business development representative (ankara) Jobs in Ankara

business development representative (ankara)

customer support consultant – tier 1 - ankara Jobs in Ankara

customer support consultant – tier 1 - ankara

senior regulatory scientist - turkey Jobs in Ankara

senior regulatory scientist - turkey

territory sales engineer, ankara Jobs in Ankara

territory sales engineer, ankara

business development specialist (turkey) Jobs in Ankara

business development specialist (turkey)

senior regulatory scientist turkey

ICON plc

<div>Senior Regulatory Scientist - Turkey<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>
Completes country and, or regional Clinical Trial Regulatory deliverables according to study specifics, ICON policies, procedures, applicable regulations and the principles of ICH-GCP with sound scientific/technical principles in line with contractual agreement.</div><div><br>
Depending upon experience, become involved, when required, staff training/mentoring and contribute to the review of ICON systems and procedures as appropriate</div><div></div><div>
Responsibilities:</div><div>
Minimum of 3 years&rsquo; relevant regulatory experience<br>
Read, write and speak fluent English; fluent in host country language<br>
Travel less than 5%<br>
Recognize, exemplify and adhere to ICON's values which centre around our commitment to People, Clients and Performance<br>
As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs<br>
Ensure regulatory deliverables are performed in accordance with all relevant regulations, guidelines, policies and procedures within contractual timelines and budget with sound scientific/technical principles<br>
Advanced knowledge of ICON&rsquo;s SOPs/WIs, ICH, GCP and appropriate regulations<br>
Advanced knowledge of ICON systems applicable to role<br>
Advanced knowledge of country/region Regulatory Agency (RA), Central Ethics Committee (CEC) and other country-level authority clinical trial requirements, as applicable<br>
Input to strategic planning of submissions to RA, CEC and other country-level bodies, including proactive identification and mitigation of risks, as applicable<br>
Direct interaction with RA, CEC and other country-level bodies<br>
Ensure timely preparation/creation/adaptation/coordination/collation of submission pack/documentation according to applicable requirements<br>
Arrange internal/external review of submission/documentation according to project requirements<br>
Track and file central submission/approval progress in Clinical Trials Management System (CTMS), eTMF and other applicable systems ensuring accuracy and completeness of data/documents entered<br>
Perform translation management according to project requirements<br>
Manage submissions through lifecycle to approval in line with contractual agreement<br>
Maintain agreed timelines<br>
Ensure project team is informed of applicable clinical trial Regulatory submissions and approvals in accordance with project requirements<br>
Collaborate with other roles in-country/region to meet ICON&rsquo;s deliverables<br>
Ensure all project-specific training is completed on time, as applicable<br>
Adhere to study budget and proactively identifies out of scope activities<br>
Support the surveillance, collection, and maintenance of accurate, up-to-date clinical trial global/regional/country and regulatory clinical trial intelligence<br>
May mentor junior team members<br>
May contribute to the review of ICON systems and procedures as appropriate<br>
Any other duties deemed necessary to secure the success of ICON&rsquo;s business</div><div></div><div>
#LI-CL1</div><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>

