29 Jobs für Laboratory Medicine Expert
Stellenangebote Laboratory Medicine Expert Jobs
Job vor 2 Tagen bei Jooble gefunden
• Kemnath
[. .. ] leading global medical technology company. An estimated 5 million patients across the globe benefit every day from our innovative technologies and services in the areas of diagnostic [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and therapeutic imaging, laboratory diagnostics and molecular medicine, as well as digital health and enterprise services. care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. Setting up a profile lets us know you are interested in career opportunities with us and makes it easy for us to send you [. .. ]
Job vor 2 Tagen bei Jooble gefunden
Design Quality Assurance Expert
• Kemnath
[. .. ] leading global medical technology company. An estimated 5 million patients across the globe benefit every day from our innovative technologies and services in the areas of diagnostic [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and therapeutic imaging, laboratory diagnostics and molecular medicine, as well as digital health and enterprise services. care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. Setting up a profile lets us know you are interested in career opportunities with us and makes it easy for us to send you [. .. ]
Job vor 3 Tagen bei Jooble gefunden
• Forchheim, Landkreis Forchheim
Führungs-/ Leitungspositionen
[. .. ] stroke, and cancer. Then come and join our global team as Head of Medical Affairs Cardiovascular Care (f/m/d) . Medical Scientific Leadership : Serve as the global [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] medical expert for Cardiovascular Care; Develop, align and execute cross Healthineers medical affairs strategy for Cardiovascular Care; Ensure medical accuracy and scientific integrity across all internal and external communications. External Engagement KOL Management : Build and maintain strong relationships with global and regional Key Opinion Leaders; Drive advocacy for guidelines and reimbursement [. .. ] affairs team; Establish medical governance processes, including review of promotional and non-promotional materials. Ensure compliance with global regulations, industry codes, and company policies. You have a university degree in medicine, life sciences, or a related field (MD, Ph D, Pharm D, or equivalent preferred) in Cardiovascular Care You have many years of senior experience in Medical Affairs, clinical research, or related roles within the Med Tech or healthcare industry You have a proven track record in evidence generation, clinical study oversight, and regulatory [. .. ] leading global medical technology company. An estimated 5 million patients across the globe benefit every day from our innovative technologies and services in the areas of diagnostic and therapeutic imaging, laboratory diagnostics and molecular medicine, as well as digital health and enterprise services. care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. Setting up a profile lets us know you are interested in career opportunities with us and makes it easy for [. .. ]
Job vor 3 Tagen bei Jooble gefunden
Head of Medical Affairs-Cardiovascular Care (f/m/d)
• Forchheim, Landkreis Forchheim
Führungs-/ Leitungspositionen
[. .. ] come and join our global team as Head of Medical Affairs Cardiovascular Care (f/m/d) . Your tasks and responsibilities: Medical Scientific Leadership : Serve as the global [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] medical expert for Cardiovascular Care; Develop, align and execute cross Healthineers medical affairs strategy for Cardiovascular Care; Provide clinical input on product strategy, clinical value propositions, and innovation priorities. Ensure medical accuracy and scientific integrity across all internal and external communications. Clinical Evidence : Lead clinical evidence generation strategies; Oversee clinical studies, [. .. ] with global regulations, industry codes, and company policies. To find out more about the specific business, have a look at Your qualifications and experience: You have a university degree in medicine, life sciences, or a related field (MD, Ph D, Pharm D, or equivalent preferred) in Cardiovascular Care You have many years of senior experience in Medical Affairs, clinical research, or related roles within the Med Tech or healthcare industry You have Clinical training or a strong background in Cardiovascular Care. You have [. .. ] shape the future of healthcare. An estimated 5 million patients across the globe benefit every day from our innovative technologies and services in the areas of diagnostic and therapeutic imaging, laboratory diagnostics and molecular medicine, as well as digital health and enterprise services. Our culture: Our culture embraces different perspectives, open debate, and the will to challenge convention. Change is a constant aspect of our work. We aspire to lead the change in our industry rather than just react to it. [. .. ]
Job vor 4 Tagen bei Jooble gefunden
• Kemnath
