Aktuelle Jobs im Zusammenhang mit Medical Device Reprocessing Expert - Hamburg, Hamburg - Olympus
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Medical Device Risk Manager
vor 2 Wochen
Hamburg, Hamburg, Deutschland D Consulting GmbH VollzeitJob SummaryWe are seeking a highly skilled Medical Device Risk Manager to join our team at D.Med Consulting GmbH. As a key member of our regulatory affairs department, you will be responsible for identifying, analyzing, and evaluating product-relevant risks for medical devices in accordance with ISO standards.Your ResponsibilitiesEvaluate the safety...
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Medical Device Risk Manager
vor 2 Wochen
Hamburg, Hamburg, Deutschland D Consulting GmbH VollzeitJob SummaryWe are seeking a highly skilled Medical Device Risk Manager to join our team at D.Med Consulting GmbH. As a key member of our regulatory affairs department, you will be responsible for identifying, analyzing, and evaluating product-relevant risks for medical devices.Your ResponsibilitiesEvaluate the safety relevance of hazards in collaboration...
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Medical Device Risk Manager
vor 2 Wochen
Hamburg, Hamburg, Deutschland D Consulting GmbH Vollzeit**Job Summary**We are seeking a highly skilled Risk & Regulatory Affairs Manager to join our team at D.Med Consulting GmbH. As a key member of our team, you will be responsible for identifying, analyzing, and evaluating product-relevant risks for medical devices, ensuring compliance with regulatory requirements.**Key Responsibilities:**Collaborate with...
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Lead Auditor
vor 1 Woche
Hamburg, Hamburg, Deutschland DNV VollzeitJob Title: Lead Auditor - Medical DevicesDNV is seeking a Lead Auditor to join our team in the Medical Devices department. As a Lead Auditor, you will be responsible for planning and conducting audits against the manufacturing of medical devices, in accordance with ISO 13485, MDD 93/42/EEC, MDR 745/2017 and MDSAP standards.Key Responsibilities:Planning and...
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Medical Devices Auditor
vor 2 Wochen
Hamburg, Hamburg, Deutschland DNV VollzeitAs a Medical Devices Auditor at DNV, you will be responsible for planning and conducting international audits under ISO 13485, MDR, and MDSAP. Your tasks will also include conducting technical documentation assessments and documenting audit results according to accreditation and designation requirements.Additionally, you will develop and support the company...
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Auditor (m/f) - Medical Devices
vor 1 Monat
Hamburg, Hamburg, Deutschland Real Staffing VollzeitJob DescriptionWe are seeking a highly skilled Lead Auditor (m/w/d) for active medical products in an unlimited position. The successful candidate will be responsible for:Close collaboration with medical device manufacturers, both on-site and remotelyCreating audit reports and evaluating technical documentation for non-active medical productsSuccessful...
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Auditor (m/f) - Medical Devices
vor 1 Monat
Hamburg, Hamburg, Deutschland Real Staffing VollzeitJob DescriptionWe are seeking a highly skilled Lead Auditor (m/w/d) for active medical products in an unlimited position. The successful candidate will be responsible for:Close collaboration with medical device manufacturers, both on-site and remotelyCreating audit reports and evaluating technical documentation for non-active medical productsSuccessful...
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Lead Auditor
vor 2 Wochen
Hamburg, Hamburg, Deutschland DNV VollzeitJob SummaryDNV is seeking a Lead Auditor to join our team in the Medical Devices department. As a Lead Auditor, you will be responsible for planning and conducting audits of medical device manufacturers to ensure compliance with ISO 13485 and other relevant standards.Key ResponsibilitiesPlan and conduct audits of medical device manufacturers to ensure...
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Risk and Compliance Manager Medical Devices
vor 3 Wochen
Hamburg, Hamburg, Deutschland D Consulting GmbH VollzeitJob SummaryWe are seeking a highly skilled Risk and Regulatory Affairs Manager to join our team at D.Med Consulting GmbH. As a key member of our team, you will be responsible for identifying, analyzing, and mitigating risks associated with medical devices, ensuring compliance with regulatory requirements.Key ResponsibilitiesConduct risk assessments and...
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Risk and Compliance Manager Medical Devices
vor 3 Wochen
Hamburg, Hamburg, Deutschland D Consulting GmbH VollzeitJob SummaryWe are seeking a highly skilled Risk and Regulatory Affairs Manager to join our team at D.Med Consulting GmbH. As a key member of our team, you will be responsible for identifying, analyzing, and mitigating risks associated with medical devices, ensuring compliance with regulatory requirements.Key ResponsibilitiesConduct risk assessments and...
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Risk Management Specialist for Medical Devices
vor 2 Wochen
Hamburg, Hamburg, Deutschland D Consulting GmbH Vollzeit**Job Summary**We are seeking a highly skilled Risk Management Specialist for Medical Devices to join our team at D.Med Consulting GmbH. As a key member of our regulatory affairs team, you will be responsible for identifying, analyzing, and evaluating product-relevant risks for medical devices in accordance with ISO standards.**Key...
