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DHL Supply Chain

<div>
 Let's be the part of our #TogetherUnstoppable team!
 <br/>
 <br/>
 DHL Supply Chain is providing supply chain management and consulting like warehousing, distribution, managed transportation services and value-added services in consumer, retail, life science &amp; healthcare, technology, engineering &amp; manufacturing and automotive sectors. We are active in more than 60 countries and territories, employing around 120,000 people. DHL Supply Chain located in 2400 locations all over the world and manages approx. 23 million m2 storage area.
 <br/>
 <br/>
 DHL Supply Chain Turkey started its operations in 2000 providing warehousing, distribution, labeling, packaging, technical services, home delivery, spare parts logistics and reverse logistics services. DHL Supply Chain Turkey serving leading companies in consumer, retail, healthcare, automotive, engineering &amp; manufacturing and technology sectors with more than 2000 employees in 370 thousand m2 warehousing space.
 <br/>
 <br/>
 <strong>
  Qualifications
  <br/>
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor's degree in pharmacy, Chemistry, Chemistry Engineering, Biology, Medical Biology Genetics,
  </li>
  <li>
   Minimum 2 years' experience in life sciences and healthcare (2 years' experience will not be required for Pharmacy graduates - new graduates will also be considered)
  </li>
  <li>
   Knowledge of ISO 9001, GMP/GDP,
  </li>
  <li>
   Following GMP/GDP guidelines and manage quality systems of the LSHC site,
  </li>
  <li>
   Focusing on needs of customers, driving the team to meet service levels,
  </li>
  <li>
   Advanced level in both written and spoken English,
  </li>
  <li>
   Strong communication skills,
  </li>
  <li>
   No military obligation for male candidates,
  </li>
  <li>
   Preferably residing near to Esenyurt area,
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Job Description
  <br/>
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Assuring that quality KPIs are followed by all employees and department.
  </li>
  <li>
   Managing SOPs and ensuring that current policy and procedures are followed among the site.
  </li>
  <li>
   Preparing quarterly/monthly business review presentations and lead customer meetings
  </li>
  <li>
   Assuring that no critical observation points are received from global and local inspections.
  </li>
  <li>
   Managing and following Ministry of Health regulations, cGMP/GDP compliance activities
  </li>
  <li>
   Working as a back-up of Responsible Pharmacist
  </li>
  <li>
   Following all quality topics as Deviations, Customer Complaints, Corrective/Preventive Actions, Change Management
  </li>
  <li>
   Providing trainings to employees
  </li>
  <li>
   Attending audits and perform self-inspections.
  </li>
  <li>
   Assuring that Good Documentation Practices are followed among the site.
  </li>
 </ul>
</div>


Quality Assurance Specialist

<div></div><div><div>Let's be the part of our <div>#TogetherUnsto</div>ppable team!<br>
<br>
DHL Supply Chain is providing supply chain management and consulting like warehousing, distribution, managed transportation services and value-added services in consumer, retail, life science &amp; healthcare, technology, engineering &amp; manufacturing and automotive sectors. We are active in more than 60 countries and territories, employing around 120,000 people. DHL Supply Chain located in 2400 locations all over the world and manages approx. 23 million m2 storage area.<br>
<br>
DHL Supply Chain Turkey started its operations in 2000 providing warehousing, distribution, labeling, packaging, technical services, home delivery, spare parts logistics and reverse logistics services. DHL Supply Chain Turkey serving leading companies in consumer, retail, healthcare, automotive, engineering &amp; manufacturing and technology sectors with more than 2000 employees in 370 thousand m2 warehousing space.<br>
<br>
<div>Qualifications</div><br>
<br>
<ul><li>Bachelor's degree in pharmacy, Chemistry, Chemistry Engineering, Biology, Medical Biology Genetics,</li><li>Minimum 2 years' experience in life sciences and healthcare (2 years' experience will not be required for Pharmacy graduates - new graduates will also be considered)</li><li>Knowledge of ISO 9001, GMP/GDP,</li><li>Following GMP/GDP guidelines and manage quality systems of the LSHC site,</li><li>Focusing on needs of customers, driving the team to meet service levels,</li><li>Advanced level in both written and spoken English,</li><li>Strong communication skills,</li><li>No military obligation for male candidates,</li></ul><br>
<ul><li>Preferably residing near to Esenyurt area,</li></ul><br>
Job Description<br>
<br>
<ul><li>Assuring that quality KPIs are followed by all employees and department.</li><li>Managing SOPs and ensuring that current policy and procedures are followed among the site.</li><li>Preparing </li></ul><div>quarterly/mont</div>hly business review presentations and lead customer meetings<br>
<ul><li>Assuring that no critical observation points are received from global and local inspections.</li><li>Managing and following Ministry of Health regulations, cGMP/GDP compliance activities</li><li>Working as a back-up of Responsible Pharmacist</li><li>Following all quality topics as Deviations, Customer Complaints, </li></ul><div>Corrective/Pre</div>ventive Actions, Change Management<br>
<ul><li>Providing trainings to employees</li><li>Attending audits and perform </li></ul><div>self-inspectio</div>ns.<br>
<ul><li>Assuring that Good Documentation Practices are followed among the site.</li></ul></div></div>