[. .. ] leading global medical technology company. An estimated 5 million patients across the globe benefit every day from our innovative technologies and services in the areas of diagnostic [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and therapeutic imaging, laboratory diagnostics and molecular medicine, as well as digital health and enterprise services. care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. Setting up a profile lets us know you are interested in career opportunities with us and makes it easy for us to send you [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Design Quality Assurance Expert (m/w/d)
• Kemnath
[. .. ] leading global medical technology company. An estimated 5 million patients across the globe benefit every day from our innovative technologies and services in the areas of diagnostic [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and therapeutic imaging, laboratory diagnostics and molecular medicine, as well as digital health and enterprise services. care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. Setting up a profile lets us know you are interested in career opportunities with us and makes it easy for us to send you [. .. ]
Job vor 4 Tagen bei Jooble gefunden
• Forchheim, Landkreis Forchheim
[. .. ] to this cause. It reflects their pioneering spirit combined with our long history of engineering in the ever-evolving healthcare industry. Then come and join our global team [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as Scientific Expert (f/m/d) for clinical applications in Computed Tomography. You will assist in the preliminary development of physical algorithms and concepts for CT (computed tomography) and support their implementation in our software framework. Together with clinical partners, you will design and create studies and reports for the approval of medical [. .. ] leading global medical technology company. An estimated 5 million patients across the globe benefit every day from our innovative technologies and services in the areas of diagnostic and therapeutic imaging, laboratory diagnostics and molecular medicine, as well as digital health and enterprise services. care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. Setting up a profile lets us know you are interested in career opportunities with us and makes it easy for us to send you [. .. ]
Job vor 5 Tagen bei Jooble gefunden
Senior IT SAP Governance Professional (f/m/d)
• Erlangen
[. .. ] Article 21 must be fulfilled too. Within Co E SAP, the department CAS (Compliance, Authorization Security) proactively governs, monitors consult regarding SAP Quality, Compliance Audit towards business [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and IT by providing expert knowledge, defined frameworks innovative tool sets to safeguard SAP systems integrity security. Quality Compliance are accountable for the strategic and operational performance of the CAS department, ensuring the successful delivery of business strategy and operational goals to exceed customer expectations for product/ process quality, cost, and delivery while facilitating continuous [. .. ] shape the future of healthcare. An estimated 5 million patients across the globe benefit every day from our innovative technologies and services in the areas of diagnostic and therapeutic imaging, laboratory diagnostics and molecular medicine, as well as digital health and enterprise services. Our culture: Our culture embraces different perspectives, open debate, and the will to challenge convention. Change is a constant aspect of our work. We aspire to lead the change in our industry rather than just react to it. Thats why we invite [. .. ]
Neu Job vor 6 Std. bei Jobleads gefunden
Head of Medical Affairs-Cardiovascular Care (f/m/d)
• Forchheim, Bayern
Führungs-/ Leitungspositionen
[. .. ] Then come and join our global team as Head of Medical Affairs Cardiovascular Care (f/m/d) . Overview Responsibilities: Responsibilities Medical Scientific Leadership : Serve as the global [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] medical expert for Cardiovascular Care; Develop, align and execute cross Healthineers medical affairs strategy for Cardiovascular Care; Provide clinical input on product strategy, clinical value propositions, and innovation priorities. Ensure medical accuracy and scientific integrity across all internal and external communications. Clinical Evidence : Lead clinical evidence generation strategies; Oversee clinical studies, [. .. ] team; Establish medical governance processes, including review of promotional and non-promotional materials. Ensure compliance with global regulations, industry codes, and company policies. Qualifications: You have a university degree in medicine, life sciences, or a related field (MD, Ph D, Pharm D, or equivalent preferred) in Cardiovascular Care You have many years of senior experience in Medical Affairs, clinical research, or related roles within the Med Tech or healthcare industry You have Clinical training or a strong background in Cardiovascular Care. You have [. .. ] shape the future of healthcare. An estimated 5 million patients across the globe benefit every day from our innovative technologies and services in the areas of diagnostic and therapeutic imaging, laboratory diagnostics and molecular medicine, as well as digital health and enterprise services. Our culture: Our culture embraces different perspectives, open debate, and the will to challenge convention. Change is a constant aspect of our work. We aspire to lead the change in our industry rather than just react to it. [. .. ]
