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senior regulatory scientist - turkey Jobs in Ankara Turkey

senior regulatory scientist - turkey

regulatory affairs specialist

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>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

Sanofi

<div><p><i>About the job</i></p><p></p><p>
As <b>Strategic Partnerships Lead</b> within our Strategic Partnerships Department, you&rsquo;ll have the opportunity to support to our great vision to build a world where no one suffers or dies because of a vaccine preventable disease while chasing scientific miracles for improving people&rsquo;s lives. Ready to get started?</p><p><i>
The location of this position is Ankara; there is one coordinator &amp; one specialist within the team. This department directly linked to General Manager of Sanofi Vaccines Business Unit of Eurasia (Russia, T&uuml;rkiye, Caucasus, Levant, İran &amp; Iraq) and the responsibility of the position is limited with T&uuml;rkiye. The department supports to all franchises in regard to stakeholder engagement, access to public market through tenders and long-term partnership agreements in addition to private market through importation permit achievement. Working hand in hand with Regulatory, Quality and Business operations teams in addition to PAMA, Treasury &amp; Finance business partner teams. The external stakeholders are Public Health Directorate, Borders &amp; Shores Directorate, Religious Affairs Directorate, Turkish Medicines and Medical Devices Institution, Turkish National Control Laboratory, Turkish Health Institute, Ministry of Finance, State Supply Office, Treasury of TR.</i></p><p></p><p><b>
About Sanofi:</b></p><p>
We&rsquo;re an R&amp;D-driven, AI-powered biopharma company committed to improving people&rsquo;s lives and delivering compelling growth. Our deep understanding of the immune system &ndash; and innovative pipeline &ndash; enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people&rsquo;s lives.</p><p></p><p><b>
Main responsibilities:</b></p><p></p><ul><li><p>
Developing and maintaining strong relationships with key people in the T.R. Ministry of Health and all other relevant governmental institutions, acquiring information that will provide strategic added value to company objectives</p></li><li><p>
Supporting both to the strategical partnership projects of the company with short term and limited strategic scope and to establishment of strategical partnership pursuing long term and extensive strategical relations</p></li><li><p>
Discussion and negotiation with internal and external stakeholders, health authorities to achieve the permissions and solutions to issues related to responsibilities of the department
</p></li><li><p>Ensuring our company's participation to the tenders of ministry of health within the frame of our products</p></li><li><p>
Planning the quality control tests before the delivery of the tender vaccines and following the stages of the laboratory analyses, reporting and payment of fees after the delivery of the vaccines to the MoH warehouses
</p></li><li><p>Under global competitive environment ensuring of the visibility of our company value for public health and improving the company image</p></li></ul><p></p><p><i>
About you
</i></p><ul><li><p><b>Experience</b>: Market access/Regulatory/Project Management/Public Procurement experience in a pharma co.
</p></li><li><p><b>Soft and technical skills</b>: Commercial acumen, Strategic thinking, Negotiation skills, Influencing others, Analytical skills, People leadership, Forward thinking, Comfortable working in complex, matrixed environments with global counterparts. Self-starter with a passion for innovation and a strong sense of initiative</p></li><li><p><b>
Languages</b>: Fluent in English</p></li></ul><p></p><p><i>
Why choose us?</i></p><ul><li><p>
Work at the forefront of AI-powered science that accelerates discovery and improves outcomes.</p></li><li><p>
Collaborate beyond your expertise, sparking new ideas with diverse, multidisciplinary teams.</p></li><li><p>
Explore bold career paths &ndash; with opportunities to grow through scientific, leadership, and cross-functional moves.</p></li><li><p>
Help protect half a billion people every year, contributing to one of the largest global vaccination efforts in healthcare.</p></li></ul><p></p><p><b>
Pursue</b> <i>Progress</i>. <b>Discover </b><i>Extraordinary</i>.</p><p>
Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what&rsquo;s never-been-done-before. You&rsquo;ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people&rsquo;s lives? Let&rsquo;s Pursue <i>Progress</i> and Discover <i>Extraordinary</i> &ndash; together.</p><p>
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.</p>
null</div>

