hr specialist

regulatory consultant

accounting specialist

compensation & benefits sr. specialist/ specialist Jobs in Istanbul

compensation & benefits sr. specialist/ specialist

compensation benefits specialist Jobs in Istanbul

compensation benefits specialist

regulatory compliance specialist

DEXIS

<div>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 Interprets federal/state/international regulations as they apply to our products, processes and/or procedures advises on impact of regulations, devises strategies for compliance, and liaison with regulatory bodies. Investigates and resolves compliance problems, questions and complaints. Audits and evaluates current policies, procedures, and documentation for compliance with regulations and statutes. Determine the need for and prepare regulatory submissions, negotiate the resolution of agency questions, and secure market clearance and/or approval and appropriate country licenses and certificates for new products and/or changes to existing products. Executes appropriately on product recalls. Respond to regulatory agency inquiries. Support the manufacturing lines when nonconformance exists to ensure appropriate regulatory assessments and requirements.
 <br/>
 <br/>
 <strong>
  Job Requirements
  <br/>
  <br/>
 </strong>
 <strong>
  Reports to Role
 </strong>
 : Head of RA Regions &amp; Registrations
 <br/>
 <br/>
 <strong>
  Location
 </strong>
 (HQ or Region, Country, Site):
 <br/>
 <br/>
 Istanbul, Turkey, EH TURKEY SA&Gbreve;LIK &Uuml;R&Uuml;NLER&Idot; VE H&Idot;ZMETLER&Idot; L&Idot;M&Idot;TED &Scedil;&Idot;RKET&Idot;. Fully remote
 <br/>
 <br/>
 <strong>
  <em>
   PURPOSE
  </em>
 </strong>
 <em>
  &ndash; in a few sentences, briefly describe the overall purpose of the role, i.e. why the role exists
  <br/>
  <br/>
 </em>
 The Regulatory Affairs Specialist supports regulatory affairs activities for international product registration by providing regulatory documentation and stakeholder support to ensure the timely regulatory approvals and maintenance of products in compliance with local regulatory requirements.
 <br/>
 <br/>
 The Regulatory Affairs Specialist is accountable for timely execution of regulatory strategies to support launch activities and maintain compliance status for international product registration.
 <br/>
 <br/>
 <strong>
  <em>
   ACCOUNTABILITIES
  </em>
 </strong>
 <em>
  &ndash; describe role accountabilities/responsibilities, i.e. what the role does. Should cover the following:
  <br/>
  <br/>
 </em>
 The Regulatory Affairs Specialist is accountable for compliance and delivery for all assigned countries and registrations in Regions.
 <br/>
 <br/>
 <strong>
  Regions &amp; Registrations
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Contribute to development and execution of regulatory strategies for respective department projects, compliance projects as well as lifecycle management activities.
  </li>
  <li>
   Contribute to execution of International RA support projects for market access to REGIONS and ensure all RA related elements &amp; requirements implemented.
  </li>
  <li>
   Align with local distributors and with local RA, understand requirements, and assists with the deliverables/ files related to preparing ROW submissions; uploads deliverables/ files into repository. Consults with others on these efforts as required.
  </li>
  <li>
   Prepare, order, and maintain oversight of all Free Sales Certificates, Certificates of Foreign Government and Country of Origin certificates requested for international regulatory approvals
  </li>
  <li>
   Prepare core documentation "regulatory submission packages" for new product registrations in international markets
  </li>
  <li>
   Prepare country specific documents for international regulatory approvals including, but not limited to manufacturer statements, Letters of Authorization and Power of Attorney
  </li>
  <li>
   Review submission documents prepared by local RA to be used in country registrations
  </li>
  <li>
   Support provision of regulatory guidance for Nobel Biocare IFU and labeling processes
  </li>
  <li>
   Conduct regulatory release and delisting of products using specialized regulatory software
  </li>
  <li>
   Is aware of procedures and only makes decisions in line with procedure on simple topics
  </li>
  <li>
   Plan out workload to deliver on time, able to make adjustments when required and prioritizing work together with manager
  </li>
  <li>
   Prepare, and follow-up on International regulatory assessments for product changes
  </li>
  <li>
   Closely monitoring together with local country representatives guidelines, regulations, changes in the marketplace and regulator positions for the assigned markets to ensure new requirements are caught, impact assessed and escalated if required
  </li>
  <li>
   Close gaps created due to changed or new local country requirements by initatin projects and/or incorporating into global processes.
  </li>
  <li>
   Support the provision of regulatory guidance to project teams in assigned projects and markets, in terms of requirements and related submission to support optimal timelines and required compliance levels.
  </li>
  <li>
   Support the assembly of documents and the submission to authorities in countries of responsibility
  </li>
  <li>
   Supports the monitoring of the regulatory environment and maintenance of the information resources
  </li>
  <li>
   Support internal and external audits in the audit preparation and audit back office
  </li>
  <li>
   Contributes and participates in the review of change requests to ensure compliance and the potential for regulatory submissions
  </li>
  <li>
