food safety and quality manager Jobs in Istanbul

food safety and quality manager

incoming quality control manager Jobs in Istanbul

incoming quality control manager

laboratory manager

quality assurance engineer Jobs in Istanbul

quality assurance engineer

quality compliance senior manager Jobs in Istanbul

quality compliance senior manager

quality manager

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-Onsite</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><br>
<b>Posting Type:</b> DNI</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>
 DNI
 <br/>
 <br/>
</div>


Teva Pharmaceuticals

<div>
 <strong>
  Who We Are
  <br/>
  <br/>
 </strong>
 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.
 <br/>
 <br/>
 <strong>
  The opportunity
  <br/>
  <br/>
 </strong>
 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.
 <br/>
 <br/>
 <strong>
  How You&rsquo;ll Spend Your Day
  <br/>
  <br/>
 </strong>
 <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
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Your Experience And Qualifications
  <br/>
  <br/>
 </strong>
 <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
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Already Working @TEVA?
  <br/>
  <br/>
 </strong>
 If you are a current Teva employee, please apply using the internal career site available on "Employee Central". 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
 <br/>
 <br/>
 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.
 <br/>
 <br/>
 <strong>
  Teva&rsquo;s Equal Employment Opportunity Commitment
  <br/>
  <br/>
 </strong>
 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.
 <br/>
 <br/>
 <strong>
  Ki&scedil;isel Verilerin Korunmas&inodot;
  <br/>
  <br/>
 </strong>
 Teva &Idot;la&ccedil;lar&inodot; San ve Tic. A.&Scedil;., 6698 say&inodot;l&inodot; Ki&scedil;isel Verilerin Korunmas&inodot; Kanunu&rsquo;na uygun olarak ki&scedil;isel veri i&scedil;lemektedir. Bu kapsamda, hangi ki&scedil;isel verilerinizi i&scedil;ledi&gbreve;imiz, hangi ama&ccedil;la i&scedil;ledi&gbreve;imiz, aktarma bi&ccedil;imimiz dahil gerekli t&uuml;m hususlarda veri ilgililerini ayd&inodot;nlatmay&inodot; &ouml;nemsemektedir. &Idot;&scedil;e al&inodot;m s&uuml;reci kapsam&inodot;nda siz de&gbreve;erli &ccedil;al&inodot;&scedil;an adaylar&inodot;m&inodot;z&inodot;, ki&scedil;isel verilerin i&scedil;lenmesi ile ilgili ayd&inodot;nlatmak isteriz. &Ccedil;al&inodot;&scedil;an Aday&inodot; Ayd&inodot;nlatma Metnimize, resmi web sitemizde yer alan &Ccedil;ALI&Scedil;AN ADAYLARI - K&Idot;&Scedil;&Idot;SEL VER&Idot;LER&Idot;N &Idot;&Scedil;LENMES&Idot;NE &Idot;L&Idot;&Scedil;K&Idot;N AYDINLATMA METN&Idot; linki &uuml;zerinden eri&scedil;ebilir ve bu konuda detayl&inodot; bilgilere ula&scedil;abilirsiniz.
 <br/>
 <br/>
 Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.
</div>


Third Party Operations Quality Manager & Qualified Person (QP)