TCI Aircraft Interiors

<div>
 <p>
  TCI Aircraft Interiors was founded in 2010, and in 2023, it entered a new era with the merger of three subsidiary companies under Turkish Airlines.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>
 </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>
  <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>


Nestlé

<div><p>Nestl&eacute; is one of the world&rsquo;s leading food and beverage company, with 2000 global iconic brands and operating in 188 countries.</p><p>
At Nestl&eacute; we work for unlocking the power of food to enhance quality of life for everyone, today and for generations to come. That is our purpose.</p><p>
We are the <b><i>Good food, Good</i></b><i> </i><b><i>life</i></b> company. We believe in the power of food to enhance lives. Good food nourishes and delights the senses. It helps children grow healthy, pets thrive, parents age gracefully and everyone live life to the fullest. Good food brings us together. Good food also respects our planet and protects resources for future generations.</p><p>
Get to know us better at <b>www.nestle.com</b></p><p><b>
Join Nestl&eacute; Team and be a Force For Good!</b></p><p>
We are currently looking for a <b>Quality Assurance System Specialist </b>to join our <b>Bal&#305;kesir Factory </b>team.</p><p>
Location: Bal&#305;kesir</p><p>
Type of contract: Permanent</p><p><b>
As a Quality Assurance System Specialist,</b> <b>you will have the following responsibilities;</b></p><ul><li>
SAP Quality Module Super User: To ensure that the quality processes in the SAP system work correctly and uninterruptedly from end to end; to regularly monitor system controls (Health Check), to analyse user needs and to direct development requests.</li><li>
Product Release Processes: To follow up the results of analyses for finished products and semi-finished products on PO (Purchase Order) basis, and to carry out release processes through the system. To ensure the correction of missing or incorrect data points by coordinating with the relevant departments when necessary.</li><li>
Analysing and Reporting Quality Data: Analysing quality data from production processes, identifying trends and possible deviations; reporting these analyses to management and contributing to decision support processes.</li><li>
Customer Complaint Management: To record customer complaints via SAP or related systems, perform root cause analyses and ensure the implementation of sustainable actions. Coordination with relevant units in feedback processes.</li><li>
Legal and Corporate Compliance Support: To support the sustainability of quality systems to ensure compliance with Nestl&eacute; Quality Standards, NQMS (Nestl&eacute; Quality Management System) and legal regulations. To actively contribute to the preparation processes for internal and external audits.</li><li>
System Performance Monitoring and Improvement: Monitoring the effectiveness of quality data entry processes, leading projects to simplify and error-free workflows in SAP quality module.</li><li>
Training and User Support: Providing training and continuous support to the quality team and related user groups on the use of SAP quality module, data entry and analysis processes.</li><li>
Contribution to Improvement Projects: Supporting data-based improvement projects under Nestl&eacute; Continuous Excellence; developing projects in the areas of efficiency, error reduction and process standardisation.</li></ul><p><b>
Which profile are we looking for?</b></p><ul><li>
Excellent command of English</li><li>
Graduated from Food Engineering, Chemical Engineering or similar departments of universities,</li><li>
Experienced in SAP QM module and preferably with super user experience,</li><li>
Minimum 2 years of experience in quality assurance processes,</li><li>
Competent in data analysis and reporting; MS Excel and preferably Power BI knowledge,</li></ul><p></p><p><b><br>
</b></p><p><b>What are our employee community values?</b></p><p>
Safety, quality, compliance and respect are pillars for our community existence.</p><p>
Respect is our overaching value in Nestl&eacute;. We RESPECT eachother, others, environment and all life around.</p><p>
We work in a supportive, caring, elevating environment. It is crucial for us to preserve our culture of solidarity.</p><p><b>
What are our working values at Nestl&eacute;?</b></p><p>
Multinational experience at one of the world&rsquo;s leading food and beverage company</p><p>
International and domestic career opportunities</p><p>
Development opportunities and trainings</p><p>
Exclusive employee discounts</p><p>
Employee Assistance Program, 24/7 expert support</p><p>
Sport benefit program (benefit from more than 350 sport centers)</p><p>
A paid birthday leave</p><p>
4 weeks paternity leave</p><p>
The Nestl&eacute; Companies are an equal employment opportunity and affirmative action employer seeking diversity in qualified applicants for employment. All applicants will receive consideration for employment without regard to race, ethnicity, color, gender, gender identity, age, religion, national origin, ancestry, disability, perceived disability, genetic information, veteran status, sexual orientation, or any other protected status, as defined by applicable law. <b><i>Be a force for good.</i></b></p><p>
..</p></div>