   May assist with reviews of promotional materials.
  </li>
  <li>
   Has a yearly training program in place specified by manager.
  </li>
  <li>
   Support the creation and maintenance of regulatory procedures and templates.
  </li>
  <li>
   Can revise or create Technical Files.
  </li>
  <li>
   Support the review of labels and IFUs
  </li>
  <li>
   Support provision of regulatory guidance for Nobel Biocare IFU and labeling processes
  </li>
  <li>
   Tracks and maintains files on current status of licenses, registrations and product information as per agreed formats in the different systems in use by the organization
  </li>
  <li>
   Can collect the regulatory compliance status of main countries, contribute to regulatory status of other regions of devices affected by HHE/Deviation/CAPA/Recall.
  </li>
  <li>
   Provide internal trainings on requirements for area under their responsibility.
  </li>
  <li>
   Knows and understands the EBS philosophy and employs it in daily RA activities and standard work.
  </li>
  <li>
   Able to provide input in terms of activities required to be added to a DM or VPM.
  </li>
  <li>
   Trained on PSP procedures to solve standard problems; analyzes information and standard practices to make judgments.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  <em>
   KNOWLEDGE, SKILLS &amp; EXPERIENCE
  </em>
 </strong>
 <em>
  &ndash;
 </em>
 <em>
  Functional/technical competencies specific to the role and required to perform the role
  <br/>
  <br/>
 </em>
 <strong>
  Critical Knowledge and Qualifications:
 </strong>
 <em>
  (what the role holder must know; including any required general or professional qualifications/education)
  <br/>
  <br/>
 </em>
 <ul>
  <li>
   A minimum of a Bachelor&rsquo;s degree from accredited college or university is required.
  </li>
  <li>
   Basic knowledge of medical device quality management systems such as 21 CFR Part 820 and ISO 13485.
  </li>
  <li>
   Basic knowledge of international legislation in some countries.
  </li>
  <li>
   Knowledge of main general documents required as FSC &amp; legalization process
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Critical Skills/technical know-how:
 </strong>
 <em>
  (what the role holder must be able to do)
  <br/>
  <br/>
 </em>
 <ul>
  <li>
   Fluency in English a must. Further languages is an advantage.
  </li>
  <li>
   Able to communicate effectively with team members, project team members, manager and other stakeholders; this includes: able to listen and grasp key information, able to clearly convey straightforward information, able to read non-verbal communication, such as reading body language and able to give short presentations to RA team on straightforward information
  </li>
  <li>
   Demonstrates and advocates for working together in the spirit of openness, honesty and transparency that encourages engagement, collaboration, respectful interactions and trust.
  </li>
  <li>
   Seeks out diverse ideas, opinions and insights, and applies them in workplace.
  </li>
  <li>
   Works closely with direct team and project teams and starts building up network of colleagues, stakeholders, SMEs and customers.
  </li>
  <li>
   Is aware of procedures and regulations and is able to assess situation on simple topics
  </li>
  <li>
   Creates clarity and direction amid complexity and develops solutions
  </li>
  <li>
   Never compromises on patient safety.
  </li>
  <li>
   Have a positive attitude and 'can do' spirit
  </li>
  <li>
   Ability to be flexible and adaptable. Maintain a professional demeanor under pressure.
  </li>
  <li>
   Demonstrate a commitment to getting the job done right and on time and prioritizing work together with manager.
  </li>
  <li>
   Be able to manage several projects, tasks products and/or countries work load and takes ownership.
  </li>
  <li>
   Have attention to detail to task in hand but also start seeing bigger picture / wider process.
  </li>
  <li>
   Know when to ask questions.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Critical Experience
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Minimum 2 years' experience in regulatory affairs or associated field within medical device industry.
   <br/>
   <br/>
  </li>
 </ul>
 COMPETENCIES &ndash; Essential for the role
 <br/>
 <br/>
 <em>
  Determine max. 6 competencies, refer to List and Definition of Competencies
  <br/>
  <br/>
 </em>
 <ul>
  <li>
   Continuous Improvement
  </li>
  <li>
   Planning and Organizing
  </li>
  <li>
   Strategy execution
  </li>
  <li>
   Driving Execution
  </li>
  <li>
   Learning Orientation
  </li>
  <li>
   Actively contribute to successful team
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Operating Company
  <br/>
  <br/>
 </strong>
 DEXIS
 <br/>
 <br/>
 Envista and its family of companies (Envista) will not accept unsolicited resumes from any source other than directly from a candidate. Envista will consider unsolicited referrals and/or resumes submitted by vendors such as search firms, staffing agencies, professional recruiters, fee-based referral services and recruiting agencies (Agency) to have been referred by the Agency free of charge and Envista will not pay a fee for any placement resulting from the receipt such unsolicited resumes. An Agency must obtain advance written approval from Envista's internal Talent Acquisition or Human Resources team to submit resumes, and then only in conjunction with a valid fully-executed contract approved by the Global Talent Acquisition leader and in response to a specific job opening. Envista will not pay a fee to any Agency that does not have such agreement and written approval in place.
</div>


