food safety and quality manager Jobs in Istanbul

food safety and quality manager

qa engineer

regulatory affairs manager Jobs in Istanbul

regulatory affairs manager

corporate quality engineer Jobs in Istanbul

corporate quality engineer

health and safety manager Jobs in Istanbul

health and safety manager

quality assurance manager

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><p>
Ensure compliance with local Good Clinical Practice (GCP) Quality System as well as compliance with applicable T&uuml;rkiye MOH regulations.</p><p></p><p><b>
Technical training, personal skills and experience required:</b></p><ul><li><p>
A university degree in Pharmacy from T&uuml;rkiye.</p></li><li><p>
Minimum 2 years&rsquo; experience in quality assurance applied to the pharmaceutical industry.</p></li><li><p>
Working knowledge of GCP regulations and quality system implementation and the ability to interpret and apply them for Quality Assurance (QA) responsibilities</p></li><li><p>
Fluent in English (conversational, writing and reading) Knowledge and mastery of basic computing tools (Microsoft office).</p></li><li><p>
Good interpersonal relations Ability to train working groups.</p></li><li><p>
Good analytical skills and attention to details.</p></li><li><p>
High initiative, learning agility and a flexible, positive attitude.</p></li><li><p>
High degree of accuracy and attentive to details.</p></li></ul><p></p><p><b>
The Responsible Manager Delegate for Clinical Trial Materials is responsible for:</b></p><ul><li><p>
Act as delegated Responsible Manager to Perform Quality checks for the release of the Clinical Trial Products upon arrival to T&uuml;rkiye.</p></li><li><p>
Release clinical trial product shipments that meet all quality specifications and local regulations as a delegated Responsible Manager.</p></li><li><p>
Support inspection readiness activities for MOH inspections. Assure that <b>deviations, change management processes, root cause investigations, and corrective/preventive actions</b> are effectively managed, documented, escalated, and completed in a timely manner.</p></li><li><p>
Monitor compliance with the external party which is responsible for storage and distribution of Clinical Trial Materials.</p></li><li><p>
Assist on training programs to external vendors which might have impact on Clinical Trial Material operations.</p></li><li><p>
Review the returned products, ensure that any potential quality issue or failure that could have originated the return will be reported appropriately and coordinate if new provision applies to these products Support Quality Manager on reviewing/ updating Quality Agreements related to Clinical Trial Products Act as a point of contact for quality release of clinical trial materials in T&uuml;rkiye affiliate.</p></li><li><p>
Provide appropriate escalation of issues clinical teams and affiliate Responsible Manager.</p></li><li><p>
Understand performance metrics related to CT material and identify areas for improvement and simplification.</p></li><li><p>
Understand SOPs and processes for CT materials.</p></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>