Neu Job vor 6 Std. bei Jobleads gefunden
Head of Medical Affairs-Cardiovascular Care (f/m/d)
• Forchheim, Bayern
Führungs-/ Leitungspositionen
[. .. ] Then come and join our global team as Head of Medical Affairs Cardiovascular Care (f/m/d) . Your tasks and responsibilities Medical Scientific Leadership: Serve as the global [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] medical expert for Cardiovascular Care; Develop, align and execute cross Healthineers medical affairs strategy for Cardiovascular Care; Provide clinical input on product strategy, clinical value propositions, and innovation priorities. Ensure medical accuracy and scientific integrity across all internal and external communications. Clinical Evidence: Lead clinical evidence generation strategies; Oversee clinical studies, research [. .. ] and company policies. To find out more about the specific business, have a look at the relevant products and services. Your qualifications and experience You have a university degree in medicine, life sciences, or a related field (MD, Ph D, Pharm D, or equivalent preferred) in Cardiovascular Care You have many years of senior experience in Medical Affairs, clinical research, or related roles within the Med Tech or healthcare industry You have Clinical training or a strong background in Cardiovascular Care. You have [. .. ] shape the future of healthcare. An estimated 5 million patients across the globe benefit every day from our innovative technologies and services in the areas of diagnostic and therapeutic imaging, laboratory diagnostics and molecular medicine, as well as digital health and enterprise services. Our culture Our culture embraces different perspectives, open debate, and the will to challenge convention. Change is a constant aspect of our work. We aspire to lead the change in our industry rather than just react to it. [. .. ]
Neu Job vor 6 Std. bei Jobleads gefunden
• München, Bayern
[. .. ] a Project Manager for our EU CRO Pre-clinical Department, based in our offices in Munich (KLIFOVET Gmb H) . KLIFOVET Gmb H, part of Argenta, is an [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] internationally recognised provider of expert services in the veterinary medicine and animal feed sector based in Munich. We support our customers from the idea, through development, to approval and beyond. Service for our customers determines our actions. Founded in 1997, we are considered as a global leader in animal health product development. Argenta and KLIFOVET have been awarded multiple times [. .. ] a: Position Project Manager Pre-Clinical Studies (m/f/x) Full-time Your tasks Complying with the responsibilities as defined by VICH GCP (Veterinary Good Clinical Practice) , GLP (Good Laboratory Practice) , and all applicable regulatory requirements Advising clients on study design and placement of GCP/ GLP field and laboratory studies in Europe and internationally Building, coordinating and leading multidisciplinary teams across individual studies, including selection and training of investigators, study set-up activities, among others Monitor activities during the [. .. ]
Neu Job vor 6 Std. bei Jobleads gefunden
Lead Mechatronics Engineer: Next-Generation Live-Cell AFM Nano-Imaging
• Zürich Zuerich
Führungs-/ Leitungspositionen
Lead Mechatronics Engineer: Next-Generation Live-Cell AFM Nano-Imaging The
Laboratory of Molecular
Medicine, led by Prof. Yohei Yamauchi, is developing the Vi Vi D-AFM V2.0 a next-generation nano-imaging system. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] This project focuses on transitioning from academic prototypes to commercial-grade industrial systems while ensuring complete IP independence from legacy V1.0 patents. Project background The Laboratory of Molecular Medicine, led [. .. ] sub-nanometer control systems and high-precision scanning devices. Specialized Mechatronics: Substantial track record in the physical realization of high-speed AFM hardware specifically for soft cell surfaces. Control Systems: Expert-level knowledge of sub-nanometer control systems, exceeding the scope of generic mechatronics. Collaborative Design: Proven ability to work in tight technical tandem with architects to solve complex system integration problems. Academic/ Industrial Background: Experience in high-precision scanning mechanisms and a history of research-to-industry transition. Technical Synchronization: [. .. ]
Job gestern bei Jobleads gefunden
• Zürich Zuerich
Führungs-/ Leitungspositionen
The
Laboratory of Molecular
Medicine, led by Prof. Yohei Yamauchi, is developing the Vi Vi D-AFM V2.0a next-generation nano-imaging system. This project focuses on transitioning from academic prototypes [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to commercial-grade industrial systems while ensuring complete IP independence from legacy V1.0 patents. Project background The Laboratory of Molecular Medicine, led by [. .. ] sub-nanometer control systems and high-precision scanning devices. Specialized Mechatronics: Substantial track record in the physical realization of high-speed AFM hardware specifically for soft cell surfaces. Control Systems: Expert-level knowledge of sub-nanometer control systems, exceeding the scope of generic mechatronics. Collaborative Design: Proven ability to work in tight technical tandem with architects to solve complex system integration problems. Academic/ Industrial Background: Experience in high-precision scanning mechanisms and a history of research-to-industry transition Technical Synchronization: [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Senior IT SAP Governance Professional (f/m/d)
