53 Jobs für Biomedical Expert
Stellenangebote Biomedical Expert Jobs
Neu Job vor 4 Std. bei StepStone gefunden
ZEISS
• Oberkochen (Baden- Württemberg)
Teilzeit
[. .. ] will allow you create the ideal con-ditions for your future career. In a spacious modern setting full of opportunities for further development, ZEISS employees work in a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] place where expert knowledge and team spirit reign supreme. All of this is supported by a special ownership structure and the long-term goal of the Carl Zeiss Foundation: to bring science and society into the future together. Join us today. Inspire people tomorrow. Diversity is a part of ZEISS. We look forward [. .. ] skills and passion to tackle open real-world challenges. Work on potential AI and/or digital twin features for future medical devices Design solutions for computer vision problems towards advanced biomedical visualisations Evaluate and refine your approach on real-world data Build proof-of-principle demonstrators test your solution with product management and our clinical partners Work closely in an interdisciplinary team of AI Digital Twin experts and application experts Participate in lively student community at ZEISS Enrolled in a bachelor/ [. .. ]
Job gestern bei Mindmatch.ai gefunden
Roche
Clinical Evaluation Manager-Freelancer (m/f/d)
• AT- 9 Wien
Freiberuflich
[. .. ] activities for my Sugr/ Roche products, including systematic literature reviews, data appraisal, and the authoring of regulatory-compliant Clinical Evaluation Reports (CERs) to demonstrate device safety and performance. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] You will provide expert medical input to medical risk management and vigilance across the full product lifecycle, from development to post-market. Additionally, you will be responsible for facilitating team backlog grooming and prioritisation of deliverables to ensure efficient, scalable working practices. Essential skills for your mission: Experience: 13 years of experience with regulatory/ CER writing for medical devices or in vitro diagnostics Education: Advanced degree (e. g. , MSc, Ph D, MD, Pharm D, etc) in medicine, life sciences, pharmacology, biomedical engineering, biostatistics/ epidemiology or other related fields Skills and Competencies: Strong analytical and problemsolving skills; Excellent written and verbal communication skills in English; Detailoriented with the ability to manage multiple tasks and deadlines; Capability to make riskbased decisions Technical Proficiency: Basic understanding of clinical research and biostatistics; Proficiency in Google [. .. ]
Job gestern bei Mindmatch.ai gefunden
F. Hoffmann- La Roche Gruppe
• AT- 9 Wien
Freiberuflich
[. .. ] evaluation activities for my Sugr/ Roche products, including systematic literature reviews, data appraisal, and the authoring of regulatorycompliant Clinical Evaluation Reports (CERs) to demonstrate device safety and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] performance. You will provide expert medical input to medical risk management and vigilance across the full product lifecycle, from development to postmarket. Additionally, you will be responsible for facilitating team backlog grooming and prioritisation of deliverables to ensure efficient, scalable working practises. Essential skills for your mission: Experience: 1-3 years of experience with regulatory/ CER writing for medical devices or in vitro diagnostics Education: Advanced degree (e. g. , MSc, Ph D, MD, Pharm D, etc) in medicine, life sciences, pharmacology, biomedical engineering, biostatistics/ epidemiology or other related fields Skills and Competencies: Strong analytical and problemsolving skills Excellent written and verbal communication skills in English Detailoriented with the ability to manage multiple tasks and deadlines Capability to make riskbased decisions Technical Proficiency: Basic understanding of clinical research and biostatistics Proficiency in Google [. .. ]
Job gestern bei Mindmatch.ai gefunden
F. Hoffmann- La Roche AG
Clinical Evaluation Manager-Freelancer (m/f/d)
• AT- 9 Wien
Freiberuflich
[. .. ] activities for my Sugr/ Roche products, including systematic literature reviews, data appraisal, and the authoring of regulatory-compliant Clinical Evaluation Reports (CERs) to demonstrate device safety and performance. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] You will provide expert medical input to medical risk management and vigilance across the full product lifecycle, from development to post-market. Additionally, you will be responsible for facilitating team backlog grooming and prioritisation of deliverables to ensure efficient, scalable working practises. Essential skills for your mission: Experience: + 1-3 years of experience with regulatory/ CER writing for medical devices or in vitro diagnostics Education: + Advanced degree (e. g. , MSc, Ph D, MD, Pharm D, etc) in medicine, life sciences, pharmacology, biomedical engineering, biostatistics/ epidemiology or other related fields Skills and Competencies: + Strong analytical and problem-solving skills + Excellent written and verbal communication skills in English + Detail-oriented with the ability to manage multiple tasks and deadlines + Capability to make risk-based decisions Technical Proficiency: + Basic understanding [. .. ]