Proterial

<div><p><b>Location:
</b></p>Istanbul, Turkey
<p></p><p><b>Job ID:
</b></p>R0112450
<p></p><p><b>Date Posted:
</b></p>2025-11-27
<p></p><p><b>Company Name:
</b></p>HITACHI ENERGY TURKEY ELEKTRIK SANAYI ANONIM SIRKETI
<p></p><p><b>Profession (Job Category):
</b></p>Quality Management
<p></p><p><b>Job Schedule:
</b></p>Full time
<p></p><p><b>Remote:
</b></p>No
<p></p><p><b>Job Description:
</b></p><p><b>The Opportunity
</b></p><p>At Hitachi Energy, our purpose is advancing a sustainable energy future for all. We bring power to our homes, schools, hospitals, and factories. Join us and work with fantastic people, while learning and developing yourself on projects that have a real impact to our communities and society. Bring your passion, bring your energy, and be part of a global team that appreciates a simple truth: Diversity + Collaboration = Great Innovation.
</p><p></p><p><b>How you&rsquo;ll make an impact
</b></p><ul><li>Plan routine and non-routine inspections of incoming materials &amp; suppliers
</li><li>Verify incoming materials and their documentation meet specification of requirements.
</li><li>Manage labeling of all components with identification and status tag to visualize their compliance with requirements.
</li><li>Identify and manage non-conformances.
</li><li>Conduct non-conformance analysis and report findings. Document inspection records in SAP QM.
</li><li>Maintain quality inspection tools and equipment. Support 5S program in the work environment. Collaborate with Manufacturing, Engineering, Quality, Test Room, and Supply teams.
</li><li>Responsible to ensure compliance with applicable external &amp; internal regulations, procedures &amp; guidelines.
</li><li>Managers are responsible for ensuring compliance with applicable external and internal regulations, procedures, and guidelines.
</li></ul><p></p><p><b>Your background
</b></p><ul><li>Bachelor&rsquo;s degree in engineering.Mechanical or Materials and Metallurgical Engineering is a plus.
</li><li>Min 10 years&rsquo; experience in a production environment, mainly in transformer quality processes. Strong knowledge of industry standards and regulatory compliance, such as ISO 9001 and other relevant standards.
</li><li>Excellent analytical skills for data analysis and non-conformance investigations.
</li><li>Performed Internal Audit, Experienced in leading external audits
</li><li>Knowledge of problem-solving methods such as 8D, root cause analysis, Ishikawa. Developed job follow-up and problem-solving skills, paying attention to details.
</li><li>Excellent command of written and spoken English and Turkish.
</li></ul><p></p><p><b>More About Us
</b></p><p>We pride ourselves on offering a holistic range of competitive benefit programs to support your financial, physical and mental wellbeing and personal development. We want you to truly thrive with us &ndash; in work and out.
</p><p>For this role, depending on grade and experience, we offer the following employee benefits;
</p><p></p><ul><li>Access to a comprehensive wellbeing program,
</li></ul><ul><li>Private health insurance,
</li></ul><ul><li>Transportation allowance
</li></ul><p></p><h2 class="jobSectionHeader"><b>Qualified individuals with a disability may request a reasonable accommodation if you are unable or limited in your ability to use or access the Hitachi Energy career site as a result of your disability. You may request reasonable accommodations by completing a </b><b>general inquiry form </b><b>on our website. Please include your contact information and specific details about your required accommodation to support you during the job application process.
</b></h2><p></p><h2 class="jobSectionHeader"><b>This is solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes will not receive a response.</b></h2></div><p></p>