Junior Responsible Manager Delegate for Clinical Trial Materials

Teva Pharmaceuticals

<div><div><div><div><p>Apply now &raquo;</p>
</div></div><div><div><div><div><div><p>Third Party Operations Quality Manager &amp; Qualified Person (QP)
</p></div></div></div></div><div></div><div><div><div><div><b>Date: </b>Nov 3, 2025
</div></div></div></div><div><div><div><div><b>Location:
</b>Istanbul, Turkey, 34000
</div></div></div></div><div><div><div><div><b>Company: </b>Teva Pharmaceuticals
</div></div></div></div><div><div><div><div><b>Job Id: </b>64617
</div></div></div></div><div><div><div><div><div><div><div><div><b>Who we are</b></div>
</div><div>Together, we&rsquo;re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It&rsquo;s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world&rsquo;s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization&rsquo;s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we&rsquo;re always looking for new ways to continue making a difference, and new people to make a difference with.</div></div><div><div><div><b>
The opportunity</b></div>
</div><div><div>
Third Party Operations Quality Manager &amp; Qualified Person (QP) will support business units by managing quality problems in local manufacturers in a way that does not disrupt local production plans and supply, and will manage technical activities (analytical, process, technology etc.) at CMO site level and Change Management Projects between CMOs, API/excipient Vendors and prepare technical dossiers for MOH submissions.</div></div></div><div><div><div><b>
How you&rsquo;ll spend your day</b></div>
</div><div><ul><li>Market release operations for batches both imported and local to local products (from local CMOs)</li>
<li>Ensure GDP compliance support while working at the 3rd party distribution center (sales warehouse)</li>
<li>Accountable for technology transfer projects by having analytical transfers and process validations (including design of the studies, review/approve protocol and reports, attend production of validation batches as an observer etc.) executed at CMOs in timely manner.</li>
<li>Support KPI reporting &amp; evaluation and discussion at global level in Quality Councils</li>
<li>Accountable for successful QMS (preferred Trackwise, Veeva) forpost-marketin quality issues such as customer complaints, returns etc.</li>
<li>Identify Quality / Compliance risks at CMOs, resolve issues and minimize risks and input, review and endorse investigations in the local manufacturers</li>
<li>Drive continuous improvement /CAPA processes at the CMOs through target setting, quality expert meetings, regular Business Review Meetings</li>
<li>To have active role in the process/quality improvement/ technical troubleshooting projects to drive risk reduction activities to ensure product robustness, sustainability and capability at CMO.</li>
<li>Maintain product risk oversight by reviewing PQR, stability data, BMR, validation report etc. and proactively drive risk reduction program</li>
<li>Provide to maintain the robust quality assurance system with the company SOP &amp; Training management</li>
<li>Provide maintenance of company QMS to ensure compliance to local and global regulations</li>
<li>Manage/follow up new &amp; cuurent regulatory compliance necessities &amp; ensure changes and improvements in the QMS accordingly</li>
<li>Support global QMS projects on behalf of Teva Affiliate</li>
<li>Support Vendor Qualification and Maintenance</li>
</ul></div></div><div><div><div><b>Your experience and qualifications</b></div>
