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associate director gvp gcp quality assurance auditor

Organon Pharmaceuticals

<p></p><div><p><b>The Position</b></p><p>
The Associate Director, GVP/GCP Quality Assurance Auditor, is responsible for ensuring quality and compliance with local and international regulatory requirements by conducting audits of Organon Processes, Affiliates, Vendors, Business Partners, and Investigator sites. The Associate Director is responsible for accepting audit assignments, performing audit pre-work, conducting audits and ensuring post audit activities are completed within defined timeframes. This role provides guidance to internal stakeholders, assisting in the establishment of the company's compliance strategy and the resolution and prevention of compliance risks.</p><p></p><p><b>
Responsibilities</b></p><ul><li><p>
Schedule and conduct assigned GVP/GCP audits in accordance with the global audit plan ensuring compliance with local and international guidelines and regulations.</p></li><li><p>
Prepare audit reports and manage follow-up activities within established timelines.</p></li><li><p>
Maintain broad-based expertise in Organon Policies, Procedures and Guidelines, local and global regulatory requirements, etc., pertinent to GCP and GVP. Maintain awareness of evolving industry and regulatory trends/regulations.</p></li><li><p>
Obtain and maintain cutting-edge knowledge, and application, for various Quality auditing topics.</p></li><li><p>
Generate and present comprehensive presentations/summary of audit issues for effective communication to all levels, as needed.</p></li><li><p>
Leads initiatives / drive results in various projects, as assigned, to maintain the effectiveness and efficiency of the audit program, and to ensure the audit program continues to meet company and regulatory expectations.</p></li><li><p>
Supports the implementation and maintenance of the GVP/GCP risk-based strategy, including assistance in the development of the annual audit plan and maintenance of the audit tool.</p></li><li><p>
Reviews and provides input into the quality sections of the Pharmacovigilance System Master File (PSMF)</p></li><li><p>
Supports regulatory inspections and external audits, when required.</p></li><li><p>
Train and mentor junior team members.</p></li></ul><p></p><p><b>
Required Education, Experience, and Skills
</b></p><ul><li><p>A minimum of a Bachelor&rsquo;s degree in a relevant scientific field (Pharmacy, Life Sciences, etc.).</p></li><li><p>
Fluency in written and spoken English; additional language skills a plus.</p></li><li><p>
Minimum of ten (10) years of experience in the pharmaceutical industry or regulatory agency related to Quality Systems and Quality Assurance (e.g., clinical trial quality, pharmacovigilance, regulatory)</p></li><li><p>
Minimum of one (1) years of experience in GVP and/or GCP auditing with EU/FDA /global regulatory requirements</p></li><li><p>
Strong knowledge of EMA, FDA and ICH guidelines in GCP and GVP and proficiency in interpreting and applying regulatory requirements and guidelines</p></li><li><p>
Attention to detail and ability to work independently in a virtual environment</p></li><li><p>
Proficiency in Microsoft applications (Word, Excel, PowerPoint, Outlook)</p></li><li><p>
Excellent/accomplished communication, negotiation, facilitation, influencing, and strategic thinking skills at all levels of organization Availability to travel up to 20% of time.</p></li></ul><p></p><p>
Primary skills include but are not limited to:</p><p></p><p>
Collaboration and Partnering: Demonstrates ability to work in partnership with others within the Company and external partners to accomplish quality goals; possesses advanced leadership skills.</p><p></p><p>
Communication Skills: Strong verbal skills and experienced effective writing skills.</p><p></p><p>
Project Management: Demonstrates ability to organize work efforts, prioritization of tasks and utilize appropriate resources to deliver or support work products in accordance with timelines and appropriate regulations.</p><p></p><p>
Decision Making: Demonstrates skills to utilize knowledge, networks, and data to make rapid and appropriate decisions and to determine when escalation of issues is necessary.</p><p></p><p>
Business Operations/Knowledge of Field: Demonstrates knowledge of regulations. Regulatory and business trends and applies this knowledge to optimize daily activities and ensure the functional areas within Research and Development are compliant with regulations and appropriate procedures.</p><p></p><p><b>
Secondary Job Description</b></p><p></p><p><b>
Who We Are:
</b></p><p>Organon delivers ingenious health solutions that enable people to live their best lives. We are a $6.5 billion global healthcare company focused on making a world of difference for women, their families and the communities they care for. We have an important portfolio and are growing it by investing in the unmet needs of Women&rsquo;s Health, expanding access to leading biosimilars and touching lives with a diverse and trusted portfolio of health solutions. Our Vision is clear: A better and healthier every day for every woman.</p><p></p><p>
As an equal opportunity employer, we welcome applications from candidates with a diverse background. We are committed to creating an inclusive environment for all our applicants.</p><p></p><p><b>
Search Firm Representatives Please Read Carefully</b><br>
Organon LLC, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.</p><p></p><p><b>
Annualized Salary Range</b></p><p></p><p><b>
Annualized Salary Range (Global)</b></p><p><b>
Annualized Salary Range (Canada)</b></p><p><b>
Please Note: Pay ranges are specific to local market and therefore vary from country to country.</b></p><p></p><p><b>
Employee Status:
</b></p>Regular<p></p><p><b>
Relocation:</b></p>
No relocation<p></p><p><b>
VISA Sponsorship:</b></p><p></p><p><b>
Travel Requirements: Organon employees must be able to satisfy all applicable travel and credentialing requirements, including associated vaccination prerequisites</b></p><p></p><p><b>
Flexible Work Arrangements:</b></p><p></p><p><b>
Shift:</b></p><p></p><p><b>
Valid Driving License:</b></p><p></p><p><b>
Hazardous Material(s):</b></p><p></p><p><b>
Number of Openings:
</b></p>1<p><b><br>
Requisition ID:</b>R537874</p></div>

