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operations manager

quality assurance manager

Teva Pharmaceuticals

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

Third Party Operations Quality Manager & Qualified Person (QP)

VERO Digital Solutions

WHO WE ARE:VERO Digital Solutions has been dealing with the digitalization of the construction industry since 2018. We help our customers to better manage, control and plan their daily business. Our focus is on excellent user experience and performant mobile app solutions. Our 20 employees are spread across our development sites in Germany and Bulgaria.YOUR TASKS:&middot; Test of Product Components: Conduct thorough testing of our product components, including Android, iOS, Web-Portal, and API, to ensure seamless functionality across all platforms.&middot; Integration Tests before Release: Perform comprehensive integration tests prior to product releases to guarantee smooth and bug-free launches.&middot; Test Automation: Utilize your expertise in test automation to streamline the testing process, improve efficiency, and enhance the reliability of our software products.&middot; Preparing Test-Data: Prepare and manage test data to simulate real-world scenarios, enabling accurate and effective testing.&middot; Set-Up Test Processes and Integrate into Development Processes: Establish and integrate robust test processes into our development lifecycle, ensuring continuous improvement and adherence to best practices.&middot; Formalize Test-Cases to avoid Regression: Develop and formalize test cases to prevent regression issues and maintain the stability and performance of our software over time.YOUR SKILLS:&middot; Proven experience in software quality assurance, with a strong understanding of testing principles and methodologies.&middot; Proficiency in testing multiple product components (Android, iOS, Web-Portal, API).&middot; Hands-on experience with test automation tools and frameworks.&middot; Strong analytical and problem-solving skills, with the ability to prepare and manage test data effectively.&middot; Excellent communication and collaboration skills to work seamlessly with development teams.&middot; Detail-oriented with a commitment to delivering high-quality software products&middot; Fluent English in spoken &amp; writtenWHAT WE OFFER:&middot; Work with the latest technology and modern methods&middot; Flexible working from home office&middot; Competitive compensationIf you possess the qualifications and skills mentioned above and want to be part of adynamic team, please send your complete application, including your resume and a cover letter. Non-English Applications will be rejected.It is necessary that you own up-to-date hardware that you can use for your work.Job Type: Full-time

