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Regulatory Affairs (IVDR) Manager / Sr Manager
Regulatory Affairs (IVDR) Manager / Sr ManagerSOPHiA GENETICS • Rolle, Vaud, Switzerland
Regulatory Affairs (IVDR) Manager / Sr Manager

Regulatory Affairs (IVDR) Manager / Sr Manager

SOPHiA GENETICS • Rolle, Vaud, Switzerland
Vor 30+ Tagen
Stellenbeschreibung

Do you bring a background in Regulatory Affairs, and a passion for driving innovative solutions? Have you driven Reagent or Software products through IVDR approval with notified bodies?

If this sounds like you and you are driven by purpose, Join the SOPHiA GENETICS Regulatory Affairs Team as a IVDR Regulatory Affairs Manager / Senior Manager, and enable us to make a positive impact on the outcomes for cancer and rare disease patients worldwide.

Enjoy the flexibility of a hybrid work schedule allowing 2 days PW home working, collaborating closely with colleagues in either our Rolle, CH or Boston, MA corporate offices.

Our mission

We believe there is a smarter, more data-driven way to make decisions in healthcare and our cloud-native AI powered SOPHiA DDM Platform makes that vision a reality on a daily basis. You will have direct input to our mission to democratize data-driven medicine for the ultimate benefit of cancer and rare disease patients across the globe.

Your mission

Reporting to the Head of Regulatory Affairs you’ll be directly responsible for driving the strategy and delivering the execution on submission for our transition to IVDR.

The value you bring

  • Provide strategic regulatory guidance for IVDR Class C and higher IVD and CDx products.
  • Drive and coordinate the development and execution of regulatory strategies and submission plans to support timely product approvals and market access.
  • Lead regulatory submission efforts including EU Clinical Trial Assays (CTAs), Ethical Approvals, and Notified Body filings.
  • Serve as the primary point of contact for IVDR-related projects internally and externally ( with Notified Bodies).

Requirements

We know that every background is different, but to be best set for success we see you bringing :

  • 8+ Years Regulatory Affairs experience within Diagnostics or Medical Devices
  • Proven track record of successful IVDR Class C or higher submissions and approval
  • Direct working knowledge of either IVDR submission for software-based devices or NGS-based diagnostics (ideally both). EN / IEC 62304 Beneficial.
  • Experience of working is EU Notified Bodies / Regulatory Authorities essential, international bodies (US / Japan) Beneficial.
  • Knowledge of oncology regulatory frameworks and companies diagnostic development highly beneficial
  • As a public organisation facing ongoing commercial growth, you will bring a success-orientated and solutions-focused mindset that embraces team collaborations, change, growth and inclusion.

    As an international organisation, English is our primary business language and you will need to bring full fluency in English. As part of your recruitment journey, you should expect to meet English-only speakers, so for best chances of success, you should include your CV in English. Non-English CVs have a high likelihood of being rejected at application stage.

    Benefits

    You will be joining an organisation with the patient at the heart of every decision and action, driven by purpose as we pursue exponential growth.

    Business recognition and accolades include :

  • World's most innovative companies (Top 10)
  • World's smartest companies (Top 50)
  • 100 Best Places to Work in Boston
  • Top 10 European Tech Startup
  • Top 10 European biotechs startup to watch
  • Top 25 East-Coast Biotech to watch
  • Our benefits package is comprehensive, but varies internationally in-line with local standards and laws. You can discuss a full breakdown with us, but as a brief overview :

    US :

  • Outstanding Medical, Dental & Vision with 90% Employer Contribution
  • Company matched 401K at 4%
  • Company-paid short & long-term disability insurance
  • FSA commuter benefits
  • 20 Days PTO, increasing to 25 with tenure; 5 Days Sick and 14 Public Holidays
  • Free EAP
  • CH

  • Sickness and Accident coverage through Helsana
  • Meal Vouchers at 90CHF PM with our partner cafeteria
  • A fun and engaging work environment, with Rest & Entertainment space, full stocked free coffee machine and free fruit / snacks
  • Free parking in an easy to access location
  • A strong social committee whose purpose is to make SOPHiA GENETICs both enjoyable as well as rewarding
  • As our global HQ, you’ll have direct interaction and exposure to senior leadership and our executive team locally
  • Our DNA

    Like the strands of DNA itself, SOPHiA GENETICS and the team are deeply interconnected and reliant on each other to deliver. There are common threads across the team. Things that bind us together. Those things are Relentless Curious; Resilient & Nimble and Fearlessly Adventurous

    Our Virtues

    At SOPHiA GENETICS we established our 7 Virtues to clarify how our principles show up each day through action. We Decide; We Do; We Collaborate; We Innovate; We Empower; We Adapt and We Learn.

    At the centre of our Virtues is our Mantra, We Care, which provides a constant reminder of the compassionate, benevolent, and hopeful nature of our mission and how it should be threaded through each of our Virtues and everything we do. Learn more about our DNA and Virtues on our Careers portal

    The Process

    We use the power of AI to help our partners make decisions. If you’re utilising AI in your search and application process, why not use some of these prompts, or read our AI guide.

    ‘What impact can I expect to have on the world by working at SOPHiA GENETICS?’

    ‘I have an interview with SOPHiA GENETICS. What should I know before I meet with them?’

    ‘I am a

  • job title
  • What can SOPHiA GENETICS offer my career?’
  • Apply now with your CV and any supporting information.

    Suitably qualified candidates will be invited through an interview and screening process where you will speak with members of our Talent Acquisition Team, the hiring leader alongside key colleagues and stakeholders from across the business. If you need additional support for accessibility, please contact our TA team for assistance.

    We appreciate the value external partners can bring, but we operate a direct-hiring model and we are not looking to utilise agency support at this time. All hiring is controlled by Talent Acquisition, potential partners should liaise through TA and not our hiring teams please.

    Starting Date : Q1 2026

    Location : Boston, MA or Rolle, CH - Hybrid work schedule

    Contract : Permanent, full time

    MA Pay Range : $88K - $168K (Manager) / $104K - $186K (Sr Manager)

    Disclaimer :  The estimated pay range represents a good faith estimate of what the Company expects to pay a successful applicant for the listed position and applies specifically to candidates based in Massachusetts. Due to various factors, the estimated pay range may vary in other locations. Should the level or location of the role change during the hiring process, the applicable base range may be updated accordingly. Compensation decisions are dependent on several factors including, but not limited to, an individual’s qualifications, job related skills, years of experience, location, relevant education or training, internal equity, and alignment with market data. The range does not include benefits, and if applicable, bonus, commission, or equity.​

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