Durchführung von Audits nach MDR, ISO 13485, und ggf. MDSAP.* Beurteilung von Änderungen an Produkten und QM-Systemen, SSCPs, PSURs, und Vigilanz, im Rahmen der kontinuierlichen Überwachung ...
New
Durchführung von Audits nach MDR, ISO 13485, und ggf. MDSAP.* Beurteilung von Änderungen an Produkten und QM-Systemen, SSCPs, PSURs, und Vigilanz, im Rahmen der kontinuierlichen Überwachung ...
New
Work with ASMGi MDR / MSOC plus Service clients as part of the overall service and specifically the Incident Response Program Development including Incident Response Policy, Incident Response Plan ...
Work with ASMGi MDR / MSOC plus Service clients as part of the overall service and specifically the Incident Response Program Development including Incident Response Policy, Incident Response Plan ...
Durchführung von Audits nach MDR, ISO 13485, und ggf. MDSAP.* Beurteilung von Änderungen an Produkten und QM-Systemen, SSCPs, PSURs, und Vigilanz, im Rahmen der kontinuierlichen Überwachung ...
New
Durchführung von Audits nach MDR, ISO 13485, und ggf. MDSAP.* Beurteilung von Änderungen an Produkten und QM-Systemen, SSCPs, PSURs, und Vigilanz, im Rahmen der kontinuierlichen Überwachung ...
New
$79.93 - $102.76/hr
Du koordinierst Verifikations- und Validierungsaktivitäten für medizinische Softwareprojekte gemäß IEC 62304, ISO 13485 und MDR, sicherst Traceability im V-Modell und agierst als Schnittstelle ...
New
$79.93 - $102.76/hr
Du koordinierst Verifikations- und Validierungsaktivitäten für medizinische Softwareprojekte gemäß IEC 62304, ISO 13485 und MDR, sicherst Traceability im V-Modell und agierst als Schnittstelle ...
New
$75 - $95/hr
You coordinate and carry out verification and validation activities - in accordance with IEC 62304, ISO 13485, MDR and customer-specific requirements. * You accompany requirements throughout their ...
New
$75 - $95/hr
You coordinate and carry out verification and validation activities - in accordance with IEC 62304, ISO 13485, MDR and customer-specific requirements. * You accompany requirements throughout their ...
New
$70.28 - $93.71/hr
Sicherstellung, Pflege und strategische Weiterentwicklung des Qualitätsmanagementsystems gemäß ISO 13485, MDR (EU) 2017/745 sowie FDA 21 CFR Part 820 inklusive regelmäßiger Wirksamkeitsbewertung ...
New
$70.28 - $93.71/hr
Sicherstellung, Pflege und strategische Weiterentwicklung des Qualitätsmanagementsystems gemäß ISO 13485, MDR (EU) 2017/745 sowie FDA 21 CFR Part 820 inklusive regelmäßiger Wirksamkeitsbewertung ...
New
$68.51 - $97.05/hr
Durchführung von Labortests * Kommunikation mit Lieferanten * Pflege und Erstellung MDR-konformer Produktakten * Technische Dokumentation, Stammdatenpflege und Regulatory Affairs * Sicherstellung ...
New
$68.51 - $97.05/hr
Durchführung von Labortests * Kommunikation mit Lieferanten * Pflege und Erstellung MDR-konformer Produktakten * Technische Dokumentation, Stammdatenpflege und Regulatory Affairs * Sicherstellung ...
New
This position requires a deep understanding of how to translate intricate regulatory requirements from diverse global authorities (e.g., FDA, EU MDR) and environmental directives (e.g., WEEE, PPWR ...
This position requires a deep understanding of how to translate intricate regulatory requirements from diverse global authorities (e.g., FDA, EU MDR) and environmental directives (e.g., WEEE, PPWR ...
IS0 9001, ISO 13485, MDSAP and CFR Part 820/211, EU MDR, and other applicable standards. The Quality Director will lead teams of quality managers and engineers responsible for product and service ...
