Clinical Engineering Stellenangebote


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Jobbörse Stellenangebote Clinical Engineering Jobs gefunden bei Jobbörse StepStone

Stellenangebote Clinical Engineering Jobs bei StepStone


Stellenangebot Clinical Engineering Job bei Daiichi Sankyo Europe GmbH Neu Job vor 7 Std. gefunden Daiichi Sankyo Europe GmbH

Tech Management Lead (m/f/x) Monoclonal Antibodies

• Pfaffenhofen an der Ilm Führungs-/ Leitungspositionen Work-Life-Balance
MEHR[...] and external sites and development projects Act as main interface to internal and external sites Review technical documentation (protocols, reports) associated with manufacturing, tech transfer, site- to- site transfers and PPQ as needed Conduct scouting activities and recommend CDMOs for clinical and launch site selection from Tech Mgmt. Monoclonal Antibodies perspective Communicate and implement manufacturing plans at the site which are [...] of regulatory submissions (INDs/ IMPDs, NDAs, BLAs, etc. ) , responses to regulatory questions, briefing books Coordinate with lab units, SC, RACMC, QA to drive collaboration and solves issues in Tech Mgmt. Monoclonal Antibodies team Ph. D. (biochemistry, chemistry, pharmaceutics, engineering, or related disciplines) or masters degree with equivalent work experience to doctoral degree within pharmaceutical/ biotechnology sciences Multiple years of [...]
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Jobbörse Stellenangebote Clinical Engineering Jobs gefunden bei Jobbörse Neuvoo.com

Stellenangebote Clinical Engineering Jobs bei Neuvoo.com


Neu Job vor 7 Std. gefunden Aesculap AG part of the B. Braun Group Internship (w/m/d) Usability/ Human Factors Engineer • Tuttlingen
MEHR[...] and summative usability evaluations and recommend optimizations. You support the development of all necessary usability- related documents according to IEC 62366- 1 and FDA Guidance Documents You support the usability- related risk analysis according to ISO 14971. You collaborate with clinical advisors, healthcare professionals, risk managers, quality managers, UX UI designers, UX researchers, and developers Professional competencies Currently enrolled and successfully completed at least 2 years of study, preferably in Human Factors Engineering, Psychology Engineering, Product Design, UX UI Design, or Medical Engineering Initial experience (e. g. , via internships) in the corporate [...]
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Job vor 10 Tagen gefunden Takeda GmbH

Process Validation Engineer (f/m/d)

• Singen
MEHR[...] to the Senior Manager, Vaccines MS T Validation. What you bring to Takeda: You have completed studies in the natural sciences field Several years of experience in lifecycle process validation in manufacturing operations onsite and with CMOs for commercial and clinical manufacturing Extended knowledge in Process Performance Qualification, Continued Process Verification, and risk management Practical experience in vaccine production Expertise in [...]
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Job vom 24.10.2024 Aesculap AG part of the B. Braun Group Senior Regulatory Affairs Manager (f/m/d) • Freiburg im Breisgau
MEHR[...] electrode based on thin- film technology that allows us to selectively stimulate specific fibers in the nerve. Our first product, the baroloop stimulator, is specifically designed for the treatment of high blood pressure. Our main focus is to provide excellent clinical effectiveness while minimizing risks and side effects for the patient and a simple and safe use for the caregiver. Duties [...] policies, standards and guidelines that affect the assigned product portfolio. You will conduct post- market surveillance and report adverse events/ field safety corrective actions to the authorities In your role you will be supporting currently marketed products, e. g, review engineering changes, product labeling and promotional materials Professional competencies You have a degree in natural sciences, technology, engineering, medicine or a [...]
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Jobbörse Stellenangebote Clinical Engineering Jobs gefunden bei Jobbörse Stellenanzeigen.de

Stellenangebote Clinical Engineering Jobs bei Stellenanzeigen.de


Stellenangebot Clinical Engineering Job bei Seleon GmbH Job vom 23.10.2024 Seleon GmbH