Regulatory Affairs Specialist

Yordas Group

<div><h3 class="jobSectionHeader"><b>Description</b></h3><div><br>
Yordas Group is a leading international provider of scientific and consultancy services, regulatory advice and training to industry in sustainability, chemicals management and risk assessment. We help ensure companies are compliant and up-to-date with the regulations affecting their supply chains and product portfolios. Yordas is headquartered in the UK, with offices and representation across the globe.</div><div></div><div><br>
<b>
Job title:</b> Regulatory Consultant</div><div>
<b>Grade:</b> Dependent on experience</div><div>
<b>Location:</b> Istanbul, Turkey</div><div>
<b>Salary range:</b> Dependent on experience, full time position</div><div>
<br>
<b>Summary</b></div><div><br>
</div><div>
We are looking for a Regulatory Consultant to support our growing regulatory services under EU-REACH, KKDIK and UK-REACH which entered into force on 1st January 2021.<br>
</div><div>As a member of the regulatory team, you will deliver regulatory and technical services to clients to fulfil compliance requirements for EU-REACH, KKDIK and UK-REACH. You will oversee and coordinate the Only Representative contracts for manufacturers and formulators based outside of these regions, in addition to supporting clients within these regions as necessary.<br>
</div><div>You will deliver and expand our services in a customer facing role and be able to communicate effectively and efficiently with colleagues, clients, international partners and authorities.</div><h3 class="jobSectionHeader"><b><br>
Role and Responsibilities<br>
</b></h3><br>
<ul><li>Provide regulatory and technical advice and support for clients with regard to KKDIK, UK-REACH and EU-REACH regulation</li>
<li>Interpret and understand complex EU, Turkish and UK law and in turn communicate these clearly to clients</li>
<li>Project management of UK-REACH, KKDIK and EU-REACH Registrations and Notifications<br>
Setup and management of Only Representative contracts</li>
<li> Management and expansion of business in strategic regions</li>
<li>Close cooperation with colleagues from all departments within the company to deliver multi-disciplinary services</li>
<li>Implementation of customer-oriented services such as training and webinars</li></ul><br>
<h3 class="jobSectionHeader"><b>
Profile and Qualifications</b></h3><div><br>
For a Regulatory Consultant position, the candidate is expected to have the following skills and qualifications.</div><ul>
<li>Fluent English (spoken and written), additional European languages would be an advantage</li>
<li>Comprehensive knowledge of the EU-REACH and KKDIK regulation and guidance, with strong appreciation of how the UK&rsquo;s exit from the EU impacts on complex supply chains</li>
<li>Good working knowledge of other chemicals legislation is desirable, e.g. CLP, safety data sheets, biocidal products</li>
<li>Demonstrable experience in delivering EU-REACH and KKDIK Registration services, including providing accurate quotations, managing large projects involving internal and external stakeholders, data sharing discussions and contractual negotiations</li>
<li>Demonstrable experience with the IUCLID 6 software for creating Inquiry and Registration dossiers for submission to ECHA (experience with Lead Registration dossiers would also be desirable, though not essential)</li>
<li>Experience using ECHA&rsquo;s REACH-IT platform for submissions</li>
<li>Experience using Turkey&rsquo;s KKS platform for submissions</li>
<li>At least 3 years professional experience in a similar role (Regulatory Consultant role)</li>
<li>University degree in a natural science such as (eco)toxicology, chemistry or environmental sciences</li>
<li>Attention to detail and strong problem-solving skills</li>
<li>Strong communication skills, customer orientation and business acumen</li>
<li>Adaptable and capable of working under pressure towards deadlines</li>
<li> Independent and well organised</li><br>
</ul><br>
<h3 class="jobSectionHeader"><b>Staff Benefits</b></h3><div><br>
Dependent on location, we offer an excellent range of staff benefits, including:</div><ul>
<li>Pension Scheme and Medical Benefits</li>
<li>Generous holidays</li>
<li>Professional Development</li>
<li>Social Culture</li>
<li>Flexible working</li></ul><br>
<h3 class="jobSectionHeader"><b>
About Yordas Group</b></h3><div>
<br>
Yordas Group is a leading provider of scientific, environmental, human health, and global regulatory consulting services. We offer chemical regulatory support, expert scientific services and support on chemicals management and product stewardship, global hazard communication, hazard and risk assessment, analytical and (eco)tox testing.<br>
<br>
Our international client base includes chemical producers, manufacturers, formulators, importers, distributors, retailers as well as trade associations. Yordas serves various industry sectors such as Aerospace, Biocides, Cleaning, Electronics, Lubricants, Nanomaterials, Oil, Gas &amp; Mining, Plastics or Textiles.<br>
<br>
We are an equal opportunity employer and welcome applications from all suitably qualified persons regardless of their race, sex, disability, religion/belief, sexual orientation, gender reassignment or age.<br>
<br>
Yordas Group embraces diversity and promotes equal opportunities. As such, we run a Disability Confident Scheme (DCS) for candidates with disabilities who meet the minimum selection criteria.</div></div><div></div>

