12 Jobs für Medical Device Coordinator
Stellenangebote Medical Device Coordinator Jobs
Job am 20.01.2026 bei Jooble gefunden
INM- Leibniz- Institut für Neue Materialien gGmbH
• Saarland
Work-Life-Balance
[. .. ] are Engineered Living Materials (ELMs) , an emergent class of materials at the interface between materials science and synthetic biology, with huge potential for sustainable innovation in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] different technological and medical fields. Our institute develops safe-by-design concepts for responsible ELM innovation. Project Manager in Regulatory Affairs related to biotechnology/ biomedical products (f, m, d) The project manager will coordinate a knowledge-exchange network that links multiple stakeholders (academic institutions, industry, consultants and regulatory agencies) and experts with interest in [. .. ] development. Conceptualization of the outreach action plan (website, online platform, workshops) in cooperation with scientists in Material Vital Hub and communication experts at INM and partner institutions. Reporting to project coordinator, partners and funding agencies. Masters degree in Regulatory Affairs and at least 2 years of related work experience. Alternatively, university degree in natural, engineering or life sciences and several years experience in regulatory science or regulatory affairs. A Ph D in biomedical materials, microbiology, or experience in clinical translation of cell therapies is considered beneficial. EU GMO regulation, medical device regulation (MDR) , ATMPs) is highly desirable. Clear writing and strong communication skills in German and English. Project management and organization skills. An interesting and timely topic with high visibility, as well as opportunities for interaction with public and private partners. A professional and supportive working environment with an open [. .. ]
Job am 20.01.2026 bei Jooble gefunden
INM- Leibniz- Institut für Neue Materialien gGmbH
• Saarland
Work-Life-Balance
[. .. ] are Engineered Living Materials (ELMs) , an emergent class of materials at the interface between materials science and synthetic biology, with huge potential for sustainable innovation in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] different technological and medical fields. Our institute develops safe-by-design concepts for responsible ELM innovation. To lead a community-driven initiative in ELMs, we seek a Project Manager in Regulatory Affairs related to biotechnology/ biomedical products (f, m, d) to develop guidelines and best practices for the development of safe and sustainable ELM-[. .. ] network. Conceptualization of the outreach action plan (website, online platform, workshops) in cooperation with scientists in Material Vital Hub and communication experts at INM and partner institutions. Reporting to project coordinator, partners and funding agencies. Your profile Master s degree in Regulatory Affairs and at least 2 years of related work experience. Alternatively, university degree in natural, engineering or life sciences and several years experience in regulatory science or regulatory affairs. A Ph D in biomedical materials, microbiology, or experience in clinical translation of cell therapies is considered beneficial. Experience in regulatory frameworks relevant to biotechnology and biomedical products (e. g. EU GMO regulation, medical device regulation (MDR) , ATMPs) is highly desirable. Strong analytical skills and attention to detail. Clear writing and strong communication skills in German and English. Project management and organization skills. Structured working style. We offer An interesting and timely topic with high visibility, as well as opportunities for interaction with public [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
Project Manager in Regulatory Affairs (f/m/D)
• Kaiserslautern, Rheinland- Pfalz
Work-Life-Balance
[. .. ] are Engineered Living Materials (ELMs) , an emergent class of materials at the interface between materials science and synthetic biology, with huge potential for sustainable innovation in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] different technological and medical fields. Our institute develops safe-by-design concepts for responsible ELM innovation. To lead a community-driven initiative in ELMs, we seek a Project Manager in Regulatory Affairs related to biotechnology/ biomedical products (f, m, d) to develop guidelines and best practices for the development of safe and sustainable ELM-[. .. ] network. Conceptualization of the outreach action plan (website, online platform, workshops) in cooperation with scientists in Material Vital Hub and communication experts at INM and partner institutions. Reporting to project coordinator, partners and funding agencies. Your profile Master s degree in Regulatory Affairs and at least 2 years of related work experience. Alternatively, university degree in natural, engineering or life sciences and several years experience in regulatory science or regulatory affairs. A Ph D in biomedical materials, microbiology, or experience in clinical translation of cell therapies is considered beneficial. Experience in regulatory frameworks relevant to biotechnology and biomedical products (e. g. EU GMO regulation, medical device regulation (MDR) , ATMPs) is highly desirable. Strong analytical skills and attention to detail. Clear writing and strong communication skills in German and English. Project management and organization skills. Structured working style. We offer An interesting and timely topic with high visibility, as well as opportunities for interaction with public [. .. ]
Job am 20.01.2026 bei Jobleads gefunden
Project Manager in Regulatory Affairs (f/m/D)
• Saarbrücken, Saarland
Work-Life-Balance