</div><div><ul><li>Bachelor&rsquo;s degree in pharmacy/chemical engineering/chemist or equivalent scientific degree</li>
<li>In pharmaceutical industry, minimum 7 years of experience in a similar position in local manufacturing related business models or manufacturing environment itself.</li>
<li>Background in R&amp;D or/and Quality Control Laboratory is strongly preferred in parallel with Quality Assurance. Proven experience working with technical and operational teams troubleshooting.</li>
<li>Experience in production &amp; method validation processes, quality oversights in different culture local manufacturers, technology transfer projects, knowledge about the technology of different types of finished product and raw material characteristics such as sterile, non-sterile, non-beta lactams and beta-lactam-penicillin, biotech etc.</li>
<li>Excellent planning, co-ordination, communication skills</li>
<li>Ability to manage multiple tasks and strong daily follow up skills.</li>
<li>Energetic and committed to continuous improvement, meeting evolving Quality compliance expectations.</li>
<li>Result-oriented, analytic, and well-disciplined.</li>
<li>Advanced level of English, good knowledge of MS Office applications and being experienced with computerized Quality Systems is preferred.</li>
<li>Ability to work as part of a team within an international and multicultural team at various level of organizational leadership.</li>
<li>Knowledge of local current and upcoming legislation and current Quality Standards and advanced knowledge of cGMP requirements</li>
<li>Advanced understanding and insight into the different aspects of quality functions like QC, QA, Quality Systems, Compliance, Documentation etc.</li>
<li>Advanced negotiation, interpersonal and presentation skills</li>
<li>Change Management Experience within the complex MoH, Vendor, CMO environment</li>
<li>Able to travel to local contracted manufacturers</li>
</ul></div></div><div><div><div><b>Already Working @TEVA?</b></div>
</div><div><div>
If you are a current Teva employee, please apply using the internal career site available on &quot;Employee Central&quot;. By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site
</div><div>The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.</div></div></div><div><div><div><b>
Teva&rsquo;s Equal Employment Opportunity Commitment</b></div>
</div><div>Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.</div></div><div><div><div><b>
Ki&#351;isel Verilerin Korunmas&#305;</b></div>
</div><div><div>
Teva &#304;la&ccedil;lar&#305; San ve Tic. A.&#350;., 6698 say&#305;l&#305; Ki&#351;isel Verilerin Korunmas&#305; Kanunu&rsquo;na uygun olarak ki&#351;isel veri i&#351;lemektedir. Bu kapsamda, hangi ki&#351;isel verilerinizi i&#351;ledi&#287;imiz, hangi ama&ccedil;la i&#351;ledi&#287;imiz, aktarma bi&ccedil;imimiz dahil gerekli t&uuml;m hususlarda veri ilgililerini ayd&#305;nlatmay&#305; &ouml;nemsemektedir. &#304;&#351;e al&#305;m s&uuml;reci kapsam&#305;nda siz de&#287;erli &ccedil;al&#305;&#351;an adaylar&#305;m&#305;z&#305;, ki&#351;isel verilerin i&#351;lenmesi ile ilgili ayd&#305;nlatmak isteriz. &Ccedil;al&#305;&#351;an Aday&#305; Ayd&#305;nlatma Metnimize, resmi web sitemizde yer alan &Ccedil;ALI&#350;AN ADAYLARI - K&#304;&#350;&#304;SEL VER&#304;LER&#304;N &#304;&#350;LENMES&#304;NE &#304;L&#304;&#350;K&#304;N AYDINLATMA METN&#304; linki &uuml;zerinden eri&#351;ebilir ve bu konuda detayl&#305; bilgilere ula&#351;abilirsiniz.</div></div></div></div>
</div></div></div></div></div><p></p><div><p>Apply now &raquo;</p></div></div></div><div></div>