Job vor 13 Tagen bei Mindmatch.ai gefunden
Medtronic plc
• AT- 9 Wien
[. .. ] and attending meetings with key hospital stakeholders to track progress and ensure smooth implementation. Support the coordination of surgeon training programs, including scheduling off-site training sessions and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] arranging for expert guidance during their initial cases. Help develop training plans for hospital staff, ensuring they receive the necessary education and hands-on support to confidently use the robotic system. Gain hands-on experience by observing and assisting during robotic-assisted surgeries, supporting surgeons and staff as they become comfortable with the [. .. ] engineers (FSEs) and hospital teams to prepare operating rooms for robotic surgery. Track key project milestones and document the impact of the surgical robotics program. Qualifications : Bachelors degree in Biomedical Engineering or Medical Technology or other technical field. Fluent in English and German. Eager to learn and passionate about medical technology and surgical innovation. Strong communication and interpersonal skills, with the ability to work in a hospital environment and collaborate with healthcare professionals. Excellent problem-solving skills and a proactive [. .. ]
Job am 04.11.2025 bei Mindmatch.ai gefunden
Medtronic
Clinical Specialist Surgical Robotics (m/w/d) - DACH
• AT- 9 Wien
[. .. ] organizing and attending meetings with key hospital stakeholders to track progress and ensure smooth implementation. Support the coordination of surgeon training programs, including scheduling offsite training sessions [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and arranging for expert guidance during their initial cases. Help develop training plans for hospital staff, ensuring they receive the necessary education and handson support to confidently use the robotic system. Gain handson experience by observing and assisting during roboticassisted surgeries, supporting surgeons and staff as they become comfortable with the technology. Work alongside [. .. ] service engineers (FSEs) and hospital teams to prepare operating rooms for robotic surgery. Track key project milestones and document the impact of the surgical robotics program. Qualifications Bachelors degree in Biomedical Engineering or Medical Technology or another technical field. Fluent in English and German. Eager to learn and passionate about medical technology and surgical innovation. Strong communication and interpersonal skills, with the ability to work in a hospital environment and collaborate with healthcare professionals. Excellent problemsolving skills and a proactive attitude [. .. ]
Job am 14.09.2025 bei Jobleads gefunden
• Basel, Basel- Stadt
[. .. ] be based in London, Basel, Dublin or Barcelona. Major Accountabilities Leads the GCT, represents Clinical Development on the Global Program Team (GPT) May serve as the Clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Development Representative on Biomedical Research clinical/ project teams to drive transition of pre-Po C (Proof of Concept) projects to Development Decision Point (DDP) May support Business Development Licensing (BD L) activities Post-DDP, leads the development and execution of the clinical strategy. Develops an endorsed Integrated Development Plan (IDP) in line with the Target [. .. ] drug safety profile, including safety monitoring of clinical studies and signal detection from post-marketing surveillance. Serves as a core member of the Safety Management Team (SMT) As the medical expert, leads interactions with external stakeholders (e. g. , regulatory authorities, key opinion leaders, data monitoring committees, advisory boards, patient advocacy groups) , internal stakeholders (e. g. , Research, Translational Medicine, Global Medical Affairs (GMA) , Marketing, Health Economics Outcomes Research) , and internal decision boards. Minimum Requirements What youll bring [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Medical Science Liaison-Switzerland
• Zug