Senior Regulatory Scientist - Turkey

<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.
 <br/>
 <br/>
 Completes country and, or regional Clinical Trial Regulatory deliverables according to study specifics, ICON policies, procedures, applicable regulations and the principles of ICH-GCP with sound scientific/technical principles in line with contractual agreement.
 <br/>
 <br/>
 Depending upon experience, become involved, when required, staff training/mentoring and contribute to the review of ICON systems and procedures as appropriate
 <br/>
 <br/>
 <strong>
  Responsibilities
  <br/>
  <br/>
 </strong>
 Minimum of 3 years&rsquo; relevant regulatory experience
 <br/>
 <br/>
 Read, write and speak fluent English; fluent in host country language
 <br/>
 <br/>
 Travel less than 5%
 <br/>
 <br/>
 Recognize, exemplify and adhere to ICON's values which centre around our commitment to People, Clients and Performance
 <br/>
 <br/>
 As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs
 <br/>
 <br/>
 Ensure regulatory deliverables are performed in accordance with all relevant regulations, guidelines, policies and procedures within contractual timelines and budget with sound scientific/technical principles
 <br/>
 <br/>
 Advanced knowledge of ICON&rsquo;s SOPs/WIs, ICH, GCP and appropriate regulations
 <br/>
 <br/>
 Advanced knowledge of ICON systems applicable to role
 <br/>
 <br/>
 Advanced knowledge of country/region Regulatory Agency (RA), Central Ethics Committee (CEC) and other country-level authority clinical trial requirements, as applicable
 <br/>
 <br/>
 Input to strategic planning of submissions to RA, CEC and other country-level bodies, including proactive identification and mitigation of risks, as applicable
 <br/>
 <br/>
 Direct interaction with RA, CEC and other country-level bodies
 <br/>
 <br/>
 Ensure timely preparation/creation/adaptation/coordination/collation of submission pack/documentation according to applicable requirements
 <br/>
 <br/>
 Arrange internal/external review of submission/documentation according to project requirements
 <br/>
 <br/>
 Track and file central submission/approval progress in Clinical Trials Management System (CTMS), eTMF and other applicable systems ensuring accuracy and completeness of data/documents entered
 <br/>
 <br/>
 Perform translation management according to project requirements
 <br/>
 <br/>
 Manage submissions through lifecycle to approval in line with contractual agreement
 <br/>
 <br/>
 Maintain agreed timelines
 <br/>
 <br/>
 Ensure project team is informed of applicable clinical trial Regulatory submissions and approvals in accordance with project requirements
 <br/>
 <br/>
 Collaborate with other roles in-country/region to meet ICON&rsquo;s deliverables
 <br/>
 <br/>
 Ensure all project-specific training is completed on time, as applicable
 <br/>
 <br/>
 Adhere to study budget and proactively identifies out of scope activities
 <br/>
 <br/>
 Support the surveillance, collection, and maintenance of accurate, up-to-date clinical trial global/regional/country and regulatory clinical trial intelligence
 <br/>
 <br/>
 May mentor junior team members
 <br/>
 <br/>
 May contribute to the review of ICON systems and procedures as appropriate
 <br/>
 <br/>
 Any other duties deemed necessary to secure the success of ICON&rsquo;s business
 <br/>
 <br/>
 <strong>
  What ICON Can Offer You
  <br/>
  <br/>
 </strong>
 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.
 <br/>
 <br/>
 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.
 <br/>
 <br/>
 <strong>
  Our Benefits Examples Include
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Various annual leave entitlements
  </li>
  <li>
   A range of health insurance offerings to suit you and your family&rsquo;s needs.
  </li>
  <li>
   Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
  </li>
  <li>
   Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family&rsquo;s well-being.
  </li>
  <li>
   Life assurance
  </li>
  <li>
   Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
   <br/>
   <br/>
  </li>
 </ul>
 Visit our careers site to read more about the benefits ICON offers.
 <br/>
 <br/>
 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.
 <br/>
 <br/>
 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 or submit a request here
 <br/>
 <br/>
 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.
 <br/>
 <br/>
 Are you a current ICON Employee? Please click here to apply
 <br/>
 <br/>
</div>


PaneraTech, Inc.

