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Produktentwickler & Qualitätsmanager (wmd)

Deine AufgabenBeobachtung von Markt Wettbewerb und Produkttrends sowie Entwicklung neuer Produktideen für die HAWLIK-MarkenEntwicklung und Bewertung von Produktkonzepten und Rezepturen einschließlich Inhaltsstoffen Dosierungen Geschmack und Zielkosten in Abstimmung mit den relevanten FachbereichenKo...

Yesterday
Full Time

Quality Engineer (mwd) Complaint Handlingpost Mark...

Work Flexibility: Hybrid or Onsite(Senior) Quality Engineer Post-Market Surveillance (m/f/d)As a (Senior) Quality Engineer (m/f/d) in Post-Market Surveillance you will be part of our Post-Market Surveillance team at our Freiburg site. Your primary responsibility will be to investigate complaints fro...

Yesterday
Full Time

Teamlead Regulatory Affairs (mwd)

Die Refresco Deutschland GmbH mit Hauptsitz in Mönchengladbach gehört als Hersteller von Fruchtsäften und Erfrischungsgetränken für Industrie- und Handelskunden zu den führenden Anbietern von Getränkelösungen in Deutschland.Das Unternehmen beschäftigt deutschlandweit rund 1.800 Mitarbeiterinnen und...

3 days ago
Full Time

Senior Regulatory Affairs Officer (mfx)

Über unsKoch-Chemie ist Teil der französischen Novarc-Gruppe einer international aufgestellten Industriegruppe mit über 60 Gesellschaften und rund 1.900 Mitarbeitenden weltweit. Gemeinsam stehen wir für technologische Exzellenz industrielle Kompetenz und nachhaltige Innovation. Koch-Chemie steht sei...

4 days ago
Full Time

Recruitment Data Policies Rwe Strategy Lead Respir...

Make your mark for patientsWe are looking for a Real-World Evidence Strategy Lead Respiratory who is strategic collaborative and results-driven to join us in our Real-World Evidence team based in Monheim Germany. This is a hybrid role requiring 40% weekly onsite presence.About the roleYou will lead...

5 days ago
Full Time

Clinical Affairs Medical Expert (md)

We are seeking a medically qualified clinical expert to provide independent medical and scientific input across Brainlabs portfolio of image-guided surgery surgical planning navigation medical imaging and related technologies. The role combines clinical evaluation and medical documentation review wi...

6 days ago
Full Time

Medical Devices Product Security Engineer

Take responsibility for the cybersecurity of our Windows-based medical devices throughout the entire product lifecycle.Analyze and implement regulatory requirements and relevant standards (e.g. IECIEC 62304 ISO 14971).Conduct threat modeling risk assessments and vulnerability analyses.Develop implem...

6 days ago
Full Time

Global Regulatory Strategy Lead

The PositionWe are seeking a dynamic individual to provide global strategic regulatory guidance and leadership throughout the product lifecycle on assigned this pivotal role you will develop and be accountable for the Global Regulatory Strategy of your projects lead the Regulatory Excellence Team (R...

8 days ago
Full Time

Qm Associate – Product Registrations (part-time 20...

At Brainlab we develop innovative medical devices to make an impact for healthcare providers physicians and their patients. As a QM Associate Product Registrations you will be part of the international Regulatory Affairs team overseeing and managing medical device approvals around the world. Your go...

11 days ago
Part-time

Senior Gxp & Ai Compliance Business Analyst (all G...

DUanalysierst komplexe fachliche technische und regulatorische Anforderungen in digitalen datengetriebenen und KI-gestützten Umgebungenübersetzt Vorgaben aus GxP Data Integrity Datenschutz und weiteren regulatorischen Rahmenwerken in konkrete Business- und Systemanforderungenführst Gap-Analysen Risi...

11 days ago
Full Time

Senior Regulatory Affairs Manager, Fda & Us Market...

Shape the US regulatory strategy for a specialist medical technology companyOur client is an internationally active medical technology company developing products for clinical use.To strengthen its Regulatory Affairs function the company is seeking an experienced professional to lead regulatory acti...

12 days ago
Employee

(senior Advanced) Clinical Study Manager

We are looking for an experienced proactive and self-driven (Senior / Advanced) Clinical Study Manager to join our Clinical Affairs team at Brainlab.In this role you will independently lead clinical studies and medical device investigations from concept to completion ensuring high-quality execution...

13 days ago
Full Time

Senior Data Scientist Fokus Pharma (mwd)

StartdatumWir suchen Dich ab sofortan einem unserer deutschen Standorte in München Nürnberg Leipzig Berlin Essen oderFrankfurt am Main!Deine AufgabenDataundAIsind Dein Zuhause Des Weiteren gestaltet sich Deine neue Herausforderung wie folgt:Du gestaltest zielstrebig anspruchsvolle Data Science und A...

14 days ago
Full Time

Head Of Regulatory And Prrc For A Core Product Inc...

At Vivalyx a medical technology startup based in Cologne were on a mission to save the lives of those suffering from organ failure.Our innovative approach aims to significantly improve the vitality and availability of donor organs. As we gear up for certification and related studies were seeking ded...

14 days ago
Employee

Associate Director, Regulatory Affairs, Europe Reg...

Welcome to AbbVie! As part of an international company with ca. 57000 employees worldwide and around 3500 employees in Germany you will have the opportunity of addressing some of tomorrows unmet medical needs in close collaboration with your colleagues. Are you passionate about improving global heal...

14 days ago
Full Time

Manager Regulatory Affairs And Audit Management (m...

Regulatory Affairs & Compliance: Sie identifizieren bewerten und dokumentieren relevante gesetzliche regulatorische und normative Anforderungen und stellen deren transparente Kommunikation sowie wirksame Umsetzung im Qualitätsmanagementsystem (QMS) sicher.Normen- und Änderungsmanagement: Sie überwac...

15 days ago
Full Time

Manager Regulatory Affairs And Audit Management (m...

Regulatory Affairs & Compliance: Sie identifizieren bewerten und dokumentieren relevante gesetzliche regulatorische und normative Anforderungen und stellen deren transparente Kommunikation sowie wirksame Umsetzung im Qualitätsmanagementsystem (QMS) sicher.Normen- und Änderungsmanagement: Sie überwac...

15 days ago
Full Time

Configuration Manager Medizintechnik (all Gender)

DUübernimmst die Verwaltung und Pflege produktbezogener Konfigurationen über den gesamten Product Lifecycle hinwegstellst die Konsistenz zwischen Anforderungen Spezifikationen Risiken Testfällen und Freigabedokumenten sicherkoordinierst und dokumentierst Change Requests Änderungsbewertungen sowie Ve...

15 days ago
Full Time

Quality Management & Regulatory Affairs Manager (m...

Willkommen bei Unora! Mit Hauptsitz in Berlin und einer Niederlassung im Vereinigten Königreich vereinen wir jahrzehntelange Erfahrung in der Stomaversorgung. Entstanden aus den Stärken von ForLife und Oakmed entwickelt unser Team seit vielen Jahren Produkte die Komfort bieten Sicherheit geben und e...

16 days ago
Full Time

Program Manager – Regulatory Programs & Capability...

Lead global regulatory transformation programs and implementation initiativesTranslate regulatory requirements into operating models roadmaps and delivery plansManage program governance milestones risks dependencies and executive reportingFacilitate Steering Committees and executive decision-making...

17 days ago
Full Time

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