Incoming Quality Control Manager

Hitachi Energy

<div><p><b>About Us</b>
</p><p>We pride ourselves on offering a holistic range of competitive benefit programs to support your financial, physical and mental wellbeing and personal development. We want you to truly thrive with us &ndash; in work and out.</p><p><b>
Description</b>
</p><p><b>The Opportunity</b></p><p>
At Hitachi Energy, our purpose is advancing a sustainable energy future for all. We bring power to our homes, schools, hospitals, and factories. Join us and work with fantastic people, while learning and developing yourself on projects that have a real impact to our communities and society. Bring your passion, bring your energy, and be part of a global team that appreciates a simple truth: Diversity + Collaboration = Great Innovation.</p><p></p><p><b>
How you&rsquo;ll make an impact</b></p><ul><li>
Plan routine and non-routine inspections of incoming materials &amp; suppliers</li><li>
Verify incoming materials and their documentation meet specification of requirements.</li><li>
Manage labeling of all components with identification and status tag to visualize their compliance with requirements.</li><li>
Identify and manage non-conformances.</li><li>
Conduct non-conformance analysis and report findings. Document inspection records in SAP QM.</li><li>
Maintain quality inspection tools and equipment. Support 5S program in the work environment. Collaborate with Manufacturing, Engineering, Quality, Test Room, and Supply teams.</li><li>
Responsible to ensure compliance with applicable external &amp; internal regulations, procedures &amp; guidelines.</li><li>
Managers are responsible for ensuring compliance with applicable external and internal regulations, procedures, and guidelines.</li></ul><p></p><p><b>
Your background
</b></p><ul><li>Bachelor&rsquo;s degree in engineering.Mechanical or Materials and Metallurgical Engineering is a plus.</li><li>
Min 10 years&rsquo; experience in a production environment, mainly in transformer quality processes. Strong knowledge of industry standards and regulatory compliance, such as ISO 9001 and other relevant standards.</li><li>
Excellent analytical skills for data analysis and non-conformance investigations.</li><li>
Performed Internal Audit, Experienced in leading external audits</li><li>
Knowledge of problem-solving methods such as 8D, root cause analysis, Ishikawa. Developed job follow-up and problem-solving skills, paying attention to details.</li><li>
Excellent command of written and spoken English and Turkish.</li></ul><p></p><p><b>
More About Us</b></p><p>
We pride ourselves on offering a holistic range of competitive benefit programs to support your financial, physical and mental wellbeing and personal development. We want you to truly thrive with us &ndash; in work and out.</p><p>
For this role, depending on grade and experience, we offer the following employee benefits;</p><p></p><ul><li>Access to a comprehensive wellbeing program,</li><li>Private health insurance,</li><li>Transportation allowance</li></ul><p></p><h2 class="jobSectionHeader"><b>
Qualified individuals with a disability may request a reasonable accommodation if you are unable or limited in your ability to use or access the Hitachi Energy career site as a result of your disability. You may request reasonable accommodations by completing a </b><b>general inquiry form</b><b> on our website. Please include your contact information and specific details about your required accommodation to support you during the job application process.</b></h2><p></p><h2 class="jobSectionHeader"><b>
This is solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes will not receive a response.</b></h2></div><p></p>