[. .. ] Article 21 must be fulfilled too. Within Co E SAP, the department CAS (Compliance, Authorization Security) proactively governs, monitors consult regarding SAP Quality, Compliance Audit towards business [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and IT by providing expert knowledge, defined frameworks innovative tool sets to safeguard SAP systems integrity security. Quality Compliance are accountable for the strategic and operational performance of the CAS department, ensuring the successful delivery of business strategy and operational goals to exceed customer expectations for product/ process quality, cost, and delivery while facilitating continuous [. .. ] shape the future of healthcare. An estimated 5 million patients across the globe benefit every day from our innovative technologies and services in the areas of diagnostic and therapeutic imaging, laboratory diagnostics and molecular medicine, as well as digital health and enterprise services. Our culture Our culture embraces different perspectives, open debate, and the will to challenge convention. Change is a constant aspect of our work. We aspire to lead the change in our industry rather than just react to it. That s why we [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
• Erlangen, Bayern
[. .. ] Article 21 must be fulfilled too. Within Co E SAP, the department CAS (Compliance, Authorization Security) proactively governs, monitors consult regarding SAP Quality, Compliance Audit towards business [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and IT by providing expert knowledge, defined frameworks innovative tool sets to safeguard SAP systems integrity security. Quality Compliance are accountable for the strategic and operational performance of the CAS department, ensuring the successful delivery of business strategy and operational goals to exceed customer expectations for product/ processquality, cost, and delivery while facilitating continuous improvement. [. .. ] shape the future of healthcare. An estimated 5 million patients across the globe benefit every day from our innovative technologies and services in the areas of diagnostic and therapeutic imaging, laboratory diagnostics and molecular medicine, as well as digital health and enterprise services. Our culture: Our culture embraces different perspectives, open debate, and the will to challenge convention. Change is a constant aspect of our work. We aspire to lead the change in our industry rather than just react to it. Thats why we invite [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Global Trial Associate (GTA) - Global Clinical Operations Leadership Development Program 2026
• Neuss, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] expertise in Innovative Medicine and Med Tech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https:/ / Job Function Job Function: R D Operations Job Sub Function: Clinical Trial Support Job Category: Professional [. .. ] leadership, and negotiating skills. Excellent organizational skills and the ability to collaborate and handle multiple priorities within a matrix environment. Ability to perform activities in a timely and accurate manner. Expert proficiency with Word, Power Point, Excel. Travel While in the Site Manager rotation, approximately 25 travel. Skills Required Skills: Analytical Reasoning, Business Behavior, Business English, Clinical Data Management, Clinical Trials, Clinical Trials Operations, Execution Focus, Issue Escalation, Laboratory Operations, Process Improvements, Process Oriented, Project Support, Regulatory Environment, Research and Development, Research Ethics, Study Management, Time Management #J-18808-Ljbffr 79020126 [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Senior IT SAP Governance Professional (f/m/d)
• Erlangen, Bayern
[. .. ] Article 21 must be fulfilled too. Within Co E SAP, the department CAS (Compliance, Authorization Security) proactively governs, monitors consult regarding SAP Quality, Compliance Audit towards business [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and IT by providing expert knowledge, defined frameworks innovative tool sets to safeguard SAP systems integrity security. Quality Compliance are accountable for the strategic and operational performance of the CAS department, ensuring the successful delivery of business strategy and operational goals to exceed customer expectations for product/ process quality, cost, and delivery while facilitating continuous [. .. ] shape the future of healthcare. An estimated 5 million patients across the globe benefit every day from our innovative technologies and services in the areas of diagnostic and therapeutic imaging, laboratory diagnostics and molecular medicine, as well as digital health and enterprise services. Our culture Our culture embraces different perspectives, open debate, and the will to challenge convention. Change is a constant aspect of our work. We aspire to lead the change in our industry rather than just react to it. Thats why we invite [. .. ]