[. .. ] symposia and publication planning. Provide input to the Medical Affairs Manager and Medical Director to develop appropriate strategic and tactical plans (e. g. MAC) for the country. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Be the team expert on all aspects of the MSL role including: process improvements and sharing of best practice. Foster a collaborative working relationship with Medical Representatives and Commercial colleagues to ensure strategies and business plans are both patient and business focused. Work with the Swiss team to bring the voice of the fieldbased [. .. ] to Medical Information as per the Alnylam Adverse Event Reporting Policy. Qualifications Advanced academic background in a scientific or healthcarerelated field. A university degree in medicine, natural sciences, pharmacology, or biomedical sciences is required; an advanced degree (e. g. , Ph D or MD) is strongly preferred. Minimum of 2 years of experience in the healthcare industry or in a related role preferred; open to candidates with transferable skills. Ability to organize and prioritize own work schedule. Well developed social and relationship [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
• Ralingen, Rheinland- Pfalz
[. .. ] a strategic priority of the University of Luxembourg and is in a phase of ambitious development. This provides opportunities for broadening our research topics to include cuttingedge [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] trends in medical/ biomedical sciences. This strategic development requires additional expertise in teaching pharmacology in various fields (Medicine, Life sciences, Nursing, and Allied Health Professions) . About the role. . . You are an expert in Pharmacology/ Toxicology and will lead your own research group. Candidates applying computational tools (e. g. machine learning, artificial intelligence or other approaches) are also encouraged to apply. You will teach pharmacologyrelated courses in the Bachelors of Life Sciences, Medicine, Nursing, and Allied Health Professions, as well as in related [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Staff Machine Learning Engineer (dfm)
• Berlin
[. .. ] frameworks and systems for model training, evaluation and inference across different pathology applications. Consult : Guide the CTO office, product management and fellow engineering leads through complex [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] decisions by providing expert consultation on feasibility, architecture tradeoffs and risk mitigation strategies while ensuring alignment with our technical vision. Coordinate : Foster technical alignment across teams by establishing shared architectural principles and best practices, facilitating crossteam design reviews to enable consistent decisionmaking across domains. Lead : Champion technical excellence by leading strategic initiatives [. .. ] systems. Contribute to opensource projects and technical publications. Worked in a regulated environment e. g. financial services, aerospace or healthcare. Have knowledge of digital pathology or experience with working with biomedical data. Our offer Join a purposedriven startup. We are working collectively to fight cancer and improve patient outcomes. Come help us make a difference Cuttingedge AI research and development with involvement of Charit, TU Berlin and other partners. Work with a welcoming, diverse and highly international team of colleagues. Opportunity [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Clinical Evaluation Manager-Freelancer (m/f/d)
• Wien
Freiberuflich
[. .. ] evaluation activities for my Sugr/ Roche products, including systematic literature reviews, data appraisal, and the authoring of regulatorycompliant Clinical Evaluation Reports (CERs) to demonstrate device safety and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] performance. You will provide expert medical input to medical risk management and vigilance across the full product lifecycle, from development to postmarket. Additionally, you will be responsible for facilitating team backlog grooming and prioritisation of deliverables to ensure efficient, scalable working practises. Essential skills for your mission: Experience: 1-3 years of experience with regulatory/ CER writing for medical devices or in vitro diagnostics Education: Advanced degree (e. g. , MSc, Ph D, MD, Pharm D, etc) in medicine, life sciences, pharmacology, biomedical engineering, biostatistics/ epidemiology or other related fields Skills and Competencies: Strong analytical and problemsolving skills Excellent written and verbal communication skills in English Detailoriented with the ability to manage multiple tasks and deadlines Capability to make riskbased decisions Technical Proficiency: Basic understanding of clinical research and biostatistics Proficiency in Google [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Medical Device Clinical Safety Scientist-Bs
• Basel, Basel- Stadt
Homeoffice möglich
