Medical Device Specialist Stellenangebote


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Stellenangebote Medical Device Specialist Jobs


Job vor 2 Tagen bei StepStone gefunden Edwards Lifesciences GmbH

Field Clinical Specialist TMTT, Bonn/ Siegen

• Bonn, Siegen Beratungs-/ Consultingtätigkeiten Homeoffice möglich [. .. ] patients around the world. Driven by a passion to help patients live healthier and more productive lives, our Field teams embrace Edwards Lifesciences values to build trusting, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] lasting relationships with medical professionals and industry partners. Your insight and dedication will help deepen and broaden clinical knowledge of our companys innovative technologies, while creating connections between providers and teams across our businesses to ensure patients receive the highest quality of care. Patients with mitral and tricuspid heart valve disease often have complex [. .. ] force to help patients live longer and healthier lives. Join us and be part of our inspiring journey. The successful candidate will be providing expertise and clinical support on the device, procedure and protocol during cases and focusing on growing the market share by identifying, developing and closing new sales opportunities within TMTT portfolio business unit. Territory: Germany (Bonn/ Siegen) travelling required How youll make an impact: Throughout commercial procedures, provide physicians and medical staff with required follow-up support to [. .. ] full details regarding the entitlement and conditions for the benefits. Benefit policy and components may vary by location. . Edwards Lifesciences Gmb H sucht in Bonn, Siegen eine/n Field Clinical Specialist TMTT, Bonn/ Siegen (ID-Nummer: 13849179) 86138801 [. .. ]

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Job vor 2 Tagen bei StepStone gefunden Edwards Lifesciences GmbH Field Clinical Specialist-Imaging • Nordrhein- Westfalen, Rheinland- Pfalz Beratungs-/ Consultingtätigkeiten Homeoffice möglich [. .. ] Since 2017, Edwards TMTT launched more than 4 products transformational therapies in Europe led by its PASCAL and EVOQUE programs. Every patient is different-be an expert on [...]
MEHR INFOS ZUM STELLENANGEBOT[...] our EVOQUE device/ therapy and help patients suffering from mitral and tricuspid diseases The Field Clinical Specialist-Imaging is responsible for educating physicians on EVOQUE technologies, device handling, implantation and troubleshooting techniques and case support by assigned hospitals/in assigned territories/ regions. Territory: Germany (Nordrhein-Westfalen, Rheinland-Pfalz ) travelling required How you will make an impact Educate and train physicians, hospital personnel and hospital staff on [. .. ] assessment of potential cases Other incidental duties Education and Experience: Bachelors Degree in in technical field (e. g. , clinical physiology, echocardiography) , 3 years years experience of previous related medical device and/or clinical experience Required Working experience in clinical/ technical environment advantageous Minimum of 2 years of previous related medical device and/or clinical experience required Valid driving license-travelling approx. 40 Additional Skills: Good imaging analysis software skills (e. g. 3Mensio, Tom Tec, Vitrea, Circle VI, etc. ) [. .. ]

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Job vor 9 Tagen bei StepStone gefunden Becton Dickinson

Field Clinical Specialist Central Lower Saxony-Nurse Biomedical APM (m/w/d)

• Nordrhein- Westfalen Teilzeit [. .. ] external technicians Ensure Complaint handling in accordance with BD Advanced Patient Monitoring SOP and perform Field Corrective Actions Coordinate the organization of BD Advanced Patient Monitoring participation [...]
MEHR INFOS ZUM STELLENANGEBOT[...] to local seminars, medical exhibitions and trainings Coordinate Customers participation at educational events and congresses organized by BD Advanced Patient Monitoring or the third party Implement marketing strategies. Collaborate with sales colleagues on the effective use of selling process and tools Manage installed base of control monitors: transfers, fixed assets, update software including profitability [. .. ] office machinery Strong written and verbal communication skills, presentation, and interpersonal relationship skills including negotiating and relationship management skills Excellent problem-solving and critical thinking skills Full understanding of medical device regulatory requirements and documents, device accountability and adverse events reporting Fluent German and English is a Must Click on apply if this sounds like you Becton, Dickinson and Company is an Equal Opportunity/ Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, [. .. ] or expression, genetics, disability, military eligibility or veteran status, or any other protected status. Primary Work Location DEU Heidelberg-Tullastrasse. Becton Dickinson sucht in Nordrhein-Westfalen eine/n Field Clinical Specialist Central Lower Saxony-Nurse Biomedical APM (m/w/d) (ID-Nummer: 13783648) 85650886 [. .. ]