[. .. ] are Engineered Living Materials (ELMs) , an emergent class of materials at the interface between materials science and synthetic biology, with huge potential for sustainable innovation in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] different technological and medical fields. Our institute develops safe-by-design concepts for responsible ELM innovation. Project Manager in Regulatory Affairs related to biotechnology/ biomedical products (f, m, d) to develop guidelines and best practices for the development of safe and sustainable ELM-based technologies in the future. The project manager will coordinate a [. .. ] network. Conceptualization of the outreach action plan (website, online platform, workshops) in cooperation with scientists in Material Vital Hub and communication experts at INM and partner institutions. Reporting to project coordinator, partners and funding agencies. Your profile Masters degree in Regulatory Affairs and at least 2 years of related work experience. Alternatively, university degree in natural, engineering or life sciences and several years experience in regulatory science or regulatory affairs. A Ph D in biomedical materials, microbiology, or experience in clinical translation of cell therapies is considered beneficial. Experience in regulatory frameworks relevant to biotechnology and biomedical products (e. g. EU GMO regulation, medical device regulation (MDR) , ATMPs) is highly desirable. Strong analytical skills and attention to detail. Clear writing and strong communication skills in German and English. Project management and organization skills. Structured working style. We offer An interesting and timely topic with high visibility, as well as opportunities for interaction with public [. .. ]
Job am 12.12.2025 bei Jobleads gefunden
• München, Bayern
[. .. ] and submit your application in English. Medpace Overview Medpace is a fullservice clinical contract research organisation (CRO) . We provide Phase IIV clinical development services to the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, antiviral and antiinfective. Headquartered in Cincinnati, Ohio, employing more [. .. ]
Job am 21.11.2025 bei Jobleads gefunden
Clinical Project Coordinator
• München, Bayern
[. .. ] your application in English. Medpace Overview Medpace is a full-service clinical contract research organisation (CRO) . We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, [. .. ]
Job am 11.09.2025 bei Jobleads gefunden
• München, Bayern
[. .. ] have a desire to transfer and apply analytical and academic skills in clinical project administration and management. Responsibilities Communicate and collaborate on global study activities; working closely [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with the project coordinator and clinical trial manager Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy Compile and maintain project-specific status reports within the clinical trial management system Interact with the internal project team, Sponsor, study sites, and third-party vendors Manage and perform quality control of our [. .. ] but will be advantageous Medpace Overview Medpace is a full-service clinical contract research organization (CRO) . We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, [. .. ]
Neu Job vor 5 Std. bei Neuvoo gefunden
IQVIA
• Mainz, Rhineland- Palatinate
Betriebliche Altersvorsorge
[. .. ] integrierte Projektansätze entlang des IQVIA Lösungsportfolios, die wir individuell an die Kundenbedürfnisse anpassen und aus einer Hand anbieten. Für ein spannendes Projekt bei einem rennomierten Pharmaunternehmen suchen [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] wir Documentation Training Coordinator (m/w/d) zum nächstmöglichen Zeitpunkt Einsatzort: Ingelheim Aufgaben: Management von Dokumentenworkflows: Du übernimmst die Verwaltung von Dokumentenworkflows im elektronischen Dokumentenmanagementsystem (Vault Quality) , einschließlich der Anlage und Überwachung aller Workflows. Dokumentenbearbeitung und Archivierung: Du unterstützt bei der Bearbeitung, dem formalen Review und der Archivierung von internen und externen GMP- und non-GMP-Dokumenten innerhalb der Abteilung Device Development und bietest 1st Level Support. Trainingskoordination: Du bist verantwortlich für die Anlage und Dokumentation von Trainings sowie die Pflege von Trainingsplänen im Trainingsmanagementsystem. Troubleshooting: Als Ansprechpartner für die Abteilung Device Development stehst du bei Fragen und Problemen rund um Dokumentenmanagement und Trainingsdokumentation zur Verfügung. Best Practice Dokumentation: Du erstellst [. .. ] Draht zu uns: Kandidaten-Hotline: 0621-84508113 oder sende uns gerne direkt Deine Bewerbung per Mail an: Recruitment. #LI-CES #LI-DNP #LI-SS2 #Pharma #Medical #Chemie #Pharmazie #Pharma-Innendienst IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population [. .. ]
Job am 17.01.2026 bei Neuvoo gefunden
INM- Leibniz- Institut für Neue Materialien gGmbH
• Saarbrücken, Saarland
Work-Life-Balance
[. .. ] job here INM is an internationally leading centre for interdisciplinary research on (bio) hybrid materials, and their exploitation in materials-based solutions for a sustainable world with increasing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] digitalization and medical needs. Our research integrates materials chemistry, biological processes, physical analysis, and process engineering. We aim for leadership in the fields of opto-interactive, electro-integrative and bio-intelligent material systems. In these areas, we actively seize opportunities to transfer our scientific results into materials-driven innovation. Project Manager in Regulatory [. .. ] network. Conceptualization of the outreach action plan (website, online platform, workshops) in cooperation with scientists in Material Vital Hub and communication experts at INM and partner institutions. Reporting to project coordinator, partners and funding agencies. Your profile Masters degree in Regulatory Affairs and at least 2 years of related work experience. Alternatively, university degree in natural, engineering or life sciences and several years experience in regulatory science or regulatory affairs. A Ph D in biomedical materials, microbiology, or experience in clinical translation of cell therapies is considered beneficial. Experience in regulatory frameworks relevant to biotechnology and biomedical products (e. g. EU GMO regulation, medical device regulation (MDR) , ATMPs) is highly desirable. Strong analytical skills and attention to detail. Clear writing and strong communication skills in German and English. Project management and organization skills. Structured working style. We offer An interesting and timely topic with high visibility, as well as opportunities for interaction with public [. .. ]
