procurement specialist

accounting specialist

it support specialist

qa engineer

clinical specialist

quality control specialist

Biruni Üniversitesi

<div>
 
 
 
 Manufacturing &amp; QC Specialists (GMP) &ndash; Advanced Cell &amp; Viral Vector Production
 
 
 
 
 
 
 
 Location:
 
 Zeytinburnu, Istanbul, T&uuml;rkiye (On-site)
 
 
 
 Employment Type:
 
 Full-Time
 
 
 
 
 
 
 About Biruni University
 
 
 
 Biruni University is building T&uuml;rkiye&rsquo;s leading center for cell &amp; gene therapy. Our GMP cleanroom facility (completion this year) will support clinical-grade manufacturing of viral vectors and engineered immune-cell products. To accelerate know-how transfer, we offer a fully funded
 
 3-month training placement at Harvard University
 
 for eligible hires (advanced bioprocessing &amp; QC systems).
 
 
 
 
 
 
 Position Overview
 
 
 
 We are hiring
 
 two complementary profiles
 
 under one posting:
 
 <ul>
 <li>
 
 Manufacturing Specialist
 
 &ndash; lead clinical-grade cell processing and viral vector&ndash;enabled workflows.
 </li>
 <li>
 
 QC Specialist
 
 &ndash; lead release/stability testing, method validation, and GMP quality systems.
 </li>
 </ul>
 
 
 
 
 
 Candidates may be considered for either track based on experience.
 
 
 
 
 
 
 
 Core Responsibilities
 
 
 
 
 Manufacturing:
 
 
 <ul>
 <li>
 
 Cell processing:
 
 Isolate, activate, transduce, expand, and harvest human immune cells using aseptic and closed-system techniques.
 </li>
 <li>
 
 Viral vector integration:
 
 Execute upstream/downstream steps for ex-vivo engineering (transduction parameters, MOI optimization, harvest/hold).
 </li>
 <li>
 
 GMP operations:
 
 Support facility/equipment qualification (IQ/OQ/PQ), environmental monitoring awareness, and cleanroom behaviors.
 </li>
 <li>
 
 Tech transfer &amp; scale-up:
 
 Run engineering and validation lots; contribute to batch records (BPRs), SOPs, deviations/CAPA
 
 .
 
 </li>
 <li>
 
 Equipment oversight:
 
 Incubators, biosafety cabinets, automated/closed expansion systems, cell counters/flow cytometry (user level).
 </li>
 </ul>
 
 
 QC:
 
 
 <ul>
 <li>
 
 Release &amp; stability testing:
 
 Execute in-process controls and lot-release assays (e.g., cell identity/viability, purity, potency), manage stability pulls.
 </li>
 <li>
 
 Method lifecycle:
 
 Assist with method qualification/validation, reference standards, and trending
 
 .
 
 </li>
 <li>
 
 Documentation &amp; QMS:
 
 Maintain GMP-compliant records (SOPs, test methods, raw data, LIMS/ELN entries); support deviations/CAPA, change control
 
 .
 
 </li>
 <li>
 
 Environment &amp; compliance:
 
 Coordinate with EM/Microbiology for cleanroom trend reviews; support data integrity and audit readiness.
 </li>
 </ul>
 
 
 
 
 
 Qualifications:
 
 
 <ul>
 <li>
 PhD in Biotechnology, Molecular Biology, Immunology, Biomedical Engineering, or related field
 
 (MSc with strong industry GMP experience considered).
 