Regulatory Consultant

<div>
 <p>
  <strong>
   Department:
  </strong>
  STAR Regulatory
 </p>
 <p>
  <strong>
   Location:
  </strong>
  Remote Turkey
  <br/>
  <br/>
 </p>
 <strong>
  Description
  <br/>
  <br/>
 </strong>
 Yordas Group is a leading international provider of scientific and consultancy services, regulatory advice and training to industry in sustainability, chemicals management and risk assessment. We help ensure companies are compliant and up-to-date with the regulations affecting their supply chains and product portfolios. Yordas is headquartered in the UK, with offices and representation across the globe.
 <br/>
 <br/>
 <strong>
  Job title:
 </strong>
 Regulatory Consultant
 <br/>
 <strong>
  Grade:
 </strong>
 Dependent on experience
 <br/>
 <strong>
  Location:
 </strong>
 Istanbul, Turkey
 <br/>
 <strong>
  Salary range:
 </strong>
 Dependent on experience, full time position
 <br/>
 <br/>
 <strong>
  Summary
  <br/>
  <br/>
 </strong>
 We are looking for a Regulatory Consultant to support our growing regulatory services under EU-REACH, KKDIK and UK-REACH which entered into force on 1st January 2021.
 <br/>
 <br/>
 As a member of the regulatory team, you will deliver regulatory and technical services to clients to fulfil compliance requirements for EU-REACH, KKDIK and UK-REACH. You will oversee and coordinate the Only Representative contracts for manufacturers and formulators based outside of these regions, in addition to supporting clients within these regions as necessary.
 <br/>
 <br/>
 You will deliver and expand our services in a customer facing role and be able to communicate effectively and efficiently with colleagues, clients, international partners and authorities.
 <br/>
 <br/>
 <strong>
  Role and Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Provide regulatory and technical advice and support for clients with regard to KKDIK, UK-REACH and EU-REACH regulation
  </li>
  <li>
   Interpret and understand complex EU, Turkish and UK law and in turn communicate these clearly to clients
  </li>
  <li>
   Project management of UK-REACH, KKDIK and EU-REACH Registrations and Notifications
   <br/>
   Setup and management of Only Representative contracts
  </li>
  <li>
   Management and expansion of business in strategic regions
  </li>
  <li>
   Close cooperation with colleagues from all departments within the company to deliver multi-disciplinary services
  </li>
  <li>
   Implementation of customer-oriented services such as training and webinars
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Profile and Qualifications
  <br/>
  <br/>
 </strong>
 For a Regulatory Consultant position, the candidate is expected to have the following skills and qualifications.
 <ul>
  <li>
   Fluent English (spoken and written), additional European languages would be an advantage
  </li>
  <li>
   Comprehensive knowledge of the EU-REACH and KKDIK regulation and guidance, with strong appreciation of how the UK&rsquo;s exit from the EU impacts on complex supply chains
  </li>
  <li>
   Good working knowledge of other chemicals legislation is desirable, e.g. CLP, safety data sheets, biocidal products
  </li>
  <li>
   Demonstrable experience in delivering EU-REACH and KKDIK Registration services, including providing accurate quotations, managing large projects involving internal and external stakeholders, data sharing discussions and contractual negotiations
  </li>
  <li>
   Demonstrable experience with the IUCLID 6 software for creating Inquiry and Registration dossiers for submission to ECHA (experience with Lead Registration dossiers would also be desirable, though not essential)
  </li>
  <li>
   Experience using ECHA&rsquo;s REACH-IT platform for submissions
  </li>
  <li>
   Experience using Turkey&rsquo;s KKS platform for submissions
  </li>
  <li>
   At least 3 years professional experience in a similar role (Regulatory Consultant role)
  </li>
  <li>
   University degree in a natural science such as (eco)toxicology, chemistry or environmental sciences
  </li>
  <li>
   Attention to detail and strong problem-solving skills
  </li>
  <li>
   Strong communication skills, customer orientation and business acumen
  </li>
  <li>
   Adaptable and capable of working under pressure towards deadlines
  </li>
  <li>
   Independent and well organised
   <br/>
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Staff Benefits
  <br/>
  <br/>
 </strong>
 Dependent on location, we offer an excellent range of staff benefits, including:
 <ul>
  <li>
   Pension Scheme and Medical Benefits
  </li>
  <li>
   Generous holidays
  </li>
  <li>
   Professional Development
  </li>
  <li>
   Social Culture
  </li>
  <li>
   Flexible working
  </li>
 </ul>
</div>


