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health and safety manager

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internal control assistant manager

quality systems manager

Danone

<div>About the job
<p><b>
Danone T&uuml;rkiye</b> is looking for a talented colleague for the position of <b>Quality Manager, Bursa.</b><br>
Take this opportunity to <b>GROW</b> together!</p>
<p>
This is a <b>team management role</b> reporting to an experienced <b>Senior </b>F<b>actory Manager</b>.</p><br>
<p></p>
<div>
Key Responsibilities:<br>
Quality Systems &amp; Standards<br>
<ul><li>Lead the implementation,and continuous improvement of site-wide quality systems in alignment with corporate standards and applicable regulations</li><li>Ensure consistent application of quality control measures throughout production, from raw material receipt to final product release</li><li>Maintain and audit all relevant documentation to ensure traceability, consistency, and compliance</li></ul>
Audit &amp; Compliance Oversight<br>
<ul><li>Prepare for and manage external and internal audits, including those from customers, certification bodies, and regulatory authorities</li><li>Ensure up-to-date knowledge and application of applicable standards (e.g., ISO 9001, regulatory frameworks, internal policies)</li><li>Lead root cause investigations and the timely execution of corrective/preventive actions</li></ul>
Performance Monitoring &amp; Process Improvement<br>
<ul><li>Analyze quality performance indicators and identify trends, deviations, and areas for process optimization</li><li>Collaborate closely with production, engineering, and maintenance teams to proactively solve quality-related challenges</li><li>Support the site&rsquo;s broader operational efficiency and reliability goals by contributing to improvement initiatives</li></ul>
Team Development &amp; Leadership<br>
<ul><li>Lead, coach, and develop a team of quality professionals responsible for in-process control, laboratory testing, and system compliance</li><li>Drive ownership and engagement by building a site-wide culture focused on quality, accountability, and continuous improvement</li><li>Coordinate and deliver training related to quality awareness, operational standards, and inspection protocols</li></ul>
Risk &amp; Incident Management<br>
<ul><li>Ensure robust product traceability and recall procedures are in place and regularly tested</li><li>Lead the investigation and management of any quality-related incidents or escalations</li><li>Actively participate in plant risk assessments and crisis preparedness activities</li></ul></div>
About you
<ul><li>Bachelor&rsquo;s or Master&rsquo;s degree in Engineering, Science, or a related technical discipline</li><li>At least 5&ndash;7 years of experience in quality assurance or quality control within manufacturing environments</li><li>Demonstrated experience managing compliance audits, system improvements, and cross-functional quality initiatives</li><li>Fluent in English (verbal and written); comfortable operating in an international work environment</li><li>Familiarity with ERP systems (e.g., SAP) and quality data tools is a plus</li></ul>
Core Competencies<br>
<ul><li>Strong leadership, influencing, and communication skills</li><li>Results-oriented mindset with a structured approach to problem-solving</li><li>Analytical thinking with attention to detail</li><li>Comfortable working under pressure and managing multiple priorities</li></ul>
About us
<p>
Being a Danoner means that you create your own working experience.</p><br>
<p></p>
<ul>
<li><p>Danone offers various types of leave days to support Danoners&rsquo; work-life balance and well-being. We have a wide variety of leave types, such as in your first year 5 days of &quot;Im New in Danone Leave&quot;; 1 day of &quot;My Future is Good Leave&quot; for our social responsibility activities. These options cater to different aspects of employees' lives and needs, reflecting the company's commitment to not only professional growth but also personal and social responsibilities.</p></li></ul><br>
<p></p>
<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><br>
<p></p>
<p>
All nominations will be considered regardless of origin, background, religion, sex, sexual orientation, age, gender identity, disability.</p><br>
<p></p>
<p>
Working with us is about being able to do things your way. The way you work, the way you develop, the way you progress, it&rsquo;s all up to you.</p><p><br>
<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><br>
<p>
Be innovative and entrepreneurial and the impact you could make might just amaze you. Join our movement for a healthier world. One Planet One Health BY YOU.</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><br>
<p></p>
<p>
What we offer</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>
#LT-U</p></div><p></p>

Quality Manager (Bursa)

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)

