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Mondelēz International

<div>
 
 Job Description
 
 
 
 
 Are You Ready to Make It Happen at Mondel&emacr;z International?
 
 
 
 
 Join our Mission to Lead the Future of Snacking. Make It With Pride.
 
 
 
 You execute the regulatory affairs strategy for your respective category or categories and geographical area using your technical and regulatory knowledge. You ensure our policies, regulatory programs and requirements of our portfolio carried out.
 
 
 
 How You Will Contribute
 
 
 
 You will deliver on the regulatory affairs strategy and compliance agenda and work with cross-functional stakeholders to assess regulatory business risks and opportunities. You will provide regulatory affairs expertise for technical regulatory developments and help in responses to challenges and crisis management. In this role, you will ensure that ingredients, product composition, claims and labelling compliance are within applicable regulations and company policies. In addition, you will provide guidance to stakeholders on developments in regulatory affairs, support regulatory impact assessments and change management, help develop regulatory affairs tools, and further develop your knowledge of regulatory, science and nutrition risks and opportunities in your market.
 
 
 
 What You Will Bring
 
 
 
 A desire to drive your future and purpose, accelerate your career and the following experience and knowledge:
 
 
 <ul>
 <li>
 Bachelor's Degree, preferably, in Food /Nutrition/Chemistry fields,
 </li>
 <li>
 Good organizational and communication skills,
 </li>
 <li>
 An open-minded attitude on problem solving and solution seeking,
 </li>
 <li>
 Experience in food regulatory field will be treated as an asset,
 </li>
 <li>
 Fluency in English &amp; Turkish,
 </li>
 <li>
 Networking and communication skills,
 </li>
 <li>
 Reliability and accuracy and an efficient work style,
 </li>
 <li>
 Meeting deadlines,
 </li>
 <li>
 Attending to detail,
 </li>
 <li>
 Project management,
 </li>
 <li>
 Regulatory affairs in an international and multi-functional environment.
 
 
 
 </li>
 </ul>
 
 More About This Role
 
 
 
 
 What you need to know about this position:
 
 
 
 
 What extra ingredients you will bring:
 
 
 
 
 Education / Certifications:
 
 
 
 
 Job specific requirements:
 
 
 
 
 Travel requirements:
 
 
 
 
 Work schedule:
 
 
 
 
 Relocation Support Available?
 
 
 
 No Relocation support available
 
 
 
 Business Unit Summary
 
 
 
 We value our talented employees, and whenever possible strive to help one of our associates grow professionally before recruiting new talent to our open positions. If you think the open position you see is right for you, we encourage you to apply!
 
 
 
 Our people make all the difference in our succes
 
 
 
 Mondel&emacr;z International is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law.
 
 
 
 Excited to grow your career?
 
 
 
 We value our talented employees, and whenever possible strive to help one of our associates grow professionally before recruiting new talent to our open positions. If you think the open position you see is right for you, we encourage you to apply!
 
 
 
 IF YOU REQUIRE SUPPORT TO COMPLETE YOUR APPLICATION OR DURING THE INTERVIEW PROCESS, PLEASE CONTACT THE RECRUITER
 
 
 
 
 Job Type
 
 
 
