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quality assurance specialist

Kenvue

<div><div><div><div><div><div><div><div><p>Kenvue is currently recruiting for a:</p></div></div></div></div></div></div></div>
Commercial Quality Specialist (Fixed term)<p></p><p><b>
What we do</b></p><p>
At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we&rsquo;re the house of iconic brands - including NEUTROGENA&reg;, AVEENO&reg;, TYLENOL&reg;, LISTERINE&reg;, JOHNSON&rsquo;S&reg; and BAND-AID&reg; that you already know and love. Science is our passion; care is our talent.</p><p></p><p><b>
Who We Are</b></p><p>
Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage &ndash; and have brilliant opportunities waiting for you! Join us in shaping our future&ndash;and yours.</p><p></p><p><b>
Role reports to:</b></p>
Ticari Kalite M&uuml;d&uuml;r&uuml;, T&uuml;rkiye &amp; CIS<p></p><p><b>
Location:</b></p>
Europe/Middle East/Africa, Turkey, Istanbul, Istanbul<p></p><p><b>
Work Location:</b></p>
Hybrid<p></p><p><b>
What you will do</b></p><p>
Kenvue is currently recruiting for:</p><p>
Commercial Quality Specialist (Fixed term)</p><p>
This position reports into Commercial Quality Manager and is based in Istanbul, Turkey.</p><p><b>
What we do
</b></p><p>At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we&rsquo;re the house of iconic brands - including NEUTROGENA&reg;, AVEENO&reg;, LISTERINE&reg;, JOHNSON&rsquo;S&reg; and BAND-AID&reg; that you already know and love. Science is our passion; care is our talent.</p><p><b>
Who we are</b></p><p>
Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage &ndash; and have brilliant opportunities waiting for you! Join us in shaping our future&ndash;and yours. For more information, click here.</p><p><b>
Role reports to:</b> Commercial Quality Manager</p><p><b>
Location:</b> Istanbul, Turkey</p><p><b>
Travel %: Minimal</b></p><p><b>
Pay:</b> 24</p><p><b>
What you will do</b></p><p>
Establishes and maintains quality assurance programs, procedures and controls, ensuring that performance parameters of both the products and quality system elements are continually measured to drive improvement initiatives. The Commercial Quality Specialist is responsible for monitoring and tracking quality detractors, ensuring compliance with company policies and procedures, and releasing commercial products to the market. This role will have cluster wide responsibilities in AMET which will provide a lot of room for growth, development opportunities with other departments. In addition, this position could be an opportunity to work with FMCG and even products such as dietary supplements.</p><p></p><p><b>
Key Responsibilities</b></p><ul><li>Develop and implement quality control processes for commercial products</li><li>Analyze data to identify trends and opportunities for improvement in product quality</li><li>Collaborate with cross-functional teams to ensure compliance with quality standards and regulations.</li><li>Conduct audits and inspections to assess product quality and identify areas for enhancement.</li><li>Provide training and guidance to team members on quality control best practices</li><li>Collaborate with cross-functional teams to monitor and track quality detractors utilizing various databases</li><li>Ensure compliance with company policies, procedures, quality standards, safety, and environmental regulations</li><li>Write and assist others in writing standard operating procedures</li><li>Generate and identify significant trends, reporting them to management and cross functional teams</li><li>Provide advanced technical assistance in information mapping technology</li><li>Support product review and release functions</li><li>Generate complex statistical summaries</li><li>Provide support to good manufacturing practice auditing.</li><li>Establish and maintain quality assurance programs, procedures, and controls to drive improvement initiatives.</li></ul><p><b>
What we are looking for</b></p><p><b>
Required Qualifications</b></p><ul><li>Education: Bachelor&rsquo;s degree in pharmacy, Medical, Engineering, or a Chemistry discipline.</li><li>Licensed as a Qualified Person from Turkish Health Authority, or eligible for qualification based on the below criteria is preferred:</li><li>He/she should have 2 years of practical experience in a manufacturing site authorized by the Drugs &amp; Devices Agency.</li><li>Minimum 2-4 years of experience in Pharma or FMCG segments, with specific Quality Assurance, regulatory and regulatory compliance competencies or involved in batch release activities.</li><li>Proven working experience in quality assurance programs and controls</li><li>Proficiency in written and spoken Turkish and English is a must.</li><li>Experience in writing standard operating procedures</li><li>Experience in supporting product review and release functions</li></ul><p><b>
Desired Qualifications</b></p><ul><li>Strong analytical skills with the ability to interpret data and make informed decisions</li><li>Excellent communication and interpersonal skills to collaborate effectively with team members</li><li>Detail-oriented with a focus on accuracy and precision in quality control processes</li><li>Experience in generating and identifying significant trends</li><li>Experience in generating statistical summaries</li><li>Experience in good manufacturing practice auditing</li></ul><p><b>
What&rsquo;s in it for you</b></p><ul><li>
Competitive Benefit Package</li><li>
Learning &amp; Development Opportunities</li><li>
Kenvuer Impact Networks</li><li>
This list could vary based on location/region</li></ul><p>
Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on merit without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.</p><p></p><p>
If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.</p></div>