Job am 24.01.2026 bei Jobleads gefunden
(Junior) Expert Biocompatibility (m/f/d) Fixed-Term (2 Years)
• Sankt Wendel, Saarland
Absolventen, Einsteiger, Trainees
[. .. ] also manages regulatory and quality data governance and provides critical product-related business services across global operations. Join our passionate team and help shape healthcare worldwide In your [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] roleas (Junior) Expert Biocompatibility (m/f/d) you willbe responsible forbiocompatibilityevaluation of medical devices in the framework of Regulation (EU) 2017/ 745 on medical devices (MDR) , ISO 10993-seriesand other regulatory guidelines/ requirements. Yourtasks Support Performance of safety and risk assessments for medical devicesbasedon the used raw materials, on extractable and leachable [. .. ] in internal and externallaboratories Ensure sufficient support ofbiocompatibilityprojects and coordinate how to apply overarching strategies Align sampling and testing strategies and support productresponsibleshow to apply these Coordinate global alignment of laboratory partners (internal and external) as well as methods applied Overall responsibility for theassignedproduct groups and relatedbiocompatibility files Contribute to supplier agreements and specifications for biocompatibility requirements as well as materialselection Observe upcoming regulation changes and ensuretimelyimplementation considering state-of-the artmethodology Yourprofile Successfully completed bachelors ormastersdegree in scientific or engineering [. .. ] are an expert and how much experience you have-all dedicated to your professional journey. Whether in front of or behind the scenes-you are helping to make ever better medicine available to more and more people around the world Individual opportunities for self-determined career planning and professional development A corporate culture in which there is enough room for innovative thinking-to find the best solution together, not the quickest one A large number of committed people with a wide [. .. ]
Job am 24.01.2026 bei Jobleads gefunden
• Sankt Wendel, Saarland
Beratungs-/ Consultingtätigkeiten
[. .. ] and quality data governance and provides critical product-related business services across global operations. Join our passionate team and help shape healthcare worldwide Your role In your role [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as (Senior) Expert Biocompatibility (m/f/d) you will be responsible for biocompatibility evaluation of medical devices in the framework of Regulation (EU) 2017/ 745 on medical devices (MDR) , ISO 10993-series and other regulatory guidelines/ requirements. Your responsibilities Performance of safety and risk assessments for medical devices based on the used [. .. ] Ensure sufficient support of biocompatibility projects and coordinate how to apply overarching strategies Align sampling and testing strategies and support product responsibles how to apply these Coordinate global alignment of laboratory partners (internal and external) as well as methods applied Overall responsibility for the assigned product groups and related biocompatibility files Contribute to supplier agreements and specifications for biocompatibility requirements as well as material selection Observe upcoming regulation changes and ensure timely implementation considering state-of-the art methodology Your profile [. .. ] are an expert and how much experience you have-all dedicated to your professional journey. Whether in front of or behind the scenes-you are helping to make ever better medicine available to more and more people around the world Individual opportunities for self-determined career planning and professional development A corporate culture in which there is enough room for innovative thinking-to find the best solution together, not the quickest one A large number of committed people with a wide [. .. ]
Job am 23.01.2026 bei Jobleads gefunden
(Junior) Expert Biocompatibility (m/f/d) Fixed-Term (2 Years)
• Bad Homburg vor der Höhe, Hessen
Absolventen, Einsteiger, Trainees
[. .. ] also manages regulatory and quality data governance and provides critical product-related business services across global operations. Join our passionate team and help shape healthcare worldwide In your [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] role as (Junior) Expert Biocompatibility (m/f/d) you will be responsible for biocompatibility evaluation of medical devices in the framework of Regulation (EU) 2017/ 745 on medical devices (MDR) , ISO 10993-series and other regulatory guidelines/ requirements. Your tasks Support Performance of safety and risk assessments for medical devices based on the [. .. ] Ensure sufficient support of biocompatibility projects and coordinate how to apply overarching strategies Align sampling and testing strategies and support product responsibles how to apply these Coordinate global alignment of laboratory partners (internal and external) as well as methods applied Overall responsibility for the assigned product groups and related biocompatibility files Contribute to supplier agreements and specifications for biocompatibility requirements as well as material selection Observe upcoming regulation changes and ensure timely implementation considering state-of-the art methodology # Your [. .. ] are an expert and how much experience you have-all dedicated to your professional journey. Whether in front of or behind the scenes-you are helping to make ever better medicine available to more and more people around the world Individual opportunities for self-determined career planning and professional development A corporate culture in which there is enough room for innovative thinking-to find the best solution together, not the quickest one A large number of committed people with a wide [. .. ]