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Job am 20.03.2026 bei StepStone gefunden Medicaroid Europe GmbH Robotic Implementation Specialist (f/m/d) • Düsseldorf Homeoffice möglich Medicaroid is a leading Japanese medical device company, established in 2013 as a joint venture between Kawasaki Heavy Industries and the medical diagnostics solutions provider Sysmex Corporation. Our flagship product, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] hinotori, is a state-of-the-art robotic-assisted surgery system, currently approved for use in Japan, Singapore, and Malaysia, supporting procedures in urology, gynecology, general surgery, [. .. ] to join our Medicaroid Europe Gmb H headquarter in Düsseldorf, Germany, founded in 2020, to help drive the adoption and advancement of robotic-assisted surgery across Europe. As a Robotic Implementation Specialist at Medicaroid Europe Gmb H, you will play a pivotal role in driving the implementation and adoption of the hinotori robotic surgery system in the hospital. you will engage and collaborate with internal external stakeholders to deliver comprehensive technical support, enabling confident and efficient use of the hinotori in the OR. [. .. ]

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Job am 10.03.2026 bei StepStone gefunden Novanta

Medical Affairs Manager Medical Devices (m/f/d)

• Berlin [. .. ] Advanced Surgery (AS) business unit group. Novanta offers highly reliable, precise and safe solutions that enhance system performance and improve patient outcomes. Insufflators, pumps and disposable tube [...]
MEHR INFOS ZUM STELLENANGEBOT[...] sets, along with medical visualization and operating room integration technologies are the preferred solution for minimally invasive surgery applications. Summary The Medical Affairs (Clinical Affairs) Manager is held responsible for keeping a product or product group compliant with regulations and guidelines. The employee ensures the proper implementation of procedures that demonstrate the conformity of [. .. ] clinical experience and innovation General Tasks Strict compliance with the quality, occupational safety and environmental regulations Implementation of the instructions of the quality/ environmental management representative and the occupational safety specialist University degree (Diploma/ Master) in life science/ natural science or an equivalent qualification; Ph D would be a plus Professional experience in the medical device industry or similar field of work is required Basic understanding of Medical Affairs processes and tasks is required Expert knowledge and experience in medical writing (literature as well as vigilance search, evaluation and review; database management) is required Proven track record in creation, editing and proof-reading of Clinical Evaluation [. .. ]

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Job am 03.03.2026 bei StepStone gefunden Edwards Lifesciences GmbH Field Clinical Specialist Münster-Hannover • Bielefeld, Münster, Hannover Beratungs-/ Consultingtätigkeiten Homeoffice möglich [. .. ] our inspiring journey. The goal will be to help make each site independent on procedures, product preparation and support. Field Clinical Specialists will provide guidance on the [...]
MEHR INFOS ZUM STELLENANGEBOT[...] use of the device, thereby enabling physicians and staff to reach expert proficiency and deliver positive patient outcomes. This role will collaborate with multiple departments including Sales, Clinical Affairs, Marketing, Quality, Regulatory, and Education. After extensive training, a Field Clinical Specialist will travel frequently within an assigned territory, clinically training customers on the THV technology. Territory: Germany (Bielefeld, Münster, Hannover) How you will make an impact: Working independently in the areas of valve crimping, case management, pre-case planning, post-case management, 3 Mensio management, Therapy Awareness program management and clinical [. .. ] and critical thinking skills Knowledge and understanding of cardiovascular science Understanding of cardiovascular anatomy, pathology and physiology including the applications and language of the market and Edwards Lifesciences and of medical device regulatory requirements and documents, device accountability and adverse events reporting Moderate imaging analysis software skills (e. g. 3Mensio, Tom Tec, Vitrea, Circle VI, etc. ) Excellent interpersonal skills, interfacing with multiple constituencies including cardiologists, support staff and sales in order to effectively build relationships with external customers and internal [. .. ]

