20 beste Stellen als developer it expert – aktuell auf Personalsuche

Head of QRA - Full Time - CH
RetinAI Medical —Bern, BE
- 100%
- Hybrides Arbeiten
- Doktorat
- Englisch
- Master
Direkt bewerben
Internal Auditor/Internal Audit Manager (with experience in Operations and/or Project Management)
Lonza —Basel, BS
- 100%
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- Englisch
- Master
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Major Account Manager - DACH
SonarSource —Genf, GE
- 100%
- Salesforce
- Englisch
- Erfahrung in der IT
Forward Deployed Engineer I, Google Cloud Consulting (French, German)
Google —Zürich, ZH
- 100%
- Microsoft Excel
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3 Tage
Product Designer
Ethereum Community Fund —Home Office
- 100%
- Homeoffice
- Englisch
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PaPM Senior Consultant (m/f/d)
msg global solutions —Zürich, ZH
- 100%
- Schreibfähigkeiten
- Englisch
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Manager Terminal Design & Operations
MSC Mediterranean Shipping Company S.A. —Genf, GE
- Microsoft Powerpoint
- AutoCAD
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BBVA —Zürich, ZH
- 100%
- Spanisch
- Englisch
- Erfahrung in der IT
3 Tage
PaPM Principal Consultant (m/f/d)
msg global solutions —Zürich, ZH
- 100%
- Informatik
- Englisch
- Bachelor
Equipment Engineering Manager
MSC Mediterranean Shipping Company S.A. —Genf, GE
- Management-Erfahrung
- Englisch
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Senior Technical Consultant SAP Development (Transportation Management)
Sika —Zürich, ZH
- 100%
- Management-Erfahrung
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Senior Lead - Computational and Robotics Engineer, Lightspray
On AG —Zürich, ZH
- Doktorat
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- Produktion
Senior Robotic Middleware Software Engineer
ABB Robotics Switzerland Ltd —Zürich, ZH
- 100%
- C++
- Linux
- Python
Direkt bewerben
9 Tage
Senior ProServe Cloud Architect, Healthcare and Life Sciences (HCLS), AWSI Sales
AWS EMEA SARL (Switzerland Branch) —Genf, GE
- 100%
- Management-Erfahrung
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12 Tage
Senior Engineer Technology Infrastructure
MSC Mediterranean Shipping Company S.A. —Genf, GE
- Management-Erfahrung
- Englisch
- Master
Senior Lead - Apparel Development
On AG —Zürich, ZH
- Englisch
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- Bachelor
Head of Product Development | Accessories
On AG —Zürich, ZH
- Erfahrung in der IT
- Produktion
- Führungserfahrung
Principal Delivery Consultant- Technical Lead GenAI/ML & Data Science, Professional Services, AWS Industries
AWS EMEA SARL (Switzerland Branch) - G96 —Zürich, ZH
- 100%
- Datenbanken
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2 Tage
Professional Services Consultant (German-Speaking)
Ripple —Genf, GE
- 100%
- Englisch
- Rechnungswesen
- Kommunikationsfähigkeit
- Eltern-/Erziehungsurlaub
Direkt bewerben
12 Tage
Senior Relationship Manager
BNP Paribas —Zürich, ZH
- 100%
- Management-Erfahrung
- Schreibfähigkeiten
- Englisch

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Head of QRA - Full Time - CH

RetinAI Medical
Bern, BE

Direkt bewerben

Details zur Stelle

100% | Pensum: 90-100%

Leistungen

Events zur Teambildung

Qualifikationen

Doktorat
Englisch
Master
Analysefähigkeit
Bachelor
Betriebswirtschaftslehre
Doktorat in Rechtswissenschaften
Kommunikationsfähigkeit
ISO 13485

Vollständige Stellenbeschreibung

About Us

Ikerian AG (formerly RetinAI Medical) is a fast-growing medical device software company headquartered in Bern, Switzerland. Our mission is to enable the right decisions sooner in healthcare, through transformative AI & data management solutions for disease screening and monitoring. Join our diverse team of entrepreneurs, developers, researchers, and commercial experts who are collectively shaping the future of healthcare.