Job am 22.01.2026 bei Jobleads gefunden
(Senior) Expert Biocompatibility (m/f/d)
• Bad Homburg vor der Höhe, Hessen
Beratungs-/ Consultingtätigkeiten
[. .. ] also manages regulatory and quality data governance and provides critical product-related business services across global operations. Join our passionate team and help shape healthcare worldwide In your [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] roleas (Senior) Expert Biocompatibility (m/f/d) you willbe responsible forbiocompatibilityevaluation of medical devices in the framework of Regulation (EU) 2017/ 745 on medical devices (MDR) , ISO10993-series and other regulatory guidelines/ requirements. Yourtasks Performance of safety and risk assessments for medical devices based on the used raw materials, on extractable and [. .. ] Ensure sufficient support of biocompatibility projects and coordinate how to apply overarching strategies Align sampling and testing strategies and support product responsible show to apply these Coordinate global alignment of laboratory partners (internal and external) as well as methods applied Overall responsibility for the assigned product groups and related biocompatibility files Contribute to supplier agreements and specifications for biocompatibility requirements as well as material selection Observe upcoming regulation changes and ensure timely implementation considering state-of-the art methodology Yourprofile Successfully [. .. ] are an expert and how much experience you have-all dedicated to your professional journey. Whether in front of or behind the scenes-you are helping to make ever better medicine available to more and more people around the world Individual opportunities for self-determined career planning and professional development A corporate culture in which there is enough room for innovative thinking-to find the best solution together, not the quickest one A large number of committed people with a wide [. .. ]
Job am 22.01.2026 bei Jobleads gefunden
(Senior) Expert Biocompatibility (m/f/d)
• Bad Homburg vor der Höhe, Hessen
Beratungs-/ Consultingtätigkeiten
[. .. ] also manages regulatory and quality data governance and provides critical product-related business services across global operations. Join our passionate team and help shape healthcare worldwide In your [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] role as (Senior) Expert Biocompatibility (m/f/d) you will be responsible for biocompatibility evaluation of medical devices in the framework of Regulation (EU) 2017/ 745 on medical devices (MDR) , ISO 10993-series and other regulatory guidelines/ requirements. # Your tasks Performance of safety and risk assessments for medical devices based on [. .. ] Ensure sufficient support of biocompatibility projects and coordinate how to apply overarching strategies Align sampling and testing strategies and support product responsibles how to apply these Coordinate global alignment of laboratory partners (internal and external) as well as methods applied Overall responsibility for the assigned product groups and related biocompatibility files Contribute to supplier agreements and specifications for biocompatibility requirements as well as material selection Observe upcoming regulation changes and ensure timely implementation considering state-of-the art methodology # [. .. ] are an expert and how much experience you have-all dedicated to your professional journey. Whether in front of or behind the scenes-you are helping to make ever better medicine available to more and more people around the world Individual opportunities for self-determined career planning and professional development A corporate culture in which there is enough room for innovative thinking-to find the best solution together, not the quickest one A large number of committed people with a wide [. .. ]
Job am 13.12.2025 bei Jobleads gefunden
Senior Machine Learning Engineer-AI Integration Engineer
• Berlin
Homeoffice möglich
[. .. ] for clinical and healthcare applications. The company addresses a fundamental challenge in modern healthcare: the need for objective, scalable, and accessible movement diagnostics. Traditional gait and movement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] analysis requires expensive laboratory equipment, specialized facilities, and expert personnelcreating barriers to widespread clinical adoption and limiting access for patients who would benefit most. LINDERA transforms movement analysis through smartphone-based 3D motion tracking technology. Using proprietary AI algorithms, the companys platform analyzes gait parameters and movement patterns through standard smartphone cameras, eliminating the need for specialized hardware while [. .. ] in 3D Motion Tracking, we set global standards in Mobility Assessment and Decision Intelligence. You will not only work with a unique product but also contribute to transforming care and medicine through our innovative technology. Effective Structures and Open Communication We operate in a taskoriented manner with a flat hierarchy, allowing us to quickly adapt and fully leverage our teams potential. Our open communication fosters collaboration across all departments, ensuring that our products thrive on the collective expertise and ideas of [. .. ]