IS0 9001, ISO 13485, MDSAP and CFR Part 820/211, EU MDR, and other applicable standards. The Quality Director will lead teams of quality managers and engineers responsible for product and service ...
IS0 9001, ISO 13485, MDSAP and CFR Part 820/211, EU MDR, and other applicable standards. The Quality Director will lead teams of quality managers and engineers responsible for product and service ...
IS0 9001, ISO 13485, MDSAP and CFR Part 820/211, EU MDR, and other applicable standards. The Quality Director will lead teams of quality managers and engineers responsible for product and service ...
Support post-market surveillance obligations per applicable US and global requirements (including MDR) * Ensure finished product artwork and labels are clear, comprehensible, and user-friendly ...
Support post-market surveillance obligations per applicable US and global requirements (including MDR) * Ensure finished product artwork and labels are clear, comprehensible, and user-friendly ...
Support post-market surveillance obligations per applicable US and global requirements (including MDR) * Ensure finished product artwork and labels are clear, comprehensible, and user-friendly ...
Support post-market surveillance obligations per applicable US and global requirements (including MDR) * Ensure finished product artwork and labels are clear, comprehensible, and user-friendly ...
$81 - $115/hr
Du stellst sicher, dass Release-Prozesse, Qualitätsstandards sowie regulatorische Anforderungen (ISO 13485, ISO 9001, MDR, IEC 62304) zuverlässig eingehalten werden. * Compliance-Prüfungen ...
New
$81 - $115/hr
Du stellst sicher, dass Release-Prozesse, Qualitätsstandards sowie regulatorische Anforderungen (ISO 13485, ISO 9001, MDR, IEC 62304) zuverlässig eingehalten werden. * Compliance-Prüfungen ...
New
$70.28 - $93.71/hr
Medizintechniker (m/w/d) oder eine vergleichbare Ausbildung * Berufserfahrung im Bereich Medizintechnik sowie Kenntnisse gesetzlicher Vorgaben (MDR, MPBetreibV, etc.) wünschenswert
New
$70.28 - $93.71/hr
Medizintechniker (m/w/d) oder eine vergleichbare Ausbildung * Berufserfahrung im Bereich Medizintechnik sowie Kenntnisse gesetzlicher Vorgaben (MDR, MPBetreibV, etc.) wünschenswert
New
Dispatcher
Cincinnati, OH · On-site
Track/Maintain yard report, MDR, CNI, and Divisional Pool * Actively participate in driver recruiting and retention * Distributes and keeps track of the Nextel radios and fleet truck assignments
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Dispatcher
Cincinnati, OH · On-site
Track/Maintain yard report, MDR, CNI, and Divisional Pool * Actively participate in driver recruiting and retention * Distributes and keeps track of the Nextel radios and fleet truck assignments
Partner with Quality and Regulatory to ensure compliance with FDA, CE/MDR, ISO 13485, and applicable global regulatory requirements. * Serve as senior technical interface with strategic OEM customers ...
Partner with Quality and Regulatory to ensure compliance with FDA, CE/MDR, ISO 13485, and applicable global regulatory requirements. * Serve as senior technical interface with strategic OEM customers ...
Director - Cyber Security at GE Renewable Energy Power and Aviation Cincinnati, OH
Cincinnati, OH · On-site
$130 - $170/hr
This role manages the strategy for working with Managed Detection and Response (MDR) partners and is focused on continuous improvement to increase performance against KRIs and KPIs. Roles and ...
Director - Cyber Security at GE Renewable Energy Power and Aviation Cincinnati, OH
Cincinnati, OH · On-site
$130 - $170/hr
This role manages the strategy for working with Managed Detection and Response (MDR) partners and is focused on continuous improvement to increase performance against KRIs and KPIs. Roles and ...