Quality Assurance System Specialist

Amerikan Hastanesi

<div>
 <p>
  Stembio (a Koc Holding/Koc Healthcare company) is a cutting-edge cGMP laboratory specializing in the production and preparation of cellular products such as CAR-T/TILs, Mesenchymal Stem Cells (MSCs), exosomes, immunotherapy products, cord blood banking and tissue grafts. We are committed to delivering high-quality, regulatory-compliant cell therapy products through rigorous quality control and validation processes.
 </p>
 <p>
  <br/>
 </p>
 <p>
  We are seeking a highly skilled and motivated
  <strong>
   Quality Assurance (QA) Expert for Stembio
  </strong>
  to ensure compliance with cGMP, regulatory requirements, and company quality standards for our cell therapy products.
 </p>
 <p>
  <br/>
 </p>
 <p>
  The QA Expert will oversee quality management systems, support regulatory audits, manage deviations, and drive continuous improvement initiatives. The ideal candidate will have a strong background in quality assurance, risk management, and compliance within a cGMP-regulated environment.
 </p>
 <p>
  <br/>
 </p>
 <p>
  If you are passionate about quality assurance in advanced cell therapies and have the expertise to uphold the highest standards, we encourage you to apply!
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Master&rsquo;s degree or higher in Biology, Biotechnology, Biochemistry, or a related field.
  </li>
  <li>
   Minimum of 3+ years of experience in a cGMP-regulated Quality Assurance environment, preferably in cell therapy, regenerative medicine, or biopharmaceuticals.
  </li>
  <li>
   Strong knowledge of quality assurance principles, risk management, and regulatory compliance (EMA, TITCK, FDA, ICH guidelines).
  </li>
  <li>
   Experience in managing QMS, deviation handling, CAPA, and change control processes.
  </li>
  <li>
   Ability to interpret and apply regulatory guidelines and quality standards to ensure compliance.
  </li>
  <li>
   Excellent analytical, problem-solving, and decision-making skills.
  </li>
  <li>
   Strong communication and leadership skills, with the ability to work independently and in a team.
  </li>
  <li>
   Experience with electronic QMS, document control systems, and LIMS is a plus.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Responsibilities
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Ensure compliance with cGMP, EMA, TITCK, and other relevant regulatory requirements for cell therapy products.
  </li>
  <li>
   Develop, implement, and maintain Quality Management Systems (QMS), including deviation management, CAPA, change control, and risk assessments.
  </li>
  <li>
   Support and participate in regulatory inspections, audits, and internal quality reviews.
  </li>
  <li>
   Review and approve SOPs, batch records, validation protocols, and quality-related documents.
  </li>
  <li>
   Conduct investigations for deviations, out-of-specification (OOS) results, and non-conformances, ensuring timely resolution and implementation of corrective and preventive actions (CAPAs).
  </li>
  <li>
   Oversee the training program to ensure all personnel are adequately trained in quality procedures and regulatory requirements.
  </li>
  <li>
   Collaborate with cross-functional teams including Quality Control (QC), Production, and Regulatory Affairs to maintain high-quality standards.
  </li>
  <li>
   Monitor and improve quality metrics to ensure continuous improvement of quality systems and processes.
  </li>
  <li>
   Manage supplier and raw material quality assurance, including vendor qualification and material release processes.
  </li>
  <li>
   Ensure timely approval and release of raw materials, intermediates, and final products based on quality assurance criteria.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <u>
   Your personal data is processed for the purpose of receiving and evaluating your job application. You can find detailed information about your processed personal data and rights from the "Employee Candidate Clarification Text" under the "Human Resources" heading of our website.
  </u>
 </p>
 <p>
 </p>
</div>