<div>
 <strong>
  Who We Are
  <br/>
  <br/>
 </strong>
 PaneraTech is a high-tech company that serves manufacturers in over 40 countries. Our disruptive technology offers unparalleled solutions that are often patent protected. Industries that use high-temperature processes, such as glass and steel, rely on PaneraTech to solve the major challenges they face. We leverage both AI and human expertise to improve efficiency, worker knowledge, and safety. We help in two major areas:
 <br/>
 <br/>
 <ul>
  <li>
   Asset Life Extension - With our patented solution in the glass and steel industry, we help manufacturers make data-driven decisions using sensors, data, and AI. This results in longer asset campaigns safely with higher annual production
  </li>
  <li>
   Enabling the next generation of workers - Heavy industries have relied on the experience of employees who worked for 20-30 years in one plant. As a generation of operators and engineers retire, we bridge the experience gap with technology, data, and expertise. We offer solutions to our customers to make their process more data-driven so that an early career workforce can flourish.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  <strong>
   Working at PaneraTech
   <br/>
   <br/>
  </strong>
 </strong>
 At PaneraTech, you will be part of a global, innovative and hybrid working team. Our corporate office is based in the United States with employees spread across Europe, Asia, and South America. Turkey office is in the Hacettepe Teknokent. In this collaborative and inspiring culture that is fostered by a creative and intellectually stimulating work environment, you will be encouraged to bring the best out of yourself and your colleagues. We are looking for professionals willing to work in a fast-paced environment, cannot wait to excel in their work and are crazy about improvement! We recognize our colleagues' achievements and both individual and team performance is valuable to us.
 <br/>
 <br/>
 <strong>
  About The Job
  <br/>
  <br/>
 </strong>
 We are looking for a highly motivated Senior Data Scientist to take active role in development of industrial AI systems for prediction and data analytics (using operational data) performances. You will propose robust solutions which are in turn employed in predictive/preventive maintenance AI architecture to optimize glass and steel manufacturing processes.
 <br/>
 <br/>
 This is a hybrid position with 3 office days per week at our office in Hacettepe Teknokent.
 <br/>
 <br/>
 <strong>
  Requirements
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s degree from a reputable university in Mathematics, Engineering, Statistics, Physics, or a related field
  </li>
  <li>
   MS/PHD Degree in machine learning is preferred
  </li>
  <li>
   At least 5 years of experience on AI
  </li>
  <li>
   At least 5 years of experience building predictive models, preferably in a business or industrial setting
  </li>
  <li>
   Experience in MATLAB (or R) and python
  </li>
  <li>
   Solid understanding of object-oriented programming
  </li>
  <li>
   Good command of the English language, both written and verbal
  </li>
  <li>
   Natural and strong curiosity with strong analytical and problem-solving skills
  </li>
  <li>
   Excited and motivated by technical challenges
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Key Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Establishing best practices for data collection and analysis
  </li>
  <li>
   Evaluating data quality to develop procedures that will ensure high quality of data
  </li>
  <li>
   Working closely with technical leaders to understand business side of data (industrial AI)
  </li>
  <li>
   Developing scalable data processing pipelines
  </li>
  <li>
   Developing data analytics tools to extract insights on manufacturing processes
  </li>
  <li>
   Building machine learning models for prediction and data insights
  </li>
  <li>
   Developing predictive/preventive maintenance AI algorithms to enhance manufacturing process
  </li>
  <li>
   Collaborating with other engineers and scientists to find effective solutions to technical challenges
  </li>
  <li>
   Helping the team develop predictive/preventive maintenance AI algorithms to optimize manufacturing processes
  </li>
  <li>
   Leading the team members to excel in their roles with a sense of contribution
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Benefits
  <br/>
  <br/>
 </strong>
 At PaneraTech, we recognize that our employees are the driving force behind our success. We are committed to creating a positive and supportive work environment.
 <br/>
 <br/>
 <strong>
  We Offer
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Competitive monthly net salary
  </li>
  <li>
   Private health insurance
  </li>
  <li>
   18 days holiday per annum
  </li>
  <li>
   A transparent work environment
  </li>
  <li>
   An agile structure that values open communication and instant feedback
  </li>
  <li>
   Opportunities for personal and professional growth
  </li>
  <li>
   A global and diverse team dedicated to improving the company and every single colleague within
  </li>
 </ul>
</div>


