6 Jobs für Medical Documentation Specialist
Stellenangebote Medical Documentation Specialist Jobs
Job am 22.02.2026 bei Mindmatch.ai gefunden
Teccon GmbH Co. KG
• 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 management, and [...]
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[...] 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 81514692 [. .. ]
Job am 31.01.2026 bei Mindmatch.ai gefunden
Teccon GmbH Co. KG
• 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 [. .. ]
Job am 03.03.2026 bei Jobleads gefunden
• München, Bayern
Jobticket
Your mission Im Fusion is an independent R D company based in Munich. We help our customers to drive innovation in
Medical Imaging based on our software platform for Image [...]
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[...] Processing, Computer Vision, AI and Robotics. We wish to expand our team with talented and motivated people to help us develop and commercialize advanced medical products in collaboration with renowned customers. As Senior Quality Management and Regulatory Affairs Manager in the Quality [. .. ] team you will have the following responsibilities: Provide guidance on regulatory and quality requirements, including MDR and FDA requirements, for our in-house and our customer software projects Create technical documentation for our industry projects together with our software development teams Provide guidance and support on MDR and FDA conformant documentation of medical AI models Maintain and continuously improve our QMS in alignment with ISO 13485 Develop, implement, and monitor quality policies, procedures, and KPIs Coordinate internal audits and prepare for [. .. ]
Job am 07.12.2025 bei Jobleads gefunden
Documentation Design Control Specialist (m/w/d) Medical Devices
• Kundl, Tirol
[. .. ] 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 [. .. ]
Job am 26.02.2026 bei Neuvoo gefunden
Im Fusion GmbH
Quality Systems Technical Documentation Specialist Medical Device Software (SaMd/SiMD)
• Munich, Bavaria
Jobticket
Your mission As a Quality Systems Technical
Documentation Specialist in our Quality Management team, you will support the creation of technical documentation for both our in-house Sa MD product and [...]
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[...] customer projects where our software is integrated into medical device systems (Si MD) , especially in the area of interventional navigation and planning. You will work closely with our software development teams and contribute to scalable documentation processes aligned with ISO 13485, MDR and FDA expectations. Your responsibilities Create technical documentation for customer solutions developed using our SDK together with [. .. ]
Job am 06.12.2025 bei Neuvoo gefunden
Sysmex
• Hamburg
Jobticket Work-Life-Balance
[. .. ] our company is dedicated to providing essential products that help people worldwide on their healthcare journey. If this opportunity appeals to you, come and join us in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the position of Specialist for Technical Documentation and QM coordinator (f/m/x) in Medical Technology Your responsibilities Handling of technical improvement campaigns for the EMEA region. Initiation, tracking and follow up of these campaigns in direct communication with our customers, our technical field service staff. Editorial of technical documents, including release and maintenance of technical documents. Quality management handling of technical department processes. Continuous [. .. ]
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 6 offene Stellenanzeigen für Medical Documentation Specialist Jobs.
In welchen Bundesländern werden die meisten Medical Documentation Specialist Jobs angeboten?
Die meisten Stellenanzeigen für Medical Documentation Specialist Jobs werden derzeit in Bayern (1 Jobs), Hamburg (1 Jobs) und Berlin (0 Jobs) angeboten.
Zu welchem Berufsfeld gehören Medical Documentation Specialist Jobs?
Medical Documentation Specialist Jobs gehören zum Berufsfeld Technische Dokumentation / Redaktion.