Associate Director, GVP/GCP Quality Assurance Auditor

PwC Türkiye

<div>
 <p>
  <strong>
   At PwC, our purpose is to build trust in society and solve important problems
  </strong>
 </p>
 <p>
  We&rsquo;re a network of firms in 151 countries with more than 360,000 people who are committed to delivering quality in assurance, advisory and tax services. PwC has been providing services to the Turkish business world since 1981, with a professional staff of 2.800 in &Idot;stanbul, Ankara, Bursa, &Idot;zmir and Eski&scedil;ehir.
 </p>
 <p>
  <br/>
 </p>
 <p>
  At PwC, we are a group of employees with a rich variety of knowledge, skills and competencies. PwC&rsquo;s problem-solving teams come together in unusual, untraditional new ways from various disciplines to create The New Equation strategy. The New Equation is our global strategy with a human-centered and tech-powered approach, that focuses on our clients and all stakeholders, and helps them build trust and drive sustainable results.
 </p>
 <p>
  <br/>
 </p>
 <p>
  As part of the continuous growth of our Risk Modelling practice and significantly increasing further market opportunities, PwC &ldquo;
  <strong>
   Risk Assurance &ndash; Risk Modelling&rdquo;
  </strong>
  ' team is looking for new
  <strong>
   Associate / Senior Associates
  </strong>
  to be a part of our expanding practice.
 </p>
 <p>
  <br/>
 </p>
 <p>
  As an Associate/Senior Associate in Risk Assurance Services at PwC, you will play a crucial role in assisting clients with identifying, managing, and mitigating risks related to their business operations. Working within our dynamic and collaborative team, you will contribute to delivering high-quality risk management solutions that help clients maintain trust and confidence in their financial reporting, regulatory compliance, and overall business processes.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Qualifications
   </u>
  </strong>
 </p>
 <ul>
  <li>
   Graduated from University&rsquo;s related Engineering, Economics, Statistics, Econometrics or Mathematics departments (Master&rsquo;s degree in business, finance or a quantitative field is preferred)
  </li>
  <li>
   Minimum of 2 years of experience in Financial Risk Management and machine learning models is a plus
  </li>
  <li>
   Prior experience in financial risk management with a focus of credit risk is a plus
  </li>
  <li>
   Strong analytical and statistical skills with the ability to think critically and solve complex problems.
  </li>
  <li>
   Experience in IRB and/or IFRS9 concepts and modeling techniques is a plus
  </li>
  <li>
   Excellent communication skills, both written and verbal, to articulate findings and recommendations effectively.
  </li>
  <li>
   High attention to detail and a commitment to delivering accurate and reliable work.
  </li>
  <li>
   Proficiency in MS Excel
  </li>
  <li>
   Excellent writing and communications skills (in English)
  </li>
  <li>
   Project management experience is a plus
  </li>
  <li>
   Experience in working with large datasets is a plus
  </li>
  <li>
   Proficiency in SQL, SAS, Python,R is a plus (knowledge of at least two of these languages at an advanced level)
  </li>
  <li>
   Ability to work effectively in a team environment and collaborate with diverse groups of professionals.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Job Description
   </u>
  </strong>
 </p>
 <p>
  The prospective candidates are expected to deliver risk management and measurement solutions to the financial and non-financial institutions through engagements and practice development. Prospective candidates are expected to:
 </p>
 <ul>
  <li>
   Coordinate with clients to identify their risk management needs especially in the area of financial risks and risk modelling and develop strategies within these frameworks and gather information and understand client organization and processes
