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quality assurance consultant Jobs in Ankara

quality assurance consultant

quality assurance specialist (qa-2505) Jobs in Ankara

quality assurance specialist (qa-2505)

quality assurance specialist qa 2505

Milsoft Software Technologies

<div><div>MilSOFT / Ankara
<div>Yay&#305;n Tarihi: 5.11.2025</div>
<div><div>&Ccedil;al&#305;&#351;ma Yeri: Yerinde</div></div>
<div><p>We were the first company in Europe that earned the highestlevel of Capability Maturity Model Integration (CMMI 5) which is accomplishedonly by the few companies around the world.</p>
<p>
We are the only company in the Turkish Defense Industry that hasbeen appraised at CMMI Maturity Level 5 by implementing Agile practices</p>
<p>
We as MilSOFT, continuously improve our genuine technology andto be the best in our field.</p>
<p>
In our field, we dedicated to create the best career developmentand learning resources as our principle.</p>
<p>
In that international contest we invite those who areself-confident, has believe in success, wants to take the success of theTurkish engineers to new horizons, are interested in providing real engineeringsolutions to projects that are issued with using the latest technologies.</p>
<p>
MilSOFT, first CMMI-Level 5 Company in Turkey, invites talented&ldquo;<b>Quality Assurance Engineer(s)</b>&rdquo; that will join the team that executesall CMMI Level 5 related activities in an agile manner.</p>
<p><b>
Quality Assurance Engineer (QA-2505)</b></p>
<p><b>
What you will be doing:</b></p>
<ul><li>Being responsible to the Quality Assurance Manager/QM Directorfor all quality assurance activities.</li></ul>
<ul><li>Defining QA requirements in proposal phase and developingQuality Plan and Audit Schedule for each project,</li></ul>
<ul><li>Performing internal process and subcontractor audits according,</li></ul>
<ul><li>Participate in peer review activities and review projectartifacts,</li></ul>
<ul><li>Providing agile coaching</li></ul>
<ul><li>Witnessing test activities,</li></ul>
<ul><li>Collecting related metrics and reporting quality assuranceactivities to senior management and Customer,</li></ul>
<ul><li>Participating/Leading process improvement activities.</li></ul>
<ul><li>Participating/leading 3rd party external audits performed bycertification audits.</li></ul>
<ul><li>Interfacing with the customer on quality problems</li></ul>
<ul><li>Performing release verification.</li></ul>
<ul><li>Performing software installation</li></ul>
<ul><li>Delivering QA related trainings.</li></ul>
<ul><li>Managing enterprise risk management activities</li></ul>
<p><b>
Required Qualifications:</b></p>
<p><b>
MUST:</b></p>
<p><b>
a. Qualifications:</b></p>
<ul><li>Bachelor&rsquo;s degree, in Software Engineering or Computer Scienceor Electrical &amp; Electronics Engineering or Industrial Engineering orrelated equivalent disciplines.</li></ul>
<p><b>
b. Experience:</b></p>
<p>
 Practicalworking experience</p>
<ul><li>in the field of quality management, quality assurance, andquality control activities for software intensive systems,</li></ul>
<ul><li>in ISO 9000 series standards and guidelines,</li></ul>
<ul><li>in process audits and product peer reviews</li></ul>
<p><b>
c. Skills:</b></p>
<ul><li>Continuous Learner</li></ul>
<ul><li>Analytical thinking, analysis andproblem-solving,</li></ul>
<ul><li>Ability to work independently as well as collaboratively in ateam environment,</li></ul>
<ul><li>Being result oriented,</li></ul>
<ul><li>Willing to improve oneself.</li></ul>
<p><b>
Preferred Qualifications:</b></p>
<p><b>
PREFERRED:</b></p>
<ul><li>Hands-on experience in an agile environment,</li></ul>
<ul><li>Knowledge on DevOps practices,</li></ul>
<ul><li>Knowledge on CMMI, NATO AQAP 2110, AQAP 2210, AS 9100, ISO12207, DO178 standards,</li></ul>
<ul><li>Performing one of software engineering practices (requirementanalysis, design, coding, testing, configuration management, etc.) as a memberof development team,</li></ul>
<ul><li>Familiarity with C/C++ and Java Programming Languages,</li></ul>
<ul><li>Familiarity with UML and object oriented analysis and design,</li></ul>
<ul><li>Use of statistical process control techniques,</li></ul>
<ul><li>Working on business process management and modeling.</li></ul>
<p></p>
<p>Candidates must be proficient in English. Military service mustbe completed or be deferred at least 2 years for male candidates. Workplace isin ODT&Uuml; Teknokent Ankara. Short listed candidates will be contacted only.</p></div></div></div><p></p>