Third Party Operations Quality Manager & Qualified Person (QP)

Danone

<div>About the job
<p><b>
Danone T&uuml;rkiye </b>is looking for a talented colleague for the<b>&quot;Quality Assurance Executive (L&uuml;leburgaz)</b>&quot; position.</p><br>
<p></p>
<p><i>
If you are looking for a job to work in a dynamic, diverse, and growing business, you may be the perfect match for this position! Take this opportunity to GROW together!</i></p><br>
<p></p>
<p><b>
Quality &amp; Food Safety Management</b></p>
<p>
Ensure quality requirements are met across all production stages.</p>
<p>
Maintain and monitor food safety standards.</p>
<p>
Implement and oversee GMP (Good Manufacturing Practices).</p><br>
<p></p>
<p><b>
Audit &amp; Monitoring Activities
</b></p><p>Manage internal and external audits, including follow-up actions.</p>
<p>
Coordinate pre- and post-audit processes.</p>
<p>
Conduct traceability and recall tests to assess accessibility and performance during potential crisis situations.</p><br>
<p></p>
<p><b>
KPI &amp; Performance Tracking
</b></p><p>Monitor and report factory quality KPIs regularly.</p>
<p>
Track and report FSPM (Food Safety Preventive Maintenance) points monthly.</p>
<p>
Develop monitoring and action plans for delayed maintenance and deviations in FSPM points, including risk analysis.</p><br>
<p></p>
<p><b>
Consumer Complaint Management
</b></p><p>Perform root cause analysis of consumer complaints.</p>
<p>
Manage and report complaints, including presentation preparation.</p><br>
<p></p>
<p><b>
Product &amp; Equipment Controls
</b></p><p>Collaborate with relevant teams during new product development processes.</p>
<p>
Conduct machine cleaning and foreign material inspections. Perform pre- and post-maintenance checks.</p>
About you
<ul><li>Bachelor&rsquo;s degree in Food Science, Food Engineering, Chemistry, Biology, or a related discipline.</li>
<li>Max 3 years of experience in quality assurance or food safety roles within the food manufacturing industry.</li>
<li>Experience in dairy, beverage, or similar sectors is an advantage.</li>
<li>Technical Competencies Solid understanding of food safety systems (HACCP, ISO 22000, FSSC 22000).</li>
<li>Hands-on experience with GMP practices and hygiene monitoring.</li>
<li>Familiarity with traceability systems and recall procedures.</li>
<li>Ability to conduct inspections, supervise cleaning and foreign material controls.</li>
<li>Skilled in root cause analysis and corrective/preventive action planning.</li>
<li>Behavioral Competencies Strong attention to detail and commitment to quality.</li>
<li>Effective communication and reporting skills.</li>
<li>Ability to work collaboratively with production, maintenance, and quality teams.</li>
<li>Proactive, solution-oriented mindset with good organizational skills.</li>
<li>Key Performance Indicators (KPIs) Compliance rate with hygiene and quality control procedures.</li>
<li>Timely execution of corrective actions and audit findings.</li>
<li>Number and resolution time of consumer complaints.</li>
<li>Effectiveness of traceability and recall simulations.</li>
<li>FSPM deviation tracking and maintenance coordination.</li>
</ul>About us
<p>
We are proud to promote diversity and equal opportunity within our teams. We believe that our differences will make a difference, and that an inclusive work environment will drive our growth as a company, as a team, and as individuals. We will therefore consider all implementations* by fostering an inclusive work culture where everyone can feel at home.</p>
<p>
All nominations will be considered regardless of origin, background, religion, sex, sexual orientation,<b>age</b>, gender identity, disability.</p>
<p><b>
Working with us</b>is about being able to do things your way. The way you work, the way you develop, the way you progress, i<b>t&rsquo;s all up to you.</b></p><p><br>
Working here, you&rsquo;ll need to enjoy a fast-paced environment, a little complexity and challenging tasks but it is packed with opportunities. You will work for some of the best-known brands in the world, such as Activia, Danone, Danino, Danette, Aptamil, Bebelac, Hayat, and S&#305;rma, and we absolutely guarantee that you can just be yourself.</p>
<p><b>
Be innovative and entrepreneurial and the impact you could make might just amaze you</b>. Join our movement for a healthier world.<b>One Planet One Health BY YOU.</b></p><br>
<p></p>
<p>
At Danone T&uuml;rkiye, inspired by our B Corp journey, we continuously challenge ourselves to improve and measure our social and environmental impact.</p>
<p>
This journey inspires us to constantly challenge ourselves, measure what truly matters, and create long-term value &mdash; not just for our business, but for our people, partners, communities, and future generations.<br>
If you&rsquo;re looking to grow your career with purpose, you&rsquo;re in the right place.</p><br>
<p></p>
<p><b>
What we offer</b></p>
<p>
This is a visible position within the company, we offer opportunities where you can grow your expertise and have an end-to-end responsibility to drive &quot;change&quot; &amp; &quot;growth&rdquo;. You will have a chance to experience 360 ways of working with multiple stakeholders. We develop talents and growth potential to enable strong career development for our employees.</p><br>
<p></p>
<p>
At Danone T&uuml;rkiye, we do not aim to be the best company in the world, but better for the world.<br>
That&rsquo;s why, inspired by our B Corp journey, we continuously challenge ourselves to improve and measure our social and environmental impact.<br>
Through this journey, we strive to create long-term value for our employees, partners, communities, and future generations.</p><p></p><p><br>
<b>
What&rsquo;s next?</b></p>
<p>
Visit our websitewww.danone.comto discover more about us and to find out how you could be part of it all!</p><br>
<p></p>
<p>
#LI-DNI</p></div>

