Quality Manager Digital Specialist (f/m/x)

ZipRecruiter; München; Vor Ort; EUR 50.000 - 70.000; Vollzeit

Zusammenfassung

A leading company in the medical technology sector is seeking a quality management professional to support software systems for medical devices. The role involves analyzing product documentation, coordinating risk management, and ensuring compliance with quality principles. Ideal candidates will have a degree in a relevant field, several years of experience in software or product development, and strong communication skills in both German and English.

Qualifikationen

• Several years of professional experience in software development or product development of medical devices.
• Strong understanding of quality principles; able to work independently and goal-oriented.
• Proficiency in German and English.

Aufgaben

• Support quality management activities in a project team for software systems on medical devices.
• Analyze and review product documentation, ensuring process-compliant software development.
• Support and coordinate risk management activities according to ISO 14971.

Kenntnisse

Quality principles

Communication

Teamwork

Ausbildung

Degree in computer science, business administration, or comparable field

Jobbeschreibung

Job Description

Step out of your comfort zone, excel and redefine the limits of what is possible. That's just what our employees are doing every single day – in order to set the pace through our innovations and enable outstanding achievements. After all, behind every successful company are many great fascinating people.

In a spacious modern setting full of opportunities for further development, ZEISS employees work in a place where expert knowledge and team spirit reign supreme. All of this is supported by a special ownership structure and the long-term goal of the Carl Zeiss Foundation: to bring science and society into the future together.

Join us today. Inspire people tomorrow.

We are a part of ZEISS. We look forward to receiving your application regardless of gender, age, social background, philosophy of life, disability, or other personal characteristics.

Apply now! It takes less than 10 minutes.

Responsibilities

1. Support quality management activities in an interdisciplinary and cross-location project team for software systems on medical devices or medical software-only products, as advisor and supporter of the project manager and team.
2. Analyze and review product documentation, approve and contribute product-specific and quality-oriented feedback, ensuring process-compliant software development.
3. Support and coordinate risk management activities according to ISO 14971 with interdisciplinary teams.
4. Check project status and negotiate necessary measures with the team.
5. Participate in project milestones and approve milestone decisions from a quality management perspective.
6. Manage complaints and support reporting to authorities and management if necessary.
7. Contribute to post-market surveillance activities for the product.
8. Work closely with colleagues from Quality Management, Development, Product Management, Information Security, and Regulatory and Clinical Affairs.

Minimum Requirements

1. Degree in computer science, business administration, or a comparable field.
2. Several years of professional experience in software development or product development of medical devices, specifically in quality management.
3. Strong understanding of quality principles; able to work independently and goal-oriented.
4. Excellent communication and teamwork skills.
5. Proficiency in German and English.