170 Jobs für Medical Documentation Specialist
Stellenangebote Medical Documentation Specialist Jobs
Job vor 3 Tagen bei StepStone gefunden
Fresenius Kabi Deutschland GmbH
• Bad Homburg
We have a clear commitment: putting best-possible solutions in the hands of
medical professionals, enabling them to find the right answer to the challenge they face. Fresenius Kabi is a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] driver of healthcare for the coming decade. We truly live diversity and value different backgrounds and motivations. #careerswithapurpose at Fresenius Over 300, 000 people across the globe work at Fresenius to provide [. .. ] EMA, CSV, Data Integrity) and internal guidelines. Responsible for organizing and coordinating system validations and revalidations in close collaboration with Quality Assurance and IT departments. Creation and maintenance of system documentation (SOPs, work instructions, system descriptions) . Serve as the main contact for specialist departments (Regulatory Affairs, QA, IT) and external service providers. Collaborate with interdisciplinary teams to define requirements and drive system acceptance. Manage incidents, changes, releases, and support audits and inspections. Degree in life sciences, computer science, or a related discipline Extensive experience working in regulated sectors such as Pharma, Biotech, or [. .. ]
Job vor 5 Tagen bei StepStone gefunden
Fresenius Kabi Deutschland GmbH
Regulatory Compliance Specialist Enteral Nutrition (m/f/d)
• Bad Homburg
We have a clear commitment: putting best-possible solutions in the hands of
medical professionals, enabling them to find the right answer to the challenge they face. Fresenius Kabi is a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] driver of healthcare for the coming decade. We truly live diversity and value different backgrounds and motivations. #careerswithapurpose at Fresenius Over 300, 000 people across the globe work at Fresenius to provide [. .. ] to make a difference with your career and to become part of our impressive growth story. Regulatory assessment of raw materials, recipes and nutrient profiles Creation and updating of regulatory documentation (e. g. list of ingredients, nutrition information, raw material information) Review and approval of labels and communication materials in accordance with EU food law Participation in project teams on new developments and product changes Regulatory analysis and impact assessment of changes concerning raw materials, recipes and labelling Coordination of orders [. .. ] pressure Strong team player with a collaborative mindset High level of quality awareness Good communication and presentation skills. Fresenius Kabi Deutschland Gmb H sucht in Bad Homburg eine/n Regulatory Compliance Specialist Enteral Nutrition (m/f/d) (ID-Nummer: 13388229) 70937061 [. .. ]
Job am 29.10.2025 bei JobMESH gefunden
PAUL HARTMANN AG
• Baden- Wurttemberg Heidenheim
[. .. ] on time according to regulatory requirements You will assume portfolio responsibility for the products under your care Ensure compliance throughout the product lifecycle Global monitoring and improvement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of regulatory product documentation and conformity assessments You will be responsible for driving the optimization of the IT infrastructure related to regulatory documentation management Provide strategic and technical consulting on regulatory issues Evaluation of product-related regulatory requirements with focus on risk management, labeling and post-market surveillance Support complaint management Qualification: University degree in science or technical sciences or an equivalent qualification Professional experience in the medical device environment or another regulatory field of work Proven experience with MDR and ISO 13485 Knowledge and/or experience in the areas of medical devices, technical documentation and regulatory product documentation, conformity assessment and post-market surveillance Familiarity with FDA regulations and guidelines is desirable A strong interest in and [. .. ]
Job vor 4 Tagen bei Stellenanzeigen.de gefunden
GYNEMED GmbH Co. KG
Regulatory Affairs Specialist (m/f/d) - Medical Devices (Full-time)
• Schleswig- Holstein 23730
Homeoffice möglich
We are seeking an experienced and proactive Regulatory Affairs
Specialist to join our international team and strengthen our global regulatory and quality management activities. In this role, you will be [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] responsible for driving regulatory strategies and submissions not only in Europe (MDR) and the U. S. (FDA) , but also across diverse international markets. By ensuring compliance with global requirements [. .. ] fertility care by ensuring our products meet highest quality standards and global regulatory requirements. The position is based at our German subsidiary near Lübeck. Regulatory Affairs Specialist (m/f/d) Medical Devices (Full-time) Your tasks Lead and support cross-functional projects in regulatory affairs and quality management. Identify, interpret, and implement regulatory requirements across global markets, with a strong focus on international registrations outside the U. S. and EU. Independently prepare submissions and change notifications for competent authorities and international agencies. Update, and maintain technical documentation and dossiers for medical devices (Class I to III) . Collaborate with quality management in risk assessments, usability analyses, and post-market surveillance. Maintain effective communication with global regulatory authorities, international partners, and internal teams. Your qualifications University degree in medical technology, natural sciences, quality engineering, or equivalent training with [. .. ]