Reckitt

<div>
 We are Reckitt
 <br/>
 <br/>
 Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege.
 <br/>
 <br/>
 Research &amp; Development
 <br/>
 <br/>
 In Research and Development, we're full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. With nine Centres of Excellence, we continually seek out new opportunities by using science, our entrepreneurial flare and our fearless innovation to develop and enhance our existing portfolio, never compromising on quality or performance.
 <br/>
 <br/>
 We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality.
 <br/>
 <br/>
 The size of our organisation means you'll have the opportunity to learn and work in different functions within R&amp;D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation.
 <br/>
 <br/>
 <strong>
  About The Role
  <br/>
  <br/>
 </strong>
 As a Regulatory Associate, you&rsquo;ll be at the forefront of our innovation and compliance efforts. You&rsquo;ll jumpstart your career in a role that provides a blend of strategic thinking and hands-on experience within a dynamic, collaborative environment. If you have a passion for science and a drive to ensure the safety and efficacy of consumer products, your skills could be a perfect match for us. Together, we will work to navigate the exciting regulatory landscape, ensuring our diverse product range not only meets but exceeds the highest standards.
 <br/>
 <br/>
 Your responsibilities
 <br/>
 <br/>
 <ul>
  <li>
   Support the development and rollout of new products by navigating regulatory requirements and maintaining compliance.
  </li>
  <li>
   Engage with regulatory authorities, staying abreast of the changing landscape and expertly managing product compliance.
  </li>
  <li>
   Contribute to the team by formatting and compiling regulatory submission documents under guidance.
  </li>
  <li>
   Access and understand regulations and guidelines, applying them effectively to projects, as directed.
  </li>
  <li>
   Communicate and interact with cross-functional teams, playing a pivotal role in project meetings to understand objectives.
   <br/>
   <br/>
  </li>
 </ul>
 The experience we're looking for
 <br/>
 <br/>
 <ul>
  <li>
   0-3 years of experience within the regulatory field, ideally supported by a BSc or MSc in a scientific discipline such as chemistry and chemistry engineering.
  </li>
  <li>
   Ability to work under pressure while ensuring task execution and adherence to deadlines.
  </li>
  <li>
   Developing business acumen and commercial awareness, with a view to understanding product lifecycle management.
  </li>
  <li>
   Capacity for insight into consumer needs and expectations.
  </li>
  <li>
   Eagerness to collaborate, build partnerships, and continuously innovate.
   <br/>
   <br/>
  </li>
 </ul>
 The skills for success
 <br/>
 <br/>
 Task Execution Under Pressure, Business Acumen, Commercial Awareness, Objective Setting, Accountability, Consumer Insight, R&amp;D, Product Lifecycle Management, Intellectual Property, Business Partnership, Collaboration and partnership building, Adapt to changes in technological development plans, Ability to challenge the status quo and propose improvement, Innovation Processes.
 <br/>
 <br/>
 What we offer
 <br/>
 <br/>
 With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way. We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitt's potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitt's pay for performance philosophy.
 <br/>
 <br/>
 Equality
 <br/>
 <br/>
 We recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you. All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law.
</div>