$79.78 - $125.37/hr
MPDG, MDR), sowie relevanter Normen wie ISO 13485, ISO 14971, IEC 60601-1/2, IEC 62304 * Erfahrung in der Erstellung technischer Dokumentationen für internationale Zulassungen
$79.78 - $125.37/hr
MPDG, MDR), sowie relevanter Normen wie ISO 13485, ISO 14971, IEC 60601-1/2, IEC 62304 * Erfahrung in der Erstellung technischer Dokumentationen für internationale Zulassungen
Position and scope SOC-backed security services (e.g., MDR/XDR, email security and investigation, vulnerability remediation, security awareness) and align response workflows and reporting ...
Position and scope SOC-backed security services (e.g., MDR/XDR, email security and investigation, vulnerability remediation, security awareness) and align response workflows and reporting ...
IT & Security Consultant (Pre-Sales)
Independence, OH · On-site
$120 - $150/hr
Position and scope SOC-backed security services (e.g., MDR/XDR, email security and investigation, vulnerability remediation, security awareness) and align response workflows and reporting ...
IT & Security Consultant (Pre-Sales)
Independence, OH · On-site
$120 - $150/hr
Position and scope SOC-backed security services (e.g., MDR/XDR, email security and investigation, vulnerability remediation, security awareness) and align response workflows and reporting ...
Mdr information
See Ohio salary details
$17.60 - $22.04
4% of jobs
$22.04 - $26.49
3% of jobs
$26.49 - $30.94
0% of jobs
$30.94 - $35.38
7% of jobs
$36.62 is the 25th percentile. Wages below this are outliers.
$35.38 - $39.83
36% of jobs
$39.83 - $44.27
11% of jobs
$44.27 - $48.72
7% of jobs
$51.78 is the 75th percentile. Wages above this are outliers.
$48.72 - $53.16
9% of jobs
$53.16 - $57.61
10% of jobs
$57.61 - $62.06
9% of jobs
$62.06 - $66.50
4% of jobs
$17
$44
$66
How much do mdr jobs pay per hour?
As of Aug 21, 2026, the average hourly pay for mdr in Ohio is $44.86, according to ZipRecruiter salary data. Most workers in this role earn between $36.78 and $53.70 per hour, depending on experience, location, and employer.
What is an MDR?
An MDR (Market Development Representative) is a sales professional responsible for identifying and qualifying potential leads for a company's products or services. They focus on early-stage prospecting, researching target markets, and engaging with potential customers to generate sales opportunities. MDRs work closely with sales and marketing teams to ensure a seamless handoff of qualified leads for further nurturing and closing. Their role is crucial in driving business growth by expanding the company's customer base.
What does a typical day look like for a Medical Device Reprocessing (MDR) technician?
A typical day for an MDR Technician involves cleaning, disinfecting, and sterilizing surgical instruments and medical devices according to strict protocols. You'll routinely inspect equipment, assemble instrument trays, document processes, and ensure all items meet quality assurance standards. MDR Technicians frequently collaborate with surgical teams and other healthcare professionals to meet tight turnaround times for critical instruments. This is a hands-on role that requires adaptability, precision, and a commitment to patient safety, often performed in hospital central sterile departments or specialized clinics.
What are the key skills and qualifications needed to thrive in the MDR position, and why are they important?
To thrive as a Medical Device Reprocessing (MDR) Technician, you need knowledge of sterilization processes, infection control standards, and a high school diploma or equivalent, often supplemented with formal MDR certification. Familiarity with autoclaves, washer-disinfectors, and tracking systems is necessary for proper equipment handling. Attention to detail, teamwork, and effective communication are important soft skills in this role. These abilities ensure patient safety and efficient support of clinical procedures in healthcare environments.
What are popular job titles related to Mdr jobs in Ohio?
For Mdr jobs in Ohio, the most frequently searched job titles are:
What job categories do people searching Mdr jobs in Ohio look for?