Commercial Quality Specialist (Fixed term)

Roche

<div><p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><p></p><div>
The Position</div><p>
Roche fosters diversity, equity and inclusion, representing the communities we serve. When dealing with healthcare on a global scale, diversity is an essential ingredient to success. We believe that inclusion is key to understanding people&rsquo;s varied healthcare needs. Together, we embrace individuality and share a passion for exceptional care. Join Roche, where every voice matters.<br>
<br>
The Position<br>
We are looking for a Regulatory Affairs and Quality Specialist at Roche Diagnostics.<br>
 <b>What will you do?</b></p><ul><li><p><br>
You ensure all product related local and global requirements for registration.</p></li><li><p><br>
You supervise all kinds of registration procedures of the products, to obtain documentation related there of from company&rsquo;s relevant global functions. Mastery of all IVD product local registration processes and coordination with functions such as product management, sales and tenders.</p></li><li><p><br>
You coordinate regulatory documentation activities, obtain overseas documents required for tenders and other legal procedures and participate meetings with regulatory body when necessary.</p></li><li><p><br>
You update and maintain the quality assurance system aligned with global standards and local requirements.</p></li><li><p><br>
You work together with distributors in the quality assurance area and to perform controlling processes when necessary.</p></li><li><p><br>
You prepare internal and external audits in collaboration with internal stakeholders and perform the action plans.</p></li></ul><p><b><br>
Who are you?</b></p><ul><li><p><br>
You have University Degree</p></li><li><p><br>
You have Regulatory affairs and Quality experience in IVD/medical device industry</p></li><li><p><br>
You have process knowledge and experience in ISO 9001 and ISO 13485 standards</p></li><li><p><br>
You are experienced in conducting 2nd party audits &amp; 3rd party logistics processes</p></li><li><p><br>
You are proactive and team worker.</p></li><li><p><br>
You are Fluent in English</p></li></ul><p></p><div>
Who we are</div><p>
A healthier future drives us to innovate. Together, more than 100&rsquo;000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p><br>
Let&rsquo;s build a healthier future, together.</p><p></p><p><b>
Roche is an Equal Opportunity Employer.</b></p></div>

