Senior Quality Manager (Orpha Care)- fixed-term until 31.12.2028

AOP Health; Wien; On-site; EUR 45,000 - 55,000; Full time

Benefits offered by this job

Open corporate culture

Professional development

Flat hierarchies

Competitive salary package

Job summary

OrphaCare, a subsidiary of AOP Health, is seeking a Senior Quality Manager to join the QARA team. The role focuses on developing and maintaining a robust QMS for Class III implantable medical devices, aligning with ISO 13485 and MDR/FDA standards.

You will drive eQMS implementation, ensure validated processes, and collaborate with QA, RA and technical teams to harmonize quality across sites. This fixed-term role supports ongoing quality initiatives.

Qualifications

• Degree in scientific, engineering or quality-related discipline.
• 7-10 years of experience in medical device quality management.
• Practical knowledge of ISO 13485, EU MDR and FDA requirements.
• Hands-on experience with eQMS implementation and training.

Responsibilities

• Develop, maintain, and improve the QMS per ISO 13485 and MDR/FDA.
• Identify QMS gaps and drive procedures, records, and templates.
• Harmonize quality processes across sites.
• Collaborate with QA/RA/technical teams on design controls, risk, supplier management, production controls, validation, complaints, and PMS.
• Lead eQMS deployment and validation efforts.

Skills

Quality management

Cross-functional collaboration

eQMS implementation

Audits & CAPA

Education

Degree in scientific/engineering/quality

7-10 years in medical device quality management

Tools

eQMS

Job description

OrphaCare is a subsidiary of AOP Health that specializes in medical devices and patient‑support solutions for treating rare and complex diseases. To enhance our team we are looking for a:

Senior Quality Manager (Orpha Care)- fixed-term until 31.12.2028

Start: as of now

What Your Day To Day Will Look Like

• Develop, maintain, and continuously improve the Quality Management System in accordance with ISO 13485:2016 and applicable EU Medical Device Regulation (MDR) and FDA QMSR requirements.
• Identify QMS gaps and drive the development, revision, and implementation of procedures, work instructions, templates, and records.
• Harmonize quality processes and documentation across company sites.
• Collaborate closely with QA, RA, and technical teams to establish and maintain compliant quality processes covering design controls, risk management, supplier management, production controls, validation, complaints, and post-market surveillance.
• Support and lead key activities related to the implementation and deployment of the electronic Quality Management System (eQMS).
• Define user requirements, workflows, document structures, metadata, access permissions, and reporting requirements for the eQMS.
• Coordinate validation activities, user training, and go-live support to ensure the eQMS remains in a validated state.

Your Qualifications And Experience

• Degree in scientific, engineering or quality-related discipline
• 7-10 years of experience in medical device quality management.
• Practical knowledge of ISO 13485, EU MDR and FDA requirements, and quality management processes.
• Experience in developing procedures, implementing QMS continual improvements, and managing quality documentation.
• Hands‑on experience with eQMS implementation, administration, validation, and training.
• Experience with audits, CAPA, change control, and management review processes.
• Strong organizational skills, attention to detail, and the ability to work effectively across functions.
• Experience with Class III or implantable medical devices is considered a plus
• Fluent English; German is an advantage.

Our offer

• Open corporate culture with the opportunity to bring in your own ideas
• Great opportunities for personal and professional development
• Attractive work environment with excellent career opportunities and flat hierarchies
• Competitive salary package plus bonus and various benefits
• Gross annual salary provided for this function is a minimum of EUR 49.840, - based on full-time employment (38,5h/week). Any potential overpayment depends on professional experience and qualifications.

OrphaCare is a subsidiary of AOP Health that specializes in medical devices and patient‑support solutions for treating rare and complex diseases. To enhance our team we are looking for a: We are looking for an experienced and motivated Senior Quality Manager to join our OrphaCare QARA team. In this role, you will lead the development and maintenance of our Quality Management System (QMS) for Class III active implantable medical devices and play a key role in advancing our eQMS implementation and quality harmonization initiatives.

What Your Day To Day Will Look Like

• Develop, maintain, and continuously improve the Quality Management System in accordance with ISO 13485:2016 and applicable EU Medical Device Regulation (MDR) and FDA QMSR requirements.
• Identify QMS gaps and drive the development, revision, and implementation of procedures, work instructions, templates, and records.
• Harmonize quality processes and documentation across company sites.
• Collaborate closely with QA, RA, and technical teams to establish and maintain compliant quality processes covering design controls, risk management, supplier management, production controls, validation, complaints, and post-market surveillance.
• Support and lead key activities related to the implementation and deployment of the electronic Quality Management System (eQMS).
• Define user requirements, workflows, document structures, metadata, access permissions, and reporting requirements for the eQMS.
• Coordinate validation activities, user training, and go-live support to ensure the eQMS remains in a validated state.

Your Qualifications And Experience

• Degree in scientific, engineering or quality-related discipline
• 7-10 years of experience in medical device quality management.
• Practical knowledge of ISO 13485, EU MDR and FDA requirements, and quality management processes.
• Experience in developing procedures, implementing QMS continual improvements, and managing quality documentation.
• Hands‑on experience with eQMS implementation, administration, validation, and training.
• Experience with audits, CAPA, change control, and management review processes.
• Strong organizational skills, attention to detail, and the ability to work effectively across functions.
• Experience with Class III or implantable medical devices is considered a plus
• Fluent English; German is an advantage.

Our offer

• Open corporate culture with the opportunity to bring in your own ideas
• Great opportunities for personal and professional development
• Attractive work environment with excellent career opportunities and flat hierarchies
• Competitive salary package plus bonus and various benefits
• Gross annual salary provided for this function is a minimum of EUR 49.840, - based on full-time employment (38,5h/week). Any potential overpayment depends on professional experience and qualifications.