Consulta

<div>
 <p>
  <strong>
   We Are Hiring:
   <u>
    Third Part Manufacturer and Technical Transfer QA Manager&ndash; EMEA
   </u>
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  &ldquo;On behalf of our global business partner operating in the healthcare sector, we are reaching out to qualified candidates for the Third Party Manufacturer and Technical Transfer QA Manager &ndash; EMEA (Istanbul) position. This role is responsible for TPM (Third Party Manufacturer) management across the EMEA region, overseeing technical transfer processes, and providing quality assurance support particularly for biosimilar product transfer projects.&rdquo;
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Regional TPM Quality:
   </u>
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Primary responsible for Quality management related to TPM in the EMEA region, for delivering quality products through reliable supply chain.
  </li>
  <li>
   Responsible of Monitoring TPM quality performance.
  </li>
  <li>
   Primary lead for Quality Technical Agreements approval renewal
  </li>
  <li>
   Primary contact for communication of TPM Quality issues as needed.
  </li>
  <li>
   QA support for investigations, trends, complaints, corrective and preventive actions (CAPA), validation support, and product release issues as needed.
  </li>
  <li>
   Responsible for maintaining regional Approved Supplier Listing.
  </li>
  <li>
   Responsible for representing regional TPMs Quality in Management Review.
  </li>
  <li>
   Responsible for communication with Global TPM/Supplier QA regarding Global TPM Products that are supplied
  </li>
  <li>
   Responsible for supporting Global and Regional Quality Compliance and improvement initiatives.
  </li>
  <li>
   Primary QA interface for new contract manufacturing site approvals within region must approve all new contract manufacturers for EPD commercial product within responsibility.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Product Transfer and Support QA
   </u>
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   QA Lead for below quality activities during Product Transfer and ASQ including,
  </li>
  <li>
   Change Control / Stability and Change Impact Assessment
  </li>
  <li>
   Test Method Transfer/Analytical Method
  </li>
  <li>
   Validation/Verification
  </li>
  <li>
   Process Validation/Verification Program
  </li>
  <li>
   Stability program during Shelf-Life of the product Microbiological validation studies
  </li>
  <li>
   First lot quality review for release the validation batches for commercialization.
  </li>
  <li>
   Gather information from the Sending Unit, in order to assemble a data package.
  </li>
  <li>
   Evaluate the information gathered and document findings with respect to product robustness
  </li>
  <li>
   Participate to the process of creation, approval and continuous improvement of the regulatory documentation related to EPD products. Provide support for the specification setting to Regulatory Affairs and receiving unit.
  </li>
  <li>
   Provide contributions for the Product technical knowledge during and after technology transfer and ensure the product meeting the Quality Standards. Facilitate issue resolution for key investigation and compliance issues
  </li>
  <li>
   Supporting the lifecycle management strategy and supporting its operational execution as supporting the work-stream team or equivalent cross-functional team. Managing product and process quality and compliance throughout the maturity stage of the life cycle of EPD commercialized products
  </li>
  <li>
   Ensure that projects and technical activities associated with Drug Substances, Drug Products, Intermediates and non-pharma products (food supplement, medical device, cosmetics) are carried out without business interruptions and according to legal and Abbott Quality, Regulatory and business requirements.
  </li>
  <li>
   Liaison between sites QA, commercial affiliates, MS&amp;T (Manufacturing Science and Technology) and other groups as necessary.
  </li>
  <li>
   Conduct/assist in due-diligence audits for new API suppliers to provide a rapid and accurate usage decision on proposed suppliers
  </li>
  <li>
   Serve as quality technical resource of regional EPD Quality organization during process and regulatory deficiency issues, risk assessment target cost initiatives and other continues improvement initiatives.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Required Qualifications
   </u>
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Bachelor's degree in Chemistry, Pharmacy, Medical Science.
  </li>
  <li>
   8+ years of supervisorial experience in the pharmaceutical (Quality, Production, R&amp;D etc.) or related fields.
  </li>
  <li>
   GMP/GLP/GCP background related to Biotechnological, Biosimilars and Biologics, medicinal products.
  </li>
  <li>
   Good communication and report writing skill in English
  </li>
  <li>
   Strong leadership skills in bringing the best out of people, managing work teams and fostering teamwork within the department.
  </li>
  <li>
   Strong strategic Planning/ Thinking, decisive judgement, and Implementation skills.
  </li>
  <li>
   Flexible for Travel: 40 %
  </li>
 </ul>
 <p>
 </p>
</div>


Third Part Manufacturer and Technical Transfer QA Manager(Temporary)

ENKA İnşaat ve Sanayi A.Ş.