  </li>
  <li>
   Organize meetings and coordinate different project parties
  </li>
  <li>
   Analyze/map business processes in risk management, document and present business process and methodologies
  </li>
  <li>
   Contribute to the review and/or evaluation of risk measurement data and methodologies and risk management policies
  </li>
  <li>
   Contribute to the risk modeling process using statistical and econometric analysis techniques
  </li>
  <li>
   Execute appropriate analytic strategies
  </li>
  <li>
   Mine raw data sets to perform any analyses that are needed
  </li>
  <li>
   Liaison with other PwC line of services and with third party other advisors in the projects to maximize efficiency and ensure to deliver highest quality services
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Responsibilities:
  </strong>
 </p>
 <ul>
  <li>
   Utilize data analytics tools to analyze large datasets and identify patterns or anomalies that could indicate potential risks or control deficiencies.
  </li>
  <li>
   Develop and maintain positive working relationships with clients, actively listen to their concerns, and communicate effectively to address their needs.
  </li>
  <li>
   Work closely with other team members to deliver integrated solutions to clients, leveraging cross-functional expertise to provide comprehensive risk assurance services.
  </li>
  <li>
   Stay abreast of industry trends, emerging risks, and evolving best practices in risk management and assurance. Engage in continuous professional development to enhance skills and knowledge.
  </li>
  <li>
   Prepare clear and concise workpapers and reports, detailing the results of risk assessments, testing procedures, and recommendations for clients.
  </li>
  <li>
   Embrace innovative technologies and tools to optimize risk assurance processes and deliver value-added insights to clients.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  --
 </p>
 <p>
  <em>
   PwC T&uuml;rkiye &scedil;irketleri* olarak elektronik ortamda toplanan kimlik, ileti&scedil;im, &ouml;zge&ccedil;mi&scedil; ve CV&rsquo;niz&rsquo;de yer alan ki&scedil;isel verilerinizi i&scedil; ba&scedil;vurusu s&uuml;re&ccedil;lerinin y&uuml;r&uuml;t&uuml;lmesi amac&inodot;yla KVKK m. 5/2 (f) uyar&inodot;nca, hukuki ihtilaf olu&scedil;mas&inodot; halinde yasal s&uuml;re&ccedil;lerin y&uuml;r&uuml;t&uuml;lebilmesi amac&inodot;yla KVKK m. 5/2 (e) uyar&inodot;nca i&scedil;leyece&gbreve;iz. Ki&scedil;isel verilerinizi mevzuattan dolay&inodot; ki&scedil;isel verilerinizin payla&scedil;&inodot;lmas&inodot;n&inodot;n zorunlu oldu&gbreve;u hallerde, ilgili ve yetkili kamu kurum ve kurulu&scedil;lar&inodot;yla KVKK m. 5/2 (&ccedil;) uyar&inodot;nca payla&scedil;abiliriz. Ki&scedil;isel verilerinin KVKK m. 9 uyar&inodot;nca merkezi yurt d&inodot;&scedil;&inodot;nda bulunan Google sistemleri &uuml;zerinden i&scedil;lenecektir. KVKK&rsquo;n&inodot;n 11. Maddesi kapsam&inodot;ndaki haklar&inodot;n&inodot;z&inodot; https://www.pwc.com.tr/tr/hakkimizda/pwc-turkiye-kvk-basvuru-formu.pdf linkinde bulunan Ba&scedil;vuru Formu ile veya pwc.turkiye@hs03.kep.tr adresine, veya tr.dpo@tr.pwc.com adresine iletebilirsiniz.
  </em>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <em>
   *PwC T&uuml;rkiye &scedil;irketleri; PwC Dan&inodot;&scedil;manl&inodot;k Hizmetleri A.&Scedil;. &amp; PwC Ba&gbreve;&inodot;ms&inodot;z Denetim ve Serbest Muhasebeci Mali M&uuml;&scedil;avirlik A.&Scedil;. &amp; PwC Yeminli Mali M&uuml;&scedil;avirlik A.&Scedil;. &amp; PwC Y&ouml;netim Dan&inodot;&scedil;manl&inodot;&gbreve;&inodot; A.&Scedil;., PwC Serbest Muhasebeci Mali M&uuml;&scedil;avirlik Ltd. &Scedil;ti., Gago T&uuml;rkmen Avukatl&inodot;k Ortakl&inodot;&gbreve;&inodot;
  </em>
 </p>
</div>