Quality Assurance Engineer

Amgen

<div>Join Amgen&rsquo;s Mission of Serving Patients
At Amgen, if you feel like you&rsquo;re part of something bigger, it&rsquo;s because you are. Our shared mission&mdash;to serve patients living with serious illnesses&mdash;drives all that we do.
Since 1980, we&rsquo;ve helped pioneer the world of biotech in our fight against the world&rsquo;s toughest diseases. With our focus on four therapeutic areas &ndash;Oncology, Inflammation, General Medicine, and Rare Disease&ndash; we reach millions of patients each year. As a member of the Amgen team, you&rsquo;ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you&rsquo;ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Live
What you will do
Let&rsquo;s do this! Let&rsquo;s change the world! The role provides proactive end to end quality support for the development and implementation of a risk-based quality assurance strategy for the clinical development program.
The role will support end to end quality oversight of the General Medicine &amp; Obesity Therapeutic Area and will be responsible for supporting a risk-based quality strategy that advances quality by design principles for the full clinical trial lifecycle (protocol development, database lock, and regulatory submissions/ approvals).
You will play a vital role by developing deep knowledge of the clinical trials you support and provide oversight and quality management of critical data and processes for global and local study teams and all clinical trial sites who participate in Amgen sponsored trials.
Responsibilities<ul><li>
Act as a Good Clinical Practice (GCP) Subject Matter Expert, offering independent, objective quality guidance.</li><li>
Oversee quality across all clinical development stages.</li><li>
Plan and execute risk-based GCP audits (sites, affiliates, vendors, studies).</li><li>
Support regulatory inspections and guide responses, including root cause analysis and CAPAs.</li><li>
Lead quality oversight of Risk Assessment Categorization Tools (RACT) for each trial.</li><li>
Facilitate monthly quality risk reviews with clinical program leaders.</li><li>
Manage audit findings, deviations, and CAPA responses.</li><li>
Ensure regional compliance with local regulations and support vendor evaluations.</li><li>
Analyze data quality trends, identify gaps, and implement corrective actions.</li><li>
Oversee technologies for endpoint data collection (e.g., biomarkers, imaging).</li><li>
Develop and execute TA-specific QA plans and protocol-specific audit strategies.</li><li>
Support quality management activities including deviations, breaches, and inspection readiness.</li><li>
Drive innovation in quality oversight using data analytics, AI, and NLP.</li><li>
Review protocols to simplify design and identify critical data/processes.</li></ul>
Country/ Regional Quality Leadership<ul><li>
Manage analytical tools and data trends to address site/regional quality gaps.</li><li>
Provide oversight for key sites in collaboration with regional operations.</li><li>
Conduct Quality Partnership Visit at key sites within the country/Region</li><li>
Share best practices and compliance insights with stakeholders.</li><li>
Offer independent quality consultation and escalate issues as needed.</li><li>
Support local vendor assessments and pre-inspection activities.</li><li>
Conduct regional risk assessments for audit planning.</li><li>
Stay current on regulatory trends and deliver ongoing training.</li></ul>
Win
WHAT WE EXPECT OF YOU
We are all different, yet we all use our unique contributions to serve patients. The individual we seek has technological literacy and leadership skills, and has these qualifications:
Doctorate degree and 2 years of Quality Management, Quality Assurance and Good Clinical Practices experience in the pharmaceutical/biotech industry where risk-based quality management and quality by design are a core responsibility.
Or
Master&rsquo;s degree and 4 years of the previous mentioned experience
Or
Bachelor&rsquo;s degree and 6 years of the previous mentioned experience
Or
Associate&rsquo;s degree and 10 years of the previous mentioned experience<ul><li>
Oversight and implementation of Quality Management Systems and experience managing quality in electronic QMS such as Veeva or Track wise.</li><li>
Thorough understanding of Clinical R&amp;D activities and Global Regulations.</li><li>
Experience with Regulatory Submission and Inspection Management procedures.</li><li>
Quality Oversight of Clinical Trials, including clinical trial protocol development, execution, and submissions.</li><li>
Leadership or mentoring experience is ideal, in a regional capacity would be phenomenal.</li><li>
Excellent verbal and written communication skills, including strong business writing abilities and active listening. Able to understand and articulate technical concepts and literature in spoken and written English.</li><li>
Ability to transform business and stakeholder feedback into clear, efficient processes using a straightforward language and format.</li><li>
Self-driven with strong analytical, critical-thinking, prioritization, and decision-making abilities.</li></ul><h2 class="jobSectionHeader">
IMPORTANT! Please submit your resume/CV in English!</h2><h2 class="jobSectionHeader">
Thrive</h2>
WHAT YOU CAN EXPECT OF US<ul><li>
Vast opportunities to learn, develop, and move up and across our global organization.</li><li>
Diverse and inclusive community of belonging, where colleagues are empowered to bring ideas to the table, take risks, and act.</li><li>
Generous Amgen Total Rewards Plan comprising healthcare, finance, wealth and career benefits.</li><li>
Flexible work arrangements.</li></ul><h2 class="jobSectionHeader">
Apply now</h2>
In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us: Careers.amgen.com
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</div>

Quality Compliance Senior Manager

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

Kerry

<div>
 
 Requisition ID 61905
 
 
 Position Type FT Permanent
 
 
 Workplace Arrangement
 
 
 
 
 About Kerry
 
 
 
 Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment.
 
 
 
 About the role
 
 
 
 The purpose of this role is to lead and develop the food safety and quality function at the manufacturing site in Turkey. This role ensures robust implementation of food safety systems, fosters a strong quality culture, and guarantees the delivery of safe, high-quality food ingredients to customers. This is a customer-facing role requiring strong collaboration with internal and external stakeholders. Based in Tuzla factory, one of the Kerry factories located in Istanbul, Turkey, with multiple technologies under one site.
 