Job vor 2 Tagen bei Jobware gefunden
Katharinenstift Heilbronn gGmbH
• Heilbronn
Teilzeit Abgeschlossene Ausbildung
Betriebliche Altersvorsorge 30+ Urlaubstage Tarifvertrag
[. .. ] Wochenenddienst Arbeit im multiprofessionellen Team Bewohnerorientierte Pflege Dokumentation im digitalen System Umgang mit Pflegehilfsmitteln Hygienevorschriften/ Infektionsschutz Pflegequalität sichern Basale Stimulation Palliativpflege Gerontopsychiatrie Intensivpflege-Erfahrung Schmerzmanagement Praxisanleitung Registered Nurse [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (RN) Nursing Specialist Inpatient Care Residential Care Long-term Care Elderly Care/ Geriatric Care Basic Nursing Care Clinical Nursing Treatment Care Care Planning Nursing Documentation Care Assessment Nursing Process Medication Management Wound Care/ Wound Management Preventive Care/ Prophylaxis Quality Management in Nursing Patient/ Resident Monitoring Empathy Communication Skills Teamwork Reliability Responsibility Stress Resilience Patience Problem-solving skills Time Management Compassion Shift Work Weekend Shifts Working in Interdisciplinary Teams Resident-centered Care Digital Documentation Systems Use of Medical Devices/ Care Equipment Hygiene Standards/ Infection Control Quality Assurance Palliative Care Dementia Care/ Gerontopsychiatric Care Basic Stimulation Pain Management Intensive Care Experience Certified Nursing Instructor/ Practice Instructor Pflegekraft Fachkraft Pflege Examinierte Pflegekraft Qualifizierte Pflegekraft Pflegefachperson Gesundheits- und Krankenpfleger/in Altenpfleger/in Gesundheits- und Pflegefachkraft Pflegefachfrau/ Pflegefachmann Gesundheits- und Krankenpfleger/in im stationären [. .. ]
Job vor 2 Tagen bei JobMESH gefunden
Nordex Group
Civil Site Manager-Quality (m/f/d)
• Mecklenburg- Vorpommern 18069 Rostock
Flexible Arbeitszeiten Betriebliche Altersvorsorge Jobticket 30+ Urlaubstage Work-Life-Balance
[. .. ] severity codes Creation of snagging lists and ensuring the snags to be cleared Regular consultations with the project managers, customers and subcontractors Compliance with all health, safety, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and environmental regulations Documentation and proper filing of quality documents YOUR PROFILE Completed a minimum of 3 years of relevant professional training or equivalent knowledge in the civil discipline, with a Civil Engineering degree being beneficial Up to 3 years relevant professional experience in the civil construction industry Basic specialist knowledge in civil construction discipline Basic theoretical knowledge of civil construction principles, methods, and tools Good knowledge of the German and English language, both written and spoken minimum CEFR level of B2 Confident Microsoft Office user Knowledge of health, safety and environmental regulations and standards in the construction industry and the ability to enforce it accordingly The ability to work independently and as part of a team Ability to earn and maintain the GWO work at height and G41 medical examination certification EU recognized class-B drivers license High willingness to travel (approx. 75) within Germany, Netherlands, and Austria. If you have a passion for renewable energies and would like to work in a dynamic and challenging environment, we look forward to receiving your application and collaborating with you in [. .. ]
Job am 14.11.2025 bei JobMESH gefunden
PAUL HARTMANN AG
Specialist Quality Regulatory Affairs-Medical Device Environment (w/m/d)
• Bavaria 91719 Heidenheim
[. .. ] on time according to regulatory requirements You will assume portfolio responsibility for the products under your care Ensure compliance throughout the product lifecycle Global monitoring and improvement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of regulatory product documentation and conformity assessments You will be responsible for driving the optimization of the IT infrastructure related to regulatory documentation management Provide strategic and technical consulting on regulatory issues Evaluation of product-related regulatory requirements with focus on risk management, labeling and post-market surveillance Support complaint management Qualification: University degree in science or technical sciences or an equivalent qualification Professional experience in the medical device environment or another regulatory field of work Proven experience with MDR and ISO 13485 Knowledge and/or experience in the areas of medical devices, technical documentation and regulatory product documentation, conformity assessment and post-market surveillance Familiarity with FDA regulations and guidelines is desirable A strong interest in and [. .. ]
