Project Manager, Qualitätsingenieur

Wir sind ein innovatives Unternehmen, das Produkte für die minimal-invasive Behandlung vonGefäßerkrankungen herstellt. Seit der Markteinführung unseres ersten Produktes im Jahr 2012 haben wirerfolgreich weltweit expandiert und sind bereits in 80 Ländern vertreten – in einigen sogar als Marktführer. Wir möchten weiterhin mit Tempo wachsen und suchen neue Mitarbeiter, die Lust auf eininternationales, dynamisches und vielseitiges Arbeitsumfeld mit guten Aufstiegsmöglichkeitenhaben.

We are looking for the following position at our headquarters in Hechingen to start as soon as possible:

Project Manager (m/f/d)

• A young and lively corporate culture with flat hierarchies and short decision-making processes
• A dynamic and appreciative team
• Start-up mentality with the structure and power of an established company
• Areas of responsibility in which everyone can operate independently
• Training and further education opportunities according to individual needs - your development is important to us!

• You have completed commercial training or have a comparable qualification, or alternatively have relevant professional experience
• Experience in the medical technology sector or in quality management is an advantage, but not essential
• You are able to manage several projects simultaneously without losing track of the big picture
• You have strong organizational and administrative skills and work with attention to detail
• You are proficient in MS Office
• You speak and write fluent German and English

• Project responsibility in sales and marketing with a focus on operational, administrative, and regulatory tasks, in a supporting role (no management responsibilities)
• Ensuring processes and documentation comply with company guidelines, quality requirements, and medical device regulations
• Close cooperation with other departments to ensure smooth processes and compliance
• Maintaining and updating the quality management system as well as creating and approving product and marketing documents
• Supporting product evaluations, customer feedback, and clinical-technical assessments as well as accompanying product launches, updates, and phase-outs
• Creating structured documentation for product files, audits, and compliance as well as supporting tenders and customer-oriented projects

Das klingt interessant für Dich? Dann bewirb Dich noch heute! Wir freuen uns auf Deine Unterlagen über unser Bewerberportal. Bei Fragen steht Dir René Zöllner unter der Nummer 07471 /  gerne zur Verfügung.