Regulatory & Quality Consultant - SaMD

Rellia Health; Canada; Remote; CAD 83,000 - 165,000; Part time

Job summary

Rellia Health in Canada offers regulatory and quality consulting for early‑stage SaMD and medical device startups. This is virtual, project‑based, independent contractor work with no minimum hourly commitment and total flexibility in hours and rate.

You will guide clients on regulatory compliance and quality management systems, develop QMS, conduct mock audits, analyze requirements, and advise strategies for compliance and documentation.

Qualifications

• Translate regulatory standards into practical, maintainable systems (QMS, documentation)
• Guide mock audits and regulatory reviews for SaMD/medical device startups
• Know regulatory requirements for Health Canada licensing and EU/US pathways
• Understand cybersecurity and privacy regulations in health tech
• Present directly to customers and regulators with clarity and credibility
• No prior consulting experience required; capable self-starter for startups

Responsibilities

• Develop quality management systems for SaMD clients
• Conduct mock audits and analyze regulatory requirements
• Advise on FDA SaMD guidance, 510(k), De Novo, or PMA submissions
• Apply ISO 13485 / MDSAP and IEC 62304 practices for lean startup teams
• Guide cybersecurity, privacy, and product documentation to meet industry standards
• Present directly to customers and regulators with practical, maintainable compliance systems

Skills

Regulatory compliance

Quality Management Systems

FDA SaMD guidance

510(k) submissions

IEC 62304 practices

ISO 13485 familiarity

Regulatory strategy

Presenting to regulators

Lean startup adaptation

Job description

Guide early-stage SaMD and medical device startups through regulatory and quality milestones—from first 510(k) filings to QMS buildout and Health Canada licensing.

Rellia Health offers regulatory and quality consulting for early-stage startups. We work with medical device and SaMD companies at pivotal moments: their first 510(k), their first QMS, their first Health Canada licensing decision, the question of whether their software is a device at all. The clients who come to us are often navigating these questions for the first time, and they're trusting us to guide them through it.

Role Description

This is virtual, project-based, independent contractor work. There is no minimum hourly commitment and you'll have complete flexibility in your working hours and hourly rate. In this position, you will guide clients on regulatory compliance and quality management systems specific to Software as a Medical Device (SaMD). Duties include developing quality management systems, conducting mock audits, analyzing regulatory requirements, advising strategies for compliance, and ensuring product documentation meets industry standards.

We're looking for a consultant to grow alongside us and who wants to be part of building something worthwhile.

Qualifications

• ISO 13485 or MDSAP Quality Management Systems, especially those built for lean startups
• IEC 62304 Software Development Lifecycle practices
• FDA SaMD guidance documents or equivalent
• 510(k), De Novo, or PMA submissions or equivalent
• Cybersecurity and privacy regulations
• You understand what makes a QMS functional versus performative
• You can translate standards into practical systems that small teams can - actually maintain
• You are comfortable presenting directly to customers and regulators
• Experience working in the health tech or medical device industry
• No previous consulting experience is necessary
  

Who You Are

Credentials and technical knowledge matter here, but the people we work best with tend to share a few less obvious traits.

• You Make Work Fun - A lot of clients are afraid that regulatory is painful and confusing. We keep the experience light, help founders gain confidence in their understanding of compliance, and try to have a good time while we do it.
• You Know When To Be Flexible - Compliance does not have to be rigid. We are open to creative approaches that fit startups and new ways of meeting requirements. We use automations and tech tools to keep things as easy as possible for everyone.
• You Work Efficiently - If we’re working with a startup with a tight budget, we do our best to keep our work as efficient as we can for them.
• You Provide Credibility - Our clients our using our suggestions and opinions to guide major strategic decisions, so they have to trust that we’re right. If we’re not sure about something, we rely on each other to get a second opinion.
• You Have Integrity - We’re are on the same team as our clients, not an adversary. We don’t work with jerks. Don’t be a jerk either.

Role highlights

• Develop quality management systems for Software as a Medical Device (SaMD) clients
• Conduct mock audits and analyze regulatory requirements
• Advise on FDA SaMD guidance, 510(k), De Novo, or PMA submissions and equivalents
• Apply ISO 13485 / MDSAP and IEC 62304 practices for lean startup teams
• Guide cybersecurity, privacy, and product documentation to meet industry standards
• Present directly to customers and regulators with practical, maintainable compliance systems