESCRIPTION
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Oversee the development and continuous improvement of the company&rsquo;s HSE Management System in line with corporate HSE Policy and objectives.Ensure that project-specific HSE Plans, Procedures, and Policies comply with national legislation and relevant international standards.Ensure that all occupational health and safety requirements are fully integrated into high-risk operational areas, including machinery and equipment procurement, commissioning, operation, and maintenance activities. This also covers supporting logistics processes such as warehouses, storage yards, and material handling operations. These activities include, but are not limited to, concrete batching plants, lifting operations, earthmoving machinery, and heavy equipment fleets, and must be conducted in accordance with corporate procedures and legal obligations.Collaborate with senior leadership and project teams to implement HSE initiatives effectively across all project sites.Monitor and update HSE procedures in response to evolving legislation, standards, and company directives, ensuring proactive compliance and strategic alignment.Develop and lead audit and review programs across all projects. Provide expert guidance on risk management, conduct trend analyses, and deliver actionable recommendations to enhance HSE performance and mitigate emerging risks.
  </li>
 </ul>
</div>


HSE Manager

Toll Group

<p><b>Company Description</b></p><p>About Toll</p><p>At Toll, we do more than just logistics - we move the businesses that move the world. Our 16,000 team members can help solve any supply chain challenge &ndash; big or small. We have been supporting our customers for more than 130 years. Today, we support more than 20,000 customers worldwide with 500 sites in 25 countries. We are proudly part of Japan Post. &ndash; www.tollgroup.com</p><p>Toll manages and delivers case management and a range of associated services on behalf of the Australian Department of Home Affairs to support Refugee and Humanitarian Visa clients with the medical assessment process and subsequent travel to Australia.</p><p><b>Job Description</b></p><p>The Role</p><p>We are looking for an Operations Manager based in Ankara, who will own and lead core operational functions including, regional service delivery elements, operational escalations, KPI performance and service recovery processes.</p><p>Toll is proud to work on behalf of the Australian Department of Home Affairs to deliver services in support of Refugees and Humanitarian visa clients. These services support the medical assessments and subsequent travel to Australia. As an Operations Manager, you will lead a team of logistics staff who operate in the field, including those who are airport based to ensure that services are delivered effectively and appropriately.</p><p>As a senior member of the regional team, you will directly support the Regional Manager with overall Assisted Passage Program deliverables and be a recognised 2IC supporting your region.</p><p><b>About You</b></p><p>To be successful in this role you will likely have:</p><p>&middot; Comprehensive awareness of Refugee &amp; Humanitarian resettlement operations and/or the delivery of services to refugees in long term host country environments.</p><p>&middot; Experience with leading case management &amp;; service delivery teams in large organisations in cross border environments.</p><p>&middot; Experience with identifying and resolving service delivery issues or failures.</p><p>&middot; Broad experience working within global organisations (commercial or non-profit) including the management of client deliverables.</p><p>&middot; Practical experience of leading operational teams in the delivery of support services to refugees.</p><p>&middot; Practical experience of managing risks and implementing strategies to mitigate those risks.</p><p>&middot; Previous experience in delivering services within a Child Safeguarding Framework.</p><p>&middot; Current or previous experience at leading, motivating and managing diverse teams across multiple locations.</p><p>Additional information:</p><p>Be connected</p><p>With a bold vision and innovative drive, join our 16,000 colleagues as we lead industry change and transform how customers best meet their global supply chain needs in a meaningful and sustainable way. There are countless opportunities to learn and make a real impact in shaping our industry's future. Grow with diverse challenges amongst a friendly and inclusive global culture. Take pride in building relationships that matter, because being connected is at the centre of what makes Toll great &ndash; it's what makes our possibilities endless.</p><p>Are you excited about this role but are concerned you don't meet all the requirements? If you have similar skills and are willing to learn, then we encourage you to apply anyway. We know that some people hesitate to apply to jobs unless they meet every single qualification. At Toll, we value a diverse, inclusive, and authentic workplace, so if you're interested in this role but your past experience doesn't align perfectly then please talk to us &ndash; you may be just the right candidate for this or other roles we have coming up.</p><p>At Toll everyone is welcome including those of all ages, ethnicities, genders and abilities. To find out more about us visit www.tollgroup.com/careers</p><p>You must be entitled to work in T&uuml;rkiye and be prepared to undertake pre-employment checks including a criminal history check and medical.</p><p>Job Type: Full-time</p><p>Ba&#351;vuru Sorular&#305;:</p><ul><li>Do you have current full legal working rights in T&uuml;rkiye?</li></ul><p>Dil:</p><ul><li>English and Turkish (Zorunlu)</li></ul>