Risk Modelling - Associate/Senior Associate (JP00276)

Eli Lilly

<div><p>At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We&rsquo;re looking for people who are determined to make life better for people around the world.</p><p></p><h3 class="jobSectionHeader"><b>
Overview</b></h3><p></p><p>
The Clinical Research Lead (CRL) is responsible for managing clinical investigators and sites participating in Lilly clinical trials and/or Post-Marketing Safety Studies. This includes investigator/site identification and qualification, ensuring timely trial enrollment aligned with scientific objectives, database lock delivery, issue resolution at trial sites, and maintaining inspection readiness at all times.</p><p>
The CRL ensures global program delivery through comprehensive investigator and site management, leveraging data and tools for informed decisions, and fostering high-quality interactions with clinical trial sites to provide an unparalleled customer experience. Additionally, the CRL oversees vendor monitoring activities, identifying and mitigating significant findings and trends.</p><p>
In countries without an Associate Director/Director of Investigator Engagement, the CRL may represent Investigator Engagement internally and externally, including interactions with regulatory bodies and influencing the local regulatory environment and strategy.</p><p></p><h3 class="jobSectionHeader"><b>
Primary Responsibilities</b></h3><p></p><p><b>
Clinical Investigator Management</b></p><ul><li>
Manage all activities at clinical trial sites, including site identification, qualification, enrollment planning, execution, and close-out.</li><li>
Ensure timely delivery of enrollment readiness, trial recruitment, and database locks through performance management and issue resolution.</li><li>
Identify opportunities to accelerate trial enrollment while maintaining an exceptional customer experience.</li><li>
Apply scientific, therapeutic area, and regional expertise to support trial execution and quality data delivery.</li><li>
Develop strategic institutional/site relationships to optimize clinical trial programs across therapeutic areas.</li></ul><p></p><p><b>
Clinical Trial Management</b></p><ul><li>
Implement investigator/site risk plans to meet enrollment and database lock commitments.</li><li>
Maintain site and country-level inspection readiness at all times.</li><li>
Use metrics to inform site/country/regional decision-making.</li><li>
Collaborate with internal and external teams to remove barriers to trial execution.</li><li>
Understand local treatment paradigms and standard of care to support feasibility and trial allocation.</li><li>
Provide vendor oversight for site monitoring activities.</li><li>
For countries with PMS requirements: manage Post-Marketing Safety Studies, including CRO selection, regulatory documentation, and project management.</li></ul><p></p><p><b>
Business Management and Engagement</b></p><ul><li>
Build strong professional relationships with clinical investigators to expand research partnerships and deliver an exceptional trial experience.</li><li>
Collaborate cross-functionally to align priorities and deliver the portfolio.</li><li>
Prospect targeted sites in line with portfolio strategy.</li><li>
Maintain therapeutic and technical expertise for scientific discussions with investigators and site staff.</li><li>
Act as a communication bridge between sites, vendors, and Lilly.</li><li>
Influence internal and external factors to improve clinical research delivery.</li></ul><p></p><p><b>
Country/Regulatory Responsibilities</b> <i>(where applicable)</i></p><ul><li>
Engage with regulatory bodies, ethical review boards, and national authorities to represent Lilly in the clinical trial environment.</li><li>
Participate in country pharmaceutical associations and affiliated bodies.</li><li>