 </li>
 <li>
 Required: Hands-on GMP experience in either cell-therapy/biologics manufacturing or QC of advanced therapies.
 </li>
 <li>
 Solid grasp of cell biology, aseptic techniques, and (for Manufacturing) viral transduction/bioreactors; (for QC) analytical methods for ATMPs.
 </li>
 <li>
 Familiarity with EMA/FDA expectations for ATMPs, data integrity, and documentation.
 </li>
 <li>
 Strong English (written/spoken); meticulous documentation habits.
 </li>
 </ul>
 
 
 
 
 
 Why Join Us
 
 
 <ul>
 <li>
 Paid 3-month Harvard training (eligible candidates).
 </li>
 <li>
 Build a flagship cell &amp; gene therapy hub in T&uuml;rkiye.
 </li>
 <li>
 Work alongside scientists, clinicians, and regulatory experts with clear career paths across Manufacturing, QC, and CMC.
 </li>
 </ul>
 
 
 
 
 
 Application Process
 
 
 <ul>
 <li>
 Submit CV + a concise cover letter indicating your preferred track (Manufacturing or QC) and summarizing your GMP experience (e.g., # of clinical lots, methods validated, cleanroom grades, platforms used).
 </li>
 </ul>
</div>

Manufacturing Specialist

TCI Aircraft Interiors

<div>
 
 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.
 
 
 
 
 
 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.
 
 
 
 
 
 
 Qualifications
 
 
 
 
 
 <ul>
 <li>
 Graduated with at least an undergraduate degree in Engineering (Mechanical, Metallurgy and Materials, Aerospace, Industrial, Mechatronics, Electrical and Electronics, Manufacturing, etc.)
 </li>
 <li>
 Proficient in English
 </li>
 <li>
 Team-oriented, with strong communication and representation skills, able to take initiative and make decisions
 </li>
 <li>
 Skilled in interpreting measurements and measurement reports (preferably experienced in using measurement equipment)
 </li>
 <li>
 Proficient in Microsoft Office programs and competent in ERP systems
 </li>
 <li>
 Able to read and interpret technical drawings
 </li>
 <li>
 Knowledgeable and experienced in ISO9001, IATF16949, and/or EN/AS9100 Quality Management Systems
 </li>
 <li>
 Preferably, at least 2 years of experience in the automotive, defense, or aviation industries; having IPC training and being a graduate in electrical or electronics engineering, or having worked as a quality control engineer in these sectors, is also preferred
 </li>
 <li>
 Strong process monitoring and coordination skills
 </li>
 </ul>
 
 
 
 
 
 Job Description
 
 
 
 
 
 <ul>
 <li>
 Ensure that receiving inspection, process, and final quality control activities are carried out in accordance with quality control standards.
 </li>
 <li>
 Ensure and control that process quality control activities comply with quality control standards.
 </li>
 <li>
 Coordinate customer expectations within the company and with suppliers.
 </li>
 <li>
 Plan with the customer, and if necessary, the aircraft manufacturer, for On-Site Control and First Product Inspection.
 </li>
 <li>
 Ensure coordination between the customer and the aircraft manufacturer and follow up with On-Site Support companies.
 </li>
 <li>
 Ensure that the parts used and produced in production are process-controlled according to the relevant control criteria, that quality control results are entered into the system, and that acceptance approval is given if the product meets the required conditions.
 </li>
 <li>
 Conduct root cause analysis for recurring non-conformances, monitor controls, and attend relevant meetings.
 </li>
 <li>
 Ensure that the inspection, testing, and measurement instruments used in quality control activities, as well as the tools used in the production area, comply with standards.
 </li>
 <li>
 Participate in periodic meetings and finalize relevant actions.
 </li>
 <li>
 Create and update relevant procedures, instructions, or forms, and coordinate with the assurance team.
 </li>
 <li>
 Ensure that the expectations of aviation authorities such as EASA, DGCA, and FAA are met.
 </li>
 </ul>
 
 
</div>

Quality Control Engineer

ENKA İnşaat ve Sanayi A.Ş.

<div>
 
 We are looking for talents to build their career as a
 
 Planning and Scheduling Supervisor
 
 for our Project in
 
 Mozambique!
 