Quality Assurance Executive (Temporary), Lüleburgaz

TCI Aircraft Interiors

<div>
 <p>
  TCI Aircraft Interiors, initially established in 2010, entered a new era in 2023 with the merger of Turkish Airlines subsidiaries TCI Cabin Interior, TSI Seat, and Cornea. Combining over a decade of experience with an innovative vision, TCI leverages its enhanced capabilities to provide cutting-edge solutions for both wide and narrow body aircrafts. As the only company in its field operating in T&uuml;rkiye, we proudly represent our country while setting new standards in the international aviation industry and continue our mission to provide the best values in the sector.
 </p>
 <p>
  <br/>
 </p>
 <p>
  We offer in our product range; economy and business class seats, galleys, lavatories, and in-flight entertainment and satellite internet (IFEC) systems for commercial aircrafts. TCI also provides the most innovative solutions to the aviation industry with products such as service trolleys, cargo containers, and seat power systems, which are widely used in aviation operations. The company operates with design, engineering, manufacturing, and R&amp;D capabilities at its facilities in Istanbul and Seattle, serving multiple aircraft types and catering to industry leaders such as Boeing, Airbus, and some of the world&rsquo;s leading airlines.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Bachelor's Degree in related Engineering Departments
  </li>
  <li>
   At least 3 years of experience in management systems and relevant aviation regulations and standards (e.g., FAA, EASA, DGCA, and IATA regulations)
  </li>
  <li>
   Strong knowledge and experience in EASA/SHGM Part 21 and Part 145 regulations, Safety Management Systems (SMS), Aerospace Standards (AS 9100, AS 9110), ISO 9001, ISO 17025, and ISO 14001
  </li>
  <li>
   Excellent proficiency in spoken and written English is required
  </li>
  <li>
   Proficiency in computer usage, including MS Office applications
  </li>
  <li>
   Confidential, open-minded, with strong analytical and synthesis skills
  </li>
  <li>
   Strong discussion skills with the ability to lead and develop people, along with excellent interpersonal and communication skills
  </li>
  <li>
   Ability to make effective technical and business decisions and identify areas for improvement
  </li>
  <li>
   High learning capability and adaptability to change
  </li>
  <li>
   Target-oriented with the ability to set priorities for effective time management
  </li>
  <li>
   Strong organizational and teamwork abilities
  </li>
  <li>
   High sense of responsibility and resilience under stress
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Job Description
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Examining EASA/SHGM Part 21 and Part 145 regulations, Safety Management Systems (SMS), Aerospace Standards (AS) 9100, AS 9110, ISO 9001, ISO 17025, and ISO 14001 Environmental Management Systems (EMS) in detail, including concepts, purposes, content, and requirements; interpreting these and collaborating with the Manager to establish a Quality Management profile for the company.
  </li>
  <li>
   Designing, establishing, implementing, and maintaining processes and workflows for an integrated process management system.
  </li>
  <li>
   Supporting the Manager in the establishment of Quality, Safety, and Environmental Management Systems (QMS, SMS, and EMS).
  </li>
  <li>
   Managing QMS, EMS, and SMS documentation, including archiving activities, record-keeping, maintenance operations, and communication with all relevant authorities.
  </li>
  <li>
   Reporting to top management on activities, effectiveness, objectives, and issues related to improving the QMS, SMS, and EMS.
  </li>
  <li>
   Following up on external and internal corrective actions, monitoring and revising them as needed.
  </li>
  <li>
   Coordinating management review meetings and maintaining records of meeting minutes.
  </li>
  <li>
   Managing risks and opportunities within processes, participating in risk analysis studies, and coordinating with related departments.
  </li>
  <li>
   Reporting on the performance of the QMS, SMS, and EMS to top management.
  </li>
  <li>
   Managing relationships with representatives from all operational departments and regulatory authorities (FAA, DGCA, ICAO, EASA, etc.) concerning the development and management of TCI's QMS, SMS, and EMS.
  </li>
  <li>
   Implementing quality development and improvement tools such as APQP, FMEA, 8D, and 5Why analysis in TCI management systems.
  </li>
 </ul>
 <p>
 </p>
</div>


Quality Assurance Specialist

SES KİMYA A.Ş.