Quality Assurance Specialist (QA-2505)

PharmEng Technology

<div>
 <strong>
  About The Job Quality Assurance Consultant
  <br/>
  <br/>
 </strong>
 <strong>
  Job Summary:
 </strong>
 The Quality Assurance Consultant is responsible for the implementation, maintenance, and oversight of the Quality Management System (QMS) in local affiliates. This role ensures compliance with regulatory requirements, quality standards, and company policies. The Quality Assurance Consultant will manage quality risk, complaints, change controls, deviations, CAPA, authority inspections, self-inspections, GxP surveillance, product quality reviews, training, local product release, and oversight of GDP requirements for local warehousing and distribution.
 <br/>
 <br/>
 <strong>
  Key Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   QMS implementation, maintenance, and oversight in local affiliates.
  </li>
  <li>
   Maintenance of the local Quality Manual and Site Master File.
  </li>
  <li>
   Quality risk management in local affiliate, including risk identification, analysis, communication, control, and escalation as required.
  </li>
  <li>
   Complaint management, acting as the Local Complaint Coordinator for reporting, local assessment, and local investigation.
  </li>
  <li>
   Change control management, QA assessment, site change control, QA review for change implementation and closure.
  </li>
  <li>
   Deviation management for internal, external, and transport deviations.
  </li>
  <li>
   CAPA management from deviations, internal audits, external audits, and self-inspections.
  </li>
  <li>
   Management of authority inspections and self-inspections.
  </li>
  <li>
   Local GxP surveillance and assessment.
  </li>
  <li>
   Product quality review (PQR).
  </li>
  <li>
   Training management, including maintenance of training matrix, training of local staff, annual GxP refresher training, and handling of training assignments in the LMS.
  </li>
  <li>
   Local product release (local QP), shipment review of transport performance, goods receipt check, and deviation handling.
  </li>
  <li>
   Oversight of GDP requirements for local warehousing and distribution.
  </li>
  <li>
   Shipping lane qualification and local transport performance of secondary distribution.
  </li>
  <li>
   Secondary distribution transport performance review.
  </li>
  <li>
   Return management, including QA evaluation against return criteria and collaboration with distributors.
  </li>
  <li>
   Product recall management, including local recall execution, communication with customers, communication with HA, recall reconciliation, and local product destruction.
  </li>
  <li>
   GxP suppliers management, including supplier identification, qualification, approval, annual compliance status evaluation, quality audit planning, conduct quality audits, and CAPA approval and closure.
  </li>
  <li>
   Local repackaging and relabeling, including change management, protocol, execution, QA review, and release.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor's degree in Quality Management, Life Sciences, or a related field.
  </li>
  <li>
   Minimum of 5 years of experience in Quality Assurance within the pharmaceutical or healthcare industry.
  </li>
  <li>
   Strong knowledge of GxP regulations and quality standards.
  </li>
  <li>
   Excellent analytical, problem-solving, and communication skills.
  </li>
  <li>
   Ability to work independently and collaboratively in a team environment.
  </li>
  <li>
   Proficiency in using Quality Management Systems and Learning Management Systems (LMS).
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Key Competencies
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Attention to detail and accuracy.
  </li>
  <li>
   Strong organizational and time management skills.
  </li>
  <li>
   Effective leadership and team management abilities.
  </li>
  <li>
   Proactive and results-oriented mindset.
  </li>
 </ul>
</div>