Job am 28.10.2025 bei JobMESH gefunden
PAUL HARTMANN AG
Specialist Quality Regulatory Affairs-Medical Device Environment (w/m/d)
• Baden- Wurttemberg
[. .. ] on time according to regulatory requirements You will assume portfolio responsibility for the products under your care Ensure compliance throughout the product lifecycle Global monitoring and improvement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of regulatory product documentation and conformity assessments You will be responsible for driving the optimization of the IT infrastructure related to regulatory documentation management Provide strategic and technical consulting on regulatory issues Evaluation of product-related regulatory requirements with focus on risk management, labeling and post-market surveillance Support complaint management Qualification: University degree in science or technical sciences or an equivalent qualification Professional experience in the medical device environment or another regulatory field of work Proven experience with MDR and ISO 13485 Knowledge and/or experience in the areas of medical devices, technical documentation and regulatory product documentation, conformity assessment and post-market surveillance Familiarity with FDA regulations and guidelines is desirable A strong interest in and [. .. ]
Neu Job vor 4 Std. bei Neuvoo.com gefunden
Hologic
• Schleswig- Holstein
Ready to make a real impact in healthcare sales? Join our team as an Sales Support
Specialist and be the driving force behind our German Breast Skeletal Health (BSH) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Gantry Consumables business As our Sales Support Specialist youll be at the heart of our sales operations, providing expert commercial and administrative support to the BSH sales team. Youll help manage customer requests, troubleshoot order processing issues, coordinate [. .. ] compliance Create and manage purchase orders for new customers and contractors Communicate clearly with customers about training, installations, and project updates Accurately record project and installation data, and distribute necessary documentation for invoicing Proactively identify and solve blockers in the sales order process What You Bring: Commercial or technical education with experience in sales support, back-office operations, or project coordination Experience in the medical technology industry, with knowledge of the German Healthcare system and tender process Experience with tender management and procurement processes Strong communication and teamwork skills Proactive problem-solving and troubleshooting abilities Excellent attention to detail and data quality Ability to multitask and prioritize in a dynamic environment Proficiency with CRM tools [. .. ]
Neu Job vor 4 Std. bei Neuvoo.com gefunden
Paul Hartmann
Specialist Quality Regulatory Affairs-Medical Device Environment (w/m/d)
• Bavaria Heidenheim
Specialist Quality Regulatory Affairs-
Medical Device Environment (w/m/d) At HARTMANN, were all in to help, care, protect and grow. We support healthcare professionals, that they can focus on what [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] really matters: to positively impact peoples life. We realize solutions that make a difference. And with your commitment you can grow on your job [. .. ] on time according to regulatory requirements You will assume portfolio responsibility for the products under your care Ensure compliance throughout the product lifecycle Global monitoring and improvement of regulatory product documentation and conformity assessments You will be responsible for driving the optimization of the IT infrastructure related to regulatory documentation management Provide strategic and technical consulting on regulatory issues Evaluation of product-related regulatory requirements with focus on risk management, labeling and post-market surveillance Support complaint management Qualification: University degree [. .. ]
Neu Job vor 4 Std. bei Neuvoo.com gefunden
Hologic
Sales Support Specialist
• Berlin
Ready to make a real impact in healthcare sales? Join our team as an Sales Support
Specialist and be the driving force behind our German Breast Skeletal Health (BSH) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Gantry Consumables business As our Sales Support Specialist youll be at the heart of our sales operations, providing expert commercial and administrative support to the BSH sales team. Youll help manage customer requests, troubleshoot order processing issues, coordinate [. .. ] compliance Create and manage purchase orders for new customers and contractors Communicate clearly with customers about training, installations, and project updates Accurately record project and installation data, and distribute necessary documentation for invoicing Proactively identify and solve blockers in the sales order process What You Bring: Commercial or technical education with experience in sales support, back-office operations, or project coordination Experience in the medical technology industry, with knowledge of the German Healthcare system and tender process Experience with tender management and procurement processes Strong communication and teamwork skills Proactive problem-solving and troubleshooting abilities Excellent attention to detail and data quality Ability to multitask and prioritize in a dynamic environment Proficiency with CRM tools [. .. ]