Ajax Systems

<div>
 The international technology company Ajax Systems opens a full-cycle production facility in T&uuml;rkiye.
 <br/>
 <br/>
 Ajax Systems is the largest developer and manufacturer of security systems in Europe. The back office, R&amp;D department, and two full-cycle production facilities are located in Ukraine. The company has branch offices worldwide: UAE (Dubai), Italy, Spain, Germany, Poland, Canada, and many other regions. Ajax team has more than 2,200 employees, including 500 developers and 1,200 production workers. Attracting local expertise in each key market enables us to scale the product globally and grow fast.
 <br/>
 <br/>
 <strong>
  Location : Istanbul/Tuzla, DESBAS
  <br/>
  <br/>
 </strong>
 <strong>
  Reponsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   The FAI process organization and support
  </li>
  <li>
   The FAI process control, training in critical aspects of production (or training if ESD skills and certification are available)
  </li>
  <li>
   Organization, optimization, and improvement of production control processes
  </li>
  <li>
   Conducting inspections of production processes
  </li>
  <li>
   Production key quality indicators monitoring, analysis, and response to deviations
  </li>
  <li>
   Preparation of reports based on the results of the analysis of inconsistencies
  </li>
  <li>
   Regulatory documentation creation, description of processes and procedures to ensure team functioning
  </li>
  <li>
   Team management
  </li>
  <li>
   Setting clear KPIs for the team
  </li>
  <li>
   Coordination and tracking of corrective and preventive actions within the team
  </li>
  <li>
   Mentoring and training new team members
  </li>
  <li>
   Conducting meetings on inconsistencies and process quality, supporting continuous system improvements
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Higher education (technical, standardization/quality systems)
  </li>
  <li>
   More than 2 years of work experience in the field of the quality management system
  </li>
  <li>
   Experience with regulatory documentation (GOST, DSTU, ISO)
  </li>
  <li>
   Knowledge of European and Turkish legislation, regulatory documents, standards, rules, and norms related to quality management systems and technical regulations is desirable
  </li>
  <li>
   Good command of English
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
</div>


Quality Engineer

<div><div>The international technology company Ajax Systems opens a full-cycle production facility in T&uuml;rkiye.</div><div>
Ajax Systems is the largest developer and manufacturer of security systems in Europe. The back office, R&amp;D department, and two full-cycle production facilities are located in Ukraine. The company has branch offices worldwide: UAE (Dubai), Italy, Spain, Germany, Poland, Canada, and many other regions. Ajax team has more than 2,200 employees, including 500 developers and 1,200 production workers. Attracting local expertise in each key market enables us to scale the product globally and grow fast.</div><div></div><div><b><br>
Location : Istanbul/Tuzla, DESBAS</b></div>
<h3 class="jobSectionHeader"><b>Reponsibilities</b></h3><ul><li>
The FAI process organization and support</li><li>
The FAI process control, training in critical aspects of production (or training if ESD skills and certification are available)</li><li>
Organization, optimization, and improvement of production control processes</li><li>
Conducting inspections of production processes</li><li>
Production key quality indicators monitoring, analysis, and response to deviations</li><li>
Preparation of reports based on the results of the analysis of inconsistencies</li><li>
Regulatory documentation creation, description of processes and procedures to ensure team functioning</li><li>
Team management</li><li>
Setting clear KPIs for the team</li><li>
Coordination and tracking of corrective and preventive actions within the team</li><li>
Mentoring and training new team members</li><li>
Conducting meetings on inconsistencies and process quality, supporting continuous system improvements</li></ul><h3 class="jobSectionHeader"><b>
Qualifications</b></h3><ul><li>
Higher education (technical, standardization/quality systems)</li><li>
More than 2 years of work experience in the field of the quality management system</li><li>
Experience with regulatory documentation (GOST, DSTU, ISO)</li><li>
Knowledge of European and Turkish legislation, regulatory documents, standards, rules, and norms related to quality management systems and technical regulations is desirable</li><li>
Good command of English</li></ul>
<p>
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.</p></div>