Quality Assurance Consultant

ICON plc

<div>Site Specialist II, Study Start Up<div></div><div>
ICON plc is a world-leading healthcare intelligence and clinical research organization. We&rsquo;re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development</div><div></div><div>
We are currently seeking a Site Specialist II (Study Start Up Associate II) to join our diverse and dynamic team. As a Site Specialist II at ICON, you will play a pivotal role in leading the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.</div><div></div><div>
What you will be doing</div><ul><li><div>
Leading the preparation and submission of regulatory documents, including clinical trial applications, ethics committee submissions, and regulatory agency communications.</div></li></ul><ul><li><div>
Coordinating and liaising with internal and external stakeholders to obtain necessary approvals and authorizations for study initiation.</div></li></ul><ul><li><div>
Managing and maintaining comprehensive and accurate records of regulatory submissions, approvals, and correspondence</div></li></ul><ul><li><div>
Providing guidance and support to study teams on regulatory requirements and best practices for study start-up activities.</div></li></ul><ul><li><div>
Participating in process improvement initiatives to streamline study start-up processes and enhance efficiency.</div></li></ul><div></div><div>
Your profile</div><ul><li><div>
Bachelor's degree in life sciences or a related field.</div></li></ul><ul><li><div>
Minimum of 2 years of experience in clinical research or regulatory affairs, with specific experience in study start-up activities.</div></li></ul><ul><li><div>
Strong understanding of regulatory requirements and guidelines for clinical trials, including ICH-GCP and local regulatory requirements.</div></li></ul><ul><li><div>
Excellent organizational and project management skills, with the ability to prioritize and manage multiple tasks simultaneously.</div></li></ul><ul><li><div>
Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.</div></li></ul><div></div><div>
What ICON can offer you:</div><div></div><div><div><div><div><div>
Our success depends on the quality of our people. That&rsquo;s why we&rsquo;ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.</div><div></div><div>
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.</div><div></div><div>
Our benefits examples include:</div><ul><li><div>
Various annual leave entitlements</div></li><li><div>
A range of health insurance offerings to suit you and your family&rsquo;s needs.</div></li><li><div>
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.</div></li><li><div>
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family&rsquo;s well-being.</div></li><li><div>
Life assurance</div></li><li><div>
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.</div></li></ul></div></div></div></div><div></div><div>
Visit our <div>careers site</div> to read more about the benefits ICON offers.</div><div></div><div>
At ICON, inclusion &amp; belonging are fundamental to our culture and values. We&rsquo;re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.</div><div></div><div><div><div><div><div>
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know</div><div></div><div><div>
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless &ndash; there&rsquo;s every chance you&rsquo;re exactly what we&rsquo;re looking for here at ICON whether it is for this or other roles.</div></div></div></div></div></div></div><div></div>

Site Specialist II, Study Start Up

<div>CRA II<div></div><div>
ICON plc is a world-leading healthcare intelligence and clinical research organization. We&rsquo;re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development</div><div></div><div>
We are currently seeking a Clinical Research Associate II Specialist to join our diverse and dynamic team. As a Clinical Research Associate II Specialist at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies</div>
What you will be doing<ul><li>
Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.</li></ul><ul><li>
Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.</li></ul><ul><li>
Collaborating with investigators and site staff to facilitate smooth study conduct.</li></ul><ul><li>
Performing data review and resolution of queries to maintain high-quality clinical data.</li></ul><ul><li>
Contributing to the preparation and review of study documentation, including protocols and clinical study reports</li></ul>
Your profile<ul><li>
Bachelor's degree in a scientific or healthcare-related field.</li></ul><ul><li>
Minimum of 2 years of experience as a Clinical Research Associate.</li></ul><ul><li>
In-depth kNwledge of clinical trial processes, regulations, and ICH-GCP guidelines.</li></ul><ul><li>
Strong organizational and communication skills, with attention to detail.</li></ul><ul><li>
Ability to work independently and collaboratively in a fast-paced environment.</li></ul><div></div><div>
What ICON can offer you:</div><div></div><div><div><div><div><div>
Our success depends on the quality of our people. That&rsquo;s why we&rsquo;ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.</div><div></div><div>
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.</div><div></div><div>
Our benefits examples include:</div><ul><li><div>
Various annual leave entitlements</div></li><li><div>
A range of health insurance offerings to suit you and your family&rsquo;s needs.</div></li><li><div>
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.</div></li><li><div>
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family&rsquo;s well-being.</div></li><li><div>
Life assurance</div></li><li><div>
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.</div></li></ul></div></div></div></div><div></div><div>
Visit our <div>careers site</div> to read more about the benefits ICON offers.</div><div></div><div>
At ICON, inclusion &amp; belonging are fundamental to our culture and values. We&rsquo;re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.</div><div></div><div><div><div><div><div>
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know</div><div></div><div><div>
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless &ndash; there&rsquo;s every chance you&rsquo;re exactly what we&rsquo;re looking for here at ICON whether it is for this or other roles.</div></div></div></div></div></div></div><div></div>