 Regular
 
 
 Scientific Affairs &amp; Regulatory Affairs
 
 
 Product Quality, Safety and Compliance
</div>

Regulatory Affairs Scientist I

<div><div>Job Description
Are You Ready to Make It Happen at Mondel&#275;z International?
Join our Mission to Lead the Future of Snacking. Make It With Pride.
You execute the regulatory affairs strategy for your respective category or categories and geographical area using your technical and regulatory knowledge. You ensure our policies, regulatory programs and requirements of our portfolio carried out.
How you will contribute
You will deliver on the regulatory affairs strategy and compliance agenda and work with cross-functional stakeholders to assess regulatory business risks and opportunities. You will provide regulatory affairs expertise for technical regulatory developments and help in responses to challenges and crisis management. In this role, you will ensure that ingredients, product composition, claims and labelling compliance are within applicable regulations and company policies. In addition, you will provide guidance to stakeholders on developments in regulatory affairs, support regulatory impact assessments and change management, help develop regulatory affairs tools, and further develop your knowledge of regulatory, science and nutrition risks and opportunities in your market.
What you will bring
A desire to drive your future and purpose, accelerate your career and the following experience and knowledge:<ul><li>
Bachelor's Degree, preferably, in Food /Nutrition/Chemistry fields,</li><li>
Good organizational and communication skills,</li><li>
An open-minded attitude on problem solving and solution seeking,</li><li>
Experience in food regulatory field will be treated as an asset,</li><li>
Fluency in English &amp; Turkish,</li><li>
Networking and communication skills,</li><li>
Reliability and accuracy and an efficient work style,</li><li>
Meeting deadlines,</li><li>
Attending to detail,</li><li>
Project management,</li><li>
Regulatory affairs in an international and multi-functional environment.</li></ul>
More about this role
What you need to know about this position:
What extra ingredients you will bring:
Education / Certifications:
Job specific requirements:
Travel requirements:
Work schedule:
Relocation Support Available?
No Relocation support available
Business Unit Summary<div>
We value our talented employees, and whenever possible strive to help one of our associates grow professionally before recruiting new talent to our open positions. If you think the open position you see is right for you, we encourage you to apply!</div><div></div><div>
Our people make all the difference in our succes</div>
Mondel&#275;z International is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation or preference, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law.
Excited to grow your career?
We value our talented employees, and whenever possible strive to help one of our associates grow professionally before recruiting new talent to our open positions. If you think the open position you see is right for you, we encourage you to apply!
IF YOU REQUIRE SUPPORT TO COMPLETE YOUR APPLICATION OR DURING THE INTERVIEW PROCESS, PLEASE CONTACT THE RECRUITER
Job Type
Regular
Scientific Affairs &amp; Regulatory Affairs
Product Quality, Safety and Compliance</div></div>

Medtronic

<div>At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You&rsquo;ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
<h1 class="jobSectionHeader">A Day in the Life
</h1>Come and join our regional Regulatory Affairs Team as Regulatory Affairs Manager to oversee both pre-market and post-market regulatory activities in Levant, Gulf and Pakistan countries (Cyprus, Iran, Iraq, Jordan, Lebanon, Syria, Bahrain, Kuwait, Oman, Qatar, Yemen, UAE, Pakistan and Afghanistan) and work with a talented team.
 
 
The role is crucial to enable timely product launches and business continuity in the said regions by sustaining strong relations with distributors, authorities as well as internal stakeholders including country leaders. The role will report into Sr. Regulatory Affairs Manager responsible for Turkiye, West Asia, Levant and Gulf.
Responsibilities may include the following and other duties may be assigned:
<ul><li>Drives an effective product planning &amp; submission process across region with proactive alignment with relevant stakeholders
</li><li>Leads to compile all materials required in submissions, license renewal and annual registrations
</li><li>Recommends changes for labelling, manufacturing, marketing for regulatory compliance
</li><li>Ensure audit readiness in organization and continue meeting our Quality KPIs
</li><li>Ensures effective monitoring, communication and collaboration on new &amp; changing regulations and required actions
</li><li>Executes a comprehensive Q/RA advocacy strategy and may direct interaction with regulatory agencies on defined matters. Active participation in related Trade Associations
</li><li>Recommends strategies for earliest possible approvals of product dossiers in specified regions and drive optimization and foster innovation in regulatory processes
</li><li>Foster and contribute to the culture of Engagement, Inclusion and Innovation as a people manager.
</li></ul>Required Knowledge and Experience:
<ul><li>Bachelor&rsquo;s degree or equivalent
</li><li>Minimum 5 years of experience in the regulatory affairs
</li><li>Strong leadership skills including proven minimum 1 year of people management
</li><li>Ability to influence to authorities and stakeholders &amp; strong presentation skills
</li><li>Strong communication skills
</li><li>Proven success stories in Regulatory Affairs &amp; Quality Assurance
</li><li>Medical device experience and knowledge in those countries are preferred
</li><li>Strong adoption skills and ability of multi-tasking
</li><li>Strong follow-up skills with being result-oriented
</li><li>Excellent fluency in English both written and verbal.
</li></ul>Physical Job Requirements
 
 
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
<h1 class="jobSectionHeader">Benefits &amp; Compensation
</h1>Medtronic offers a competitive Salary and flexible Benefits Package
 
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. 
 
<h1 class="jobSectionHeader">About Medtronic
</h1>We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
 
Our Mission &mdash; to alleviate pain, restore health, and extend life &mdash; unites a global team of 95,000+ passionate people.
 