Regulatory Associate (Hygiene) / Fixed Term Contract

Perrigo

<p></p><div><p>At Perrigo, we are driven by our mission to <b><i>Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All</i></b>. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing <b><i>The Best Self-Care for Everyone</i></b>, we are the people behind the brands you trust. We are Opill&reg;, Compeed&reg;, Solpadeine&reg;, NiQuitin&reg;, ACO&reg;, and many more. <b>We Are Perrigo</b>. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.</p><p></p><p><br>
Join us on our One Perrigo journey as we evolve to win in self-care.</p><p></p><div><div><div><h2 class="jobSectionHeader"><b><br>
Description Overview</b></h2></div><div><p>
In this role you will be responsible for the hands on regulatory activities required to maintain existing commercial products, and support in making correct and timely new product applications of Perrigo products on the Turkish market. You will support to ensure compliance with the existing legislation for Medicines, Medical Devices, Biocides and Cosmetics. Another key aspect of the role will be supporting in the achievement of the overall Regulatory, Quality &amp; Safety objectives and timely realization of operational activities. In this position you collaborate closely with the Corporate Regulatory and Turkish Commercial colleagues to strive to help the customer the best.</p></div></div><div><div><h2 class="jobSectionHeader"><b>
Scope of the Role</b></h2></div><div><ul><li>
Support in the management of change by preparing applications and technical files in support of existing commercial product regulatory maintenance;</li><li>
Support in the regulatory activities on new product development (NPD), including artwork approvals, label claims and associated supporting documentation;</li><li>
Develop and approve label specifications (master text and local artwork text) in compliance with SOPs, as well as promotional materials from a regulatory perspective;</li><li>
Maintain regulatory files and data systems in compliance with SOPs;</li><li>
Represent regulatory affairs in project meetings with both Perrigo staff and external contacts;</li><li>
Follow up on changes in (inter)national regulations and legislations, and support in the interpretation, communication and implementation;</li><li>
Liaise with Corporate Regulatory, responding to regulatory queries and providing and review of registration documents as necessary for the Turkish and/or European territory;</li><li>
Support in the communication with local regulatory authorities regarding license applications and notice of change.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Experience Required</b></h2></div><div><ul><li>
University Degree in a Scientific Subject;</li><li>
Minimum of 2 years work experience within Regulatory Affairs required, within at least one of the following categories Medical Devices, Biocides, Cosmetics and Medicines;</li><li>
Excellent communicator in Turkish and English;</li><li>
Proficient computer skills esp. Microsoft (word, excel, powerpoint); experience with Veeva, TVT, Trackwise is an asset;</li><li>
Eye for detail, punctual, well organized;</li><li>
Being flexible and adaptable to change;</li><li>
Ability to support several concurrent projects/products simultaneously;</li></ul></div></div></div><p><b>
Benefits</b><br>
We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.</p><p>
Find out more about <b>Total Rewards</b> at Perrigo.</p><p></p><p><b><br>
Hybrid Working Approach</b><br>
We love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.</p><p></p><p><br>
We are proud to be included in the Forbes list of &quot;America's Best Employers by State 2024&quot;. Find out more <b>here</b></p><p></p><p><b><br>
Applicants please note:</b> To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) Thank you.</p><p></p><p><i><br>
We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law. #weareperrigo</i></p></div>