Consultant Clinical/ Regulatory Affairs Medizintechnik (m/w/d)

• 74072, Heilbronn, Deutschland Beratungs-/ Consultingtätigkeiten Homeoffice möglich Flexible Arbeitszeiten Betriebliche Altersvorsorge
MEHRConsulting, Heilbronn/ Mitarbeiter/ Unbefristet/ 100 Consultant Clinical/ Regulatory Affairs Medizintechnik (m/w/d) Die seleon GmbH ist seit 25 Jahren ein führender, internationaler Dienstleistungspartner für Medizintechnikunternehmen mit Konzentration auf [...] com . Klinische Bewertung von Medizinprodukten und Drug Device Combinations; klinische Studien für Medizinprodukte und Drug Device Combinations; Post Market Clinical Follow- up für Medizinprodukte und Drug Device Combinations;. . . . Elektrotechnik, Diplom- Ingenieur, Medizinphysik, physikalische, Technik, Medizintechnikerin, Biomedical, Engineering, biomedizinische, Technik, Mechanical, Medizintechnik- Ingenieur, Messtechnik, Elektromedizinisch, Servicetechniker, Instandhaltung, Reparatur 15714610 [...]
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Jobs aus mittelfrankenJOBS.de

Stellenangebote Clinical Engineering Jobs bei mittelfrankenJOBS.de


Job vom 30.10.2024 IBA Dosimetry GmbH Physicist Dosimetry Expert • 90592, Schwarzenbruck, Deutschland
MEHRMission The R D Engineer/ Scientist will play a critical role in advancing quality assurance (QA) methodologies for radiation oncology by developing solid phantoms for Plan QA and Imaging in clinical radiotherapy settings. This position involves designing, testing, and refining solid phantoms that serve as critical tools in treatment planning verification, [...] products at the cutting edge of technology. Engage in continuous improvement efforts to refine phantom designs based on clinical feedback and emerging industry trends. Qualifications and Skills Educational Background: Bachelor s, Master s or Ph. D. in Medical Physics, Biomedical Engineering, Radiation Oncology, or a related scientific/ engineering field. Experience: Prior experience in radiotherapy QA, phantom development, dosimetry, or related R [...]
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Stellenangebot Clinical Engineering Job bei PAUL HARTMANN AG Job vom 02.11.2024 PAUL HARTMANN AG

Junior Product Developer- Global Product Development (f/m/d)

• Heidenheim Absolventen, Einsteiger, Trainees
MEHRResponsibilities: Idea generation for new products and technologies with a focus on electrical engineering Development of new products in compliance with relevant regulations and standards Assist in technical design questions and support project management [...] a relevant field Experience in project collaboration and/ or project management Experience in the field of wound care and medical devices Knowledge of the medical device s regulation and the associated subject areas (e. g. , application, design control, biocompatibility, clinical evaluation, risk management, sterilization, CE conformity, FDA, etc. ) Fluent in English and German Benefits: Flexible working conditions, such as [...]
Stellenangebot Clinical Engineering Job bei PAUL HARTMANN AG Job vom 02.11.2024 PAUL HARTMANN AG Biomedical Scientist- Biological Evaluation (f/m/d) • Heidenheim
MEHR[...] of biological strategy Assistance to representatives of the Business Division and HARTMANN in working groups related to changes in legislation or standards Establish and maintain contacts with testing institutes and external service providers Collaborate with departments like R D, Manufacturing Engineering and Procurement to ensure biological evaluations comply with EN ISO 10993 Assess biocompatibility of materials, support product registration, and contribute to risk analysis and clinical evaluation reviews Qualifications: Degree in natural science, life science or engineering Knowledge in scientifc and/ or clinical working (e. g. [...]
Stellenangebot Clinical Engineering Job bei PAUL HARTMANN AG Job vom 02.11.2024 PAUL HARTMANN AG

Biological Safety Engineer- Medical Devices (f/m/d)