Calderys

<div></div><div><div><div><p>The QA Manager will be responsible for maintaining and continuously improving the Quality Management System at the Haznedar-Durer plant, in full alignment with Calderys EMEA standards and ISO 9001:2015 requirements. The role ensures compliance with customer and regulatory expectations, coordinates audits, manages documentation, and drives corrective/preventive actions. The QA Manager will also ensure that quality-related data and progress are consistently updated in the EMEA-wide global action plan. This position requires strong technical expertise, structured problem-solving, and the ability to lead quality initiatives while fostering a culture of continuous improvement within the plant.<br>
</p><p></p><p><b>Key Responsibilities:<br>
</b></p><p></p><p><b>Quality Management System (QMS):
</b></p><ul><li>Maintain and update the QMS in compliance with ISO 9001:2015 and corporate requirements.
</li><li>Ensure integration of QMS with day-to-day plant operations and business processes.
</li><li>Own and update quality documentation (manuals, procedures, instructions, forms).
</li></ul><p><b>Audits &amp; Compliance:
</b></p><ul><li>Plan and conduct internal audits; ensure findings are addressed through corrective and preventive actions.
</li><li>Coordinate external audits (customers, certification bodies, authorities) and support follow-up.
</li><li>Ensure compliance with local regulatory requirements regarding product quality and safety.
</li></ul><p><b>Reporting &amp; Coordination:
</b></p><ul><li>Provide regular updates of quality KPIs, actions, and improvement projects into the EMEA central action plan.
</li><li>Ensure quality performance and progress are properly documented and communicated.
</li><li>Collaborate with corporate QA/Opex functions to align practices and share best methods.
</li></ul><p><b>Training &amp; Awareness:
</b></p><ul><li>Promote awareness of the quality policy, objectives, and process approach among all plant employees.
</li><li>Provide training and support to teams to strengthen quality culture and operational discipline.
</li><li>Ensure alignment with Occupational Health &amp; Safety regulations in all quality practices.
</li></ul><p><b>Continuous Improvement:
</b></p><ul><li>Support problem-solving and root cause analysis for non-conformities.
</li><li>Encourage risk-based thinking and process improvement across all functions.
</li>Actively contribute to cross-functional projects (product transfer, process optimization, customer complaints resolution).<br>
<li>
</li></ul><p></p><p><b>Qualifications &amp; Education:
</b></p><ul><li>Minimum Bachelor&rsquo;s degree (Lisans) in Chemistry, Mechanical Engineering, Materials Science, or Industrial Engineering. Alternatively, a Technical Vocational School degree (MYO) in a related field, combined with relevant experience, can be considered.
</li><li>ISO 9001 knowledge or certification (internal auditor training is a plus but not mandatory at hiring stage).
</li><li>1&ndash;3 years of professional experience in quality, production, or industrial operations.
</li><li>Previous exposure to manufacturing environment (ceramics, cement, automotive, chemicals, or similar) preferred but not mandatory.
</li><li>Refractory-specific experience good to have but not mandatory.
</li><li>Good computer literacy (MS Office required; ERP/QMS software knowledge is a plus).
</li><li>At least basic English proficiency (reading documentation, reporting to corporate).
</li><li>Detail-oriented, organized, able to manage documentation rigorously.
</li><li>Proactive and problem-solving mindset, willing to grow into the role.
</li><li>Strong communication skills to liaise with production, maintenance, and corporate QA teams.</li></ul></div></div></div><div></div>

Quality Assurance Manager

Stellantis Middle East & Africa

<div>
 <p>
  <strong>
   General Mission/Purpose:
  </strong>
 </p>
 <ul>
  <li>
   Lead quality activities and reporting
  </li>
  <li>
   Work on quality alignement of xF and xP brands
  </li>
  <li>
   Implement change management for quality and ensure customer centricity project implementation
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Main Activities:
  </strong>
 </p>
 <ul>
  <li>
   Damages prevention and corrective actions to improve the quality of deliverd cars to the final customer
  </li>
  <li>
   Managment of Force Majeur events
  </li>
  <li>
   Updates of existing and new standards elaboration
  </li>
  <li>
   Downgraded and Wrecked cars management
  </li>
  <li>
   Warranty process monitoring and damages final assignement
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   COMPETENCIES &amp; QUALIFICATIONS:
  </strong>
 </p>
 <ul>
  <li>
   Education: Master degree in Quality or related field
  </li>
  <li>
   Work Experience: At least 4 years as a quality leader
  </li>
  <li>
   Language: English mandatory, French, Arabic are a plus
  </li>
  <li>
   Preferred Skills &amp; Abilities: Engineering Transport, Logistics, Quality Standards for Ooutbound Logistics
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   KEY WORKING RELATIONSHIPS
  </strong>
 </p>
 <ul>
  <li>
   Purchasing, New Vehicle Launches, Finance, Operations, Factories, Global Transport and Packaging, Flow Architectures, Claims, Regions
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <br/>
 </p>
 <p>
  At Stellantis, we assess candidates based on qualifications, merit and business needs.
 </p>
 <p>
  We welcome applications from people of all gender identities, age, ethnicity, nationality, religion, sexual orientation and disability. Diverse teams will allow us to better meet the evolving needs of our customers and care for our future.
 </p>
 <p>
  <br/>
 </p>
 <p>
  We celebrate diversity and are committed to creating an inclusive environment for all our employees. We aim to encourage a culture where people can be themselves and be valued for their contribution. We are committed to making reasonable adjustments to the recruitment process as required. Please add any adjustment requests to your application. is entrusted with the critical mission of scrutinizing the entire logistic process design and evaluating preliminary decisions in the target plant. They are expected to approach each aspect with a challenging mindset, aiming to minimize costs and investments. Their expertise will be pivotal in preparing comparative profitability analyses for alternative process scenarios, providing the management team with sensible suggestions that enable informed best-cost decision-making.
 </p>
 <p>
 </p>
</div>


Quality System Leader - MEA Region

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

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