Strategic Partnership Lead Vaccines

<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

ICMPD Türkiye Temsilciliği

<div>
 <strong>
  Functional Overview
  <br/>
  <br/>
 </strong>
 The Senior Operations Manager leads and oversees the full scope of operations, administration and resource management functions in
 <em>
  the
 </em>
 <em>
  Regional Office/Representation/Mission,
 </em>
 as applicable. The role includes safeguarding institutional compliance, strengthening efficiency and accountability and ensuring that operational, administrative and resource management functions support programme delivery in line with ICMPD's strategic objectives, donor obligations, national and other applicable regulatory frameworks. The SOM monitors and analyses efficiency of business processes, assesses emerging issues and develops solutions. The SOM acts as an administrative advisor to
 <em>
  the Head of Region/Representation/Mission
 </em>
 and the Senior Managers and is responsible for coordinating the resource management and administrative functions and teams required for the implementation of the portfolio in an efficient and cost-effective manner.
 <br/>
 <br/>
 Reporting to the Head of Region/Representation/Mission and working in close coordination with internal stakeholders in the given office/s and relevant HQ units, the SOM ensures effective planning, compliance, operational coherence and alignment of administrative processes with ICMPD's regulatory and institutional framework. The position plays a critical role in ensuring that programme implementation is supported by sound resource planning, allocation and coordination of financial, human and administrative resources and high-performing support teams.
 <br/>
 <br/>
 Proficiency in English (verbal and written) and the language of the duty station.
</div>


VA25P165V01 - Senior Operations Manager

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 an IT Specialist to manage, maintain, and continuously improve PaneraTech&rsquo;s IT infrastructure and end-user environments. In this role, you will be responsible for ensuring the reliable operation of end-point devices, networks, and peripheral systems while providing effective and timely support to employees.
 <br/>
 <br/>
 You will take an active role in the full lifecycle of IT services, including planning, procurement, installation, configuration, maintenance, and troubleshooting of hardware and software systems. IT Specialist also contributes to standardization efforts, documentation, and continuous improvement initiatives to support secure and efficient IT operations across the company.
 <br/>
 <br/>
 This is a hybrid position with 3 office days per week at our office in Hacettepe Teknokent and Ostim OSB.
 <br/>
 <br/>
 Employment type: Fixed-term contract (1 year).
 <br/>
 <br/>
 <strong>
  Requirements
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s degree in Information Systems Engineering, Management Information Systems, Electrical and Electronics Engineering, Computer Engineering, or Electronics and Communication Engineering
  </li>
  <li>
   Minimum 3 years of experience in an IT support or IT specialist role
  </li>
  <li>
   Experience with end-user systems, hardware, and software environments
  </li>
  <li>
   Knowledge of Microsoft Office 365 or Google Workspace
  </li>
  <li>
   Basic to intermediate knowledge of network technologies (LAN/WAN, TCP/IP)
  </li>
  <li>
   Familiarity with information security standards and data protection regulations (ISO 27001, KVKK, 5651)
  </li>
  <li>
   Strong analytical and troubleshooting skills
  </li>
  <li>
   Attention to documentation, reporting, and process consistency
  </li>
  <li>
   Good command of English, both written and verbal
  </li>
  <li>
   Ability to communicate technical topics clearly to non-technical users
  </li>
  <li>
   Team-oriented mindset with the ability to collaborate across departments
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Key Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Managing and maintaining end-user devices, networks, and peripheral systems
  </li>
  <li>
   Providing daily IT support and troubleshooting for technical and operational issues
  </li>
  <li>
   Installing, configuring, repairing, and maintaining personal computers and related systems
  </li>
  <li>
   Monitoring LAN/WAN network performance and supporting high network uptime
  </li>
  <li>
   Preparing and maintaining technical documentation, standard operating procedures, and knowledge base articles
  </li>
  <li>
   Supporting information security, data protection, and compliance requirements
  </li>
  <li>
   Staying up to date with emerging technologies and industry trends
  </li>
  <li>
   Supporting IT planning activities, roadmaps, and continuous improvement initiatives
   <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>