Ensure compliance with local regulatory requirements and maintain internal processes accordingly.</li><li>
Contribute to external clinical development community initiatives and incorporate learnings into internal strategies.</li><li>
Support affiliate leadership in implementing regional initiatives.</li></ul><p></p><h3 class="jobSectionHeader"><b>
Minimum Qualifications</b></h3><ul><li>
Bachelor&rsquo;s degree or equivalent (preferably in a scientific or health-related field).</li><li>
Minimum 3 years of experience in pharmaceutical industry and/or clinical research.</li><li>
Strong knowledge of Good Clinical Practice (GCP).</li><li>
Ability to acquire and maintain therapeutic expertise to support portfolio needs.</li><li>
Excellent organizational and self-management skills.</li><li>
Strong communication skills (verbal and written) and ability to influence others.</li><li>
Strategic agility and broad business acumen.</li><li>
Demonstrated leadership behaviors and ability to lead in uncertain environments.</li></ul><p></p><h3 class="jobSectionHeader"><b>
Additional Preferences</b></h3><ul><li>
Strong organizational and planning skills.</li><li>
Ability to enhance customer experience.</li><li>
Fluent in English.</li><li>
Knowledge of country regulatory guidelines.</li><li>
Strong teamwork and interpersonal skills.</li><li>
Ability to develop innovative solutions.</li><li>
Travel required (50&ndash;75%).</li></ul><p></p><p>
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.</p><p></p><p>
Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.</p><p></p><p>
#WeAreLilly</p></div>

Clinical Research Lead

IQVIA

<div>
 <strong>
  Senior Clinical Research Associate
  <br/>
  <br/>
 </strong>
 IQVIA is the Human Data Science Company oriented to drive human health outcomes forward.
 <br/>
 <br/>
 When you join
 <strong>
  IQVIA Turkey
 </strong>
 as a sponsor-dedicated CRA, you&rsquo;ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers.
 <br/>
 <br/>
 With access to world-class training and mentoring, you&rsquo;ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.
 <br/>
 <br/>
 <strong>
  Your Responsibilities Will Include
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Performing site selection, initiation, monitoring and close-out visits
  </li>
  <li>
   Supporting the development of a subject recruitment plan
  </li>
  <li>
   Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  </li>
  <li>
   Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
  </li>
  <li>
   Collaborating with experts at study sites and with client representatives
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   University degree in scientific discipline or health care
  </li>
  <li>
   At least 2 years of on-site monitoring experience
  </li>
  <li>
   Good knowledge of clinical research regulatory requirements
  </li>
  <li>
   Very good computer skills including MS Office
  </li>
  <li>
   Excellent command of Turkish and English language
  </li>
  <li>
   Organizational, time management and problem-solving skills
  </li>
  <li>
   Ability to establish and maintain effective working relationships with co-workers, managers, and clients
  </li>
  <li>
   Flexibility to travel
  </li>
  <li>
   Driver&rsquo;s license class B
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What You Can Expect
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Resources that promote your career growth
  </li>
  <li>
   Leaders that support flexible work schedules
  </li>
  <li>
   Programs to help you build your therapeutic knowledge
  </li>
  <li>
   Better Work-Life balance, optimal DOS
  </li>
  <li>
   Excellent working environment in a stabile, international, reputable company
  </li>
  <li>
   Company car, mobile phone and attractive benefits package
   <br/>
   <br/>
  </li>
 </ul>
 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
</div>