Job vor 3 Tagen bei Neuvoo.com gefunden
Nordex Group
Civil Site Manager-Quality (m/f/d)
• Baden- Württemberg
Flexible Arbeitszeiten Betriebliche Altersvorsorge Jobticket 30+ Urlaubstage Work-Life-Balance
[. .. ] qualityinspections including assigning of severity codes Creation ofsnagging lists and ensuring the snags to be cleared Regularconsultations with the project managers, customers andsubcontractors Compliance with all health, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] safety, andenvironmental regulations Documentation and proper filing ofquality documents YOUR PROFILE Completed a minimum of 3 years ofrelevant professional training or equivalent knowledge in the civildiscipline, with a Civil Engineering degree being beneficial Up to3 years relevant professional experience in the civil constructionindustry Basic specialist knowledge in civil constructiondiscipline Basic theoretical knowledge of civil constructionprinciples, methods, and tools Good knowledge of the German and English language, both written and spoken minimum CEFR level of B2 Confident Microsoft Office user Knowledge of health, safety andenvironmental regulations and standards in the constructionindustry and the ability to enforce it accordingly The ability towork independently and as part of a team Ability to earn andmaintain the GWO work at height and G41 medical examinationcertification EU recognized class-B drivers license Highwillingness to travel (approx. 75) within Germany, Netherlands, and Austria. If you have a passion for renewable energies and wouldlike to work in a dynamic and challenging environment, we lookforward to receiving your application and collaborating with you ina varied and future-oriented [. .. ]
Job vor 2 Tagen bei JobMESH gefunden
Nordex Group
• Mecklenburg- Vorpommern Rostock
Flexible Arbeitszeiten Betriebliche Altersvorsorge Jobticket 30+ Urlaubstage Work-Life-Balance
[. .. ] severity codes Creation of snagging lists and ensuring the snags to be cleared Regular consultations with the project managers, customers and subcontractors Compliance with all health, safety, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and environmental regulations Documentation and proper filing of quality documents YOUR PROFILE Completed a minimum of 3 years of relevant professional training or equivalent knowledge in the civil discipline, with a Civil Engineering degree being beneficial Up to 3 years relevant professional experience in the civil construction industry Basic specialist knowledge in civil construction discipline Basic theoretical knowledge of civil construction principles, methods, and tools Good knowledge of the German and English language, both written and spoken minimum CEFR level of B2 Confident Microsoft Office user Knowledge of health, safety and environmental regulations and standards in the construction industry and the ability to enforce it accordingly The ability to work independently and as part of a team Ability to earn and maintain the GWO work at height and G41 medical examination certification EU recognized class-B drivers license High willingness to travel (approx. 75) within Germany, Netherlands, and Austria. If you have a passion for renewable energies and would like to work in a dynamic and challenging environment, we look forward to receiving your application and collaborating with you in [. .. ]
Job am 29.10.2025 bei Jooble gefunden
PAUL HARTMANN AG
Specialist (m/w/d) Regulatory Affairs
• Heidenheim
[. .. ] on time according to regulatory requirements You will assume portfolio responsibility for the products under your care Ensure compliance throughout the product lifecycle Global monitoring and improvement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of regulatory product documentation and conformity assessments You will be responsible for driving the optimization of the IT infrastructure related to regulatory documentation management Provide strategic and technical consulting on regulatory issues Evaluation of product-related regulatory requirements with focus on risk management, labeling and post-market surveillance Support complaint management Qualification: University degree in science or technical sciences or an equivalent qualification Professional experience in the medical device environment or another regulatory field of work Proven experience with MDR and ISO 13485 Knowledge and/or experience in the areas of medical devices, technical documentation and regulatory product documentation, conformity assessment and post-market surveillance Familiarity with FDA regulations and guidelines is desirable A strong interest in and [. .. ]
Job am 29.10.2025 bei JobMESH gefunden
PAUL HARTMANN AG
Specialist Quality Regulatory Affairs-Medical Device Environment (w/m/d)
• Baden- Wurttemberg 89520 Heidenheim