We are engineers at heart&mdash; putting ambitious ideas to work to generate real solutions for real people. From the R&amp;D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.</div>

Regulatory Affairs Manager

MR DIY Türkiye

<div>
 
 MR.DIY first opened its doors in July 2005 as a small hardware store on Jalan Tuanku Abdul Rahman in Kuala Lumpur, Malaysia. Today, with more than 4000 stores worldwide, MR.DIY has expanded its store network in Europe for the first time with Malaysia, Singapore, Thailand, Brunei, Indonesia, Philippines, Cambodia, India, Spain and now Turkey is the most widespread Construction Market and It aims to become one of the Home Goods retailers.
 
 
 Most MR.DIY stores encompass about average 10,000 square feet per store, providing a comfortable and wholesome family shopping experience. MR.DIY serves more than 188 million customers yearly at all its stores worldwide.
 
 
 
 
 
 MR.DIY stores offer a wide selection of &mdash; approximately 18,000 SKUs &mdash; across 5 major categories, namely hardware; household and furnishing; electrical; stationery and sports equipment products; and others (comprising amongst others toys, car accessories, jewellery, and cosmetics).
 
 
 
 
 
 The company strives to always put customers first by operating an innovative business that is flexible when it comes to providing a wide variety of products, good quality, and value-for-money, holding true to the company motto: &ldquo;ALWAYS LOW PRICES&rdquo;.
 
 
 We are looking for a Import Specialist for the Import Department
 
 
 
 
 
 
 
 QUALIFICATIONS
 
 
 
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in Business Administration, Logistics, International Relations or related fields
 </li>
 <li>
 2+ years of experience in regulatory affairs and product compliance.
 </li>
 <li>
 Fluent in English both spoken and written.
 </li>
 <li>
 Strong communication and influencing skills.
 </li>
 <li>
 Ability to organize, prioritize, multitasking and meet deadlines
 </li>
 <li>
 Strong analytical, critical thinking and problem-solving skills.
 </li>
 <li>
 People management &amp; stakeholder management experience.
 </li>
 </ul>
 
 
 
 
 
 
 
 
 
 JOB DESCRIPTION
 
 
 
 
 
 
 <ul>
 <li>
 Stay up-to-date with local, national and international regulations and standards relevant to the company's products.
 </li>
 <li>
 Ensure that products meet all applicable regulatory requirements, including safety, environmental, and quality standards.
 </li>
 <li>
 Collaborate with cross-functional teams, including local import team, legal departments HQ purchasers&rsquo; team, etc. to align product compliance efforts with business goals.
 </li>
 <li>
 Develop and maintain databases accurately with up-to-date records of product compliance activities and documentation.
 </li>
 <li>
 Prepare compliance reports for management and regulatory authorities as required.
 </li>
 <li>
 Conduct risk assessments on new products and product changes.
 </li>
 <li>
 Identify potential compliance risks and develop mitigation plans.
 </li>
 </ul>
 
 
</div>

Import Specialist

Xiaomi Technology

<div>
 
 1. Import/Export HS code management: Professional for Turkey import/export customs HS code policy especially for phone, pad, TV, fridge and AIOT products, choose correct HS code for cost saving and compliance follow government policy.
 
 
 2. AEO Certification: well known the AEO certification application process and policy, better to have AEO application experience.
 
 
 3. Regulatory Policy Research: Proficient in the regulations and policies of various Turkey ports involved in import/export business. Responsible for monitoring changes in customs regulatory policies from customs and other relevant regulatory authorities. Combining the company's business model and current situation, this position allows for rapid and thorough interpretation, development of solutions, and implementation to ensure the healthy and compliant development of the company's business.
 
 
 
 
 
 4. Customs Relationship Maintenance: Develop, establish, and maintain strong relationships with customs and other regulatory authorities. Maintain close ties with local government departments to secure customized support policies and promote mutually beneficial government-enterprise partnerships.
 
 
 
 
 
 5. Import/Export Customs Operations: Gain a deep understanding of the platform's core customs clearance ports and declaration terminal business processes and characteristics, and be responsible for the quality of port operations. Based on the platform's business model, this position involves regular management of service providers, and ongoing assessment and optimization efforts, especially for increase the Import efficiency.
 
