Mobile Engineering Manager

Making every move matter

At Vi Centra , we’re on a mission to make living with diabetes easier, by designing simple, beautiful, and effective solutions that fit people’s lives, not the other way around.

We combine technological innovation with human-centered design to empower people with more freedom, confidence, and life on their terms. Our values;

Be Bold, Build Trust, Focus on the Customer and Deliver Excellence drive everything we create and every decision we make.

We believe that when ambition meets purpose, remarkable things happen. If you thrive in a space where ideas accelerate, challenges spark growth, and making a difference is the goal, ViCentra is your next great adventure.

As Mobile Engineering Manager
, you will play a defining role in how ViCentra builds, owns, and evolves its mobile technology. As we transition from externally developed software to a fully in‑house, scalable mobile function
, you will take end‑to‑end ownership of the Kaleido App and the engineering capability behind it.

From day one, you will define ViCentra’s 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. You will build and grow the team, shape the culture, and ensure the mobile platform is robust, compliant, and ready to scale.

This role sits at the intersection of technology, regulation, and product strategy
. Your work will directly support ViCentra’s US expansion, future device integrations, and long‑term product roadmap.

This is not a “keep‑the‑lights‑on” role. You will establish the foundations of a mobile platform that is critical to ViCentra’s growth and have lasting influence on how we build medical software for years to come.

In your role, you will:

• 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

• Ensure mobile software meets the highest standards of safety, quality, and regulatory compliance

• Support product releases tied to ViCentra’s go-to-market strategy

• Report directly into the VP of R&D and shape the future mobile roadmap

• Extensive experience in medical device software development

• 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)

• Confidence working in complex multi-disciplinary environments

• Comfortable operating with autonomy, ownership, and accountability

• Previous scale-up or rapid-growth environment experience

Working at ViCentra means joining a team defined by:

• Courage to create:
  
  We experiment, challenge norms, and learn fast.

• Trust above all:
  
  Integrity, honesty, and openness shape our relationships.

• Customer‑f…