The top searched job categories for Mdr jobs in Ohio are:
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Job description
**Ihre Rolle*** Bewertung der Technischer Dokumentationen (TD-Review) von Medizinprodukten unter MDR.* Durchführung von Audits nach MDR, ISO 13485, und ggf. MDSAP.* Beurteilung von Änderungen an Produkten und QM-Systemen, SSCPs, PSURs, und Vigilanz, im Rahmen der kontinuierlichen Überwachung.* Erstellung von Auditprogrammen und Stichprobenpläne, Zuweisung von Ressourcen, Verifizierung von Anträgen, Klassifizierung, Codierung, etc.* Mitwirkung an Konformitätsbewertungsverfahren, insbesondere bei komplexen oder neuartigen Medizinprodukten.* Fachlicher Austausch mit internen und externen Experten (z. B. Klinische Experten, Risikobewerter).* Unterstützung bei Behördenanfragen, ggf. Teilnahme an Inspektionen durch ZLG, DAkkS, und SCC.* Unterstützung von internen Verbesserungsmaßnahmen.* finale Zulassung von Medizinprodukten**Ihr Profil*** Abgeschlossenes Studium in einem relevanten Fachbereich (z. B. Medizintechnik, Biomedizin, Ingenieurwissenschaften, Naturwissenschaften).* Mehrjährige Berufserfahrung (> 4 Jahre) in der Entwicklung, Herstellung, Prüfung oder Qualitätssicherung von aktiven oder nichtaktiven Medizinprodukten.* Idealerweise mehrjährige (>10 Jahre) Berufserfahrung als Auditor und/oder Produktbewerter bei einer Benannten Stelle für die MDR-Verordnung (EU) 2017/745. Ihre professionelle Erfahrung deckt dabei nachweislich ein breites Spektrum an Medizinprodukten (MDA- und/oder MDN-Codes) sowie Technologien (MDT-Codes) ab.* Tiefgehende Kenntnisse der MDR, ISO 13485, ISO 14971, ISO 10993, IEC 62304, IEC 62366-1, IEC 60601, ISO 14155, MDSAP Dokumente, sowie weiterer regulatorischer Anforderungen, MDCG-Leitlinien und Produktnormen.* Anerkannte und nachweisliche Qualifikationen als Lead Auditor für MDR, ISO 13485 und idealerweise MDSAP.* Ausgeprägte Fähigkeit zur Bewertung komplexer technischer und klinischer Sachverhalte.* Fließende Deutsch- und Englischkenntnisse in Wort und Schrift.* Hohes Maß an Eigenverantwortung, Objektivität und professioneller Kommunikation.* Bereitschaft zu internationaler Reisetätigkeit (nach Bedarf)Es erwartet Sie ein leistungsstarkes und sympathisches Team, eine kollegiale, systematische Einarbeitung sowie interessante Möglichkeiten zur Weiterbildung. Darüber hinaus bieten wir Ihnen eine attraktive, leistungsbezogene Vergütung, die Chance, sich aktiv einzubringen und weiterzuentwickeln, sowie moderne Arbeitsbedingungen in einem internationalen Umfeld.* Hybrides Arbeiten: Büro und Remote* Flexible Arbeitszeiten* Jobticket* JobRad* 30 Tage Urlaub* Vermögenswirksame Leistung### Why Work With UsAt DQS, you will work on issues that matter - for companies and for society. Our audits and certifications not only create trust and competitive advantages, but also contribute to greater sustainability, safety, and responsibility in global supply chains. Those who work at DQS actively shape how companies worldwide live quality and fulfill their social obligations - soundly, independently, and effectively.Diversity is part of our identity at DQS. In our global team, we promote a working environment in which different perspectives, experiences, and life paths are welcome - regardless of origin, gender, age, or individual abilities. Through flexible working models, fair development opportunities, and inclusive structures, we create space for everyone to reach their full potential. #J-18808-Ljbffr