 
 6. Import/Export Customs Abnormality Management: Monitor the company's Import/ export declaration processes at ports, identifying, monitoring, and resolving Import/export customs risks.
 
 
 7. Utilize digital and visual operational tools to improve operational efficiency and quality.
 
 
 
 
 
 
 
 
 
 
 
 1. Proficient in spoken and written English and Turkish
 
 
 2. Bachelor's degree or above in a related field, such as international customs affairs, logistics management, or logistics and customs clearance supervision. Familiarity with Turkey Customs' Import/export business models. Experience with customs affairs in the cross-border electronics industry is preferred.
 
 
 3. Proficiency in Turkey customs affairs, including import and export clearance and commodity classification, with proficiency in relevant electronics products customs skills (classification, import and export controls, valuation, origin, etc.).
 
 
 4. Excellent interpersonal and communication skills, strong verbal and written communication skills, and demonstrated resource integration and business innovation capabilities.
 
 
 5. Demonstrated ability to work effectively as a team, independently handle tasks, and collaborate on cross-departmental projects. Strong sense of responsibility, ability to withstand work pressure.
 
 
 
</div>

Customs Operations Manager(A15586)

Daiichi Sankyo

<div><h2 class="jobSectionHeader">Passion for Innovation. Compassion for Patients.</h2> 

With over 120 years of experience and approximately 19,000 employees in more than 30 countries/regions, Daiichi Sankyo is dedicated to discovering, developing, and delivering new standards of care that enrich the quality of life around the world.

In Europe, we focus on two areas: The goal of our Specialty Business is to protect people from cardiovascular disease, the leading cause of death in Europe, and help patients who suffer from it to enjoy every precious moment of life.

In Oncology, we are driving innovation in solid tumours and blood cancers, founded on breakthrough science from our own labs in Japan. We aspire to create better tomorrows for people living with cancer and their loved ones.

Our European headquarters are in Munich, Germany, and we have affiliates in 15 European countries and Canada. 
We're looking for a Market Access Lead who will lead processes for pricing, reimbursement, access, stakeholder engagement processes for Daiichi Sankyo Turkey oncology portfolio. S/he will be working closely with affiliate commercial teams and with regional teams, DSTR brand teams including Pricing, Reimbursement and Access, Regulatory Affairs, marketing and medical affairs. This person will support the Market Access team in Turkey will be reporting to Market Access and Regulatory Affairs Director and will be working in close collaboration with DS International Regulatory Affairs DSE Oncology&amp; DSE Market Access OBU. 


Responsibilities:

Lead development of pricing, reimbursement, HTA and access activities working cross-functionally/regionally 
Enhance information exchange and best practice sharing across MSC and DSE; drive adoption of pricing tools and resources 
Ensure price submissions are done accurately and timely manner while working closely with DSE price team for IRP process, tracking reimbursement and pricing lists, stakeholder engagement 
Generation of reimbursement dossier in line with local requirements while generating local data and adapting Global CE models 
Insight generation and information among DSTR teams regarding competitors and DSTR portfolio pricing, reimbursement and sectoral analysis &amp; closely monitoring developments in healthcare environment 
Stakeholder engagement activities for OBU product portfolio stakeholders like KoLs, SSI &amp; MoH and TEB as well as other govermental agencies. 
Support alliance processes &amp; BC processes to ensure OBU access processes are managed flawlessly. 
Determine proactive price strategies of the products which are licensed or to be licensed and price application to Ministry of Health 
Collaborate with Regulatory &amp; Commercial &amp; Sales and Medical teams to generate access strategies. 


Knowledge and Skills:

2 or more years of hands on experience acquired at pharmaceutical companies, 
demonstrated experience with developing pricing, reimbursement and access 
Strong strategic mindset &amp; analytical &amp; pro-active approach- ability to work well in a matrix team environment and independently 
Excellent communication skills (oral and written) 
Strong process/project management skills 
Strong business acumen &amp; solution-oriented 
Fluency in English 
Agile mindset and willing to work in a dynamic environment<h2 class="jobSectionHeader">
Why work with us?</h2> 