<div>
 <p>
  QUALIFICATIONS AND JOB DESCRIPTION
 </p>
 <p>
  <br/>
 </p>
 <p>
  ENKA &Idot;n&scedil;aat ve Sanayi A.&Scedil;. has founded at 1957, is a recognized international EPC (Engineering &ndash; Procurement &ndash; Construction) Company has designed and built many Projects for Oil and Gas Process, Combined Cycle Power Plants (CCPP) Projects, Simple Cycle Power Plants (SCPP) Projects, Coal Fired Power Plants, Desalination Plants, Pipeline&amp;Pump Stations, Well Pad Facilities, and the Tank Farms in all over the world up to date.
 </p>
 <p>
  ENKA has its own `in-house` multi-disciplinary engineering team that performs all design services required for the development of above-mentioned projects. ENKA Engineering team carries out Conceptual (FEED), Basic and Detailed engineering for the Process, Piping, Mechanical, Electrical, Instrumentation and Control, Civil &amp; Structural, and Architectural disciplines.
 </p>
 <p>
  ENKA Engineering organization comprises of 3 main divisions located in Istanbul Head Quarter - Engineering Offices in Turkey.
 </p>
 <p>
  &middot; ENKA Civil, Structural and Infrastructural,
 </p>
 <p>
  &middot; ENKA Architectural Design, and
 </p>
 <p>
  &middot; ENKA Energy Engineering.
 </p>
 <p>
  ENKA Energy Engineering is seeking for new teammates who will become the member of ENKA&rsquo;s design &amp; engineering team located in Istanbul, Turkey. We are seeking to hire a Corporate Quality Engineer to be employed in Our Head Office in Istanbul.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   KEY RESPONSIBILITIES
  </strong>
 </p>
 <ul>
  <li>
   Plan, coordinate, and conduct internal quality audits across ENKA departments and projects in accordance with ISO 9001 and ISO 27001 requirements,
  </li>
  <li>
   Support and accompany external audits performed by certification bodies (BSI, ASME, etc.) and clients,
  </li>
  <li>
   Prepare audit plans, checklists, and reports; monitor corrective and preventive actions until closure,
  </li>
  <li>
   Maintain and update ENKA&rsquo;s audit schedules and certification records in line with Corporate Quality procedures,
  </li>
  <li>
   Develop and standardize Quality Assurance documentation for project bids, including Project Quality Plans (PQP), Quality Manuals, and related deliverables,
  </li>
  <li>
   Ensure compliance of documentation with ENKA corporate standards and client-specific quality requirements,
  </li>
  <li>
   Collaborate with proposal and engineering teams to provide quality-related input during tender preparation,
  </li>
  <li>
   Support the Corporate Quality Manager in the development, review, and optimization of corporate workflows and quality processes,
  </li>
  <li>
   Participate in the development and digitalization of quality management tools integrated into ENKA&rsquo;s ERP systems (e.g., EGFS, EGPS, EDMS),
  </li>
  <li>
   Monitor the performance of ENKA&rsquo;s Quality Management System and contribute to periodic management reviews,
  </li>
  <li>
   Prepare and review trend analyses related to audit findings, NCRs, and other quality performance indicators,
  </li>
  <li>
   Act as a liaison for quality-related communication with clients, partners, and certification agencies when required,
  </li>
  <li>
   Provide technical support and training to project quality teams on QMS implementation, documentation requirements, and audit preparedness.
  </li>
 </ul>
 <p>
  <strong>
   QUALIFICATIONS
  </strong>
 </p>
 <ul>
  <li>
   <strong>
    B.Sc. degree
   </strong>
   in Mechanical, Metallurgical &amp; Materials, Civil, Electrical or Electrical-Electronics Engineering,
  </li>
  <li>
   Minimum
   <strong>
    5 years of professional experience
   </strong>
   in Quality Assurance / Quality Control, preferably in construction and engineering projects,
  </li>
  <li>
   <strong>
    Certified Internal / Lead Auditor
   </strong>
   for ISO 9001 (ISO 27001 &amp; ISO 19443 Auditor certifications are an advantage),
  </li>
  <li>
   Additional certifications such as
   <strong>
    PMP, RMP or Six Sigma
   </strong>
   are considered an asset,
  </li>
  <li>
   Strong knowledge of
   <strong>
    ISO 9001 and ISO 27001
   </strong>
   standards,
  </li>
  <li>
   Experience in construction site quality control inspections and corporate-level QMS implementation,
  </li>
  <li>
   Familiarity with ERP-based construction management systems and document control tools,
  </li>
  <li>
   Advanced command of
   <strong>
    MS Office
   </strong>
   applications; familiarity with
   <strong>
    Power BI
   </strong>
   is an advantage,
  </li>
  <li>
   Excellent command of
   <strong>
    written and spoken English
   </strong>
   ,
  </li>
  <li>
   Strong analytical skills; effective communication, organization, and coordination abilities,
  </li>
  <li>
   Self-motivated, detail-oriented, and able to work both independently and within multidisciplinary teams,
  </li>
  <li>
   No restriction to travel and stay abroad.
  </li>
 </ul>
 <p>
 </p>
</div>


CORPORATE QUALITY ENGINEER

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Third Part Manufacturer and Technical Transfer QA Manager(Temporary)

CORPORATE QUALITY ENGINEER