[. .. ] on time according to regulatory requirements You will assume portfolio responsibility for the products under your care Ensure compliance throughout the product lifecycle Global monitoring and improvement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of regulatory product documentation and conformity assessments You will be responsible for driving the optimization of the IT infrastructure related to regulatory documentation management Provide strategic and technical consulting on regulatory issues Evaluation of product-related regulatory requirements with focus on risk management, labeling and post-market surveillance Support complaint management Qualification: University degree in science or technical sciences or an equivalent qualification Professional experience in the medical device environment or another regulatory field of work Proven experience with MDR and ISO 13485 Knowledge and/or experience in the areas of medical devices, technical documentation and regulatory product documentation, conformity assessment and post-market surveillance Familiarity with FDA regulations and guidelines is desirable A strong interest in and [. .. ]
Job am 29.10.2025 bei Jooble gefunden
PAUL HARTMANN AG
Regulatory Specialist (m/w/d)
• Heidenheim
[. .. ] on time according to regulatory requirements You will assume portfolio responsibility for the products under your care Ensure compliance throughout the product lifecycle Global monitoring and improvement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of regulatory product documentation and conformity assessments You will be responsible for driving the optimization of the IT infrastructure related to regulatory documentation management Provide strategic and technical consulting on regulatory issues Evaluation of product-related regulatory requirements with focus on risk management, labeling and post-market surveillance Support complaint management Qualification: University degree in science or technical sciences or an equivalent qualification Professional experience in the medical device environment or another regulatory field of work Proven experience with MDR and ISO 13485 Knowledge and/or experience in the areas of medical devices, technical documentation and regulatory product documentation, conformity assessment and post-market surveillance Familiarity with FDA regulations and guidelines is desirable A strong interest in and [. .. ]
Job am 29.10.2025 bei Jooble gefunden
PAUL HARTMANN AG
• Heidenheim
[. .. ] on time according to regulatory requirements You will assume portfolio responsibility for the products under your care Ensure compliance throughout the product lifecycle Global monitoring and improvement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of regulatory product documentation and conformity assessments You will be responsible for driving the optimization of the IT infrastructure related to regulatory documentation management Provide strategic and technical consulting on regulatory issues Evaluation of product-related regulatory requirements with focus on risk management, labeling and post-market surveillance Support complaint management Qualification: University degree in science or technical sciences or an equivalent qualification Professional experience in the medical device environment or another regulatory field of work Proven experience with MDR and ISO 13485 Knowledge and/or experience in the areas of medical devices, technical documentation and regulatory product documentation, conformity assessment and post-market surveillance Familiarity with FDA regulations and guidelines is desirable A strong interest in and [. .. ]
Job am 29.10.2025 bei Jooble gefunden
PAUL HARTMANN AG
Specialist Quality Regulatory Affairs-Medical Device Environment (w/m/d)
• Heidenheim
[. .. ] on time according to regulatory requirements You will assume portfolio responsibility for the products under your care Ensure compliance throughout the product lifecycle Global monitoring and improvement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of regulatory product documentation and conformity assessments You will be responsible for driving the optimization of the IT infrastructure related to regulatory documentation management Provide strategic and technical consulting on regulatory issues Evaluation of product-related regulatory requirements with focus on risk management, labeling and post-market surveillance Support complaint management Qualification: University degree in science or technical sciences or an equivalent qualification Professional experience in the medical device environment or another regulatory field of work Proven experience with MDR and ISO 13485 Knowledge and/or experience in the areas of medical devices, technical documentation and regulatory product documentation, conformity assessment and post-market surveillance Familiarity with FDA regulations and guidelines is desirable A strong interest in and [. .. ]
Job am 29.10.2025 bei Jooble gefunden
PAUL HARTMANN AG
• Heidenheim