[. .. ] : PCS safety team approx. 6; cross-functional project teamsmembers Hiring Manager : Simone Melega Department : Portfolio Clinical Safety (PCS) , PDS Working Hours : Standard Tasks [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Responsibilities Provide expert leadership for all clinical safety and vigilance activities related to Class II/ III medical devices throughout the product lifecycle. Oversee the full medical device vigilance process, including intake, processing, assessment and timely submission of adverse events to regulatory authorities. Review key clinical investigation documents to ensure high-quality inclusion of [. .. ] regarding safety requirements in medical device clinical investigations. Must Haves Bachelors, Masters or Ph D in a scientific or medical discipline. Minimum 3 years of relevant experience in healthcare, scientific or biomedical research with exposure to clinical safety and the use of medical devices or combination products. Strong understanding of the technical and biomedical aspects of medical devices. Solid working knowledge of relevant medical device regulations and industry standards. Demonstrated hands-on experience in safety activities for Class II and/or III [. .. ]
Job gestern bei Jobleads gefunden
• Basel- Landschaft
[. .. ] holder is expected independently and strategically to lead the development of safety deliverables for MD clinical investigations. Contract duration : 6 months/ possible extension Location : Basel [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Responsibilities : Provide expert oversight and leadership for all clinical safety and vigilance activities for Class II and/or III Medical Devices (MD) , ensuring compliance with global regulations and internal standards throughout the product lifecycle. Manage and execute the MD vigilance process, including the intake, processing, assessment, and reporting of adverse events, ensuring [. .. ] site staff on clinical investigation safety requirements, particularly those outlined in ISO 14155. Requirements : Bachelor, Masters or Ph D within the scientific fields Min. 3 years relevant Healthcare, Scientific or biomedical research background in clinical safety-with the use of MDs and/or combination products in the Medical Device industry Strong understanding of the biomedical technical aspects of MDs. Working knowledge of relevant MD regulations and industry standards. MD clinical investigations expertise : significant expertise and handson experience in safety activities [. .. ]
Job gestern bei Jobleads gefunden
Clinical Evaluation Manager-Freelancer (m/f/d)
• Wien
Freiberuflich
[. .. ] activities for my Sugr/ Roche products, including systematic literature reviews, data appraisal, and the authoring of regulatory-compliant Clinical Evaluation Reports (CERs) to demonstrate device safety and performance. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] You will provide expert medical input to medical risk management and vigilance across the full product lifecycle, from development to post-market. Additionally, you will be responsible for facilitating team backlog grooming and prioritisation of deliverables to ensure efficient, scalable working practices. Essential skills for your mission: Experience: 13 years of experience with regulatory/ CER writing for medical devices or in vitro diagnostics Education: Advanced degree (e. g. , MSc, Ph D, MD, Pharm D, etc) in medicine, life sciences, pharmacology, biomedical engineering, biostatistics/ epidemiology or other related fields Skills and Competencies: Strong analytical and problemsolving skills; Excellent written and verbal communication skills in English; Detailoriented with the ability to manage multiple tasks and deadlines; Capability to make riskbased decisions Technical Proficiency: Basic understanding of clinical research and biostatistics; Proficiency in Google [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
[. .. ] the commercial team when required to support business development and marketing activities as it grows the customer base worldwide. Perform unannounced visits to medical device manufacturers globally [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as a technical expert to check on compliance with certification. Work with Line Manager and other team leaders as required to provide reviews within area of expertise. Essential Criteria 4 or more years of Software Medical Device experience in a technical capacity, preferably within product design, development and/or testing. Interpretation and applications of [. .. ] companies operating in these spaces and current industry trends. Qualifications Degree educated (Bachelors minimum or equivalent) relevant to medical device design, development, manufacture and use i. e. electromechanical, electronic/ electrical, biomedical engineering, computer science, medical physics or similar. What We Offer BSI offers a competitive salary, ample annual leave/ paid time off, and other robust benefits depending on country. We invest strongly in the development of our experts, a highlight being an annual conference where our hundreds of experts come together [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Senior Director Statewide Operations