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Medical Devices Auditor
vor 1 Monat
Hamburg, Hamburg, Deutschland DNV VollzeitJob Title: Lead Auditor Medical DevicesYour primary responsibilities will include:Planning and conducting international audits under ISO 13485, MDR, and MDSAP standards.Conducting technical documentation assessments according to competence profiles.Documenting audit results in accordance with accreditation and designation requirements.Developing and...
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Medical Devices Auditor
vor 1 Monat
Hamburg, Hamburg, Deutschland DNV VollzeitJob Title: Lead Auditor Medical DevicesYour primary responsibilities will include:Planning and conducting international audits under ISO 13485, MDR, and MDSAP standards.Conducting technical documentation assessments according to competence profiles.Documenting audit results in accordance with accreditation and designation requirements.Developing and...
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Medical Devices Auditor
vor 4 Wochen
Hamburg, Hamburg, Deutschland DNV VollzeitJob Title: Lead Auditor Medical DevicesYour primary responsibilities will include:Planning and conducting international audits under ISO 13485, MDR, and MDSAP standards.Conducting technical documentation assessments according to competence profiles.Documenting audit results in accordance with accreditation and designation requirements.Developing and...
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Medical Devices Auditor
vor 4 Wochen
Hamburg, Hamburg, Deutschland DNV VollzeitJob Title: Lead Auditor Medical DevicesYour primary responsibilities will include:Planning and conducting international audits under ISO 13485, MDR, and MDSAP standards.Conducting technical documentation assessments according to competence profiles.Documenting audit results in accordance with accreditation and designation requirements.Developing and...
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Medical Devices Auditor
vor 3 Wochen
Hamburg, Hamburg, Deutschland DNV VollzeitJob Title: Lead Auditor Medical DevicesYour primary responsibilities will include:Planning and conducting international audits under ISO 13485, MDR, and MDSAPConducting technical documentation assessments according to competence profilesDocumenting audit results in accordance with accreditation and designation requirementsDeveloping and supporting the...
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Medical Devices Auditor
vor 3 Wochen
Hamburg, Hamburg, Deutschland DNV VollzeitJob Title: Lead Auditor Medical DevicesYour primary responsibilities will include:Planning and conducting international audits under ISO 13485, MDR, and MDSAPConducting technical documentation assessments according to competence profilesDocumenting audit results in accordance with accreditation and designation requirementsDeveloping and supporting the...
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Senior Quality Engineer
vor 2 Wochen
Hamburg, Hamburg, Deutschland Olympus VollzeitAbout the RoleWe are seeking a highly skilled Senior Quality Engineer to join our team at Olympus Medical Systems Division. As a key member of our quality team, you will be responsible for ensuring the highest standards of quality in our medical devices.Key ResponsibilitiesLead and support the development of quality standards and processes across global...
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Medical Devices Auditor
vor 1 Woche
Hamburg, Hamburg, Deutschland DNV VollzeitAs a Medical Devices Auditor at DNV, you will be responsible for planning and conducting international audits under ISO 13485, MDR, and MDSAP. Your tasks will also include conducting technical documentation assessments, documenting audit results, and developing the company culture within the Audit department.Key responsibilities include:Planning and...
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Medical Devices Auditor
vor 1 Monat
Hamburg, Hamburg, Deutschland DNV VollzeitJob Title: Lead Auditor Medical DevicesYour primary responsibilities will include:Planning and conducting international audits under ISO 13485, MDR, and MDSAP standards.Conducting technical documentation assessments according to competence profiles.Documenting audit results in accordance with accreditation and designation requirements.Developing and...
Medical Device Reprocessing Expert
vor 2 Monaten
About the Role
Olympus is seeking a highly skilled R&D Specialist to join our team in the field of medical devices. As a key member of our team, you will be responsible for ensuring the efficacy and material compatibility of medical devices throughout their product development and life cycle management.
Key Responsibilities
- Reprocess medical devices with respect to efficacy and material compatibility within product development and life cycle management
- Ensure biocompatibility and biological safety of medical devices within product development and life cycle management
- Prepare documentation for reprocessing and biocompatibility
- Collaborate with external suppliers to validate reprocessing and biocompatibility of medical devices
- Transfer results to other interface functions, including Instruction for Use and Verification/Validation
- Act as an internal and external consultant in various interfaces, including other departments and customers
- Screen and implement relevant standards and best practices
Requirements
- Bachelor's or Master's degree in Engineering, Microbiology, or equivalent
- Relevant experience in reprocessing and/or biocompatibility of medical devices or in a regulated and highly industrial or scientific environment
- Experience in collaborating with external suppliers and other partners
- Ability to read and understand technical drawings
- Excellent written and verbal English skills, as well as German language skills
- Proficiency in MS Office
- Extensive understanding of quality needs
- Strong problem-solving and communication skills
What We Offer
- 30 days of annual leave
- Up to 60% mobile work possible, with flexible work time model and overtime compensation
- Holiday and Christmas bonuses
- Corporate benefits discounts for employees
- Comprehensive company pension scheme and capital-forming benefits
- Company restaurant with live cooking and healthy food (subsidized)
- Employee Assistance Program of FamPLUS to support your health, mental, and emotional well-being
- Subsidy for public transportation (Deutschlandticket), free parking spaces, and bike or car leasing
- Various subsidized company sports groups and access to the in-house company gym