• Heidenheim
MEHR[...] of biological strategy Assistance to representatives of the Business Division and HARTMANN in working groups related to changes in legislation or standards Establish and maintain contacts with testing institutes and external service providers Collaborate with departments like R D, Manufacturing Engineering and Procurement to ensure biological evaluations comply with EN ISO 10993 Assess biocompatibility of materials, support product registration, and contribute to risk analysis and clinical evaluation reviews Qualifications: Degree in natural science, life science or engineering Knowledge in scientifc and/ or clinical working (e. g. [...]
Stellenangebot Clinical Engineering Job bei PAUL HARTMANN AG Job vom 02.11.2024 PAUL HARTMANN AG Specialist Biological Evaluation (f/m/d) - 24 months • Heidenheim
MEHR[...] of biological strategy Assistance to representatives of the Business Division and HARTMANN in working groups related to changes in legislation or standards Establish and maintain contacts with testing institutes and external service providers Collaborate with departments like R D, Manufacturing Engineering and Procurement to ensure biological evaluations comply with EN ISO 10993 Assess biocompatibility of materials, support product registration, and contribute to risk analysis and clinical evaluation reviews Qualifications: Degree in natural science, life science or engineering Knowledge in scientifc and/ or clinical working (e. g. [...]
Stellenangebot Clinical Engineering Job bei PAUL HARTMANN AG Job vom 02.11.2024 PAUL HARTMANN AG

Toxicology Specialist- Biological Evaluation (f/m/d)

• Heidenheim
MEHR[...] of biological strategy Assistance to representatives of the Business Division and HARTMANN in working groups related to changes in legislation or standards Establish and maintain contacts with testing institutes and external service providers Collaborate with departments like R D, Manufacturing Engineering and Procurement to ensure biological evaluations comply with EN ISO 10993 Assess biocompatibility of materials, support product registration, and contribute to risk analysis and clinical evaluation reviews Qualifications: Degree in natural science, life science or engineering Knowledge in scientifc and/ or clinical working (e. g. [...]
Stellenangebot Clinical Engineering Job bei PAUL HARTMANN AG Job vom 02.11.2024 PAUL HARTMANN AG Medical Device Quality Specialist- Biological Evaluation (f/m/d) • Heidenheim
MEHR[...] of biological strategy Assistance to representatives of the Business Division and HARTMANN in working groups related to changes in legislation or standards Establish and maintain contacts with testing institutes and external service providers Collaborate with departments like R D, Manufacturing Engineering and Procurement to ensure biological evaluations comply with EN ISO 10993 Assess biocompatibility of materials, support product registration, and contribute to risk analysis and clinical evaluation reviews Qualifications: Degree in natural science, life science or engineering Knowledge in scientifc and/ or clinical working (e. g. [...]
Stellenangebot Clinical Engineering Job bei PAUL HARTMANN AG Job vom 02.11.2024 PAUL HARTMANN AG

Manager Global Product Development (f/m/d) - Medical Devices

• Heidenheim
MEHRResponsibilities: Idea generation for new products and technologies with a focus on electrical engineering Development of new products in compliance with relevant regulations and standards Assist in technical design questions and support project management [...] a relevant field Experience in project collaboration and/ or project management Experience in the field of wound care and medical devices Knowledge of the medical device s regulation and the associated subject areas (e. g. , application, design control, biocompatibility, clinical evaluation, risk management, sterilization, CE conformity, FDA, etc. ) Fluent in English and German Benefits: Flexible working conditions, such as [...]
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Stellenangebot Clinical Engineering Job bei PAUL HARTMANN AG Job vom 02.11.2024 PAUL HARTMANN AG Biocompatibility Specialist- Medical Devices (f/m/d) • Heidenheim
MEHR[...] of biological strategy Assistance to representatives of the Business Division and HARTMANN in working groups related to changes in legislation or standards Establish and maintain contacts with testing institutes and external service providers Collaborate with departments like R D, Manufacturing Engineering and Procurement to ensure biological evaluations comply with EN ISO 10993 Assess biocompatibility of materials, support product registration, and contribute to risk analysis and clinical evaluation reviews Qualifications: Degree in natural science, life science or engineering Knowledge in scientifc and/ or clinical working (e. g. [...]
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Jobbörse Stellenangebote Clinical Engineering Jobs gefunden bei Jobbörse Jobleads