IT Specialist

Baker Hughes

<div><p>Field Specialist &ndash; Intelligent Production Systems</p><p></p><p>
Do you enjoy working with cutting-edge energy equipment?</p><p>
Do you enjoy being part of a successful team?</p><p>
Join our growing team</p><p>
We are the leader in well construction and production. Our innovative physical and digital solutions improve efficiency, production and maximize reservoir value.</p><p></p><p>
Partner with the best</p><p>
As a Field Specialist, you will play a vital role onsite with our customers. Leading the installation and maintenance activities, you will work with customers to troubleshoot issues and ensure safe and compliant installations. You will be the onsite expert, continually developing your knowledge and skills to deliver innovative solutions.</p><p>
As a Field Specialist, you will be responsible for:</p><ul><li>
Running multiple medium to high risk applications in IPS Product Group such as Gauges, Intelligent Well Systems</li><li>
Installing equipment following technical documentation and using a variety of tools</li><li>
Being responsible for preparation / assembly and testing of completions/ IPS equipment to required standards in workshop as required.</li><li>
Ensuring supplied equipment is compatible with well parameters and other equipment used during installation</li><li>
Installing equipment in line with operating procedures to ensure flawless execution and minimizing down-time for our customers</li></ul><p></p><p>
Fuel your passion</p><p>
To be successful in this role you will:</p><ul><li>
Have Technical Diploma or Technical knowledge &amp; solid experience in Oilfield Services</li><li>
Have At least 8 years of field experience in completion tools and accessories e.g., Downhole Gauges, Intelligent Well Systems, Intelligent Production Systems (Minimum hands-on experience with running Downhole gauges and Flow control valves in smart wells)</li><li>
Demonstrate a good mechanical &amp; electronic aptitude and a desire to learn</li><li>
Be able to work varied work schedule and be available for a 24 hour call out as necessary</li><li>
Be willing and able to ensure Competency is kept up to date and achieve new ones within allocated period of time</li><li>
Have effective computer skills with competence in basic Microsoft Office programs suite</li><li>
Deep Water Offshore operations is desired</li><li>
Have thorough knowledge of drilling and completion techniques and drilling/work over rig operations</li></ul><p></p><p>
Work in a way that works for you</p><p>
We recognize that everyone is different and that the way in which people want to work and deliver at their best is different for everyone.</p><ul><li>
Working flexible hours - flexing the times when you work in the day to help you fit in everything in and work when you are the most productive</li></ul><p></p><p>
Working with us</p><p>
Our people are at the heart of what we do at Baker Hughes. We know we are better when all of our people are developed, engaged and able to bring their whole authentic selves to work. We invest in the health and well-being of our workforce, train and reward talent and develop leaders at all levels to bring out the best in each other.</p><p></p><p>
Working for you</p><p>
Our inventions have revolutionized energy for over a century. But to keep going forward tomorrow, we know we have to push the boundaries today. We prioritize rewarding those who embrace change with a package that reflects how much we value their input. Join us, and you can expect:</p><ul><li>
Contemporary work-life balance policies and wellbeing activities</li><li>
Comprehensive private medical care options</li><li>
Safety net of life insurance and disability programs</li><li>
Tailored financial programs</li><li>
Additional elected or voluntary benefits</li></ul><p></p><b>
About Us:</b><div>
We are an energy technology company that provides solutions to energy and industrial customers worldwide. Built on a century of experience and conducting business in over 120 countries, our innovative technologies and services are taking energy forward &ndash; making it safer, cleaner and more efficient for people and the planet.</div><br>
<b>
Join Us:</b><div>
Are you seeking an opportunity to make a real difference in a company that values innovation and progress? Join us and become part of a team of people who will challenge and inspire you! Let&rsquo;s come together and take energy forward.<br>
<br>
Baker Hughes Company is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.</div></div>

Field Specialist General – Intelligent Production Systems

Explore 29+ Regulatory affairs specialist in Ankara Turkey this January. Find roles across top companies and apply now to boost your career.