Working at Daiichi Sankyo is more than just a job &ndash; it is your chance to make a difference and change patients&rsquo; lives for the better. We can only achieve this ambitious goal together. That is why we foster a culture of mutual respect and continuous learning, with a strong commitment to inclusion and diversity. Here, you will have the opportunity to grow, think boldly, and contribute your ideas. If you have a proactive mindset and passion for addressing the needs of patients, we eagerly await your application.
For more information: www.daiichi-sankyo.at</div>

TR-Market Access Lead

BNP Paribas

<div><div>GENEL N&#304;TEL&#304;KLER<ul><div>
Bankalar&#305;n Mevzuat &amp; Hukuk Dan&#305;&#351;manl&#305;k, Tefti&#351;, &#304;&ccedil; Kontrol B&ouml;l&uuml;mlerinde veya D&#305;&#351; Denetim firmalar&#305;nda en az 3 y&#305;l deneyim sahibi,</div><div>
Mevzuat takibini ve ara&#351;t&#305;rmay&#305; seven;</div><div>
Kredi, mevduat, sermaye yeterlili&#287;i, &ouml;deme sistemleri, dijital bankac&#305;l&#305;k, a&ccedil;&#305;k bankac&#305;l&#305;k vb. alanlara ilgili,</div><div>
&Ccedil;ok iyi derecede yaz&#305;l&#305; ve s&ouml;zl&uuml; &#304;ngilizce bilen,</div><div>
Ekip &ccedil;al&#305;&#351;mas&#305;na yatk&#305;n,</div><div>
S&ouml;zl&uuml; ve yaz&#305;l&#305; ileti&#351;imi, sunum becerileri kuvvetli,</div><div>
Analitik muhakeme kapasitesine sahip,</div><div>
Zaman y&ouml;netimi ve i&#351; takibinde etkin,</div><div>
Tercihen SPK lisanslar&#305;na (D&uuml;zey 3, T&uuml;rev Ara&ccedil;lar) sahip adaylar&#305;n ba&#351;vurular&#305;n&#305; bekliyoruz.</div></ul>
&#304;&#350; TANIMI<ul><div>
Bankac&#305;l&#305;k mevzuat&#305;n&#305;n takibi,</div><div>
Mevzuat de&#287;i&#351;ikliklerinin analizi, &Uuml;st Y&ouml;netim ve ilgili ekiplerin bilgilendirilmesi,</div><div>
&#350;ubelere ve Genel M&uuml;d&uuml;rl&uuml;k ekiplerine bankac&#305;l&#305;k mevzuat&#305; alan&#305;nda dan&#305;&#351;manl&#305;k verilmesi,</div><div>
Yeni &uuml;r&uuml;n ve projelerin mevzuata uygun tasar&#305;m&#305; i&ccedil;in g&ouml;r&uuml;&#351; sa&#287;lanmas&#305;,</div><div>
D&uuml;zenleyici kurumlarla ili&#351;kilerin ve resmi yaz&#305;&#351;malar&#305;n y&uuml;r&uuml;t&uuml;lmesi,</div><div>
Resmi kurumlar ile T&uuml;rkiye Bankalar Birli&#287;i nezdinde Bankan&#305;n temsil edilmesi,</div><div>
Banka s&uuml;re&ccedil;lerinin d&uuml;zenlemelere uyumunu temin i&ccedil;in takip ve g&ouml;zden ge&ccedil;irme &ccedil;al&#305;&#351;malar&#305;n&#305;n y&uuml;r&uuml;t&uuml;lmesi,</div><div>
Mesleki Etik ve Piyasa B&uuml;t&uuml;nl&uuml;&#287;&uuml; konular&#305;nda BNP Paribas Compliance Grubu d&uuml;zenlemelerinin ve projelerinin takip edilmesi,</div><div>
BNP Paribas Compliance Grubu ile ili&#351;kilerin y&ouml;netilmesi, gerekli raporlamalar&#305;n yap&#305;lmas&#305;,</div><div>
Y&uuml;r&uuml;t&uuml;len faaliyetlerle ilgili &Uuml;st Komitelere raporlama yap&#305;lmas&#305;.</div></ul></div></div>

Mevzuat ve Etik Yöneticisi

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216 regulatory affairs specialist jobs IN Istanbul

Regulatory Affairs Scientist I

Regulatory Affairs Scientist I

Regulatory Affairs Manager

Import Specialist

Customs Operations Manager(A15586)

TR-Market Access Lead

Mevzuat ve Etik Yöneticisi