Job am 15.01.2026 bei Neuvoo gefunden
GULP experts united
• Penzberg, Bavaria
Our dynamic team in the heart of picturesque Penzberg sets new standards in the development of pioneering
medical solutions. We offer ambitious talents the opportunity to contribute and develop [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] their specialist knowledge in the position of Senior Plant Technician Expert (m/f/d) . Heres what we offer Attractive salary and long-term job security through group affiliation Up to 30 days vacation per year Contribution to company [. .. ] work processes to maintain technical safety and ensure the implementation of new production processes and technologies. Implementation of qualification and validation measures of the relevant systems, equipment and cleanrooms as coordinator or expert (e. g. preparation of change requests, P I diagrams and system function descriptions, approval of plans and reports, etc. ) . reports etc. ) Processing of complex, cross-departmental or cross-functional projects in the role of a Subject Matter Expert, taking into account the requirements of the [. .. ] engineering with professional experience alternatively completed Bachelors degree in biotechnology or process engineering with relevant professional experience Very good knowledge of English Nice to Have: Experience in change management and device qualification In-depth, conceptual knowledge in a specialized field as an expert or coach 76323398 [. .. ]
Job am 25.12.2025 bei Neuvoo gefunden
West Pharmaceutical Services
Coordinator, Laboratory
• Stolberg (Rhineland) , North Rhine- Westphalia Stolberg (Rhineland)
[. .. ] project management organization. Self-reliant, diligent, flexible (with working time to fulfill requirements of a global role) . Clear communication (fluent in written and verbal English required) . [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Background in medical device or pharmaceutical industry. Knowledge of lean manufacturing and operational excellence concepts. Able to comply with the companys safety policy at all times. Able to comply with the companys quality policy at all times. Travel Requirements 5: Up to 13 business days per year Physical Requirements Sedentary-Exerting up to 10lbs/ [. .. ]
Job am 09.12.2025 bei Neuvoo gefunden
Rivian
Sr. Administrative Assistant II
• Berlin
[. .. ] discretion and integrity. Anticipate the needs of the Berlin team, resolving operational and administrative issues before they arise. Qualifications Experience: 3+ years of experience in an administrative, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] executive assistant, or coordinator role, preferably within a fast-paced tech company or startup environment. Organizational Prowess: Exceptional organizational and time-management skills with a proven ability to manage multiple priorities and deadlines without sacrificing attention to detail. Tech-Savvy: High proficiency with modern office tools, including Google Workspace (Gmail, Calendar, Docs, Sheets) . [. .. ] equity. In addition, our benefits package has been designed to support the health and wellness of our employees. Benefit offerings include Flex Time Off, retirement savings plans as well as medical, vision and dental coverage. For more information on RV Techs comprehensive benefits package for full-time employees, check out our Global Benefits Site. External candidates can apply for this role through the RV Tech Careers site (https:/ / rivianvw. tech/ #careers) . If you are a current employee, please [. .. ] laws) when you apply for employment and/or participate in our recruitment processes (Candidate Personal Data) . This data includes contact, demographic, communications, educational, professional, employment, social media/ website, network/ device, recruiting system usage/ interaction, security and preference information. Rivian and Volkswagen Group Technologies may use your Candidate Personal Data for the purposes of (i) tracking interactions with our recruiting system; (ii) carrying out, analyzing and improving our application and recruitment process, including assessing you and your application and conducting employment, [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Medical device coordinator pro Jahr?
Als Medical device coordinator verdient man zwischen EUR 45.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Medical Device Coordinator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 12 offene Stellenanzeigen für Medical Device Coordinator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Medical Device Coordinator Jobs?
Aktuell suchen 6 Unternehmen nach Bewerbern für Medical Device Coordinator Jobs.
Welche Unternehmen suchen nach Bewerbern für Medical Device Coordinator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Medical Device Coordinator Stellenangebote:
- IQVIA (1 Job)
- GULP experts united (1 Job)
- West Pharmaceutical Services (1 Job)
- Rivian (1 Job)
In welchen Bundesländern werden die meisten Medical Device Coordinator Jobs angeboten?
Die meisten Stellenanzeigen für Medical Device Coordinator Jobs werden derzeit in Bayern (4 Jobs), Rheinland-Pfalz (2 Jobs) und Saarland (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Medical Device Coordinator Jobs?
Medical Device Coordinator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
