Senior Post-Market Surveillance Manager (m/f/d)

Hilo By Aktiia

Source: WorkableLocation: Germany onlyPublished: Sep 08, 2026Confirmed active: Sep 10, 2026
Full-timeHealthcare50-200

Key points from the posting

Tech stack
FDA MDREU MDRISO 13485ISO 14971
Seniority:
Senior

Read out of the job posting automatically

Our assessment

  • Our reading of the full posting text confirms it: fully remote.
  • The posting states no salary. Comparable roles in our index (97 postings): median 4,750 euros per month, middle range 3,959 to 5,675 euros.
  • 5 more open roles from this employer in our index. 4 of them fully remote.

This section only: calculated automatically by nomado24, from our own job index and our own reading of the posting text. Not stated by the employer.

Job description

Company & Role Overview

About Hilo by Aktiia

High blood pressure is the world's most common disease, causing 18M deaths each year. At Hilo by Aktiia, we're building a world where no lives are lost to its effects — with technology that helps people take control of their health.

We're a venture-backed scale-up with $96M raised from investors in Europe and the US. Rooted in 18 years of research at the Swiss Center for Electronics and Microtechnology (CSEM), our device is the world's only medically accurate, cuffless, continuous blood pressure monitor for daily use — clinically validated and CE Marked as a Class IIa medical device, now available in 12 countries. In July, we launched in the US.

We're a remote-first company headquartered in Neuchâtel, Switzerland, united by our passion for impact and innovation.

Role overview

As Post-Market Surveillance Manager, you'll build and run our global post-market surveillance system — from complaint handling and adverse-event reporting to data trending and governance — and lead its rollout across Customer Support, QA, Regulatory, Engineering, Clinical, and Product. This is a hands-on role: you'll turn post-market insights into action that improves product quality, patient safety, and the customer experience, drawing on strong judgment, disciplined execution, and the ability to influence stakeholders globally.

Requirements

Core responsibilities

  • Design, build, and run our global post-market surveillance system — complaint handling, adverse-event/vigilance reporting, escalation, and governance — staying hands-on for complex or high-risk cases
  • Own the complaint-to-report pipeline: reportability assessments and timely, accurate adverse-event/vigilance submissions across markets (US, EU, and others)
  • Build the KPIs, dashboards, and trending methods that surface safety, quality, and customer-experience signals — and turn findings into action via CAPA, risk management, product/software fixes, and labeling updates
  • Lead the cross-functional rollout — implementation plans, priorities, dependencies, and risk — to build sustainable post-market processes and infrastructure
  • Present post-market performance and recommendations to leadership, and support PMS reports, PSURs, and management reviews
  • Act as SME during audits and inspections, and guide internal teams and external partners on post-market activities

Background & Experience

  • 7+ years in medical-device post-market surveillance, complaint handling, quality, or regulatory affairs, including leading process implementations
  • At least a bachelor's degree
  • Hands-on experience with complaint investigations, reportability assessments, and regulatory submissions (FDA MDR, EU MDR vigilance/PMS, ISO 13485, ISO 14971), plus post-market data analysis
  • Program management skills — workstreams, stakeholders, dependencies — plus an analytical mindset for turning complaint data into risk-based recommendations
  • Strong communicator, comfortable influencing cross-functional teams, leadership, and regulators
  • Hands-on, independent leadership style; able to scale processes as we grow
  • Nice to have: experience with additional international markets or digital complaint-management systems

What success looks like

  • Scalable processes for complaint intake, investigation, and resolution — with clear escalation pathways to ensure adverse events and reportable incidents are identified, assessed, and reported within regulatory timeline
  • Customer Support consistently identifies, documents, and escalates complaints and potential safety events, thanks to close partnership and training
  • KPIs and dashboards give clear visibility into complaint timeliness, resolution, regulatory reporting, and emerging trends
  • Post-market insights translate into action — product improvements, CAPAs, risk-management updates, and a better customer experience

Benefits

What Makes You A Great Fit

At Hilo by Aktiia, our values guide everything we do:

Move the Needle — You focus on what drives real impact. You let data and clarity guide your decisions, and you take accountability for results. You're a difference maker — you drive ideas to commercial success from start to end

Move Fast, Learn, Refine — You work with urgency and purpose, balancing speed with quality. You treat feedback as a chance to learn, and you're deep in customer and partner feedback — translating it to action quickly

Team First — You collaborate effectively across teams and build trust through clarity and respect. You're comfortable bridging local execution with a global team, and you communicate openly across time zones

Why Join Us?

  • Hilo by Aktiia is becoming one of the most important med-tech companies, and you can be part of this exciting story
  • Work on a mission that matters: transforming cardiovascular health at global scale
  • Be part of a high-impact, fast-growing, and venture-backed scale-up company
  • Collaborate with a diverse, passionate, and …
workableQuality and RegulatoryQuality Assurance

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