Führungs-/ Leitungspositionen
Work-Life-Balance
Add expected salary to your profile for insights Provide strategic leadership and oversight for the operational delivery of
biomedical technology services across Queenslands public health system. As a key [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] member the Biomedical Technology Services (BTS) executive team, this role ensures consistent, high-quality, and safe service delivery through hospital-based teams and centralised business support functions. The Senior Director plays a pivotal role in aligning BTS operations with Queensland Healths strategic priorities, clinical needs, and service improvement goals. What youll do Provide expert-level leadership in statewide biomedical technology services, ensuring safe, efficient, and responsive delivery across diverse clinical and operational environments. Lead the development and implementation of strategic frameworks that advance professional competence and integrate multidisciplinary services to support high-quality statewide health outcomes. Drive statewide governance, risk management, and compliance across [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
• Binningen, Basel- Landschaft
Homeoffice möglich
[. .. ] expected Team Size: PCS safety team approx. 6; cross-functional project teams 510 members Hiring Manager: Simone Melega Department: Portfolio Clinical Safety PCS, PDS Working Hours: Standard Tasks [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Responsibilities Provide expert leadership for all clinical safety and vigilance activities related to Class II/ III medical devices throughout the product lifecycle. Oversee the full medical device vigilance process, including intake, processing, assessment and timely submission of adverse events to regulatory authorities. Review key clinical investigation documents to ensure high-quality inclusion of [. .. ] regarding safety requirements in medical device clinical investigations. Must Haves Bachelors, Masters or Ph D in a scientific or medical discipline. Minimum 3 years of relevant experience in healthcare, scientific or biomedical research with exposure to clinical safety and the use of medical devices or combination products. Strong understanding of the technical and biomedical aspects of medical devices. Solid working knowledge of relevant medical device regulations and industry standards. Demonstrated handson experience in safety activities for Class II and/or III medical [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
Medical Device Clinical Safety Scientist (6754)
• Dallenwil, Basel, Nidwalden, Basel- Stadt
[. .. ] (IB) , and Reference Safety Information (RSI) . The role holder is expected independently and strategically to lead the development of safety deliverables for MD clinical investigations. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Main Responsibilities Provide expert oversight and leadership for all clinical safety and vigilance activities for Class II and/or III Medical Devices (MD) , ensuring compliance with global regulations and internal standards throughout the product lifecycle. Manage and execute the MD vigilance process, including the intake, processing, assessment, and reporting of adverse events, ensuring [. .. ] ISO 14155. Qualifications and Experience: Relevant Swiss working/ residency permit or Swiss/ EU-Citizenship required Bachelor, Masters or Ph D within the scientific fields Min. 3 years relevant Healthcare, Scientific or biomedical research background in clinical safety with the use of MDs and/or combination products in the pharmaceutical/ biotech or MD industry Background in drug safety (pharmacovigilance) is an additional asset Strong understanding of the biomedical technical aspects of MDs. Working knowledge of relevant MD regulations and industry standards. MD clinical [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
Medical Device Clinical Safety Scientist
• Basel, Basel- Stadt
[. .. ] (IB) , and Reference Safety Information (RSI) . The role holder is expected independently and strategically to lead the development of safety deliverables for MD clinical investigations. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Main Responsibilities Provide expert oversight and leadership for all clinical safety and vigilance activities for Class II and/or III Medical Devices (MD) , ensuring compliance with global regulations and internal standards throughout the product lifecycle. Manage and execute the MD vigilance process, including the intake, processing, assessment, and reporting of adverse events, ensuring [. .. ] ISO 14155. Qualifications and Experience Relevant Swiss working/ residency permit or Swiss/ EU-Citizenship required Bachelor, Masters or Ph D within the scientific fields Min. 3 years relevant Healthcare, Scientific or biomedical research background in clinical safety with the use of MDs and/or combination products in the pharmaceutical/ biotech or MD industry Background in drug safety (pharmacovigilance) is an additional asset Strong understanding of the biomedical technical aspects of MDs. Working knowledge of relevant MD regulations and industry standards. MD clinical [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Director Pharmacokinetics (PK) Quantitate Systems Pharmacology (QSP)