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Job am 21.02.2026 bei StepStone gefunden Novanta

Medical Affairs Manager (m/f/d)

• Berlin [. .. ] Advanced Surgery (AS) business unit group. Novanta offers highly reliable, precise and safe solutions that enhance system performance and improve patient outcomes. Insufflators, pumps and disposable tube [...]
MEHR INFOS ZUM STELLENANGEBOT[...] sets, along with medical visualization and operating room integration technologies are the preferred solution for minimally invasive surgery applications. Summary The Medical Affairs (Clinical Affairs) Manager is held responsible for keeping a product or product group compliant with regulations and guidelines. The employee ensures the proper implementation of procedures that demonstrate the conformity of [. .. ] clinical experience and innovation General Tasks Strict compliance with the quality, occupational safety and environmental regulations Implementation of the instructions of the quality/ environmental management representative and the occupational safety specialist Required Experience, Education, Skills, Training and Competencies University degree (Diploma/ Master) in life science/ natural science or an equivalent qualification; Ph D would be a plus Professional experience in the medical device industry or similar field of work is required Basic understanding of Medical Affairs processes and tasks is required Expert knowledge and experience in medical writing (literature as well as vigilance search, evaluation and review; database management) is required Proven track record in creation, editing and proof-reading of Clinical Evaluation [. .. ]

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Job am 14.02.2026 bei StepStone gefunden Novanta Product Manager Medical Devices (m/f/d) • Berlin [. .. ] Novantas Advanced surgery business unit. Specialized in the field of Minimally Invasive Medicine, WOM develops devices and accessories so that doctors can operate with small cuts. We [...]
MEHR INFOS ZUM STELLENANGEBOT[...] produce Cameras, Insufflators, Medical Pumps, and tubing that makes diagnosis and treatment easier for everyone. Our insufflators and pump systems dilate cavities in the body and turn previously complicated surgeries into minor procedures. Together with customers, doctors, and technical experts, our teams continuously search for new ways to innovate. Summary The Product Manager is [. .. ] a Medical product consultant General Tasks Strict compliance with the quality, occupational safety and environmental regulations. Implementation of the instructions of the quality/ environmental management representative and the occupational safety specialist. Broad and deep functional experience. Typically acquired through 3 to 8 years of relevant work experience within the medical device industry. Requires extensive research, in-depth knowledge and creativity. Requires that complex problems are anticipated, identified, defined and resolved. Recommendations made by others are analyzed in order to solve issues bearing broad and long-term impact. Complex and varied problem-solving requires extensive diagnosis. Incumbent acts as advisor to less-[. .. ]

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Job am 14.02.2026 bei StepStone gefunden Novanta

Post Market Surveillance (PMS) Specialist Medical Devices (m/f/d)

• Berlin [. .. ] Novantas Advanced Surgery business unit group. Novanta offers highly reliable, precise and safe solutions that enhance system performance and improve patient outcomes. Insufflators, pumps and disposable tube [...]
MEHR INFOS ZUM STELLENANGEBOT[...] sets, along with medical visualization and operating room integration technologies are the preferred solution for minimally invasive surgery applications. Summary This position serves as a point of contact for medical/ clinical issues and is responsible for vigilance as well as Post-Market surveillance and Post-Market Clinical Follow-Up activities, focusing on the evaluation of vigilance data, reporting adverse events and performing recalls/ FSCAs and/or corrective actions. Evaluation of adverse events based on the event description and medical device investigation results Provision of a decision on reporting obligations based on international regulatory requirements Reporting of adverse events in line with country-specific requirements Search and evaluation of vigilance data for medical devices using country-specific databases Support with risk analysis and assessment of benefit-risk-ratio Provision of a [. .. ] 7.1 rev. 4 General Tasks Strict compliance with the quality, occupational safety and environmental regulations Implementation of the instructions of the quality/ environmental management representative and the occupational safety specialist Required Experience, Education, Skills, Training and Competencies University degree in life science/ natural science or an equivalent qualification Professional experience in the medical device environment or another regulatory field of work required Knowledge of international regulatory requirements for vigilance activities required Experience in reporting adverse events in line with country-[. .. ]