CRA II

GE HealthCare

<div><h1 class="jobSectionHeader"><b>Job Description Summary</b></h1>
As a Service Business Operation Specialist, you will play a pivotal role in driving operational excellence across the service lifecycle and will be at the heart of our service ecosystem by ensuring data integrity, digitalization, standardization, process efficiency, and customer satisfaction. it's a launchpad for developing deep expertise in service business operations. You&rsquo;ll gain exposure to international teams, sharpen your analytical and communication skills, and contribute to meaningful improvements in how we serve our customers.<br>
<br>
In this dynamic role, you will:<br>
<br>
<ul><li>Own the Installed Base Lifecycle: From asset registration to end-of-life, manage and maintain accurate records that power our service operations.</li><li>Ensure Data Accuracy &amp; Timely Billing: Enter and validate customer information, warranties, and contracts in our Service ERP system to enable precise billing for both contract and non-contract services.</li><li>Drive System Excellence: Support data remediation and updates in Service CRM and ServiceMax, and contribute to seamless Channel Partner/Distributor transitions.</li><li>Lead Data Quality Initiatives: Manage data cleanup, migration, and verification activities to uphold operational standards.</li><li>Collaborate Across Functions: Work closely with cross-functional teams to align on data accuracy and streamline service processes.</li></ul><p></p><h1 class="jobSectionHeader"><b>
Job Description</b></h1><p><b>
Roles&amp; Responsibilities</b></p><ul><li>
Load, update, and maintain GEHC customer service contracts and warranties in all applicable Service ERP systems, including additions, deletions, and modifications.</li><li>
Ensure timely and accurate system and tax legal billing for both contract and non-contract services as per customer requests, minimizing delays and discrepancies.</li><li>
Maintain database accuracy by supporting field teams, internal stakeholders, and external customers via phone and email.</li><li>
Collaborate with Field Service Sales, Service Delivery, Service Marketing, and Commercial teams to resolve technical and process-related challenges.</li><li>
Assist Finance and Cash Collection teams in resolving customer disputes, including concessions, penalties, write-offs, and credit notes.</li><li>
Initiate and drive process improvement projects to standardize operations and enhance efficiency.</li><li>
Support the transition of distributors to Channel Partner ServiceMax by preparing data, executing cleanup activities, and managing migration in coordination with multiple stakeholders.</li><li>
Provide quarterly visibility into contract and non-contract profitability, highlighting areas for pricing optimization.</li><li>
Assist Finance teams during month-end, quarter-end, and year-end closing processes.</li><li>
Deliver prompt and effective support for all contract and non-contract related customer inquiries.</li><li>
Complete all required Quality &amp; Compliance training within defined deadlines.</li><li>
Follow Quality Assurance processes by properly archiving all relevant documentation, including proposals, signed contracts, service reports, and invoices.</li><li>
Comply with GEHC&rsquo;s Quality Manual, Management System, Policies, Goals, and all applicable laws and regulations.</li></ul><p></p><p><b>
Required Qualifications &amp; Requirements</b></p><ul><li>
Bachelor&rsquo;s degree in Business Administration, Finance, Economics, Engineering, or a related field.</li><li>
Minimum of 3 years of relevant professional experience in operations, service, or data management.</li><li>
Strong command of English, both written and verbal.</li><li>
Excellent organizational and time management skills.</li><li>
Proven ability to prioritize tasks, meet deadlines, and maintain attention to detail.</li><li>
Comfortable managing multiple tasks and adapting to changing priorities in a fast-paced environment.</li><li>
Ability to thrive in a dynamic, routine and high-volume work setting.</li><li>
Demonstrates a strong sense of urgency and ownership.</li><li>
Strong analytical and communication skills; able to engage effectively with internal and external stakeholders at all levels.</li><li>
Self-motivated with a proactive approach to problem-solving and decision-making.</li><li>
Focused on continuous improvement and eliminating non-value-added activities.</li></ul><p></p><h1 class="jobSectionHeader"><b>
Additional Information</b></h1><div><div><div><div><div><div><div><p><b>
Relocation Assistance Provided: </b>No</p></div></div></div></div></div></div></div></div><p></p>