Stellenangebote Clinical Engineering Jobs bei Jobleads


Job vor 10 Tagen gefunden

(Senior) Systems Immunologist

• Wien
MEHRWhat we do? Immune- mediated diseases affect hundreds of millions of people worldwide, but less than 12 of new drugs reach approval, largely due to insufficient pre- clinical understanding of the complex underlying disease biology. You will be joining a stealth techbio therapeutics company aimed at disrupting drug [...] of I I drugs. Co- develop large scale screening assays (functional, high content microscopy, multi- omics) as part of a unique lab- in- the- loop AI discovery system. Develop screening assays to support early- stage small molecule discovery, from cell engineering and chemical screens, to hit validation studies for hit- to- lead nomination. Be part of a flat cross- functional team [...]
Job vor 13 Tagen gefunden Associate Director Engineering- Device Technology (m/f/d) • Schaftenau, Tirol Führungs-/ Leitungspositionen
MEHRAssociate Director Engineering- Device Technology (m/f/d) Job ID: REQ- 10026381 Summary LOCATION: Schaftenau, TYPE: Hybrid Working, #LI Hybrid Are you looking for [...] design input requirements, global component specifications, and design verification documents. Ensure device design development is delivered to a high quality following the design control process and applicable regulatory framework. Ensure components are delivered and controlled to the required quality for clinical trials and commercial production. Support Regulatory Affairs to prepare medical device/ combination product pre- registration documents and provide input to [...]
Job vom 05.11.2024

Associate Director Engineering- Device Technology (m/f/d)

• Schaftenau, Tirol Führungs-/ Leitungspositionen
MEHR[...] who are responsible for the development of parenteral combination products to ensure that our delivery systems fulfill the highest customer expectations? If yes, then this is the opportunity for you The Device Technology Solution Center is seeking an Associate Director Engineering within the Global Device and Packaging Development (GDPD) department in Schaftenau, Austria. Job Description Key Responsibilities: Lead technical development and [...] design input requirements, global component specifications and design verification documents. Ensure device design development is delivered to a high quality following the design control process and applicable regulatory framework. Ensure components are delivered and controlled to the required quality for clinical trials and commercial production. Support Regulatory Affairs to prepare medical device/ combination product pre- registration documents and provides input to [...]
Job vom 26.09.2024 Director Medical Affairs C EE • Heidelberg, Baden- Württemberg Führungs-/ Leitungspositionen
MEHR[...] and the EMEA Medical affairs organization the role will contribute to the value maximization of current and future Medical Affairs people, processes and product portfolio for BDX. This position is responsible to conceptualize, develop and implement BDX or cross- BU Clinical and Medical Affairs strategies and programs on a Country/ Region Level in close coordination with the BU Heads of Medical [...] BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it s no small feat. It takes the imagination and passion of all of us from design and engineering to the manufacturing and marketing of our billions of Med Tech products per year to look at the impossible and [...]
Job vom 17.08.2024

Director Medical Affairs- DACH (m/w/d)

• Mainz, Rheinland- Pfalz Führungs-/ Leitungspositionen
MEHR[...] developments in Diabetes and CGM, so that we can best serve our patients and provide accurate advice and support to health care professionals. The Medical Affairs teams are our resident experts regarding the treatment of diabetes, medical device product training, clinical studies and the use of CGM as a management tool for diabetes. Where you come in: As Director Medical Affairs [...] in clinical and medical affairs and keen to support Dexcom s efforts to be leader in CGM education and driving CGM as a standard of care. Leverage your clinical expertise to provide strategic and operational support to our Product and Engineering teams to make sure our offerings meet the needs of our large network of clinicians who use them every day [...]
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