Medical Device Regulatory Affairs

As a Medical Device Specialist at Johnson & Johnson, you will play a critical role in driving sales growth and market expansion through effective strategy development and execution.The ideal candidate will possess strong analytical and negotiative skills, as well as excellent communication and presentation abilities.Responsibilities:Develop and execute...

Job Title: Medical Device Regulatory ExpertWe are seeking a seasoned Medical Device Regulatory Expert to join our team at Bioeksen R&D Technologies Inc. The successful candidate will be responsible for ensuring compliance with global regulatory requirements, including EU IVDR, FDA, and ANVISA regulations.About the RoleIn this role, you will work closely with...

Johnson & Johnson is committed to keeping people well at every age and stage of life. As a Medical Excellence and Compliance Manager, you will play a critical role in ensuring our products meet the highest standards of quality and safety.About Our ProductsWe develop innovative medical devices, pharmaceuticals, and consumer goods that improve patient outcomes...

RequirementsTo be successful in this role, you will need:A bachelor's degree in a relevant field, advanced degree preferred;At least 3-5 years of experience in Regulatory Affairs, preferably within the IVD or medical device industry;Strong project management skills, including the ability to manage multiple projects and deadlines;Excellent written and verbal...

Job Summary:The Regulatory Affairs Manager is responsible for ensuring the company's products meet all regulatory requirements in the markets where they are sold. This role involves managing regulatory submissions, ensuring compliance with national and international laws, and liaising with regulatory authorities to facilitate approvals and maintain...

Job ResponsibilitiesAs a Regulatory Affairs Specialist, you will be responsible for ensuring compliance with regulatory requirements for IVD products.Key responsibilities include:Preparation and submission of regulatory documentation for new product registrations, renewals, and amendments;Maintenance of up-to-date knowledge of regulatory...

About Fresenius Medical CareWe are a global leader in providing products and services for individuals with renal failure, and we're seeking a skilled Quality Assurance Supervisor to join our team.ResponsibilitiesSpearhead Quality & Regulatory compliance efforts across the organization, ensuring alignment with business objectives.Oversee Field Action...

Job OverviewWe are looking for a highly motivated Regulatory Affairs Trainee to join our team at GlaxoSmithKline. In this role, you will be responsible for supporting the Regulatory Department in various activities, including dossier preparations, follow-up tasks, and system updates.Key Responsibilities:Update regulatory correspondence files, trackers, and...

Job DescriptionThis role is responsible for ensuring compliance with regulatory requirements for IVD products. The ideal candidate will have a strong understanding of global regulations, including EU IVDR and FDA.The Regulatory Affairs Specialist will work closely with cross-functional teams to ensure regulatory requirements are integrated into product...

About the RoleWe are seeking a highly skilled Regulatory Compliance Specialist to join our team at EasyVit. As a key member of our regulatory affairs department, you will play a critical role in ensuring our products meet all regulatory requirements across various markets.The ideal candidate will have a strong background in regulatory affairs, with a minimum...

Job DescriptionTo provide deep medical & scientific expertise to support healthcare professionals, professional associations, patient groups and other relevant decision makers. This includes the following:Develop and deliver the local medical strategy and life-cycle clinical plans for Pfizer's inline and pipeline medicines in nominated therapy...

Our company is seeking a dedicated Regulatory Affairs Manager to join our Regulatory Affairs Department. If you're ready to make a global impact and drive compliance excellence, we want you on our team in Istanbul.ResponsibilitiesContribute to the preparation of registration and variation files according to current Ministry of Health requirements,Contribute...

The role of Expert, Regulatory Affairs HNC EMEA requires a high degree of autonomy, initiative, and problem-solving skills. As an expert in regulatory affairs, you will be responsible for supporting the HNC regional RA team for a major global roll-out activity.You will work closely with the HNC RA global segment team to ensure compliance with regulatory...

Join Our Team as a Clinical SpecialistWe are seeking a motivated and experienced Clinical Specialist to join our team at MicroPort Turkiye. The successful candidate will have a strong understanding of clinical workflows and be able to communicate complex information effectively.Responsibilities:Collaboration with Healthcare Teams:Partner with healthcare...

Medtronic is a leader in healthcare technology, pioneering innovative solutions to improve patient outcomes. We are seeking a skilled Medical Device Maintenance Specialist to join our team.A Day in the LifeThis role involves performing maintenance and calibration tasks on medical devices, ensuring they operate at optimal levels. You will work collaboratively...

About the Job:As a Medical Device Installer and Repairer at ITH Icoserve, you'll have the opportunity to work on a wide range of medical devices and equipment. Your primary responsibility will be to ensure the smooth operation of these devices by performing regular maintenance, repairs, and installations.Key Requirements:Bachelor's degree in Electronic or...

About the Role:We are seeking a highly skilled Regulatory Affairs Specialist to join our team in Turkiye. As an expert in regulatory compliance, you will be responsible for supporting the HNC regional RA team for a major global roll out activity.Your Responsibilities:Develop, manage and support the pharma and food submissions in certain regions or...

About UsFor over a century, Johnson & Johnson has been dedicated to helping people live healthier, more fulfilling lives. Our mission is to provide safe, effective, and affordable medical solutions that improve human health.We achieve this by leveraging our expertise in pharmaceuticals, medical devices, and consumer packaged goods to develop innovative...

Operasyon Tam zamanlı **Regulatory and Government Affairs Manager Turkey**İstanbul, Türkiye Advising on product and labelling-related regulatory compliance, reviewing, and advising on marketing collateral, and monitoring of and engagement on key regulatory and governmental changes that impact Red Bull's strategic interests. This involves...

About this roleWe are seeking a talented Regulatory Affairs Trainee to join our team at GlaxoSmithKline. In this role, you will support the Regulatory Department in various activities, including dossier preparations, follow-up tasks, and system updates.Key Responsibilities:Ensure regulatory correspondence files, trackers, and submission archives are...