Why we need you
We’re looking for a Junior Quality Manager to support the maintenance and improvement of our Quality Management System (ISO 13485). You’ll work hands-on with document control, CAPA tracking, internal audits, and supplier evaluations — helping us keep our compliance foundations solid as we scale in digital health. This is a great role for someone who enjoys structured work, is eager to learn, and wants real responsibility in a regulated environment.
About the Company
At nyra health, we’re building software that makes a real difference. Our tools help clinics, therapists, and patients in their neurorehabilitation journey. Our products — myReha (therapy app) and nyra insights (web platform for patient management and analysis) — deliver evidence-based, AI-powered neurotherapy at scale.
If that resonates with you, we’d love to hear from you.
What you’ll shape
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QMS maintenance & improvement: Continuously improve and track changes within our Quality Management System, keeping documentation, processes, and controls in shape.
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CAPA & document control: Support CAPA documentation with follow-ups and status updates, and assist with general document control tasks to ensure everything stays current and audit-ready.
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Software validation & supplier evaluation: Carry out software validation and supplier evaluation processes, building confidence in our toolchain and vendor relationships.
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Internal audits: Plan and take part in internal audits within the ISO 13485 and MDR frameworks, helping identify gaps and drive continuous improvement.
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Quality advocacy: Be an advocate for quality across the company — working cross-functionally with Product, Engineering, and Operations to embed quality thinking into how we build and ship.
What sets you up for success
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Interest in medical device quality: you’re curious about how quality systems work in healthcare and motivated to build expertise in ISO 13485 and MDR
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Structured & detail-oriented: you’re the kind of person who notices when something is out of place and takes pride in clean, accurate documentation
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Strong communicator: you can work effectively across teams and aren’t afraid to ask questions or flag issues
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English proficiency: our working language is English; German is a plus
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Bonus: studying or background in medical engineering, regulatory affairs, healthcare management, or a related field; basic understanding of ISO 13485
Beyond your CV
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Pragmatic and reliable: you follow through on tasks, meet deadlines, and don’t let things slip through the cracks
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Eager to learn: you’re comfortable in areas where you don’t have all the answers yet and actively seek to build your knowledge
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Comfortable with ambiguity: you can switch between policy and practice and thrive in a fast-moving environment where flexibility matters
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Quality mindset: you care about doing things right — not just checking boxes, but understanding why the process matters
Why nyra health
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Fast-growing digital health scale-up with international ambition
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Direct collaboration with our QMRA Team Lead and founders
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Hands-on experience with real-world compliance challenges
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Responsibility from day one and tangible impact on how we scale securely
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Transparent, direct communication and feedback culture
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Attractive compensation, Phantom Stock Options, and company perks (Wiener Linien Jahreskarte etc.)
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Beautiful office in Vienna’s First District with regular team events
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Some of the best Mario Kart drivers in the Austrian startup scene ;)
The Process
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Intro call (~30 mins): Background, expectations, and an overview of nyra health and the role.
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Practical exercise: A short case focused on QMS improvement (e.g. CAPA handling, document control, or audit preparation), which you will discuss with our QMRA Team Lead.
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Meet with Founders: Discuss your case and approach as the last step before joining nyra health.