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Job am 14.02.2026 bei StepStone gefunden Novanta Design Assurance Engineer Medical Devices (m/f/d) • Berlin [. .. ] Novantas Advanced Surgery business unit. Specialized in the field of Minimally Invasive Medicine, WOM develops devices and accessories so that doctors can operate with small cuts. We [...]
MEHR INFOS ZUM STELLENANGEBOT[...] produce Cameras, Insufflators, Medical Pumps, and tubing that makes diagnosis and treatment easier for everyone. Our insufflators and pump systems dilate cavities in the body and turn previously complicated surgeries into minor procedures. Together with customers, doctors, and technical experts, our teams continuously search for new ways to innovate. Job Summary As Design Assurance [. .. ] improvement of processes Failure analysis for field returns and during development Strict compliance with quality, occupational safety and environmental regulations and implementation of instructions by quality/ environmental officers and the specialist for occupational safety Required Experience, Education, Skills and Competencies Completed technical and/or physical studies At least 2 years of professional experience Experience with product quality in a highly regulated industry (medical device, automotive, aviation etc. ) Experience in theory and application of quality methods and techniques English language skills (B2) required Quality-conscious, trustworthy and reliable Team player Good communication skills Structured and systematic way of working Travel Requirements Willingness to travel to all locations and business contacts (10) #LI-UK1 [. .. ]

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Job am 14.02.2026 bei StepStone gefunden Novanta

Senior Regulatory Affairs Specialist Medical Devices (m/f/d)

• Berlin Beratungs-/ Consultingtätigkeiten [. .. ] Novantas Advanced Surgery business unit. Specialized in the field of Minimally Invasive Medicine, WOM develops devices and accessories so that doctors can operate with small cuts. We [...]
MEHR INFOS ZUM STELLENANGEBOT[...] produce Cameras, Insufflators, Medical Pumps, and tubing that makes diagnosis and treatment easier for everyone. Our insufflators and pump systems dilate cavities in the body and turn previously complicated surgeries into minor procedures. Together with customers, doctors, and technical experts, our teams continuously search for new ways to innovate. Summary As a Senior Regulatory Affairs Specialist, youll be working to obtain government approval for new products. Your responsibilities will include analyzing compliance regulations and ensuring product and process compliance. Additionally, youll carry out compliance and inspection activities, report on findings, and make recommendations. Primary Responsibilities Medical device approval: Self-responsible compilation of registration-relevant documents on request of customers in third countries incl. free sales certificates, legalizations, other declarations and certificates Self-responsible compilation of documents for documentation tests by the Notified Body of W. O. M. within the scope of approval procedures according to EU Medical [. .. ]