 
 
 Key responsibilities
 
 
 
 
 Leadership &amp; Strategy
 
 
 
 <ul>
 <li>
 Lead and mentor site and TPM Quality and Food Safety teams across the region.
 </li>
 <li>
 Train and develop competencies for the current team members in the quality function across T&uuml;rkiye Kerry Site and the TPMs
 </li>
 <li>
 Develop and execute the regional quality strategy aligned with global standards and local regulatory requirements.
 </li>
 <li>
 Champion a proactive quality culture through training, engagement, and leadership.
 
 
 </li>
 </ul>
 
 Food Safety &amp; Compliance
 
 
 
 <ul>
 <li>
 Ensure implementation and maintenance of food safety systems (e.g., HACCP, FSSC 22000, BRC) across all company-owned and TPM sites.
 </li>
 <li>
 Monitor compliance with internal standards, customer requirements, and regulatory obligations.
 </li>
 <li>
 Lead internal, supplier, and third-party audits, ensuring timely closure of non-conformities and continuous improvement.
 
 
 </li>
 </ul>
 
 Third-Party Manufacturing (TPM) Management
 
 
 
 <ul>
 <li>
 Qualify, audit, and monitor TPM partners to ensure adherence to company quality and food safety standards.
 </li>
 <li>
 Establish and maintain quality agreements with TPMs, including KPIs and escalation protocols.
 </li>
 <li>
 Collaborate with Procurement, Supply Chain, and Operations to manage quality risks and drive continuous improvement at TPM sites.
 </li>
 <li>
 Provide technical support and training to TPMs to build capability and ensure consistent product quality.
 
 
 </li>
 </ul>
 
 Operational Excellence
 
 
 
 <ul>
 <li>
 Integrate quality systems with TPM and internal site TPM initiatives to drive continuous improvement.
 </li>
 <li>
 Analyze quality KPIs and trends to identify risks and opportunities.
 </li>
 <li>
 Collaborate with operations to reduce quality-related losses and improve product consistency.
 
 
 </li>
 </ul>
 
 Customer Engagement
 
 
 
 <ul>
 <li>
 Act as the regional quality representative in customer interactions, audits, and complaint resolution.
 </li>
 <li>
 Translate customer feedback into actionable improvements at both internal and TPM sites
 </li>
 <li>
 Support new product development and commercialization from a quality perspective.
 
 
 </li>
 </ul>
 
 Qualifications and skills
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s or master&rsquo;s degree in food science, Microbiology, Chemistry, or related field.
 </li>
 <li>
 Minimum 10 years of experience in food quality and safety, with at least 3 years in a regional or multi-site leadership role.
 </li>
 <li>
 Experience in a multinational food or ingredients company is highly desirable.
 </li>
 <li>
 Demonstrated experience managing third-party manufacturing quality systems.
 </li>
 <li>
 Certification in food safety systems (e.g., FSSC 22000) and auditing (e.g., Lead Auditor certification) is a strong advantage.
 </li>
 <li>
 Familiarity with SPC methodologies , Lean, or Six Sigma methodologies will be an added advantage
 </li>
 <li>
 Expertise in hygiene and sanitation, including cleaning validation, environmental monitoring, and allergen control.
 </li>
 <li>
 Solid foundation in microbiology, including pathogen control, indicator organisms, and lab result interpretation.
 </li>
 <li>
 Proficiency in risk assessment methodologies (e.g., HACCP, TACCP, VACCP, FMEA).
 </li>
 <li>
 Demonstrated experience in auditing (internal, supplier, and third-party), including audit planning, execution, reporting, and CAPA management
 
 
 </li>
 </ul>
 Beware of scams online or from individuals claiming to represent us. A Kerry employee will not solicit candidates through a non-Kerry email address or phone number. In addition, Kerry does not currently utilise video chat rooms (e.g., Google Hangouts) to conduct interviews. Refuse any request that asks you to provide payment to participate in the hiring process (e.g., purchasing a &ldquo;starter kit,&rdquo; investing in training, or something similar). Kerry will not ask you to pay any money at any point in the hiring process with the exception of reimbursable travel expenses. In addition, any payments made by Kerry will be from official firm accounts bearing the Kerry name.
 