Job am 07.12.2025 bei Jobleads gefunden
Senior Medical Director, Early Clinical Development
• Morges, Waadt
Führungs-/ Leitungspositionen
[. .. ] Functions Of The Job (Key Responsibilities) Leads development efforts for assets post-candidate selection through first in human trials, including early dose escalation, safety and tolerability evaluation, dose [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] selection, translational medicine (proof of mechanism studies) and proof of concept studies in human (ph 1 or 2) . Participates in asset/ portfolio strategies and prioritization, internal and external messaging, governance, and cross-functional interface with all key stakeholders, including translational science, clinical pharmacology and pharmacometrics, discovery organization, regulatory and others. Provides medical [. .. ] product development including clinical study protocol, informed consents, CRFs, CSRs, meeting abstracts, scientific journal publications, strategy documents and project plans. Collaborates with external vendors such as CROs, external imaging and laboratory vendors for successful implementation and conduct of early phase clinical studies. Represents Incyte Corporation at key national and international medical and scientific meetings including participation in advisory boards with key opinion leaders. Detects and analyzes emergent issues during early clinical drug development and develops and implements mitigating strategies. Works in [. .. ] development of anticancer agents. Provides guidance for successful implementation and accomplishment of investigator-initiated trials related to product development and life cycle management of a compound. Acts as subject matter expert for business development activities Professional Competencies Business Insights MD, MD-Ph D. Hematology-oncology board certification is preferred. Training in research (wet lab) , proven track record of self-directed scientific work (e. g. , post doc, peer reviewed publications as first author) preferred. Experience in early drug development required with [. .. ]
Job am 16.11.2025 bei Jobleads gefunden
Analytical Method Expert (Associate Director AS T Lifecycle Management)
• Mainz, Rheinland- Pfalz
Führungs-/ Leitungspositionen
Press Tab to Move to Skip to Content Link Select how often (in days) to receive an alert: Analytical Method
Expert (Associate Director AS T Lifecycle Management) Mainz, Germany; [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Gaithersburg, US full time Job ID:9405 As Analytical Method Expert (Associate Director AS T Lifecycle Management) , you will be making a meaningful contribution to the ongoing product development and regulatory submission (BLA/ MAA) of our RNA and Protein-based therapeutic pipeline [. .. ] standards and in accordance with relevant industry guidelines Responsible for method validation and transfer strategies as well as method lifecycle activities (e. g. exchange of critical reagents, method performance and laboratory investigations) Participate in strategic and technical discussions within projects cross-functionally with CMC team members and external partners Evaluation and review of technical and regulatory submission documents in a timely manner for the approval and market launch of development products Act as analytical SME by providing expert knowledge for regulatory [. .. ] part of #Team Bio NTech. Bio NTech, the story At Bio NTech, we are more than just a biotechnology company we are a community of innovators, scientists, and leaders dedicated to revolutionizing medicine by translating cuttingedge science into survival. Your contributions here have the potential to improve the health of people worldwide, especially by addressing diseases with high medical needs like cancer and various infectious diseases. Experience a dynamic workplace that embraces diversity in all its forms. We foster innovation, encouragecreativity, and develop [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Laboratory medicine expert pro Jahr?
Als Laboratory medicine expert verdient man zwischen EUR 50.000,- bis EUR 90.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Laboratory Medicine Expert Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 29 offene Stellenanzeigen für Laboratory Medicine Expert Jobs.
In welchen Bundesländern werden die meisten Laboratory Medicine Expert Jobs angeboten?
Die meisten Stellenanzeigen für Laboratory Medicine Expert Jobs werden derzeit in Bayern (5 Jobs), Saarland (5 Jobs) und Baden-Württemberg (4 Jobs) angeboten.
Zu welchem Berufsfeld gehören Laboratory Medicine Expert Jobs?
Laboratory Medicine Expert Jobs gehören zum Berufsfeld Laboranten / technische Assistenten.
