Medical Devices Jobs in Baden-Württemberg
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Suchergebnisse - Medical Devices Jobs in Baden-Württemberg
Medizintechnik Karriere-Waldkirch
several times in the past with various prizes and awards.
Aufgaben
• Take responsibility for the cybersecurity of our Windows-based medical devices throughout the entire product lifecycle.
• Analyze and implement regulatory requirements and relevant...
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ACANDIS GmbH-Pforzheim
Are you an experienced FDA compliance professional with a strong scientific background, extensive knowledge of Quality Systems and a passion for driving operational excellence in the medical device industry? In this role, you will establish a DVV...
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stepstone.de -
Medizintechnik Karriere-Stuttgart
specialty is highly desirable.
Knowledge and Skills
• Proven success in high-value medical devices, implantable products, premium solutions, or operating-room sales.
• Entrepreneurial hunter mindset with a strong and consistent drive for results.
• Ability...
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6 ähnliche Jobs: Heidelberg, Karlsruhe, Freiburg im Breisgau, Ulm, Mannheim...
Brainlab-Waldkirch
Dr. Langer Medical GmbH, based in Waldkirch, Germany, which has been part of Brainlab SE in Munich since 2022, has specialized in the development and marketing of highly innovative medical technology for intraoperative neuromonitoring...
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stepstone.de -
Medizintechnik Karriere-Tuttlingen
fundierte Kenntnisse hinsichtlich der nationalen und internationalen Anforderungen an Qualitätsmanagementsysteme (z.B. ISO 13485, EU Medical Device Regulation 2017/745 [MDR], 21 CFR Part 820)
• Erfahrung in der Bewertung und Freigabe Technischer...
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Actimi GmbH-Stuttgart
Actimi is a medtech company, we build and deploy a digital health platform for realtime and on-demand data from wearables and medical devices. We're scaling our digital healthcare infrastructure, extend it with AI and are looking for a senior...
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join.com -
Acandis GmbH-Pforzheim
Stellenbeschreibung
Your responsibilities: Lead FDA remediation and compliance activities for Class III medical devices / combination products, ensuring sustainable resolution of compliance gaps and regulatory observations. Provide subject matter...
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persy.jobs -
ACANDIS GmbH-Pforzheim
We are looking to fill this position as soon as possible FDA Quality & Validation Expert (f/m/d) Medical Technology Pforzheim Your responsibilities: * Lead FDA remediation and compliance activities for Class III medical devices / combination...
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stellenonline.de -
NPA WorldWide-Stuttgart
in sophisticated automated machinery across industries including robotics, semiconductor equipment, medical devices, industrial automation, aerospace, and defense.
It has approximately 250 employees globally. The company was acquired by Bosch Rexroth in 2022...
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Acandis GmbH-Pforzheim
Your responsibilities:
• Lead FDA remediation and compliance activities for Class III medical devices / combination products, ensuring sustainable resolution of compliance gaps and regulatory observations.
• Provide subject matter expertise...
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factorialhr.de -
bayoonet AG-Mannheim
schlechter Code
• Bei Interesse an einer Tätigkeit bei BAYOOMED: Erfahrung im regulierten Umfeld (IEC 62304, ISO 13485, Medical Device Regulation) von Vorteil
• Sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift
• Erfahrung...
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Under Armour-Metzingen
Comfortable with or willing to learn technology (such as computers, hand-held and mobile devices)
Benefits & Perks
• Generous employee discount
• Ability to participate in special contests with the opportunity to win merchandise and other exclusive prizes...
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nebenjob.de -
JOTEC GmbH-Hechingen
functional teams such as Clinical, R&D, Quality, and Regulatory Affairs
• Experience with EU MDR (Medical Device Regulation), including familiarity with Clinical Evaluation Reports (CERs), Clinical Evaluation Plans (CEPs), Post-Market Clinical Follow-up (PMCF...
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finest-jobs.com -
argo Experts-Konstanz
Argo-X
Argo‑X is a specialist consultancy that delivers flexible, high‑impact staffing to pharma, biotech, medical‑device and diagnostics companies worldwide. Our consultants operate in GxP environments, helping clients accelerate product...
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join.com -
AESCULAP AG-Tuttlingen
mit dem Schwerpunkt Auditmanagement * Sie besitzen fundierte Kenntnisse hinsichtlich der nationalen und internationalen Anforderungen an Qualitätsmanagementsysteme (z.B. ISO 13485, EU Medical Device Regulation 2017/745 [MDR], 21 CFR Part 820) * Erfahrung...
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stellenonline.de -
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