<p>Kozmetik ve ki&#351;isel bak&#305;m &uuml;r&uuml;nleri &uuml;retimi alan&#305;nda faaliyet g&ouml;steren firmam&#305;z&#305;n (SESK&#304;MYA A.&#350;.) Ba&#351;ak&#351;ehir il&ccedil;esinde (Alt&#305;n&#351;ehir) yer alan tesisimizin geli&#351;en ve b&uuml;y&uuml;yen organizasyonunda; Kalite &amp; Kontrol departman&#305;nda g&ouml;revlendirilmek &uuml;zere Kimyager,Kimya m&uuml;hendisi ve &uuml;niversitelerin ilgili b&ouml;l&uuml;mlerinden mezun personel al&#305;m&#305; yap&#305;lacakt&#305;r.</p><p>&#304;&#350; TANIMI</p><p>*&Uuml;r&uuml;n kalitesinin temini ve s&uuml;reklili&#287;inin sa&#287;lanabilmesi amac&#305;yla; hammaddeden ba&#351;layarak, &uuml;retim a&#351;amalar&#305;ndaki ara kontroller ve nihai &uuml;r&uuml;ne y&ouml;nelik, laboratuvar analizlerinin do&#287;ru, g&uuml;venilir ve zaman&#305;nda yap&#305;lmas&#305;n&#305; sa&#287;lamak,</p><p>*Prosesi etkin izleyerek &uuml;retim esnas&#305;nda olas&#305; problemlerin &ccedil;&ouml;z&uuml;mlerine y&ouml;nelik &ccedil;al&#305;&#351;malarda bulunmak,</p><p>*Bitmi&#351; &uuml;r&uuml;nlerin Kalite &amp; Kontrol&uuml; takibi yapmak,</p><p>*Hammadde Sat&#305;n almalar&#305;n&#305; Takip etmek, Sat&#305;n Alma s&uuml;recini izlemek</p><p>*Kalite y&ouml;netim sistemi ve iyi &uuml;retim uygulamalar&#305; (GMP) standartlar&#305; gere&#287;i ilgili &uuml;retim s&uuml;re&ccedil;lerin uygulamak, izlemek, kay&#305;t alt&#305;na almak,</p><p>*B&ouml;l&uuml;m&uuml;ndeki personelin g&ouml;rev da&#287;&#305;t&#305;m&#305;n&#305; yapmak, performanslar&#305;n&#305; takip etmek ve de&#287;erlendirmek,</p><p>*&Ccedil;al&#305;&#351;ma d&uuml;zenini bozan sorunlar&#305; m&uuml;d&uuml;r&uuml;ne raporlamak,</p><p>*&Uuml;retimin verimli, kaliteli ve zaman&#305;nda ger&ccedil;ekle&#351;mesini sa&#287;lamak,</p><p>*Planlama kriterlerine g&ouml;re gerekli i&#351; emirlerinin ve &uuml;retim metotlar&#305;n&#305;n &uuml;retim hatlar&#305;na da&#287;&#305;t&#305;m&#305;n&#305; ve takibini yapmak,</p><p>*&Uuml;retime haz&#305;rl&#305;k, &uuml;retim ve sonras&#305; faaliyetlerin kurallara uygun &#351;ekilde ve hatas&#305;z y&uuml;r&uuml;t&uuml;lmesini sa&#287;lamak,</p><p>*Hammadde, yar&#305; mamul ve mamullerin stoklar&#305;n&#305; d&uuml;zenli olarak kontrol alt&#305;nda tutmak,</p><p>*Yapm&#305;&#351; oldu&#287;u analiz ve proses kontrollere dair kay&#305;tlar&#305; tutup formlar&#305; kay&#305;t alt&#305;na almak.</p><p>GENEL N&#304;TEL&#304;KLER:</p><p>*&Uuml;niversitelerin Kimyager, Kimya M&uuml;hendisli&#287;i b&ouml;l&uuml;m&uuml;nden mezun;</p><p>*Kalite Y&ouml;netim Sistemlerine hakim;</p><p>*Ofis programlar&#305;na h&acirc;kim olan;</p><p>*Dikkatli ve tedbirli, detaylara &ouml;nem veren, takip y&ouml;n&uuml; geli&#351;mi&#351;, ileti&#351;im kurabilen;</p><p>*Kendini ifade edebilen;</p><p>*ISO 9001:2008, GMP konusunda bilgili;</p><p>*Koordine edici, y&ouml;neticilik vasf&#305; bulunan.</p><p>&#304;&#351; T&uuml;r&uuml;: Tam zamanl&#305;</p>