(Senior) Clinical Research Associate - Sponsor dedicated - Türkiye

<div><div><div>Istanbul, T&uuml;rkiye | Full time | Field-based | R1476111</div></div><p></p><div><div><div><div><b><br>
Senior Clinical Research Associate
</b></div><div>IQVIA is the Human Data Science Company oriented to drive human health outcomes forward.</div><div>
When you join <b>IQVIA Turkey</b> as a sponsor-dedicated CRA, you&rsquo;ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers.
</div><div>With access to world-class training and mentoring, you&rsquo;ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.</div><div><b>
Your responsibilities will include:</b></div><ul><li>
Performing site selection, initiation, monitoring and close-out visits</li><li>
Supporting the development of a subject recruitment plan</li><li>
Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines</li><li>
Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution</li><li>
Collaborating with experts at study sites and with client representatives</li></ul><div><b><br>
Qualifications:</b></div><ul><li>
University degree in scientific discipline or health care</li><li>
At least 2 years of on-site monitoring experience</li><li>
Good knowledge of clinical research regulatory requirements</li><li>
Very good computer skills including MS Office</li><li>
Excellent command of Turkish and English language</li><li>
Organizational, time management and problem-solving skills</li><li>
Ability to establish and maintain effective working relationships with co-workers, managers, and clients</li><li>
Flexibility to travel</li><li>
Driver&rsquo;s license class B</li></ul><div><b>
What you can expect:
</b></div><ul><li>Resources that promote your career growth</li><li>
Leaders that support flexible work schedules</li><li>
Programs to help you build your therapeutic knowledge</li><li>
Better Work-Life balance, optimal DOS</li><li>
Excellent working environment in a stabile, international, reputable company</li><li>
Company car, mobile phone and attractive benefits package</li></ul></div></div><div>
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com</div></div></div><div></div>