[. .. ] on time according to regulatory requirements You will assume portfolio responsibility for the products under your care Ensure compliance throughout the product lifecycle Global monitoring and improvement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of regulatory product documentation and conformity assessments You will be responsible for driving the optimization of the IT infrastructure related to regulatory documentation management Provide strategic and technical consulting on regulatory issues Evaluation of product-related regulatory requirements with focus on risk management, labeling and post-market surveillance Support complaint management Qualification: University degree in science or technical sciences or an equivalent qualification Professional experience in the medical device environment or another regulatory field of work Proven experience with MDR and ISO 13485 Knowledge and/or experience in the areas of medical devices, technical documentation and regulatory product documentation, conformity assessment and post-market surveillance Familiarity with FDA regulations and guidelines is desirable A strong interest in and [. .. ]
Job am 29.10.2025 bei Jooble gefunden
PAUL HARTMANN AG
Specialist, Regulatory Affairs
• Heidenheim
[. .. ] on time according to regulatory requirements You will assume portfolio responsibility for the products under your care Ensure compliance throughout the product lifecycle Global monitoring and improvement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of regulatory product documentation and conformity assessments You will be responsible for driving the optimization of the IT infrastructure related to regulatory documentation management Provide strategic and technical consulting on regulatory issues Evaluation of product-related regulatory requirements with focus on risk management, labeling and post-market surveillance Support complaint management Qualification: University degree in science or technical sciences or an equivalent qualification Professional experience in the medical device environment or another regulatory field of work Proven experience with MDR and ISO 13485 Knowledge and/or experience in the areas of medical devices, technical documentation and regulatory product documentation, conformity assessment and post-market surveillance Familiarity with FDA regulations and guidelines is desirable A strong interest in and [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
PSI CRO
Clinical Site Technology Specialist (Nuclear Medicine)
• AT- 9 Wien
Clinical Site Technology
Specialist (Nuclear Medicine) PSI is a leading Contract Research Organization with more than 29 years in the industry offering a perfect balance between stability and innovation [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Job Description As a Site [. .. ] other technologies Determine technical resources needed for project implementation, and communicate needs to department managers Organize technical training for project teams Provide support to the project teams to ensure proper documentation of study-specific assessments related to study technologies Support site initiation preparation and perform technical visits to assist the site team with technical aspects of the study Assist and advise the site monitor in the area of study technologies Provide relevant technology-related information to Business Development for proposals Prepare for and attend Bid Defense Meetings Attend and present at Investigators Meetings Qualifications At least Bachelors degree in a relevant field (Medical Imaging, Radiologic Technology, etc. ) Licensed specialist in relevant technology. Minimum 5 years experience in the specified technology: Nuclear Medicine, Molecular imaging, etc. Experience in operation and QC procedures related to overseeing and managing PET imaging agents and therapeutic RLTs Fluent in German English Proficiency in standard MS Office applications [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Medtronic
Senior Therapy Specialist (m/w/d)
• AT- 9 Wien
Homeoffice möglich
Join to apply for the Senior Therapy
Specialist (m/w/d) role at Medtronic At Medtronic you can begin a lifelong career of exploration and innovation, while helping champion healthcare access [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and equity for all. Youll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life Atrial fibrillation affects [. .. ] clinical and technical support and training to physicians and EP Lab Staff on the optimal use of the AFFERA Mapping and Ablation System. Bring your talents to a leader in medical technology and healthcare solutions. We support your growth with the training, mentorship, and guidance you need to own your future success. Join us for a career that changes lives This fieldbased position, requiring extensive travel (80 and up to 100) , covers whole Austria and, in specific support situations, Western [. .. ] department, and marketing to ensure system efficiency, provide feedback, and contribute to new product development. Stay updated on product information, IFUs, scientific literature, and compliance with all company trainings and documentation requirements. Actively participate in congresses, symposia, and workshops regionally and internationally to represent Medtronic and share clinical best practices. Required Knowledge and Experience: Bachelors degree in electrical or medical engineering, or related scientific disciplines. A minimum of 3 years of clinical electrophysiology (EP) experience. At least 2 years of proven [. .. ]
