Senior Software & Samd Consultant (Iec 62304, Mdr, Fda) | Freelance | Remote
Pubblicato il 28-08-2026 - Vlf Consulting in Italia
About VLF Consulting
At Velferd, through our brandVLF Consulting, we help medical device and healthcare companies bring innovative products to market safely, efficiently, and in compliance with international regulations.
Our team supports manufacturers worldwide in Regulatory Affairs, Quality Assurance, Clinical, and Technical Documentation, with a strong focus on Medical Devices, SaMD, AI-based solutions, and Active Medical Devices.
We are growing and looking for an experienced consultant who can contribute to challenging and high-impact projects in the Med Tech sector.
What You'll Do
As aSoftware & Active Medical Devices Consultant, you will work with international clients on the development, compliance, and market access of innovative medical technologies.
Your activities may include:
Supporting software lifecycle processes according toIEC *****
Contributing to the development and compliance of active medical devices
Preparing and reviewing technical and regulatory documentation
Performing gap assessments and compliance reviews
Supporting risk management activities
Collaborating with multidisciplinary design and development teams
Supporting cybersecurity and information security initiatives
Providing regulatory guidance for EU and US market access
Participating in audits, inspections, and technical reviews
What We're Looking For
Mandatory
Strong experience inmedical device softwareand/oractive medical devices
Solid knowledge of:
IEC *****
IEC ***** series
EU MDR ********
FDA regulatory framework
Ability to work independently and manage client-facing activities
Excellent analytical and problem-solving skills
Fluent English (written and spoken)
Degree in Computer Science, Biomedical Engineering, Electronic Engineering, or related disciplines
Nice To Have
Experience with:
ISO *****
Cybersecurity for Medical Devices
Software Validation
Artificial Intelligence / Machine Learning in healthcare
IEC *********
FDA Cybersecurity Requirements
Previous consulting experience
Why Join Us
100% remote collaboration
Flexible workload and project-based engagement
Exposure to international Med Tech projects
Opportunity to work with innovative technologies, including Software as a Medical Device (SaMD) and AI-driven solutions
Direct collaboration with senior regulatory and quality experts
Dynamic and entrepreneurial environment where your contribution has real impact
Interested?
If you have experience in medical device software and want to work on projects that make a difference in healthcare, we'd like to hear from you.
Note: Only applications that meet the required qualifications will be considered.