KİMYAGER

Kerry

<p></p><div><div><div><div><div><div><b>Requisition ID: 61905</b><br>
<b>Position Type: FT Permanent</b><br>
<b>Workplace Arrangement: #LI-Hybrid</b></div>
<div><div><div><div><b>
About Kerry</b></div>
</div><div>Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment.</div></div><div><div><div><b>
About the role</b></div></div><div></div><div><br>
<div>
The purpose of this role is to lead and develop the food safety and quality function at the manufacturing site in Turkey. This role ensures robust implementation of food safety systems, fosters a strong quality culture, and guarantees the delivery of safe, high-quality food ingredients to customers. This is a customer-facing role requiring strong collaboration with internal and external stakeholders. Based in Tuzla factory, one of the Kerry factories located in Istanbul, Turkey, with multiple technologies under one site.</div></div></div><div></div><div><div><div><b><br>
Key responsibilities</b></div></div><div></div><div><br>
<div><b>
Leadership &amp; Strategy</b></div>
<ul>
<li>Lead and mentor site and TPM Quality and Food Safety teams across the region.</li>
<li>Train and develop competencies for the current team members in the quality function across T&uuml;rkiye Kerry Site and the TPMs</li>
<li>Develop and execute the regional quality strategy aligned with global standards and local regulatory requirements.</li>
<li>Champion a proactive quality culture through training, engagement, and leadership.</li></ul><br>
<div></div>
<div><b>
Food Safety &amp; Compliance</b></div>
<ul>
<li>Ensure implementation and maintenance of food safety systems (e.g., HACCP, FSSC 22000, BRC) across all company-owned and TPM sites.</li>
<li>Monitor compliance with internal standards, customer requirements, and regulatory obligations.</li>
<li>Lead internal, supplier, and third-party audits, ensuring timely closure of non-conformities and continuous improvement.</li></ul><br>
<div></div>
<div><b>
Third-Party Manufacturing (TPM) Management</b></div>
<ul>
<li>Qualify, audit, and monitor TPM partners to ensure adherence to company quality and food safety standards.</li>
<li>Establish and maintain quality agreements with TPMs, including KPIs and escalation protocols.</li>
<li>Collaborate with Procurement, Supply Chain, and Operations to manage quality risks and drive continuous improvement at TPM sites.</li>
<li>Provide technical support and training to TPMs to build capability and ensure consistent product quality.</li></ul><br>
<div></div>
<div><b>
Operational Excellence</b></div>
<ul>
<li>Integrate quality systems with TPM and internal site TPM initiatives to drive continuous improvement.</li>
<li>Analyze quality KPIs and trends to identify risks and opportunities.</li>
<li>Collaborate with operations to reduce quality-related losses and improve product consistency.</li></ul><br>
<div></div>
<div><b>
Customer Engagement</b></div>
<ul>
<li>Act as the regional quality representative in customer interactions, audits, and complaint resolution.</li>
<li>Translate customer feedback into actionable improvements at both internal and TPM sites</li>
<li>Support new product development and commercialization from a quality perspective.</li></ul></div></div><div></div><div><div><div><b><br>
Qualifications and skills</b></div></div><div></div><div><br>
<ul>
<li>Bachelor&rsquo;s or master&rsquo;s degree in food science, Microbiology, Chemistry, or related field.</li>
<li>Minimum 10 years of experience in food quality and safety, with at least 3 years in a regional or multi-site leadership role.</li>
<li>Experience in a multinational food or ingredients company is highly desirable.</li>
<li>Demonstrated experience managing third-party manufacturing quality systems.</li>
<li>Certification in food safety systems (e.g., FSSC 22000) and auditing (e.g., Lead Auditor certification) is a strong advantage.</li>
<li>Familiarity with SPC methodologies , Lean, or Six Sigma methodologies will be an added advantage</li>
<li>Expertise in hygiene and sanitation, including cleaning validation, environmental monitoring, and allergen control.</li>
<li>Solid foundation in microbiology, including pathogen control, indicator organisms, and lab result interpretation.</li>
<li>Proficiency in risk assessment methodologies (e.g., HACCP, TACCP, VACCP, FMEA).</li>
<li>Demonstrated experience in auditing (internal, supplier, and third-party), including audit planning, execution, reporting, and CAPA management</li></ul></div></div></div><div></div><div><br>
Beware of scams online or from individuals claiming to represent us. A Kerry employee will not solicit candidates through a non-Kerry email address or phone number. In addition, Kerry does not currently utilise video chat rooms (e.g., Google Hangouts) to conduct interviews. Refuse any request that asks you to provide payment to participate in the hiring process (e.g., purchasing a &ldquo;starter kit,&rdquo; investing in training, or something similar). Kerry will not ask you to pay any money at any point in the hiring process with the exception of reimbursable travel expenses. In addition, any payments made by Kerry will be from official firm accounts bearing the Kerry name.</div>
<div><b>Recruiter:</b> #LI-NA1<br>
<b>Posting Type:</b> LI</div></div></div></div></div></div><div></div>