Stembio - Quality Assurance (QA) Expert

Curium Pharmaceuticals

<div><div><p><b>About Curium</b></p>
</div>
<div><p>Curium is the world&rsquo;s largest nuclear medicine company with more than a century of industry experience. We develop, manufacture and distribute world-class radiopharmaceutical products to help patients around the globe. Our proven heritage combined with a pioneering approach are the hallmarks to deliver innovation, excellence and unparalleled service.</p></div><div><br>
<p>
</p></div><div><p>With manufacturing facilities across Europe and the United States, Curium delivers SPECT, PET and therapeutic radiopharmaceutical solutions for life-threatening diseases to over 14 million patients annually. The name &lsquo;Curium&rsquo; honors the legacy of pioneering radioactive researchers Marie and Pierre Curie, after whom the radioactive element curium was named and emphasizes our focus on nuclear medicine. The tagline &lsquo;Life Forward&rsquo; represents our commitment to securing a brighter future for all those we serve: An enhanced quality of care for our patients. A trusted partner to our customers. A supportive employer to our valued team.</p>
</div><div><div><div><h2 class="jobSectionHeader"><b>
Summary of Position</b></h2></div><p></p><div><br>
<p>
We are looking for a Theranostics Production Specialist to join our growing team. This role will be responsible for ensuring the production processes meet regulatory standards, maintaining production schedules, and implementing improvements in production efficiency.</p></div></div><div><div><h2 class="jobSectionHeader"><b>
Essential Functions</b></h2>
</div><div><ul><li>Production Management: Oversee and manage the production process for theranostics products, ensuring that all activities are carried out in compliance with GMP, ISO, and regulatory standards.</li>
<li>Quality Assurance: Conduct routine inspections and audits to ensure products meet quality specifications. Document all production activities, deviations, and corrective actions.</li>
<li>Equipment Maintenance: Ensure proper operation of production equipment, perform calibration, and troubleshooting equipment as needed.</li>
<li>Process Optimization: Identify and implement improvements to increase efficiency, productivity, and safety in the production processes.</li>
<li>Collaboration: Work closely with the quality control team, R&amp;D department, and other stakeholders to ensure smooth production and timely delivery of products.</li>
<li>Training: Provide training to junior staff and assist in their development in production and quality assurance practices.</li>
<li>Documentation: Maintain accurate and detailed production logs, batch records, and reports for regulatory compliance.</li>
<li>Regulatory Compliance: Ensure adherence to safety, regulatory, and compliance standards, including environmental, health, and safety protocols.</li>
<li>Continuous Improvement: Actively participate in root cause analysis and lead projects aimed at improving production processes and addressing challenges.</li>
</ul></div></div><div><div><h2 class="jobSectionHeader"><b>Requirements</b></h2>
</div><div><ul><li>Bachelor&rsquo;s degree in chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering, Radiopharmaceutical Sciences, or related fields. A master&rsquo;s degree is a plus.</li>
<li>Minimum of 2-3 years of experience in radiopharmaceutical production or theranostics, with a strong understanding of GMP guidelines.</li>
<li>Experience with radiochemical synthesis, radiolabeling, and related processes.</li>
<li>Familiarity with laboratory equipment and production systems.</li>
<li>Proficient in the use of process control software and manufacturing systems.</li>
<li>Solid understanding of GMP, GLP, GRP, ICH, and regulatory requirements.</li>
<li>Familiarity with quality control and assurance in radiopharmaceutical production.</li>
<li>Strong problem-solving abilities, with attention to detail in handling complex technical and regulatory issues.</li>
<li>Excellent communication and interpersonal skills, able to work effectively with a diverse team.</li>
<li>Collaborative attitude and willingness to work in cross-functional teams.</li>
<li>Ability to work in a cleanroom environment, including the use of protective gear.</li>
<li>Experience in theranostics and radiopharmaceutical production for personalized medicine.</li>
<li>Experience with SOPs, training programs, and regulatory inspections.</li>
<li>Familiarity with software such as SAP, LIMS, or other production management systems.</li>
</ul></div></div></div><div>
<div><p><b>Disclaimer</b></p>
</div>
<div><p>The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.</p></div></div><br>
<p>
</p><div><div><p><b>Equal Opportunity Employer</b></p>
</div>
<div><p>Curium is an equal opportunity employer and believes everyone deserves respect, dignity and equality. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.</p></div></div></div>