Quality & Regulatory Specialist

Commencis

<div><div>We are looking for a <b>Senior Quality Assurance Enginee</b>r with strong technical and communication skills to contribute throughout the development lifecycle of products in various exciting domains, which are realized with Commencis&rsquo; expertise in a fast-paced team environment.</div><div></div><div><b><br>
If you are curious by nature, adaptive, collaborative, and always one step ahead, then join us and be a Commencer!</b></div>
<h3 class="jobSectionHeader"><b>Responsibilities</b></h3><ul><li>
Reviewing test basis (stories, FSD, design docs, etc.) and give feedback about whether they are testable or not</li><li>
Creating and designing efficient test cases to provide good coverage (for both manual and automated testing)</li><li>
Performing manual testing across <b>Mobile applications, APIs, and Databases</b></li><li>
Performing required activities to apply test process (test planning, design, execution, monitoring and reporting)</li><li>
Providing feedback to software engineering and other teams and enforce that business requirements are being met in the product</li><li>
Taking a supportive role on continuous integration, continuous testing and release management</li><li>
Taking an active role in all aspects of quality within the project</li></ul><h3 class="jobSectionHeader"><b>
Qualifications &amp; Experience</b></h3><ul><li>
BSc or MSc in Software/Computer Engineering or related fields,</li><li><b>
At least 4 years of experience in software testing</b></li><li><b>
Proficiency in English, both spoken and written, with strong communication skills</b></li><li><b>
Strong experience in testing Mobile applications, APIs, and Databases</b></li><li>
Strong knowledge of software QA methodologies, tools, test design techniques and processes</li><li>
Experience with frameworks and tools like Postman</li><li>
Knowledge of SQL and/or other scripting tools</li><li>
Experience with Agile Development methodologies (Scrum, Kanban, etc.)</li><li>
Experience using a test management system, preferably Zephyr</li><li>
Strong familiarity with Agile Software Development Approach, Java/other OO languages.</li><li>
Experience with databases such as MySQL, MS SQL Server, Cosmos, MongoDB, etc. Familiarity with DB queries is mandatory.</li><li>
Accurate sense of analysis and synthesis to define root causes and possible solutions.</li><li>
Being ISTQB certified is a plus.</li></ul><div><b>
Why Commencis?</b></div><div>
</div><div>
We want people to thrive at Commencis. Here&rsquo;s what Commencers like about working here:</div><div>
</div><div><b>
Competitive Compensation &amp; Benefits:</b> We offer a competitive salary, private health insurance, pension and retirement plans through a company-backed pension system, meal card, commute compensation, work-from home support and paid birthday off.</div><div></div><div><b><br>
Happier Weekdays:</b> We offer flexible working hours including remote working option. Online events, guest speakers, refreshments in the office, meeting-light culture, and many more to enjoy the weekdays.</div><div></div><div><b><br>
Never Stop Learning: </b>We support learning and development programs for almost anything. Additionally, we provide access to leading online e-learning platforms like Udemy and various libraries.</div><div></div><div><b><br>
Community &amp; Socials:</b> We are a tight-knit community that loves gathering. Our social activities include happy hours, workshops, new year party, breakfast &amp; lunch get-togethers, movie nights, and our Summer Festival.</div><div></div><div><b><br>
Open Culture:</b> We maintain a flat organizational structure with a culture of direct and open communication. We value Commencers&rsquo; voices and address any suggestions and questions you may have.</div><div></div><div><b><br>
About Commencis</b></div><div></div><div><br>
Join us in paving the way for a thriving digital society!</div><div></div><div><br>
Commencis has more than two decades of expertise in the world of experience design, software engineering and cloud technologies. Our products and solutions are used by leading brands in financial services, insurance, airlines and retail in more than 20 countries.</div><div></div><div><br>
We help our clients around the globe to commence their next evolution and pave the way for a thriving digital society. We love discovering what&rsquo;s next. We value collaboration, curiosity, and an open mindset at work.</div><div></div><div><br>
If you share the same passion with our fellow Commencers, then let us unleash your world-class potential!</div><div></div><div><b><br>
We will process your personal data as part of our recruitment procedures. To find out more, please consult our </b><b>Candidate Privacy Notices</b><b>.</b></div>
<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>

Senior Quality Assurance Engineer

Eli Lilly

<div><p>At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We&rsquo;re looking for people who are determined to make life better for people around the world.</p><p></p><p><b>
Job Description</b></p><p></p><ul><li>
Ensure that all deviation occurred are properly reported, investigated, and closed in accordance with standard procedure. Must ensure that the corresponding plan of corrective and preventive actions, involving relevant areas, is established and completed on time.</li><li>
Inspect and release batches of finished products for sale.</li><li>
Manage product complaints as a Responsible Complaint Person.</li><li>
Support Monitoring tests of cold chain passive containers which are used for the shipment of Refrigerated products.</li><li>
Report immediately suspected theft, tampering or other situations that could jeopardize the product quality.</li><li>
Ensure that local customization is performed following the guidelines established by the quality area and according to global policies and standard operating procedures that apply locally.</li><li>
Monitor compliance with the external party.</li><li>
Ensure that the process of Change Control follows as indicated in the standard procedure for local operation and any proposed change (internal or external) that could potentially affect product quality.</li><li>
Prepare all quality documentation relating to GMP/GDP operations.</li><li>
Assist on training programs to external customers.</li></ul><p></p><p><b>
Qualifications/Requirements</b></p><p></p><ul><li>
A bachelor's degree in Faculty of Pharmacy from T&uuml;rkiye</li><li>
Minimum 2 years of experience in the area of quality assurance applied to the pharmaceutical industry</li><li>
Fluent in English (conversational, writing and reading)</li><li>
Knowledge and mastery of basic computing tools (Microsoft office).</li><li>
Good interpersonal relations</li><li>
Ability to train working groups</li><li>
Good analytical skills and attention to details</li></ul><p></p><p>
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.</p><p></p><p>
Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.</p><p></p><p>
#WeAreLilly</p></div>