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Job am 14.02.2026 bei StepStone gefunden Novanta Senior Systems Engineer (m/f/d) • Berlin [. .. ] Novantas Advanced surgery business unit. Specialized in the field of Minimally Invasive Medicine, WOM develops devices and accessories so that doctors can operate with small cuts. We [...]
MEHR INFOS ZUM STELLENANGEBOT[...] produce Cameras, Insufflators, Medical Pumps, and tubing that makes diagnosis and treatment easier for everyone. Our insufflators and pump systems dilate cavities in the body and turn previously complicated surgeries into minor procedures. Together with customers, doctors, and technical experts, our teams continuously search for new ways to innovate. Summary Responsible for the technical [. .. ] between the individual departments Technical management of the technical project components and content-related support for the associated work packages (target definition, Do D) together with the project manager and the specialist departments Creation and maintenance of the technical documentation together with the project manager Responsible for product-specific risk management in collaboration with the risk manager Responsible for the product-specific verification plans and their successful implementation Technical management of the device constructions (Alpha, Beta, Vali) Responsible for the review and approval of assembly instructions, Transfer (design transfer) of the products to production Responsible for the standard tests of the device Support of the production processes up to the pilot series (NPI) ; technical support of production (PE) Responsible for integration of [. .. ]

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Job am 14.02.2026 bei StepStone gefunden Novanta

Systems Engineer Disposables (f/m/d)

• Berlin Teilzeit [. .. ] Novantas Advanced Surgery business unit group. Novanta offers highly reliable, precise and safe solutions that enhance system performance and improve patient outcomes. Insufflators, pumps and disposable tube [...]
MEHR INFOS ZUM STELLENANGEBOT[...] sets, along with medical visualization and operating room integration technologies are the preferred solution for minimally invasive surgery applications. We are looking for an Systems Engineer for our Disposables Team Summary This job is responsible for the technical implementation of products based on defined architecture and master specifications in accordance with company-wide design [. .. ] set constructions (Alpha, Beta, Vali) . Transfer (design transfer) of the products to production. Responsible for the review and approval of assembly instructions. Responsible for the standard tests of the device and tube sets. Support of manufacturing processes up to pilot series (NPI) ; Technical support of production (PE) . Control of material and BOM creation/ management. Preparation and maintenance of technical documentation together with the project manager. Responsible for the technical approval of the products by the customer. Technical contact [. .. ] (e. g. project acquisition General Tasks Strict compliance with the quality, occupational safety, and environmental regulations. Implementation of the instructions of the quality/ environmental management representative and the occupational safety specialist. Required Experience, Education, Skills, Training and Competencies Training/ Education: Dipl. -Ing. / Master of Medical Technology/ Mechanical Engineering/ Materials Engineering/ Biology or equivalent 3+ years of relevant work experience required. Preferably in the development of medical device disposable products. Good knowledge in the fields of mechanics, sterility, biocompatibility. Experience in Design [. .. ]

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Job am 14.02.2026 bei StepStone gefunden Novanta Systems Engineer Medical Devices (m/f/d) • Berlin [. .. ] Novantas Advanced Surgery business unit. Specialized in the field of Minimally Invasive Medicine, WOM develops devices and accessories so that doctors can operate with small cuts. We [...]
MEHR INFOS ZUM STELLENANGEBOT[...] produce Cameras, Insufflators, Medical Pumps, and tubing that makes diagnosis and treatment easier for everyone. Our insufflators and pump systems dilate cavities in the body and turn previously complicated surgeries into minor procedures. Together with customers, doctors, and technical experts, our teams continuously search for new ways to innovate. Summary Responsible for the technical [. .. ] between the individual departments Technical management of the technical project components and content-related support of the associated work packages (target definition, Do D) together with the project manager and the specialist departments Creation and maintenance of technical documentation together with the project manager Responsible for product-specific risk management in cooperation with the risk manager Responsible for the product-specific verification plans and their successful implementation Technical management of equipment and hose set construction (Alpha, Beta, Vali) Transfer (design transfer) of products into production Responsible for the review and approval of assembly instructions Responsible for standard testing of the device and hose sets Support of manufacturing processes up to the pilot series (NPI) ; Technical support of production (PE) Control of material and parts list creation/ management Creation and maintenance of technical documentation together with the project manager Responsible for the technical release of the products by the customer Technical [. .. ]