Arup

<div></div><div><div><div><div><div><div>Energy
 </div></div></div><div></div><div><p>Europe Region</p>
 </div><div></div><div><p>IST000013</p></div></div><p></p><div><div><br>
</div></div></div><div><p><b>Shape a future with purpose at Arup in Istanbul &amp; Ankara.</b></p><p>
Arup&rsquo;s purpose, shared values and collaborative approach has set us apart for over 75 years, guiding how we shape a better world.</p><p><b>
The Opportunity</b></p><p>
Play a key role in shaping sustainable and energy-efficient solutions by joining our Sustainability Team as an Industrial Energy Auditor! Your expertise will directly influence the transition to greener buildings and corporate sustainability practices, making a tangible difference in combating climate change.</p><p>
Drive innovation in energy efficiency and collaborate on impactful policies at city and national levels.</p><p><b>
As an Industrial Energy Auditor at Arup, you will:</b></p><ul><li><p>
Work closely with multidisciplinary design teams to help building designs to be energy efficient at the concept design stage.</p></li><li><p>
Develop sustainability policies and capacity assessments for municipalities and ministries,</p></li><li><p>
Able to audit mechanical and electrical equipment in commercial and industrial facilities, develop ECM's (energy conversation measures) and calculate the energy and cost savings associated to each ECM,</p></li><li><p>
Developing 2050 zero-emission pathways for buildings or building portfolios,</p></li><li><p>
Staying up to date with T&uuml;rkiye, EU and global energy/resource efficiency policies.</p></li></ul><p>
 <b>Does this role inspire you?</b></p><p>
We're looking for someone who is passionate about advancing energy efficiency and sustainable building design. We also value:</p><ul><li><p>
Bachelor's degree in mechanical engineering,</p></li><li><p>
Having energy auditor and preferably energy manager certifications from Ministry or Energy and Natural Resources (Certified Energy Auditor - CEA and Certified Energy Manager -CEM),</p></li><li><p>
Excellent command of both Turkish and English,</p></li><li><div>
At least 5 years' experience in combination of the following responsibilities:<br>
<ul><li>(building) mechanical designer</li><li>energy auditor</li><li>technical engineer working in sustainability, decarbonization or climate change projects.</li></ul></div></li><li><p>
Have a driver's license,</p></li><li><p>
No travel restrictions (national &amp; internationally).</p></li></ul><p><b>
Preferred Qualifications</b></p><ul><li><p>
Competency in OpenStudio (EnergyPlus) building energy modelling software,</p></li><li><p>
 Knowledge or competence or building life-cycle assessment,</p></li><li><p>
Knowledge of embodied carbon in buildings,</p></li><li><p>
Knowledge of solar power, biomass and deep geothermal (renewables),</p></li><li><p>
Experience working in global firms, projects funded by IFI's, working with municipalities and ministries is a plus.</p></li></ul><p><b>
Why Arup?</b></p><p>
At Arup, we believe in rewarding our members for their contributions to our shared success. As a trust-owned company, we have the freedom to pursue meaningful work that aligns with our purpose and values. We also offer a unique profit share program, allowing our members to share in the results of our collective efforts.</p><p><b>
Benefits that work for you:</b></p><ul><li><b>
Professional Growth &amp; Development</b>: Benefit from continuous learning opportunities, training programs, and mentorship to enhance your skills and advance your career at Arup.</li><li><b>
Global Opportunities</b>: Collaborate with colleagues worldwide and explore potential short-term or long-term assignments at other Arup offices and project locations.</li><li><b>
Financial Well-being &amp; Ownership</b>: Receive a competitive salary and benefits package and share in Arup's success through our global profit-sharing programme.</li></ul><p>
At Arup, you belong to an extraordinary collective where individuality is encouraged. Our strength comes from how we respect, share, and connect our diverse experiences, perspectives, and ideas. You'll have the opportunity to do socially useful work that has meaning &ndash; to Arup, to your career, and to the clients and communities we serve.</p><p>
We are proud to be an equal opportunity employer and are committed to building a workplace that reflects the rich diversity of the world around us. We actively promote a culture of inclusion where everyone feels welcome, respected, and valued.</p><p>
We welcome applications from talented individuals of all backgrounds, regardless of age (within legal limits), gender identity or expression, disability, ethnicity, religion, sexual orientation, or any other protected characteristic. We are committed to making our recruitment process and workplaces accessible. If you need any assistance or adjustments, please visit our Candidate Support page for contact information and assistance. We're happy to help.</p><p><b>
Do you want to join us in shaping a better world?</b></p><p>
Apply using the &quot;&quot; button above</p></div></div><div></div>