Senior Data Scientist

<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.
 <br/>
 <br/>
 <strong>
  The Role
  <br/>
  <br/>
 </strong>
 In this position, you will be responsible for negotiating and finalising Clinical Trial Agreements and amendments with sites across Turkey. You will work closely with local site teams and ICON&rsquo;s internal stakeholders to remove contracting barriers, protect ICON and client interests, and ensure studies progress according to planned timelines. Your ability to communicate clearly in both Turkish and English, manage risks, and maintain accurate contract documentation will be key to delivering successful site activation.
 <br/>
 <br/>
 <strong>
  Key Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Negotiate and finalise CTAs and amendments with Turkish sites to enable timely site activation while ensuring full compliance with Turkish legislation, ICON SOPs, and client requirements.
  </li>
  <li>
   Act as the primary contracting contact for Turkish sites, building strong relationships and ensuring clear, culturally appropriate communication throughout the contracting process.
  </li>
  <li>
   Maintain proactive communication with internal teams to keep study stakeholders aligned on contracting progress, risks, and expected timelines.
  </li>
  <li>
   Track the status of all contracts in ICON and client systems so that study teams have accurate visibility and can plan start-up activities effectively.
  </li>
  <li>
   Identify potential risks or delays early and propose realistic mitigation strategies to protect study timelines.
  </li>
  <li>
   Review all contract documents for accuracy and compliance, ensuring that agreements meet legal, financial, and operational standards specific to Turkey.
  </li>
  <li>
   Collaborate cross-functionally with SSU, Legal, Regulatory, and Clinical Operations to ensure contract terms reflect site requirements and support smooth initiation.
  </li>
  <li>
   Participate in study calls and internal meetings to align contracting work with overall study goals.
  </li>
  <li>
   Maintain organised, audit-ready contract files in accordance with ICON and client requirements.
  </li>
  <li>
   Support continuous improvement initiatives within the department and provide mentorship when needed.
  </li>
  <li>
   Complete mandatory training and adhere to SOPs to ensure consistent, high-quality delivery.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What You Need
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s degree.
  </li>
  <li>
   3&ndash;6 years of experience in clinical research, site contracts, or a related field.
  </li>
  <li>
   Fluency in both Turkish and English (written and spoken) is essential.
  </li>
  <li>
   Strong understanding of Turkish site contracting practices and local regulatory expectations.
  </li>
  <li>
   Excellent communication and relationship-building skills with both internal teams and investigative sites.
  </li>
  <li>
   Strong organisational skills and the ability to independently manage multiple priorities.
  </li>
  <li>
   High attention to detail and confidence in managing site-facing negotiations.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What ICON Can Offer You
  <br/>
  <br/>
 </strong>
 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.
 <br/>
 <br/>
 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.
 <br/>
 <br/>
 <strong>
  Our Benefits Examples Include
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Various annual leave entitlements
  </li>
  <li>
   A range of health insurance offerings to suit you and your family&rsquo;s needs.
  </li>
  <li>
   Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
  </li>
  <li>
   Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family&rsquo;s well-being.
  </li>
  <li>
   Life assurance
  </li>
  <li>
   Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
   <br/>
   <br/>
  </li>
 </ul>
 Visit our careers site to read more about the benefits ICON offers.
 <br/>
 <br/>
 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.
 <br/>
 <br/>
 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 or submit a request here
 <br/>
 <br/>
 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.
 <br/>
 <br/>
 Are you a current ICON Employee? Please click here to apply
 <br/>
 <br/>
</div>


Site Contracts Negotiator II

<div>Site Contracts Negotiator 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>
The Role</div><div>
In this position, you will be responsible for negotiating and finalising Clinical Trial Agreements and amendments with sites across Turkey. You will work closely with local site teams and ICON&rsquo;s internal stakeholders to remove contracting barriers, protect ICON and client interests, and ensure studies progress according to planned timelines. Your ability to communicate clearly in both Turkish and English, manage risks, and maintain accurate contract documentation will be key to delivering successful site activation.</div><div></div><div>
Key Responsibilities:</div><ul><li><div>
Negotiate and finalise CTAs and amendments with Turkish sites to enable timely site activation while ensuring full compliance with Turkish legislation, ICON SOPs, and client requirements.</div></li><li><div>
Act as the primary contracting contact for Turkish sites, building strong relationships and ensuring clear, culturally appropriate communication throughout the contracting process.</div></li><li><div>
Maintain proactive communication with internal teams to keep study stakeholders aligned on contracting progress, risks, and expected timelines.</div></li><li><div>
Track the status of all contracts in ICON and client systems so that study teams have accurate visibility and can plan start-up activities effectively.</div></li><li><div>
Identify potential risks or delays early and propose realistic mitigation strategies to protect study timelines.</div></li><li><div>
Review all contract documents for accuracy and compliance, ensuring that agreements meet legal, financial, and operational standards specific to Turkey.</div></li><li><div>
Collaborate cross-functionally with SSU, Legal, Regulatory, and Clinical Operations to ensure contract terms reflect site requirements and support smooth initiation.</div></li><li><div>
Participate in study calls and internal meetings to align contracting work with overall study goals.</div></li><li><div>
Maintain organised, audit-ready contract files in accordance with ICON and client requirements.</div></li><li><div>
Support continuous improvement initiatives within the department and provide mentorship when needed.</div></li><li><div>
Complete mandatory training and adhere to SOPs to ensure consistent, high-quality delivery.</div></li></ul><div></div><div>
What You Need</div><ul><li><div>
Bachelor&rsquo;s degree.</div></li><li><div>
3&ndash;6 years of experience in clinical research, site contracts, or a related field.</div></li><li><div>
Fluency in both Turkish and English (written and spoken) is essential.</div></li><li><div>
Strong understanding of Turkish site contracting practices and local regulatory expectations.</div></li><li><div>
Excellent communication and relationship-building skills with both internal teams and investigative sites.</div></li><li><div>
Strong organisational skills and the ability to independently manage multiple priorities.</div></li><li><div>
High attention to detail and confidence in managing site-facing negotiations.</div></li></ul><div></div><div>
#LI-MK1</div><div>
#LI-Remote</div><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>