Service Business Operation Specialist

<div>Site Specialist II<div></div><div>
ICON plc is a world-leading healthcare intelligence and clinical research organization. We&rsquo;re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development</div><div></div><div>
What you will be doing</div><ul><li><div>
Leading the preparation and submission of regulatory documents, including clinical trial applications, ethics committee submissions, and regulatory agency communications.</div></li></ul><ul><li><div>
Coordinating and liaising with internal and external stakeholders to obtain necessary approvals and authorizations for study initiation.</div></li></ul><ul><li><div>
Managing and maintaining comprehensive and accurate records of regulatory submissions, approvals, and correspondence</div></li></ul><ul><li><div>
Providing guidance and support to study teams on regulatory requirements and best practices for study start-up activities.</div></li></ul><ul><li><div>
Participating in process improvement initiatives to streamline study start-up processes and enhance efficiency.</div></li></ul><div></div><div>
Your profile</div><ul><li><div>
Bachelor's degree in life sciences or a related field.</div></li></ul><ul><li><div>
Minimum of 2 years of experience in clinical research or regulatory affairs, with specific experience in study start-up activities.</div></li></ul><ul><li><div>
Strong understanding of regulatory requirements and guidelines for clinical trials, including ICH-GCP and local regulatory requirements.</div></li></ul><ul><li><div>
Excellent organizational and project management skills, with the ability to prioritize and manage multiple tasks simultaneously.</div></li></ul><ul><li><div>
Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.</div></li></ul><div></div><div>
What ICON can offer you:</div><div></div><div><div><div><div><div>
Our success depends on the quality of our people. That&rsquo;s why we&rsquo;ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.</div><div></div><div>
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.</div><div></div><div>
Our benefits examples include:</div><ul><li><div>
Various annual leave entitlements</div></li><li><div>
A range of health insurance offerings to suit you and your family&rsquo;s needs.</div></li><li><div>
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.</div></li><li><div>
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family&rsquo;s well-being.</div></li><li><div>
Life assurance</div></li><li><div>
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.</div></li></ul></div></div></div></div><div></div><div>
Visit our <div>careers site</div> to read more about the benefits ICON offers.</div><div></div><div>
At ICON, inclusion &amp; belonging are fundamental to our culture and values. We&rsquo;re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.</div><div></div><div><div><div><div><div>
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know</div><div></div><div><div>
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless &ndash; there&rsquo;s every chance you&rsquo;re exactly what we&rsquo;re looking for here at ICON whether it is for this or other roles.</div></div></div></div></div></div></div><div></div>

Site Specialist II

<div>
 At EY, we&rsquo;re all in to shape your future with confidence.
 <br/>
 <br/>
 We&rsquo;ll help you succeed in a globally connected powerhouse of diverse teams and take your career wherever you want it to go.
 <br/>
 <br/>
 Join EY and help to build a better working world.
 <br/>
 <br/>
 <strong>
  The opportunity
  <br/>
  <br/>
 </strong>
 EY is a global leader in Assurance, Consulting, SaT (Strategy &amp;Transactions) and Tax services.
 <br/>
 <br/>
 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.
 <br/>
 <br/>
 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.
 <br/>
 <br/>
 Together, all in, to build a better working world.
 <br/>
 <br/>
 <strong>
  IFRS Desk Manager &ndash; &Idot;stanbul &amp; Ankara
  <br/>
  <br/>
 </strong>
 We are seeking for a IFRS Desk Manager to join our Assurance &ndash; Audit and Accounting Services team in Istanbul or Ankara with the following qualifications;
 <br/>
 <br/>
 <strong>
  What We Look For
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Strong academic background, including Bachelor&rsquo;s or Master&rsquo;s degree in Business, Finance, Economics or related field
  </li>
  <li>
   Minimum of 5 years of relevant experience in audit, technical accounting, or advisory services
  </li>
  <li>
   Strong technical knowledge of IFRS and Turkish local GAAP (TFRS/BOBI FRS).In-depth understanding of financial reporting regulations
  </li>
  <li>
   Compliance with and understanding of regulatory requirements
  </li>
  <li>
   English language skills - excellent written and verbal communication
  </li>
  <li>
   Strong analytical, problem-solving, and critical thinking abilities
  </li>
  <li>
   Strong interpersonal skills, with the ability to communicate effectively at all levels
  </li>
  <li>
   Professional accountancy qualification (SMMM, CPA, SPK) will be asset
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Your Key Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Provide high-quality technical IFRS support and guidance to engagement teams and clients
  </li>
  <li>
   Review and assess financial statements for compliance with IFRS and local GAAP
  </li>
  <li>
   Interpret new and complex IFRS standards and assess their implications for clients
  </li>
  <li>
   Contribute to the development of EY publications, training sessions, and tools related to IFRS
  </li>
  <li>
   Collaborate with global IFRS desks and industry specialists on technical consultations
  </li>
  <li>
   Monitor changes in accounting standards and regulations and assist in assessing their impact on EY clients
  </li>
  <li>
   Develop people through effectively supervising, coaching and mentoring all levels of staff
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What We Offer You
  <br/>
  <br/>
 </strong>
 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.
 <br/>
 <br/>
 Are you ready to shape your future with confidence? Apply today.
 <br/>
 <br/>
 To help create the best experience during the recruitment process, please describe any disability-related adjustments or accommodations you may need.
 <br/>
 <br/>
 <strong>
  EY
 </strong>
 | Building a better working world
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 EY is building a better working world by creating new value for clients, people, society and the planet, while building trust in capital markets.
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 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.
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EY Türkiye - IFRS Desk Manager (İstanbul & Ankara)

Explore 92+ Quality assurance specialist qa 2505 in Ankara this December. Find roles across top companies and apply now to boost your career.