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Neu Job vor 4 Std. bei Jooble gefunden Becton Dickinson Field Clinical Specialist Central Lower Saxony-Nurse Biomedical APM (m/w/d) • Gronau, Kreis Borken [. .. ] external technicians Ensure Complaint handling in accordance with BD Advanced Patient Monitoring SOP and perform Field Corrective Actions Coordinate the organization of BD Advanced Patient Monitoring participation [...]
MEHR INFOS ZUM STELLENANGEBOT[...] to local seminars, medical exhibitions and trainings Coordinate Customers participation at educational events and congresses organized by BD Advanced Patient Monitoring or the third party Implement marketing strategies. Collaborate with sales colleagues on the effective use of selling process and tools Manage installed base of control monitors: transfers, fixed assets, update software including profitability [. .. ] office machinery Strong written and verbal communication skills, presentation, and interpersonal relationship skills including negotiating and relationship management skills Excellent problem-solving and critical thinking skills Full understanding of medical device regulatory requirements and documents, device accountability and adverse events reporting Fluent German and English is a Must Click on apply if this sounds like you Becton, Dickinson and Company is an Equal Opportunity/ Affirmative Action Employer. xwminpx We do not unlawfully discriminate on the basis of race, color, religion, age, [. .. ]

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Job vor 3 Tagen bei Mindmatch.ai gefunden MED- EL Global Hearing Rehab Specialist-Flexible Hours Growth • AT- 7 Innsbruck A leading medical device manufacturer is seeking professionals for a full-time role in Innsbruck, Austria. The position involves supporting global rehabilitation services and managing materials for hearing rehabilitation. Candidates should [...]
MEHR INFOS ZUM STELLENANGEBOT[...] hold an academic degree in relevant fields and have experience with hearing loss. The role offers a minimum salary of 47, 810.14 [. .. ]

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Job vor 5 Tagen bei Mindmatch.ai gefunden MED- EL

Hearing Solutions Clinical Support Training Specialist

• AT- 7 Innsbruck A leading medical device manufacturer in Innsbruck seeks a Clinical Support Professional to provide technical assistance for hearing solutions like VIBRANT and BONEBRIDGE. Responsibilities include training medical professionals and addressing [...]
MEHR INFOS ZUM STELLENANGEBOT[...] inquiries. The ideal candidate has a degree in a technical field or life sciences, great communication skills in English, and a flexible, team-oriented [. .. ]

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Job vor 6 Tagen bei Mindmatch.ai gefunden MED- EL Global SEO SEA Specialist Data-Driven Growth • AT- 7 Innsbruck A leading medical device manufacturer in Innsbruck is seeking a dedicated SEO Specialist to enhance its online presence. Responsibilities include conducting SEO analyses, on-page audits, and managing Google Ads [...]
MEHR INFOS ZUM STELLENANGEBOT[...] campaigns. The ideal candidate has a strong educational background in marketing and in-depth SEO experience. Excellent organizational skills and fluency in English and German are required. Join a dynamic team and help [. .. ]

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Job vor 6 Tagen bei Mindmatch.ai gefunden Flinn. ai

Senior Regulatory Affairs Specialist

• AT- 9 Wien As a Senior Regulatory Affairs Specialist, you are Flinns in-house regulatory domain expert. You deliver high-quality regulatory intelligence services directly to our Med Tech customers across a broad range [...]
MEHR INFOS ZUM STELLENANGEBOT[...] of regulatory challenges monitoring new regulations, identifying gaps, interpreting requirements, and supporting market expansion. This is a generalist role by design : you will work across different regulatory frameworks, across MDSAP and EU geographies, with a broad variety of device categories. You will work inside the Product Tech team, alongside our Product Manager feeding your field expertise and customer observations as a knowledgeable domain partner, while the PM owns the product direction. You bring the regulatory know-how; they translate it into software. Over time, you will help codify your [. .. ] and spoken English is required; German is a strong plus given our core European customer base. Attributes we are looking for: 7+ years of professional experience in regulatory affairs for medical devices, with demonstrated competence in evaluating and applying MDR/ IVDR and/or FDA requirements across real customer or project scenarios. Experience in a regulatory consulting firm is strongly preferred; time spent inside a medical device manufacturer is an additional plus candidates who have seen both perspectives bring a uniquely practical [. .. ]