Product Quality Associate

MARPORT

<div>
 <p>
  <strong>
   JOB DESCRIPTION:
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  Senior Procurement Specialist/Procurement Specialist is expected to work in the Procurement Department of Arkas Holding Port and Terminal Services Group located at Marport Terminal Operators in Beylikduzu/Istanbul.
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Organize demands of customers accordance with procurement procedure of company
  </li>
  <li>
   Follow contracts renewal processes and seasonal procurement processes
  </li>
  <li>
   Research alternative suppliers through conducting meetings and making a field visit
  </li>
  <li>
   Negotiate contracts, terms, and pricing agreements with suppliers to achieve cost savings and quality assurance
  </li>
  <li>
   Monitoring supplier performance and reporting any issues or discrepancies
  </li>
  <li>
   Prepare contracts of goods and services with relevant departments and follow approval process
  </li>
  <li>
   Carry out procurement contracts on SAP SRM module, follow pricing changes of goods and services
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   QUALIFICATIONS:
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s Degree in Business Administration, Economics, Engineering or related fields
  </li>
  <li>
   Excellent verbal and written skills in English
  </li>
  <li>
   Advanced Level of MS Office Programs is required
  </li>
  <li>
   Have an experience on SAP-SRM/MM mod
  </li>
  <li>
   Min 5 years of experience in procurement preferably have a knowledge about construction and technical purchasing,
  </li>
  <li>
   Have a class B driver license
  </li>
  <li>
   Completed Military Obligation for male candidates
  </li>
 </ul>
 <p>
 </p>
</div>


Procurement Specialist/Sr. Procurement Specialist

<div><b>Company Description</b><p><br>
At H&amp;M Group, we believe in making great design available to everyone. It&rsquo;s essential in everything we do. Our family of brands &mdash; H&amp;M, COS, Monki, Weekday, Cheap Monday, &amp;Other Stories, H&amp;M Home and ARKET &mdash; offer customers around the world a wealth of fashion, beauty, accessories and homeware, as well as modern menus with fresh and local produce at some of the brands&rsquo; in-store eateries.</p><p>
At H&amp;M Production we transform design ideas into real products. The direct point of contact for local suppliers in over 20 sourcing markets, we ensure that top-quality products are made as sustainably and cost-effectively as possible.</p><b><br>
Job Description</b><ul><li><p><br>
Ensure H&amp;M&rsquo;s brand quality standards are met throughout the product lifecycle, from development to customer experience.</p></li><li><p>
Ensure the product fit, technical risk assessment, and consumption optimization in the sample stage based on different product sample workflow.</p></li><li><p>
Work with proactive approach to secure product quality early, demonstrate problem solving mindset keeping right business deliveries on time.</p></li><li><p>
Conduct quality inspection either on-site at factory or in Centralized Facility Services (CFS). Business trips are required weekly basis.</p></li><li><p>
Maintain great understanding of customer expectations, which you translate to our suppliers and support creating their quality capabilities.</p></li><li><p>
Monitor supplier performance and governance routine follow up.</p></li></ul><b><br>
Qualifications</b><br>
<ul><li>
Strong product and technical knowledge with customer focus.</li><li>
Always maintain entrepreneurial mindset value with strong sense of ownership and urgency, with product focus.</li><li>
Create effective communication to build trust and respect among stakeholders, with a solution-oriented mindset.</li><li>
Build strong, collaborative relationships with cross-functional teams and suppliers.</li><li>
Live and demonstrate H&amp;M values in your daily work.</li></ul><br>
<b>
Additional Information</b><p><i><br>
At H&amp;M Group, we&rsquo;re determined to create and maintain inclusive, diverse and equitable workplaces throughout our organization. Our teams should consist of a variety of people that share and combine their knowledge, experience and ideas. Having a diverse workforce leads to a positive impact on how we address challenges, on what we perceive possible and on how we choose to relate to our colleagues and customers all over the world. Hence all diversity dimensions are taken into consideration in our recruitment process.</i></p><p>
If all of this sounds like it might be your kind of thing, then you should get in touch. We&rsquo;re more about personality and competence than qualifications, so don&rsquo;t worry if your skills aren&rsquo;t a perfect match. If your CV is selected then a recruiter will invite you for a phone / video call, followed by a couple of interviews at one or more of our offices.</p></div><p></p>

Quality Product Technologist H&M

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

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