Regulatory Affairs, Associate Specialist

Vodafone

<div><div><div><div><h2 class="jobSectionHeader"><b>Join Us</b></h2>
</div><div><p>
At Vodafone, we&rsquo;re not just shaping the future of connectivity for our customers &ndash; we&rsquo;re shaping the future for everyone who joins our team. When you work with us, you&rsquo;re part of a global mission to connect people, solve complex challenges, and create a sustainable and more inclusive world. If you want to grow your career whilst finding the perfect balance between work and life, Vodafone offers the opportunities to help you belong and make a real impact.</p></div></div><div><div><h2 class="jobSectionHeader"><b>
What you&rsquo;ll do</b></h2>
</div><div><p>
&bull; To support implementation of fixed telecom regulatory issues within the company. &bull; Support to organize all functions to secure compliance with different Fixed Line Authorizations given by BTK/ICTA these are (Internet Service Provider (ISP), Fixed Infrastructure Management Service (AIS), Fixed Telephony Services (STH), MVNO, Satellite Service Provider (UHH), Cable Broadcasting Service (KYH) licences and regulations in force.</p><ul><li>To act as an internal regulatory partner providing fixed regulatory issues and compliance advice to the other fixed teams to support achievement of regulatory targets.</li><li>Leading official communication with the Authority Bodies.</li><li>To support related departments for assurance of compliance with the fixed regulatory obligations.</li><li>Reviewing regulations announced for public opinion and consolidating company change requests and comments.</li><li>Ensure that ICTA/BTK regular reports are delivered accurately and on time.</li><li>Representing company and creating sustainable/credible relationship at Government Authorities such as Ministry of Infrastructure and Transportation, BTK, Digital Transformation Office and NGOs such as Telkoder etc.</li><li>To initiate updating relevant procedures according to the regulatory changes together with related departments.</li><li>To support business units to secure procedures are up-to-date and meet latest regulatory requirements.</li><li>To research regulatory risks and give feedback to the other functions to secure protective &amp; solution actions.</li><li>Follow up day-to-day Regulatory developments, comments and shared related departments</li><li>To inform and follow up related department actions to be prepared against any regulatory investigation or audit.</li><li>To represent Company during meeting/investigations/audits.</li><li>To prepare report on the audits and investigations and provide necessary documentation.</li><li>To inform management about predicted risks on audits and investigations.</li><li>Following up the issues that need to be improved with the outcomes after the audits and investigations and directing the relevant units for compliance.</li><li>Following up new technologies that would affect regulatory strategy, preparing international benchmarks and conducting whitepapers to support company&rsquo;s position.</li><li>To assist Techfin / Fintech regulation colleagues for mobile payment, e-money, digital wallet, qr code payment, financing products.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Who you are</b></h2>
</div><div><ul><li>University degree in Engineering, Business Administrations or Similar Disciplines</li><li>With up to 4 years of experience/interest in the fields of Telecommunication Regulation</li><li>Excellent writing and reporting skills</li><li>Fluent English</li><li>Knowledge of Telecom or similar field legislations</li><li>Excellent team work culture</li><li>Business and commercial sense</li><li>Communication and negotiation skills</li><li>Excellent writing and reporting skills</li><li>Excellent command of MS Office applications</li><li>Influence and Impact</li><li>Initiative</li><li>Solutions Driven</li><li>Strategic Approach</li><li>Working together</li><li>Self-development</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Not a perfect fit?</b></h2>
</div><div><p>
Worried that you don&rsquo;t meet all the desired criteria exactly? At Vodafone we are passionate about empowering people and creating a workplace where everyone can thrive, whatever their personal or professional background. If you&rsquo;re excited about this role but your experience doesn&rsquo;t align exactly with every part of the job description, we encourage you to still apply as you may be the right candidate for this role or another opportunity.</p></div></div><div><div><h2 class="jobSectionHeader"><b>
What's in it for you</b></h2>
</div><div><p>
We like to keep them flexible:</p><ul><li>Vflexy: Flexible Benefits Program</li><li>Hybrid working kit</li><li>Ergonomic kit allowance</li><li>Digital meal voucher</li><li>Flexible transportation allowance.</li><li>Employee assistance hotline &amp; counselling</li><li>Comprehensive and flexible private health insurance</li><li>Discounted price deals for wide range of products &amp; services</li></ul><p><br>
Plus, plenty more to enjoy!If you want to know more about us and what we do, then visit our website: www.vodafone.com.tr</p><p>
https://www.vodafone.com.tr/insan-kaynaklari</p><p>
Instagram: https://www.instagram.com/vodafonekariyer/</p><p>
Youtube: https://www.youtube.com/user/VFTurkiye</p><p><br>
Data Privacy<br>
By applying for this job, you accept the Vodafone Privacy Policy. Please visit Privacy Policy web page at https://careers.vodafone.com/privacy-policy/turkey/ for further details.</p></div></div><div><div><h2 class="jobSectionHeader"><b>
Who we are</b></h2>
</div><div><p>
We are a leading international Telco, serving millions of customers. At Vodafone, we believe that connectivity is a force for good. If we use it for the things that really matter, it can improve people's lives and the world around us. Through our technology we empower people, connecting everyone regardless of who they are or where they live and we protect the planet, whilst helping our customers do the same.</p><p>
Belonging at Vodafone isn't a concept; it's lived, breathed, and cultivated through everything we do. You'll be part of a global and diverse community, with many different minds, abilities, backgrounds and cultures. ;We're committed to increase diversity, ensure equal representation, and make Vodafone a place everyone feels safe, valued and included.</p><p>
If you require any reasonable adjustments or have an accessibility request as part of your recruitment journey, for example, extended time or breaks in between online assessments, please refer to https://careers.vodafone.com/application-adjustments/ for guidance.</p><p>
Together we can.</p></div></div></div></div>