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Job vor 7 Tagen bei Mindmatch.ai gefunden IQVIA Clinical Associate Regulatory Submissions, Austria, IQVIA Biotech • AT- 9 Wien [. .. ] accordance with applicable local and/or international regulations, standard operating procedures (SOPs) , project requirements and contractual/ budgetary guidelines. May also include maintenance activities. Essential Functions As Regulatory [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Start-Up Specialist, you will work and lead complex projects under general supervision, serve as Single Point of Contact in assigned studies for investigative sites, Site Activation Manager, Project Management team, and other departments as necessary. You will also ensure adherence to standard operating procedures (SOPs) , Work Instructions, quality of designated deliverables [. .. ] experience, specifically in submissions. Experience in EUCTR and CTIS submission procedures, feasibility and Country Inform Consent adaptation for DACH regions. Experience in Site Contract negotiations with DACH sites. Experience in medical device submissions is beneficial. In-depth knowledge of clinical systems, procedures, and corporate standards. Skills Good negotiating and communication skills in local language. Effective communication, organizational, and interpersonal skills. Ability to work independently and to effectively prioritize tasks. Ability to manage multiple projects. Knowledge and ability to apply GCP/ ICH and [. .. ]

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Job vor 7 Tagen bei Mindmatch.ai gefunden Alexander von Humboldt- Stiftung SEO SEA Growth Strategist: Drive Visibility • AT- 7 Innsbruck A leading medical device manufacturer in Innsbruck is seeking a skilled SEO Specialist to enhance online visibility through data-driven analyses and strategic campaigns. The ideal candidate brings extensive [...]
MEHR INFOS ZUM STELLENANGEBOT[...] knowledge in SEO, Google Ads management, and strong coordination skills. A higher education in marketing and fluency in English and German are essential. This role offers an opportunity to contribute to a global B2B [. .. ]

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Job vor 8 Tagen bei Mindmatch.ai gefunden IQVIA LLC Clinical Associate Regulatory Submissions, Austria, IQVIA Biotech • AT- 9 Wien [. .. ] accordance with applicable local and/or international regulations, standard operating procedures (SOPs) , project requirements and contractual/ budgetary guidelines. May also include maintenance activities. Essential Functions As Regulatory [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Start-Up Specialist, you will work and lead complex projects under general supervision, serve as Single Point of Contact in assigned studies for investigative sites, Site Activation Manager, Project Management team, and other departments as necessary. You will also ensure adherence to standard operating procedures (SOPs) , Work Instructions, quality of designated deliverables [. .. ] experience, specifically in submissions. Experience in EUCTR and CTIS submission procedures, feasibility and Country Inform Consent adaptation for DACH regions. Experience in Site Contract negotiations with DACH sites. Experience in medical device submissions is beneficial. In-depth knowledge of clinical systems, procedures, and corporate standards. Skills Good negotiating and communication skills in local language. Effective communication, organizational, and interpersonal skills. Ability to work independently and to effectively prioritize tasks. Ability to manage multiple projects. Knowledge and ability to apply GCP/ ICH and [. .. ]