 
 
 
 
 
 In ENKA family, you can;
 
 <ul>
 <li>
 Have a chance to work for the largest engineering and construction company of Turkey,
 </li>
 <li>
 Be a part of a global company of 17.000 employees,
 </li>
 <li>
 Build your career in a company with experience over 65 years,
 </li>
 <li>
 Gain experience in corporate culture with a global management approach,
 </li>
 <li>
 Have access to future opportunities for working in other countries over 5 continents where we are currently operating after the successful completion of this assignment.
 </li>
 </ul>
 
 
 
 
 
 QUALIFICATIONS
 
 
 <ul>
 <li>
 B.Sc. degree in
 
 Materials Engineering
 
 ,
 
 Metallurgical &amp; Materials Engineering
 
 , or related engineering fields,
 </li>
 <li>
 Minimum
 
 5&ndash;7 years
 
 of experience in quality control, material inspection, or material receiving processes,
 </li>
 <li>
 Experience in industrial construction projects (preferably power plants, industrial facilities, infrastructure or similar),
 </li>
 <li>
 Good knowledge of material test methods, certification processes, and international standards (ASME, ASTM, EN, etc.),
 </li>
 <li>
 Experience in material receiving, visual inspection, measurement, and traceability processes,
 </li>
 <li>
 Good command of MS Office applications and strong reporting skills,
 </li>
 <li>
 Strong communication skills and ability to work in a multicultural environment,
 </li>
 <li>
 No restriction to travel and stay abroad.
 </li>
 </ul>
 
 
 
 
 If you apply for this job posting, you can review the clarification text prepared within the scope of KVKK s. 6698 regarding your personal data to be processed at www.enka.com.
 
 
 
</div>

Quality Control Material Controller

Eli Lilly

<div>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.
Job Description<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>
Qualifications/Requirements<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>
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.
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.
#WeAreLilly</div>

Product Quality Associate

REWE Group

<div></div><div><div><div>Istanbul</div>
<div>Full time</div>
<div>Quality Assurance</div>
<div>November 13, 2025</div>
<div>Candidate@rewe-fareast.com</div></div> 
<div>We are currently inviting a talented professional to join our Istanbul office, Turkey for the exciting role below.

The Job
<ul>
<li>Support the sourcing process by conducting preliminary assessments of production sites, reviewing technical documentation, advising improvement and corrective actions for potential suppliers in assigned regions (Turkey, Egypt, India, Thailand).</li>
<li>Work closely with international buyers, suppliers and Merchandising teams managing quality aspects for new and repeated orders, from supplier audits and specifications approval to production monitoring and shipment release.</li>
<li>Organize and manage pre-shipment inspection, sampling and testing activities, review documentations and provide professional advice and recommendations on the results.</li>
<li>Manage the performance of testing and inspection houses, proactively report potential quality and shipment risks, and provide solutions.</li>
<li>Coordinate complaints investigations, provide feedback based on suppliers&rsquo; data and monitor the implementation of corrective actions to close deviations.</li>
<li>Maintain accurate and timely data and documentation in the systems.</li></ul> 


Requirements 

<ul><li>Degree holder in food science, food engineering or equivalent.</li>
<li>At least 3 years&rsquo; work experience in food quality assurance, plus prior experience in ambient (canned, dry) and frozen (fish, fruits) product categories.</li>
<li>Familiar with legal and quality standards for processed food products in the EU market.</li>
<li>Previous experience with the Turkish and Indian supply base of advantage.</li>
<li>Self-disciplined and equipped with time- and project management skills, capable to deliver within agreed deadlines.</li>
<li>Good communication and interpersonal skills, with the ability to work effectively as part of the team in a cross-cultural environment.</li>
<li>Solution-oriented, attention to details, and always striving for customer success and excellent service. 
Mature personality with a high level of independence and integrity.</li>
<li>Advance level in both spoken and written English.</li>
<li>Proficient in MS Office applications (e.g. Excel, Word, PowerPoint, and Outlook).</li>
<li>Flexible with business trips (both in the country and abroad).</li></ul> 