Industrial Energy Auditor

RINA

<p></p><div><div><div><div><div><b>Posting Date: </b>5 Dec 2025
</div></div></div></div><div><div><div><div><b>City: </b>Istanbul
</div></div></div></div><div><div><div><div><b>Location:
</b>Istanbul, TR, 34742
</div></div></div></div><div><div><div><div><b>Contract Type: </b>Permanent
</div></div></div></div><div><div><div><div><b>Division: </b>International Certification
</div></div></div></div><div><div><div><div><b>Level of experience: </b>Senior
</div></div></div></div><div><div><div><div><div>RINA is currently recruiting for a <b>T&uuml;rkiye Certification Lead Auditor</b> to join its office in Turkiye within the <b>International Certification</b> Division.</div><div><div><div><div><b>
Mission</b></div>
</div><div><div>
The role focuses on planning, conducting, and managing audits within our certification business related to the different certification schemes.</div>
<div>
#LI-PV1</div></div></div><div><div><div><b>
Key Accountabilities</b></div>
</div><div><ul><li>Prepare, manage and control the audit programme, ensuring alignment with organizational goals and relevant standads</li></ul>
<ul><li>Document Review, including manuals, procedures, instructions, files, records</li></ul>
<ul><li>Plan audits and coordination with the relevant parties</li></ul>
<ul><li>Participate in /lead the audits</li></ul>
<ul><li>Identify/define/record/follow up the audit results by using the relevant softwares</li></ul>
<ul><li>Draw up/follow up the audit reports detailing all the findings</li></ul>
<ul><li>Manage the follow up process within the determined time frames</li></ul>
<ul><li>Conduct technical reviews and certification decisions if needed</li></ul>
<ul><li>Monitoring the performance of the resources involved in the certification process, providing guidance and support as needed</li></ul>
<ul><li>Maintain updated records and other information relevant to the audit process</li></ul>
<ul><li>Manage technical meetings with the customers, and support internal staff including scheduling and commercial if needed</li></ul>
<ul><li>Provide trainings in compliance with relevant qualified standards</li></ul>
<ul><li>Support the qualification/monitoring of the others if needed</li></ul>
<ul><li>Other adhoc activities assigned by the top management</li></ul></div></div><div><div><div><b>
Education</b></div>
</div><div><div>Bachelor&rsquo;s Degree in Engineering General</div></div></div><div><div><div><b>
Qualifications</b></div>
</div><div><ul><li>4+ years of experience in auditing, specifically within management systems or industry standards (ISO, etc.).</li></ul>
<ul><li>certified Lead Auditor courses from an internationally recognized body at least for ISO 9001, ISO 14001, ISO 45001.</li></ul>
<ul><li>Demonstrated ability to plan, conduct, and report audits per ISO 19011 guidelines</li></ul>
<ul><li>Strong understanding of audit planning, execution and reporting processes,proven ability to lead and manage auditing activities.</li></ul>
<ul><li>Previous professional experiences in Certification sector related to the auditing activities completed the qualification process as Lead Auditor for ISO 9001, ISO 14001, ISO 45001 are required as minimum. ISO 50001 and ISO 27001 Lead Auditor qualifications are plus.</li></ul>
<ul><li>In dept knowledge of industry standards, regulations and continous improvement of methodologies</li></ul>
<ul><li>Up to date qualifications and certifications</li></ul>
<ul><li>Languages: Turkish and English should be in advanced level</li></ul>
<ul><li>Driver's license holde</li></ul></div></div><div></div><div><div><div><b><br>
Competencies</b></div>
</div><ul><li>PROMOTE SUSTAINABLE DEVELOPMENT - Promote commitment by keeping promises as a Role Model
</li><li>MANAGE EMOTIONS - Recognise one's and other's emotions and express and regulate one's reactions
</li><li>PIONEER CHANGE - Actively embrace change and benefit from the new circumstances
</li><li>BUILD NETWORK - Forge trust relationships, across departments, and outside the organization
</li><li>MAKE EFFECTIVE DECISIONS - Structure activities according to priorities, actions, resources and constraint
</li><li>ADDRESS THE WAY - Have a big picture of different situations and reinterpret it in a perspective way
</li><li>THINK FORWARD - Capitalise on experiences and translate them into action plans for the future
</li><li>CLIENT INTIMACY - Embrace internal and external client needs, expectations, and requirements to ensure maximum satisfaction
</li><li>EARN TRUST - Take everyone's opinion into account and remain open to diversity</li></ul></div></div><br>
<div></div>
<div>
RINA is a multinational company providing a wide range of services in the energy, marine, certification, infrastructure &amp; mobility, industry, research &amp; development sectors. Our business model covers the full process of project development, from concept to completion.</div><br>
<div></div>
<div><i>
At RINA, we endeavor to create a work environment where every single person is valued and encouraged to develop new ideas. We provide equal employment opportunities and are committed to creating a workplace where everyone feels respected and safe from discrimination or harassment of any kind. We are also compliant to the Italian Law n. 68/99.</i></div></div></div></div></div></div><p></p>

Türkiye Certification Lead Auditor

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