21 ago - Italia
Velferd
About VLF Consulting
At Velferd, through our brand
VLF 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 MedTech sector.
What You'll Do
As a
Software & 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 to
IEC 62304
- 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 in
medical device software
and/or
active medical devices
Solid knowledge of:
- IEC 62304
- IEC 60601 series
- EU MDR 2017/745
- 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 27001
- Cybersecurity for Medical Devices
- Software Validation
- Artificial Intelligence / Machine Learning in healthcare
- IEC 81001-5-1
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