Job Description

We are looking for a Head of Quality & Regulatory Affairs (QRA) to join our company in Bern, Switzerland. This role is pivotal in driving our internal operational maturity and ensuring global compliance across our expanding product portfolio. Following Ikerian’s acquisition by EssilorLuxottica, you will lead the evolution of the QRA department from a high-growth startup environment to a world-class subsidiary operation. You will oversee global product clearances for Software as a Medical Device (SaMD), optimize our Quality Management System (QMS), and serve as a strategic partner to internal R&D, Research, and global sister companies like Heidelberg Engineering.

Key Responsibilities

Lead and mentor a global QRA team located across various time zones, establishing a supportive, high-performance team culture driven by clear accountability, structured goal-setting, and skills development.
Act as the legal Person Responsible for Regulatory Compliance (PRRC) under EU MDR to ensure device conformity, keep technical documentation up to date, and oversee post-market surveillance and vigilance reporting obligations.
Develop and execute robust global regulatory strategies with an emphasis on securing and maintaining rapid market access via FDA submissions and CE-MDR compliance frameworks.
Govern and scale a world-class Quality Management System (QMS) ensuring continuous organizational readiness for ISO 13485 and the Medical Device Single Audit Program (MDSAP).
Serve as the primary corporate representative during all internal, Notified Body, partner, and health authority audits to ensure the continuous validation of corporate certifications.
Establish structured cross-functional alignment with R&D to seamlessly integrate design controls, risk management, and software lifecycles into early product development stages.
Partner with the IT Infrastructure and Security functions to support data privacy governance frameworks including GDPR and HIPAA compliance while aligning quality processes with emerging cybersecurity standards.
Translate market intelligence and evolving global regulations into proactive compliance roadmaps to ensure customer specifications and changing health authority standards are built into the corporate lifecycle.

Requirements

University degree in Life Sciences, Biomedical Engineering, Law, or a relevant scientific discipline; a PhD or MBA is a strong asset.
A minimum of 10 years of professional experience with a documented track record of successfully leading, managing, and mentoring cross-functional quality and regulatory teams.
A minimum of 8-10 years of dedicated industry experience in medical device Quality and Regulatory Affairs specifically focused on Software as a Medical Device (SaMD).
Proven track record as a legal Person Responsible for Regulatory Compliance (PRRC) with deep experience managing complex technical files for EU MDR and FDA submissions.
Expert technical knowledge of ISO 13485, EU MDR, IEC 62304 software lifecycles, ISO 14971 risk management, and FDA 21 CFR Part 820. Formal Lead Auditor certification is highly valued.
Demonstrated ability to manage multi-faceted projects involving complex technical, clinical data, and regulatory evaluation components across international borders.
Excellent verbal and written English communication skills.
Strong analytical and problem-solving abilities with an exceptional eye for process detail, operational efficiency, and structural quality.
Demonstrated entrepreneurial and collaborative mindset with excellent team-building and conflict-resolution capabilities.
Ability to work independently as a leader.
Available to work during Central European Time (CET) business hours with a regular physical presence at our Bern headquarters.

Benefits

What We Offer

A chance to be part of an exceptional global team driving innovation in healthcare.
A competitive salary in a supportive work environment that fosters work-life balance.
Opportunities for professional growth and development in an international setting.
A culture of collaboration and inclusion, which is fundamental to our ethos.
Occasional travel to our HQ in Switzerland, immersing you in our core operations and company culture.

Direkt bewerben

Erweiterte Suche

developer it expert Jobs

Head of QRA - Full Time - CH

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Major Account Manager - DACH

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Manager Terminal Design & Operations

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Equipment Engineering Manager

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Senior Lead - Computational and Robotics Engineer, Lightspray

Senior Robotic Middleware Software Engineer

Senior ProServe Cloud Architect, Healthcare and Life Sciences (HCLS), AWSI Sales

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Senior Lead - Apparel Development

Head of Product Development | Accessories

Principal Delivery Consultant- Technical Lead GenAI/ML & Data Science, Professional Services, AWS Industries

Professional Services Consultant (German-Speaking)

Senior Relationship Manager

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