Theranostics Production Specialist

<div><p>Nestl&eacute; is one of the world&rsquo;s leading food and beverage company, with 2000 global iconic brands and operating in 188 countries.</p><p>
At Nestl&eacute; we work for unlocking the power of food to enhance quality of life for everyone, today and for generations to come. That is our purpose.</p><p>
We are the <b><i>Good food, Good</i></b><i> </i><b><i>life</i></b> company. We believe in the power of food to enhance lives. Good food nourishes and delights the senses. It helps children grow healthy, pets thrive, parents age gracefully and everyone live life to the fullest. Good food brings us together. Good food also respects our planet and protects resources for future generations.</p><p>
Get to know us better at <b>www.nestle.com</b></p><p><b>
Join Nestl&eacute; Team and be a Force For Good!</b></p><p>
We are currently looking for a <b>Quality Assurance Executive </b>to join our <b>Operations </b>team.</p><p>
Location: Karacabey, Bursa</p><p>
Type of contract: Permanent</p><p><b>
As a </b><b>Quality Assurance Executive</b><b>, you will have the following responsibilities;</b></p><ul><li>
Provide technical expertise as quality specialist to resolve internal and external quality defects by leading food safety management program and facilitating quality improvement initiatives,
</li><li>Ensure food safety management system documentation is updated and effective. Assess the Nestl&eacute; Food Safety Management System is in place, and is obtaining expected results,
</li><li>Promote quality awareness across the company by delivering training for their specific areas of expertise e.g. hygiene, foreign body, haccp, pest control, cleaning validation. Promote GMP standarts at whole factory as Hygiene Champion,</li><li>
Implement specific quality procedures, instruction and tools, which are directly related to their area of concern and implement Nestle quality instructions e.g.pathogen monitoring,</li><li>
Ensure consumer complaints, specifically foreign body complaints are properly evaluated and acted upon to prevent re-occurrence,</li><li>
Provide Risk Assessment analysis. Manage issues with non-conforming product to assure proper control, minimize losses and ensuring consumer expectations. Undertake root cause analyses for Quality and Food Safety stock holds, disposals and consumer complaints. Implementing robust, sustainable corrective actions which will reduce or eliminate reoccurrence,</li><li>
Coordinate management changes in order to ensure no food safety related risk introduced to site,</li><li>
Review and approve food safety compliance relevant system tools such as PB, PV, NEB, recipes.
</li></ul><p><b>Which profile are we looking for?</b></p><ul><li>
Bachelor&rsquo;s or master&rsquo;s degree and 5+ years of experience in food manufacturing environment</li><li>
Excellent command of English</li><li>
Experience in analysing and interpreting complex data and use it to drive improvement
</li><li>Prior experience in managing Food Safety Management System</li><li>
Conversant in Continuous Improvement tools and methodologies</li><li>
SAP QM module</li></ul><p><b>
What are our employee community values?</b></p><p>
Safety, quality, compliance and respect are pillars for our community existence.</p><p>
Respect is our overaching value in Nestl&eacute;. We RESPECT eachother, others, environment and all life around.</p><p>
We work in a supportive, caring, elevating environment. It is crucial for us to preserve our culture of solidarity.</p><p><b>
What are our working values at Nestl&eacute;?</b></p><p>
Multinational experience at one of the world&rsquo;s leading food and beverage company</p><p>
International and domestic career opportunities</p><p>
Development opportunities and trainings</p><p>
Exclusive employee discounts</p><p>
Employee Assistance Program, 24/7 expert support</p><p>
Sport benefit program (benefit from more than 350 sport centers)</p><p>
A paid birthday leave</p><p>
4 weeks paternity leave</p><p>
The Nestl&eacute; Companies are an equal employment opportunity and affirmative action employer seeking diversity in qualified applicants for employment. All applicants will receive consideration for employment without regard to race, ethnicity, color, gender, gender identity, age, religion, national origin, ancestry, disability, perceived disability, genetic information, veteran status, sexual orientation, or any other protected status, as defined by applicable law. <b><i>Be a force for goo</i></b></p><p>
..</p></div>

Quality Assurance Executive

Explore 1041+ Quality assurance specialist in Turkey this October. Find roles across top companies and apply now to boost your career.

1041 quality assurance specialist jobs IN Turkey

Quality Assurance Specialist

Quality Assurance Specialist

Quality Assurance Specialist

Quality Assurance System Specialist

Stembio - Quality Assurance (QA) Expert

Theranostics Production Specialist

Quality Assurance Executive