Job vor 3 Tagen bei Mindmatch.ai gefunden
Teccon GmbH Co. KG
Medical Devices Documentation Design Controls Specialist
• AT- 7 Kundl
A technology group specializing in
documentation solutions is seeking an expert to optimize documentation processes. The ideal candidate will have a strong background in
medical device regulation, document [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] management, and collaboration with cross-functional teams. Responsibilities include improving design control procedures and preparing clinical evidence documentation. The role offers a gross annual salary starting at EUR 69, 000, flexible working conditions, and opportunities for professional growth. J-18808-Ljbffr 71022548 [. .. ]
Job vor 4 Tagen bei Mindmatch.ai gefunden
Medtronic plc
Senior Therapy Specialist (m/w/d)
• AT- 9 Wien
Homeoffice möglich
Senior Therapy
Specialist (m/w/d) page is loaded # # Senior Therapy Specialist (m/w/d) remote type: Remotelocations: Vienna, Vienna, Austriatime type: Full timeposted on: Posted Todaytime left to apply: End [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Date: December 2, 2025 (4 days left to apply) job requisition id: R25987At Medtronic you can begin a life-long [. .. ] clinical and technical support and training to physicians and EP Lab Staff on the optimal use of the AFFERA Mapping and Ablation System. Bring your talents to a leader in medical technology and healthcare solutions. We support your growth with the training, mentorship, and guidance you need to own your future success. Join us for a career that changes lives This field-based position, requiring extensive travel ( 80 and up to 100 ) , covers whole Austria and, in specific [. .. ] ensure system efficiency, provide feedback, and contribute to new product development. Regulatory and Scientific Compliance Stay updated on product information, IFUs, scientific literature, and compliance with all company trainings and documentation requirements. Professional Representation Actively participate in congresses, symposia, and workshops regionally and internationally to represent Medtronic and share clinical best practices. Required Knowledge and Experience: Bachelors degree in electrical or medical engineering, or related scientific disciplines. A minimum of 3 years of clinical electrophysiology (EP) experience. At least 2 years [. .. ]
Job vor 4 Tagen bei Mindmatch.ai gefunden
Teccon GmbH Co. KG
Documentation Design Control Specialist (m/w/d) Medical Devices
• AT- 7 Kundl
[. .. ] for prestigious clients, aiming to discover and nurture human potential by creating tailored connections between companies and talents. Bring your expertise to our projects and actively shape [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the future. Responsibilities Documentation Excellence: Drive lean, compliant, and scientifically sound documentation processes by optimizing and digitalizing Design History Files (DHF) for efficient knowledge management. Cross-Functional Collaboration: Partner with R D, Quality, and Regulatory teams to streamline technical development processes for faster and more effective product development. Data-Driven Process Improvement: Leverage data [. .. ] Design Control procedures, ensuring alignment with global quality and compliance standards. Qualifications Education Experience: Bachelors, Masters, or Ph D in Engineering or Natural Sciences with 35 years of relevant experience in Medical Devices, Quality, or R D documentation. Regulatory Knowledge: Solid understanding and practical experience with EU Medical Device Regulation (MDR) , ISO 13485, and US FDA regulations (21 CFR Part 4 and 21 CFR Part 820) . Process Quality Focus: Proven track record in improving development, documentation, or quality management processes [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Medical Documentation Specialist pro Jahr?
Als Medical Documentation Specialist verdient man zwischen EUR 45.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Medical Documentation Specialist Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 170 offene Stellenanzeigen für Medical Documentation Specialist Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Medical Documentation Specialist Jobs?
Aktuell suchen 39 Unternehmen nach Bewerbern für Medical Documentation Specialist Jobs.
Welche Unternehmen suchen nach Bewerbern für Medical Documentation Specialist Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Medical Documentation Specialist Stellenangebote:
- Planet Pharma (11 Jobs)
- PAUL HARTMANN AG (10 Jobs)
- Nordex Group (3 Jobs)
- BD (3 Jobs)
In welchen Bundesländern werden die meisten Medical Documentation Specialist Jobs angeboten?
Die meisten Stellenanzeigen für Medical Documentation Specialist Jobs werden derzeit in Bayern (23 Jobs), Baden-Württemberg (17 Jobs) und Berlin (14 Jobs) angeboten.
Zu welchem Berufsfeld gehören Medical Documentation Specialist Jobs?
Medical Documentation Specialist Jobs gehören zum Berufsfeld Technische Dokumentation / Redaktion.