 
 
 Recruiter
 
 
 
 
 Posting Type
 
 DNI
 
 
</div>

Food Safety and Quality Manager

<div>
 At EY, we&rsquo;re all in to shape your future with confidence.
 
 
 We&rsquo;ll help you succeed in a globally connected powerhouse of diverse teams and take your career wherever you want it to go.
 
 
 Join EY and help to build a better working world.
 
 
 
 The opportunity
 
 
 
 EY is a global leader in Assurance, Consulting, SaT (Strategy &amp;Transactions) and Tax services.
 
 
 Enabled by data, AI and advanced technology, EY teams help clients shape the future with confidence and develop answers for the most pressing issues of today and tomorrow. The insights and quality services we provide help build trust and confidence in the capital markets and in economies the world over. Our offices around the world use the same methodology and are linked through an integrated technology platform to enable instantaneous communication and collaboration among team members, regardless of location. As a member of EY Global, in T&uuml;rkiye we operate in 6 offices located in &Idot;stanbul, Ankara, Bursa, &Idot;zmir and Adana, with more than 1800 people for over 40 years.
 
 
 At EY, we empower our 400.000 people in more than 150 countries with the right mindsets and skills to navigate what&rsquo;s next, become the transformative leaders the world needs, pursue careers as unique as they are, and build their own exceptional EY experiences. We work together across our full spectrum of services and skills so that business, people and the planet can thrive together.
 
 
 Together, all in, to build a better working world.
 
 
 
 Audit &ndash; Senior Manager
 
 
 
 We are seeking for a Senior Manager to join our Assurance &ndash; Audit and Accounting Services team in Istanbul with the following qualifications;
 
 
 
 What We Look For
 
 
 
 <ul>
 <li>
 Strong academic background, including a Bachelor&rsquo;s or Master&rsquo;s degree in Business, Finance, Economics or other related field
 </li>
 <li>
 Minimum 8 years of relevant work experience in risk-based auditing and risk and control strategies
 </li>
 <li>
 Professional accountancy qualification (SMMM, KGK)
 </li>
 <li>
 Excellent knowledge of IFRS and local GAAP
 </li>
 <li>
 Compliance with and understanding of regulatory requirements
 </li>
 <li>
 English language skills - excellent written and verbal communication
 
 
 </li>
 </ul>
 
 Your Key Responsibilities
 
 
 
 <ul>
 <li>
 Manage the financial aspects of assurance engagements and communicate significant issues, fees and estimates-to-complete to partners and clients
 </li>
 <li>
 Making technical contribution to audit client engagements and internal projects
 </li>
 <li>
 Planning and executing complex assurance engagements
 </li>
 <li>
 Develop and maintain productive working relationships with clients
 </li>
 <li>
 Assist partners to generate new business opportunities and build client networks and relationships
 </li>
 <li>
 Develop people through effectively supervising, coaching and mentoring all levels of staff
 
 
 </li>
 </ul>
 
 What We Offer You
 
 
 
 At EY, we&rsquo;ll develop you with future-focused skills and equip you with world-class experiences. We&rsquo;ll empower you in a flexible environment, and fuel you and your extraordinary talents in a diverse and inclusive culture of globally connected teams. Learn more.
 
 
 Are you ready to shape your future with confidence? Apply today.
 
 
 To help create the best experience during the recruitment process, please describe any disability-related adjustments or accommodations you may need.
 
 
 
 EY
 
 | Building a better working world
 
 
 EY is building a better working world by creating new value for clients, people, society and the planet, while building trust in capital markets.
 
 
 Enabled by data, AI and advanced technology, EY teams help clients shape the future with confidence and develop answers for the most pressing issues of today and tomorrow.
 
 
 EY teams work across a full spectrum of services in assurance, consulting, tax, strategy and transactions. Fueled by sector insights, a globally connected, multi-disciplinary network and diverse ecosystem partners, EY teams can provide services in more than 150 countries and territories.
</div>

EY Türkiye - Istanbul Audit - Senior Manager

ENKA İnşaat ve Sanayi A.Ş.

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

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