Food Safety and Quality Manager

<div>
 <strong>
  Requisition ID 61905
  <br/>
  <br/>
  Position Type FT Permanent
  <br/>
  <br/>
  Workplace Arrangement
  <br/>
  <br/>
 </strong>
 <strong>
  About Kerry
  <br/>
  <br/>
 </strong>
 Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment.
 <br/>
 <br/>
 <strong>
  About the role
  <br/>
  <br/>
 </strong>
 The purpose of this role is to lead and develop the food safety and quality function at the manufacturing site in Turkey. This role ensures robust implementation of food safety systems, fosters a strong quality culture, and guarantees the delivery of safe, high-quality food ingredients to customers. This is a customer-facing role requiring strong collaboration with internal and external stakeholders. Based in Tuzla factory, one of the Kerry factories located in Istanbul, Turkey, with multiple technologies under one site.
 <br/>
 <br/>
 <strong>
  Key responsibilities
  <br/>
  <br/>
 </strong>
 <strong>
  Leadership &amp; Strategy
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Lead and mentor site and TPM Quality and Food Safety teams across the region.
  </li>
  <li>
   Train and develop competencies for the current team members in the quality function across T&uuml;rkiye Kerry Site and the TPMs
  </li>
  <li>
   Develop and execute the regional quality strategy aligned with global standards and local regulatory requirements.
  </li>
  <li>
   Champion a proactive quality culture through training, engagement, and leadership.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Food Safety &amp; Compliance
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Ensure implementation and maintenance of food safety systems (e.g., HACCP, FSSC 22000, BRC) across all company-owned and TPM sites.
  </li>
  <li>
   Monitor compliance with internal standards, customer requirements, and regulatory obligations.
  </li>
  <li>
   Lead internal, supplier, and third-party audits, ensuring timely closure of non-conformities and continuous improvement.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Third-Party Manufacturing (TPM) Management
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Qualify, audit, and monitor TPM partners to ensure adherence to company quality and food safety standards.
  </li>
  <li>
   Establish and maintain quality agreements with TPMs, including KPIs and escalation protocols.
  </li>
  <li>
   Collaborate with Procurement, Supply Chain, and Operations to manage quality risks and drive continuous improvement at TPM sites.
  </li>
  <li>
   Provide technical support and training to TPMs to build capability and ensure consistent product quality.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Operational Excellence
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Integrate quality systems with TPM and internal site TPM initiatives to drive continuous improvement.
  </li>
  <li>
   Analyze quality KPIs and trends to identify risks and opportunities.
  </li>
  <li>
   Collaborate with operations to reduce quality-related losses and improve product consistency.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Customer Engagement
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Act as the regional quality representative in customer interactions, audits, and complaint resolution.
  </li>
  <li>
   Translate customer feedback into actionable improvements at both internal and TPM sites
  </li>
  <li>
   Support new product development and commercialization from a quality perspective.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications and skills
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s or master&rsquo;s degree in food science, Microbiology, Chemistry, or related field.
  </li>
  <li>
   Minimum 10 years of experience in food quality and safety, with at least 3 years in a regional or multi-site leadership role.
  </li>
  <li>
   Experience in a multinational food or ingredients company is highly desirable.
  </li>
  <li>
   Demonstrated experience managing third-party manufacturing quality systems.
  </li>
  <li>
   Certification in food safety systems (e.g., FSSC 22000) and auditing (e.g., Lead Auditor certification) is a strong advantage.
  </li>
  <li>
   Familiarity with SPC methodologies , Lean, or Six Sigma methodologies will be an added advantage
  </li>
  <li>
   Expertise in hygiene and sanitation, including cleaning validation, environmental monitoring, and allergen control.
  </li>
  <li>
   Solid foundation in microbiology, including pathogen control, indicator organisms, and lab result interpretation.
  </li>
  <li>
   Proficiency in risk assessment methodologies (e.g., HACCP, TACCP, VACCP, FMEA).
  </li>
  <li>
   Demonstrated experience in auditing (internal, supplier, and third-party), including audit planning, execution, reporting, and CAPA management
   <br/>
   <br/>
  </li>
 </ul>
 Beware of scams online or from individuals claiming to represent us. A Kerry employee will not solicit candidates through a non-Kerry email address or phone number. In addition, Kerry does not currently utilise video chat rooms (e.g., Google Hangouts) to conduct interviews. Refuse any request that asks you to provide payment to participate in the hiring process (e.g., purchasing a &ldquo;starter kit,&rdquo; investing in training, or something similar). Kerry will not ask you to pay any money at any point in the hiring process with the exception of reimbursable travel expenses. In addition, any payments made by Kerry will be from official firm accounts bearing the Kerry name.
 <br/>
 <br/>
 <strong>
  Recruiter
  <br/>
  <br/>
 </strong>
 <strong>
  Posting Type
 </strong>
 LI
 <br/>
 <br/>
</div>


Explore 712+ Quality assurance manager in Istanbul this November. Find roles across top companies and apply now to boost your career.

712 quality assurance manager jobs IN Istanbul

Junior Responsible Manager Delegate for Clinical Trial Materials

Third Party Operations Quality Manager & Qualified Person (QP)

Quality Assurance Executive (Temporary), Lüleburgaz

Quality Assurance Specialist

KİMYAGER

Food Safety and Quality Manager

Food Safety and Quality Manager