AKO Grup

<div>
 <p>
  AKO GRUP, which consists of 6 large-scale factories (PETLAS, Sumitomo Rubber AKO Turkey, AKO AK&Uuml;, AKO JANT, AKO Lastik Kaplama, and AKO &Ouml;TL), over 30 brands, and a network of nearly 1200 dealers, is the production powerhouse of Turkey, strengthening itself for tomorrow&rsquo;s Turkey.
 </p>
 <p>
  With 100% domestic production and advanced R&amp;D activities, AKO is one of the largest manufacturers and exporters in Turkey, exporting to over 100 countries. Since its establishment, AKO has made continuous development its principle, and with more than 6,000 employees, it continues to grow by combining its experience and knowledge in the automotive industry with new technologies and investments.
 </p>
 <p>
  As the leader of the Turkish tire sector, we are looking for an
  <strong>
   &lsquo;&rsquo;Purchasing Chief&rsquo;&rsquo;
  </strong>
  to join our headquarters in Ankara with the following qualifications.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <u>
   Qualifications:
  </u>
 </p>
 <ul>
  <li>
   Graduates from relevant university departments (preferably Industrial Engineering, Chemical Engineering)
  </li>
  <li>
   Experience in purchasing processes in the manufacturing sector, preferably the automotive sector
  </li>
  <li>
   Experience in the procurement of rubber, metals, cords, carbon black, and chemicals
  </li>
  <li>
   At least 5 years of experience in purchasing
  </li>
  <li>
   Advanced level of English
  </li>
  <li>
   Proficient in MS Office and familiarity with ERP programs
  </li>
  <li>
   Experience in purchasing processes in the manufacturing sector, preferably the automotive sector
  </li>
  <li>
   Analytical thinking and problem-solving skills
  </li>
  <li>
   Ability to work quickly and results-oriented, adaptable to a busy work schedule
  </li>
  <li>
   Strong communication skills and teamwork skills
  </li>
  <li>
   High sense of discipline and responsibility
  </li>
 </ul>
 <p>
  Candidate applications will be evaluated.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <u>
   Operational Duties and Responsibilities:
  </u>
 </p>
 <ul>
  <li>
   Procurement of products, materials, etc. Conducting market research,
  </li>
  <li>
   Ensuring the purchasing and supply of raw materials and materials from domestic and international markets,
  </li>
  <li>
   Examining market prices for products, materials, etc., and gathering information about the company from which the purchase will be made.
  </li>
  <li>
   Controlling and coordinating the operations of purchasing personnel,
  </li>
  <li>
   Keeping records of purchasing transactions and costs,
  </li>
  <li>
   Monitoring developments in the domestic and international markets and identifying alternative suppliers with suitable price, quality, and delivery performance,
  </li>
  <li>
   Ensuring optimal and timely meeting internal customer expectations and ensuring internal customer satisfaction,
  </li>
  <li>
   Preparing and managing contracts and service agreements with suppliers,
  </li>
  <li>
   Monitoring daily the material/raw material requirements determined by the MRP module of the existing ERP system and ensuring their delivery on time.
  </li>
 </ul>
 <p>
 </p>
</div>