• Glattbrugg, Zürich
Führungs-/ Leitungspositionen
[. .. ] therapeutic areas. Main Responsibilities Strategic Leadership Scientific Expertise Lead the development and execution of integrated PK, PBPK, and QSP modeling strategies across multiple therapeutic programs. Serve as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the subject matter expert (SME) in modeling and simulation, advising project teams on optimal study design, dose selection, and risk assessment. Champion model-informed drug development (MIDD) approaches to enhance translational understanding and regulatory confidence. PK and Model Development Lead the design and execution of nonclinical PK and TK studies to support research and [. .. ] and mentor a team of Principal and Senior scientists. Foster a culture of scientific excellence, innovation, and continuous learning. Qualifications And Experience Requirements Ph. D. in Pharmacokinetics, Systems Pharmacology, Pharmacometrics, Biomedical Engineering, or a related field. 10+ years of pharmaceutical industry experience in PK/ PD, PBPK, and/or QSP modeling. Proven track record of applying modeling to support drug development and regulatory submissions. Proficiency in modeling software for PK/ PD, PBPK, and QSP. Strong understanding of ADME, pharmacology, and translational science. [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Medical Device Clinical Safety Scientist
[. .. ] for medical devices, interpreting clinical safety data to inform decisions. Apply risk management principles in line with ISO 14971 to ensure safety in clinical processes. Serve as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a subject matter expert for safety-related activities in medical device clinical investigations. Apply ISO 14155:2020 standards to the design, conduct, monitoring, and reporting of clinical investigations, focusing on safety reporting and subject protection. Provide guidance to clinical teams, investigators, and site staff on safety requirements for clinical investigations. Key Skills and Requirements: Degree in a scientific field (Bachelors, Masters, or Ph D) . Background in healthcare, scientific, or biomedical research with experience in clinical safety for medical devices or combination products. Strong understanding of the technical and biomedical aspects of medical devices. Knowledge of relevant medical device regulations and industry standards. Expertise in safety activities related to Class II and/or III medical device clinical investigations. Proficiency in applying [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Medical Device Clinical Safety Scientist (m/f/d) (LSW) - BS
• Basel, Basel- Stadt
Homeoffice möglich
[. .. ] expected Team Size: PCS safety team approx. 6; cross-functional project teams 510 members Hiring Manager: Simone Melega Department: Portfolio Clinical Safety PCS, PDS Working Hours: Standard Tasks [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Responsibilities Provide expert leadership for all clinical safety and vigilance activities related to Class II/ III medical devices throughout the product lifecycle. Oversee the full medical device vigilance process, including intake, processing, assessment and timely submission of adverse events to regulatory authorities. Review key clinical investigation documents to ensure high-quality inclusion of [. .. ] regarding safety requirements in medical device clinical investigations. Must Haves Bachelors, Masters or Ph D in a scientific or medical discipline. Minimum 3 years of relevant experience in healthcare, scientific or biomedical research with exposure to clinical safety and the use of medical devices or combination products. Strong understanding of the technical and biomedical aspects of medical devices. Solid working knowledge of relevant medical device regulations and industry standards. Demonstrated handson experience in safety activities for Class II and/or III medical [. .. ]
Job am 17.11.2025 bei Jobleads gefunden
Scientific Consultant-Neuroimaging (m/f/d)
• Berlin
Beratungs-/ Consultingtätigkeiten