As a team member, you will enjoy:
<ul>
<li>A diverse and inclusive work environment</li>
<li>Exposure to international trade</li>
<li>Learning and development opportunities</li>
<li>Competitive compensation package</li>
<li>A 5-day work week with the option of working remotely for 2 days</li>
<li>25 days of paid annual holiday</li>
<li>Medical insurance coverage</li></ul> 


If you are looking for a challenging and rewarding career opportunity, do contact our HR Team via candidate@rewe-fareast.com in English to collect the form of &Ccedil;ALI&#350;AN ADAYI K&#304;&#350;&#304;SEL VER&#304;LER&#304;N KORUNMASI HAKKINDA AYDINLATMA. 


For personal data protection purpose, we only receive Resume together with the filled form of &Ccedil;ALI&#350;AN ADAYI K&#304;&#350;&#304;SEL VER&#304;LER&#304;N KORUNMASI HAKKINDA AYDINLATMA. 


NOTES

6698 say&#305;l&#305; Ki&#351;isel Verilerin Korunmas&#305; Kanunu (&lsquo;&lsquo;KVKK&rsquo;&rsquo;)kapsam&#305;nda Veri Sorumlusu s&#305;fat&#305;na haiz olan &#350;irketimizin KVKK&rsquo;n&#305;n 10.Maddesinden do&#287;an ayd&#305;nlatma y&uuml;k&uuml;ml&uuml;l&uuml;&#287;&uuml;n&uuml; yerine getirmek &uuml;zere ki&#351;isel verilerinizi ve &ouml;zel nitelikli ki&#351;isel verilerinizi payla&#351;madan &ouml;nce &#351;irketimizin www.rewe-fareast.com/privacy adresli internet sitesinden &Ccedil;ALI&#350;AN ADAYI K&#304;&#350;&#304;SEL VER&#304;LER&#304;N KORUNMASI HAKKINDA AYDINLATMA VE REFERANS TAAHH&Uuml;D&Uuml; metnini okuman&#305;z&#305; ve metnin sonunda ki b&ouml;l&uuml;m&uuml; doldurup CV&rsquo;nizle beraber g&ouml;ndermenizi rica ederiz.</div></div>

Quality Technologist (Food)

SES KİMYA A.Ş.

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

KİMYAGER

Huhtamaki

<div>
 
 Enjoy a career, packaged with care, whilst helping protect food, people and the planet
 
 
 
 We are a key global provider of sustainable packaging solutions. We&rsquo;re on a mission to make all packaging recyclable, reusable, or compostable. Every day, we ensure the hygiene and safety of food and drink for people around the world. We are Huhtamaki.
 
 
 You could be part of our vision. Because it&rsquo;s our talented people that make it happen. Our people on the shop floor producing innovative, sustainable products. Our people in our offices delivering excellence for our customers every day. It&rsquo;s every one of us working together.
 
 
 We offer a place where you can feel safe, be supported, and make an impact so we can all focus on the future together.
 
 
 <ul>
 <li>
 Process audit system build up
 </li>
 <li>
 Preparing CoAs with packaging compliance checks
 </li>
 <li>
 Monitoring results before Positive Release
 </li>
 <li>
 Performing dimensional mechanical and final controls (Zwick machine tests)
 </li>
 <li>
 Visual inspection (BST, Rubby)
 </li>
 <li>
 Managing internal complaints with RCA methods
 </li>
 <li>
 Tracking and isolating blocked materials
 </li>
 <li>
 Conducting FMEA workshops for risk reduction
 </li>
 <li>
 Performing internal process &amp; product audits
 </li>
 <li>
 Reporting performance indicators to Senior Quality Manager
 
 
 </li>
 </ul>
 Join us. Help protect food, people and the planet.
</div>

Process Quality Manager (Grade 15-16)

Explore 665+ Quality control specialist in Istanbul this November. Find roles across top companies and apply now to boost your career.