Purchasing Chief

<div>
 <p>
  <strong>
   <u>
    About Zes &amp; Electrip
   </u>
  </strong>
 </p>
 <p>
  Since 2018,
  <strong>
   Zes
  </strong>
  aims to help electric vehicle users and speed up the electric vehicle revolution in Turkey with its intracity and intercity stations. Besides the fast-charging services offered at open public spaces, upon demand, station installation is also available for users&rsquo; homes and offices. Zes is new, clean, and fast energy of the roads, with more than 4.000 fast charging stations all over Turkey. Powered by 100% renewable energy.
 </p>
 <p>
  Our Global brand,
  <strong>
   Electrip
  </strong>
  excels in charging point operations and energy efficiency services as a fresh brand. Having two strong pillars on energy and infrastructure; Electrip aims to contribute for a better world in line with Sustainable Development Goals (SDG). Electrip is dedicated to the development of innovative solutions to meet the needs of the present and shape the future, continuously expanding its service solutions and refining its customer-centered approach.
 </p>
 <p>
  To work on software solutions for both Zes and Electrip brands, we are looking for a
  <strong>
   Software Technical Product Management Senior Specialist (Mobile Applications)
  </strong>
  located in Ankara. This is an exciting opportunity to be part of a fast-growing, innovative environment and play a leading role in the expanding electric vehicle (EV) market.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    What You'll Be Doing
   </u>
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  As the
  <strong>
   Software Technical Product Management Senior Specialist (Mobile Applications)
  </strong>
  , you will take ownership of our mobile application planning, and execution. You will be based in Ankara and will report to
  <strong>
   Software Technical Product Management Executive (Mobile Applications)
  </strong>
  in Technology and Digital Solutions Directorate.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <em>
    Your main responsibilities will include, but aren&rsquo;t limited to:
   </em>
  </strong>
 </p>
 <ul>
  <li>
   Lead the implementations of our EV charging station mobile applications.
  </li>
  <li>
   Work closely with product management teams, regional teams to understand local needs and seek for global best practices/use cases to define and manage the short and long-term product roadmap, review continuously to keep it up to date.
  </li>
  <li>
   Collaborate closely with technical teams and third-party developers to ensure technical requirements and architecture are clearly defined.
  </li>
  <li>
   Work with the project manager to define the mobile application project strategy and delivery schedule.
  </li>
  <li>
   Responsible for the overall coordination, implementation, execution and control of mobile apps.
  </li>
  <li>
   Plan, execute, and oversee User Acceptance Testing (UAT) to ensure product quality before release.
  </li>
  <li>
   Ensuring the project is executed on time and meets quality standards.
  </li>
  <li>
   Manage integrations between mobile applications (native) and backend systems.
  </li>
  <li>
   Analyze and prioritize product backlog.
  </li>
  <li>
   Prepare the necessary functional requirements and tasks for the project and regularly compare competitors.
  </li>
  <li>
   Coordinate and manage product development with internal departments and all stakeholders.
  </li>
  <li>
   Identify and manage project-related risks and estimate their potential impact.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Required Skills
   </u>
  </strong>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree in Computer Science, Engineering, or a related field (or equivalent experience).
  </li>
  <li>
   4+ years of experience in software product development as a Product Owner, Business/Technical Analyst, Project Manager, Product Manager, or similar role.
  </li>
  <li>
   Proven track record in mobile application development projects (native or hybrid) and backend integrations
  </li>
  <li>
   Experienced or knowledge in mobile application development (Native (iOS, Android)) and optimizing mobile user experience (UX)
  </li>
  <li>
   Good understanding about backend, mobile technologies and technical integrations
  </li>
  <li>
   Used to working with IT Teams
  </li>
  <li>
   Deep knowledge of Agile, Scrum methodology, use case and user story
  </li>
  <li>
   Strong leadership skills, with the ability to work in cross-functional teams
  </li>
  <li>
   Ability to work in a fast-paced environment
  </li>
  <li>
   Strong ability to simplify and clearly communicate complex technical concepts.
  </li>
  <li>
   Hands-on experience gathering business requirements and collaborating with teams.
  </li>
  <li>
   Ability to set KPI&rsquo;s and monitor, evaluate regularly to effectively manage products&rsquo; time to market,
  </li>
  <li>
   Being able to think analytically, practical and result-oriented with strong problem-solving skills.
  </li>
  <li>
   Data-driven decision-making approach.
  </li>
  <li>
   Excellent written and verbal communication skills in English.
  </li>
  <li>
   Familiarity with Agile/Scrum principles and tools such as Jira, Confluence, or Azure DevOps.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Preferred Skills
   </u>
  </strong>
 </p>
 <ul>
  <li>
   Experience in
   <strong>
    EV charging, energy, or mobility sector
   </strong>
   .
  </li>
  <li>
   Knowledge of
   <strong>
    UX/UI best practices
   </strong>
   for mobile.
  </li>
  <li>
   Familiarity with
   <strong>
    Firebase, App Center, or similar analytics tools
   </strong>
   .
  </li>
 </ul>
 <p>
 </p>
</div>


Software Technical Product Management Senior Specialist (Mobile Apps)

Explore 100+ Senior regulatory scientist turkey in Ankara this January. Find roles across top companies and apply now to boost your career.

100 senior regulatory scientist turkey jobs IN Ankara

Senior Regulatory Scientist - Turkey

Senior Regulatory Scientist - Turkey

Senior Data Scientist

Site Contracts Negotiator II

Site Contracts Negotiator II

Purchasing Chief

Software Technical Product Management Senior Specialist (Mobile Apps)