Operations Manager - Türkiye and Central Asia

Cencora

<div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p>Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today!</p></div></div></div></div></div></div></div></div></div></div></div></div></div></div><p></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><h1 class="jobSectionHeader"><b>
Job Details
</b></h1></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div><p></p><p>Cencora Pharmalex is one of the leading service providers for the Pharmaceutical Industry globally and is specialized in all aspects of drugs and medical devices approval, of the market development and any action of effective product maintenance.</p><p></p><p><b>
Responsibilities:</b></p><ul><li>
Develop and maintain strong client relationships and actively explore opportunities for increased service support to Line Manager.</li><li>
Participation in regulatory processes to gain and maintain marketing authorizations for human and veterinary medicinal products (applications, renewals, variations) including medical devices, cosmetics, food supplements and herbal products.</li><li>
Preparation, review and compilation of documents within the framework of regulatory affairs projects.</li><li>
Communication with clients and Health Authorities.</li><li>
Support with scientific advice procedures and representation of clients with health authorities.</li><li>
Responsible for the planning and execution of client projects in accordance with KPIs. Coordination of project teams with colleagues and qualified external partners.</li><li>
General guidance (consultancy) of colleagues and clients regarding Regulatory Strategy and Procedure Management.</li><li>
Regulatory intelligence - develop and maintain personal regulatory knowledge, apply to client projects and actively share with colleagues.</li><li>
Present seminars and lectures for colleagues, clients and professional audiences. Active contribution and distribution of department relevant expertise.</li><li>
Support with regulatory strategy implementation and optimization.</li><li>
Comply with, maintain and contribute to optimizing internal processes.</li><li>
Support with commercial, marketing and business development activities including proposal input.</li><li>
Support respective lead in delivery to budget with accurate and timely reporting and provide project insights to address invoicing queries.</li><li>
In agreement with Head of REG providing on-site regulatory support to clients.</li><li>
The employee agrees to take over other reasonable tasks that are corresponding with their abilities upon agreement with their Line Manager/Practice Area Lead/Head of REG.</li></ul><p></p><p>
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Experience:</b></p><ul><li>
Proven experience, or demonstrable capability, in area of responsibility or similar field, advanced knowledge and insights required to perform complex tasks and strong practical knowledge of service area and how it impacts the related areas.</li></ul><p></p><p><b>
Education:</b></p><ul><li>
University degree in Life Science.</li></ul><p></p><p><b>
Skills:</b></p><ul><li>
Ability to implement tactical goals of customer or internal projects within daily work; ability to prioritize parallel tasks, identify potential road blocks and initiate appropriate counter measures.</li><li>
Structured, analytical, systematic and independent way of working; some discretion to take action consistent with operating policies, determines own priorities.</li><li>
Ability to analyze and solve problems and to develop pragmatic solutions for a given task or project. High service orientation.</li><li>
Ability to train and support junior/new colleagues in daily activities; ability to lead small project with clearly defined scope.</li><li>
Ability to manage internal and external (client) relationships on operational / day-to-day working level as well as client's team lead level.</li><li>
Good communication skills (written and verbally); capability to communicate issues and propose appropriate solutions to decision makers. Good presentation skills and confident appearance.</li><li>
English business fluent &amp; Turkish language</li></ul><p></p><h1 class="jobSectionHeader"><b>
What Cencora offers</b></h1><p></p><p>
Benefit offerings outside the US may vary by country and will be aligned to local market practice. The eligibility and effective date may differ for some benefits and for team members covered under collective bargaining agreements.</p><p></p>
Full time<p></p><h1 class="jobSectionHeader"><b>
Affiliated Companies</b></h1>
Affiliated Companies: PharmaLex Bulgaria, Jsc<p></p><h1 class="jobSectionHeader"><b>
Equal Employment Opportunity</b></h1><p>
Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law.</p><p></p><p>
The company&rsquo;s continued success depends on the full and effective utilization of qualified individuals. Therefore, harassment is prohibited and all matters related to recruiting, training, compensation, benefits, promotions and transfers comply with equal opportunity principles and are non-discriminatory.</p><p></p><p>
Cencora is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consistent with legal requirements. If you wish to request an accommodation while seeking employment, please call 888.692.2272 or email hrsc@cencora.com. We will make accommodation determinations on a request-by-request basis. Messages and emails regarding anything other than accommodations requests will not be returned</p></div>

Regulatory Manager

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