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Job am 19.03.2026 bei Mindmatch.ai gefunden International Atomic Energy Agency (IAEA) Microsoft 365 Platform Specialist (P3) • AT- 9 Wien [. .. ] aims at achieving the delivery of agreed levels of services to clients in compliance with best practices defined by international standards, in particular ITIL. Main Purpose The [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Microsoft 365 Platform Specialist leads the design, implementation, governance, and continuous improvement of Microsoft 365 services across the organization. The role ensures that Microsoft 365 workloads, including Power Platform (Power Automate, Power Apps, Copilot Studio) , Power BI, Microsoft Teams, One Drive for Business, and Share Point Online, are configured, integrated, and optimized to [. .. ] systems and troubleshooting IT incidents. Skilled in automation and integration using Power Shell, Microsoft Graph, REST APIs, and connecting with systems like Service Now. Information Technology: Computer Operations. Endpoint and Device Management. Proficiency in Microsoft Intune and Endpoint Manager for device security and access control. Knowledge of Microsoft 365 licensing models and strategies for cost optimisation. Information Technology: IT Security. Strong knowledge of security best practices and information security principles for Microsoft 365. Expertise in governance frameworks, data protection policies, and [. .. ] based interview. Candidates under serious consideration for selection may be subject to reference and background checks as part of the recruitment process. Appointment information Appointment is subject to a satisfactory medical report. Staff members may be assigned to any location. Candidates appointed to posts in the Professional and higher categories are subject to IAEA rotation policy and their maximum tour of service shall normally be seven years. The IAEA retains the discretion not to make any appointment to this vacancy, to [. .. ]

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Job am 15.03.2026 bei Mindmatch.ai gefunden Zoll GmbH Technical Helpdesk Specialist • AT- 9 Wien At ZOLL, we offer innovative technologies that make a real difference to peoples lives. Our medical devices, software and related services are used worldwide to diagnose and treat patients [...]
MEHR INFOS ZUM STELLENANGEBOT[...] suffering from serious cardiopulmonary and respiratory conditions. Location: Runcorn Office Onsite-5 days per week. Following successful probation period, 1 day remote working offered As a Technical Support Helpdesk Representative, you will deliver support for our medical device products, assisting both internal and external customers through phone and email. This role involves addressing product-related inquiries, as well as coordinating with other teams to escalate issues and ensure customer satisfaction. You will perform a variety of duties at ZOLL Medical UK including, but not limited to, the following [. .. ]

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Job am 15.03.2026 bei Mindmatch.ai gefunden Zoll GmbH Medical Device Helpdesk Specialist Onsite/ Remote Eligible • AT- 9 Wien A medical technology firm is seeking a Technical Support Helpdesk Representative in Vienna, Austria. You will provide support for medical device products, assisting customers with inquiries and troubleshooting. [...]
MEHR INFOS ZUM STELLENANGEBOT[...] The ideal candidate has a technical background, preferably in electronics or biomedical, with at least 2 years of technical support experience. This role requires fluency in English and excellent communication skills. The position is primarily onsite with one day of remote work after [. .. ]

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Häufig gestellte Fragen

Wieviel verdient man als Medical device specialist pro Jahr?

Als Medical device specialist verdient man zwischen EUR 50.000,- bis EUR 70.000,- im Jahr.


Wieviele offene Stellenangebote gibt es für Medical Device Specialist Jobs bei unserer Jobsuche?

Aktuell gibt es auf JobRobot 187 offene Stellenanzeigen für Medical Device Specialist Jobs.


Wieviele Unternehmen suchen nach Bewerbern für Medical Device Specialist Jobs?

Aktuell suchen 54 Unternehmen nach Bewerbern für Medical Device Specialist Jobs.


Welche Unternehmen suchen nach Bewerbern für Medical Device Specialist Stellenangebote?

Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Medical Device Specialist Stellenangebote:


  • Chronos Consulting (26 Jobs)
  • DEU Medtronic GmbH (17 Jobs)
  • Novanta (9 Jobs)
  • Cross Border Talents (7 Jobs)
  • Edwards Lifesciences GmbH (4 Jobs)
  • Boston Scientific (4 Jobs)


In welchen Bundesländern werden die meisten Medical Device Specialist Jobs angeboten?

Die meisten Stellenanzeigen für Medical Device Specialist Jobs werden derzeit in Berlin (28 Jobs), Nordrhein-Westfalen (19 Jobs) und Niedersachsen (15 Jobs) angeboten.


Zu welchem Berufsfeld gehören Medical Device Specialist Jobs?

Medical Device Specialist Jobs gehören zum Berufsfeld Medizintechnik.


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Dauer: 0.0535 s., Vers. V.2025-d-2009-Ind-141