[. .. ] and want to move the field of neuroscience forward? If this sounds like you, then joining our team as a Scientific Consultant will be a highly fulfilling [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] role. Develop an expert understanding of f NIRS technology. Stay well-read on f NIRS based and related research as well as methods and technology developments. Consult scientists on the best solution for their research questions. This requires understanding their research goals and the latest technology developments and considerations for their field. Interact with leading researchers [. .. ] scientists, engineers, project managers, grant writers and many others. Act as voice-of-the-customer to the rest of NIRx. Your Qualifications Ph. D. or Masters Degree in Neuroscience, Psychology, Biomedical Engineering, or related field. Comprehensive knowledge of the acquisition and analysis of physiological signals. Ideally, previous experience with f NIRS, EEG, and/or f MRI. Excellent English skills, oral and written. Excellent communication and interpersonal skills are crucial for excelling at this role. Experienced in public speaking. Ability to present to large [. .. ]
Job am 16.11.2025 bei Jobleads gefunden
Field Application Specialist to Gradientech
[. .. ] questions. You are a bridge between their forefront technology and the hospital laboratories daily clinical workflow, providing technical expertise, training, and scientific and application support. Key responsibilities [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Support and provide expert guidance to their valued customers and authorised sites in Germany, but also in other nearby markets, assisting them with effective implementation and evaluation of the advanced Quick MIC system. Train lab personnel on their Quick MIC instrument operation, maintenance and troubleshooting, as well as provide handson training for test kits, workflow and [. .. ] to create and maintain highquality marketing material and clear technical documentation to ensure effective knowledge transfer for various scientific presentations and competitor positioning. About you Degree in microbiology, clinical chemistry, biomedical science or a related field a Ph D degree is preferred. At least 25 years of working experience from clinical diagnostic labs or industry field application support roles. Excellent communication and training abilities. Customeroriented and comfortable working independently in the field; customer support experience is highly valued. Strong problemsolving skills, with [. .. ]
Job am 14.11.2025 bei Jobleads gefunden
Director, Non-clinical Pharmacology CVR
Führungs-/ Leitungspositionen
[. .. ] as Sr. Pharmacology lead on TA teams. Work closely with PK, Toxicology, Translational Science, to integrate pharmacology data into broader development plans. Participate in project teams and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] TAteams and provide expert input on pharmacologyrelated issues. Provide expert input into due diligence for inlicensing or partnership opportunities. Documentation Communication Prepare study reports, presentations, and regulatory documents (e. g. , IND, CTA) . Present findings to internal stakeholders and external collaborators as needed. Team Leadership Lead and mentor a team of Principal and Sr. scientists, incl. invivo lab work. Foster a culture of scientific excellence, innovation, and continuous learning. Qualifications and Experience Requirements Ph. D. in Pharmacology, Physiology, Biomedical Sciences, or a related field. 10+ years of experience in nonclinical pharmacology within the pharmaceutical or biotech industry or academic background with proven and deep understanding of pharmaceutical development. Strong expertise in invivo pharmacology, disease models, and translational science for the relevant TA (Cardiovascular and/or Renal Disease Biology) . [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Biomedical Expert pro Jahr?
Als Biomedical Expert verdient man zwischen EUR 60.000,- bis EUR 90.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Biomedical Expert Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 53 offene Stellenanzeigen für Biomedical Expert Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Biomedical Expert Jobs?
Aktuell suchen 12 Unternehmen nach Bewerbern für Biomedical Expert Jobs.
Welche Unternehmen suchen nach Bewerbern für Biomedical Expert Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Biomedical Expert Stellenangebote:
- Aignostics (2 Jobs)
- ZEISS (1 Job)
- Roche (1 Job)
- F. Hoffmann- La Roche Gruppe (1 Job)
- F. Hoffmann- La Roche AG (1 Job)
- Medtronic plc (1 Job)
In welchen Bundesländern werden die meisten Biomedical Expert Jobs angeboten?
Die meisten Stellenanzeigen für Biomedical Expert Jobs werden derzeit in Berlin (6 Jobs), Nordrhein-Westfalen (4 Jobs) und Baden-Württemberg (4 Jobs) angeboten.
Zu welchem Berufsfeld gehören Biomedical Expert Jobs?
Biomedical Expert Jobs gehören zum Berufsfeld Medizintechnik.
