Mobile Engineering Manager

ROM Utrecht Region; Utrecht; Hybrid; EUR 90,000 - 150,000; Full time

Job summary

ViCentra B.V. is seeking a Mobile Engineering Manager to own and evolve the Kaleido App and its mobile platform within a regulated medical device framework.

You will define foundations, processes, and quality standards while enabling innovation and scale. You will lead a mobile team (up to ~10) across Android and iOS, collaborate with security, systems, manufacturing, and regulatory teams, and manage external partners as we bring software in-house and strengthen Scrum practices in a compliant

Qualifications

• Proven leadership experience managing mobile engineering teams.
• Deep knowledge of medical device regulations and QMS including ISO 13485, IEC 62304, IEC 62366, FDA / 21 CFR 820.
• Strong understanding of mobile app development (Android and/or iOS) with hands-on Kotlin/Swift.
• Experience bringing externally developed software in-house.
• Lead the transition of a regulated app from external partner to internal ownership.
• Define and improve mobile software processes in a regulated environment.

Responsibilities

• Lead the transition of a medically regulated mobile app from an external development partner to internal ownership
• Define, implement, and continuously improve mobile software development processes within a regulated medical device environment
• Build and scale a mobile engineering team (growing to ~10 people) across Android, iOS, usability, and testing
• Establish and mature medical-device-compliant software development processes (ISO 13485, IEC 62304, IEC 62366)
• Own delivery of mobile software used in conjunction with medical hardware and cloud backends
• Drive collaboration across cyber security, systems, manufacturing, quality, and regulatory teams
• Act as the key technical and delivery interface with external partners and suppliers
• Introduce and strengthen Agile / Scrum ways of working within a regulated environment
• Proven leadership experience managing mobile engineering teams
• Deep knowledge of medical device regulations and QMS, including ISO 13485, IEC 62304, IEC 62366, FDA / 21 CFR 820
• Experience working with externally developed software and bringing it in-house
• Strong understanding of mobile app development (Android and/or iOS) and hands on background in Android (Kotlin) and/or iOS (Swift)
• Previous scale-up or rapid-growth environment experience

Skills

Medical device regs

Agile / Scrum

Mobile engineering leadership

Android Kotlin

iOS Swift

External partner mgmt

Regulatory QMS

Job description

ViCentra B.V. is active in designing simple, beautiful, and effective solutions for people living with diabetes. The company combines technological innovation with human-centered design to empower individuals with more freedom and confidence in their lives. ViCentra's mission is to make living with diabetes easier, and its values drive every decision and creation.

As a mobile engineering manager, you will play a defining role in how ViCentra builds, owns, and evolves its mobile technology. You will take end-to-end ownership of the Kaleido App and the engineering capability behind it, defining the mobile engineering foundations, setting development processes, quality standards, and ways of working that meet the demands of a regulated medical device environment while enabling innovation and agility. This role is critical to ViCentra's growth and will have a lasting influence on how we build medical software for years to come.

• Lead the transition of a medically regulated mobile app from an external development partner to internal ownership
• Define, implement, and continuously improve mobile software development processes within a regulated medical device environment
• Build and scale a mobile engineering team (growing to ~10 people) across Android, iOS, usability, and testing
• Establish and mature medical-device-compliant software development processes (ISO 13485, IEC 62304, IEC 62366)
• Own delivery of mobile software used in conjunction with medical hardware and cloud backends
• Drive collaboration across cyber security, systems, manufacturing, quality, and regulatory teams
• Act as the key technical and delivery interface with external partners and suppliers
• Introduce and strengthen Agile / Scrum ways of working within a regulated environment
• Proven leadership experience managing mobile engineering teams
• Deep knowledge of medical device regulations and QMS, including ISO 13485, IEC 62304, IEC 62366, FDA / 21 CFR 820
• Experience working with externally developed software and bringing it in-house
• Strong understanding of mobile app development (Android and/or iOS) and hands on background in Android (Kotlin) and/or iOS (Swift)
• Previous scale-up or rapid-growth environment experience