Regulation Senior Specialist

Yazaki

<div></div><div><div><div><div><div><div><div><h1 class="jobSectionHeader"><b>Trade Compliance Sr. Specialist
</b></h1></div></div></div></div><div><div><div><div><p><b>Join Yazaki. Connect to the future.</b></p><br>
<p></p>
<p><b>Country</b>: T&uuml;rkiye (TR)<br>
<b>City</b>: Sakarya<br>
<b>Worksite / Location</b>: Logistics Hub Istanbul</p><br>
<p></p>
<p><b>Job Function</b>: EDS_Logistics<br>
<b>Job Discipline</b>:
<br>
<b>Job Family</b>: Customs &amp; Global Trade</p><br>
<p></p>
<p>Founded in 1929, Yazaki is a Japanese full systems supplier of wire harness, electrical, data products and solutions enabling vehicle electrification, connectivity, and autonomy integration. More than 235,000 committed and highly motivated employees in 45 countries make us one of the most successful international automotive suppliers. Join a family-owned company committed to being environmentally friendly in every aspect of its business, contributing to society, and inspiring trust. To strengthen our team, we are looking for a Trade Compliance Sr. Specialist in our plant in [[location]].</p>
<p>
Trade Compliance Sr. Specialist</p>
<p>
 We are looking for an &ldquo;Trade Compliance Sr. Specialist&rdquo; to be member of our new Logistics Hub Organization based in Kurtkoy Istanbul.</p>
<p>
Key Responsibilities:</p>
<ul>
<li>Control Dual use, military application, EU correlation list Tar. code, denied parties, denied countries, US embargo&rsquo;s.</li>
<li>Ensure compliance of Logistics processes with internal and external rules</li>
<li>Leading official customs audits and investigations and export controls for responsibilty countries</li>
<li>Manage and monitor activities of customs brokers and other trade related service providers by regular audits and report its results for responsibilty counties.</li>
<li>To follow the regulations within the scope of international sanctions.</li>
<li>Preparation of Suspicious Activity Report Escalating unusual BU activities which might relate to money laundering or terrorist financing and sanction.</li>
<li>Support in the evaluation of the impacts of newly issued regulations on new and/or existing products, services, and processes</li>
<li>Monitor regulatory developments and ensure that the company stays compliant with the latest laws and regulations.</li>
<li>Provide guidance to business units on compliance matters and ensure that all business activities are conducted in compliance with relevant laws and regulations.</li>
<li>Ensure that the company has adequate systems and processes in place to detect and prevent compliance breaches.</li>
<li>Perform internal or external customs and foreign trade trainings and To offer solutions to ongoing and future foreign trade transactions to be realized in the most effective way and according to the regulatory compliance at the same time.</li>
</ul>
<p> Qualifications:</p>
<ul>
<li>Has a Bachelor's Degree from related departments (industrial engineering, business management etc.)</li>
<li>Has an excellent command of written and spoken English</li>
<li>Has minimum 4 years of previous experience in same position,</li>
<li>Will be able to reside in Istanbul Anatolian Side,</li>
<li>Good command of MS Office programs</li>
<li>Advance SAP knowledge</li>
<li>No military obligation for male candidates</li>
</ul><p>
At Yazaki, we are committed to providing equal employment opportunities for everyone which extends to all aspects of the employment relationship.</p><br>
<p></p>
<p>We are looking forward to receiving your application and to get to know you. Please apply by clicking the 'Apply Now' button. We wish you all the success in your application!</p><br>
<p></p>
<p>Ps. Didn't find what you are looking for?<br>
Take a look at our careers page! Be careful though, you might find your next dream job.</p></div></div></div></div></div></div></div><p></p>

Trade Compliance Sr. Specialist

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