Quality Assurance Compliance Manager

Rivia is a technology company building a data engine that powers the future of clinical trial intelligence. Rivia was founded on the belief that new drugs can be brought to market more successfully with a fraction of today's capital.

Biotechs are the source of most therapeutic innovation, yet clinical development is constantly constrained by fragmented data and outdated tooling. Rivia unifies clinical trial data at scale through a core engine built as a reusable intelligence layer, comprising hundreds of configurations and trial-specific logic, independent of source structure. This vertical stack of data engine, workflows, and agents creates a distinct advantage in how trials are operated.

Over the past two years, European and US based biotechs running global clinical trials on Rivia have demonstrated measurable impact, from earlier understanding of therapeutic potential to significantly more efficient trial execution. In March 2026, Rivia raised its $15M Series A led by Earlybird Venture Capital.

Rivia’s ambition is to become the standard infrastructure for modern drug development, transforming how trials are executed end-to-end.

As QA Manager at Rivia, you will take full ownership of the company's compliance and quality function. You will be the single point of accountability for GCP compliance and required certification including ISO 27001 (ISMS), ISO 9001 (QMS), and GAMP 5 software validation. You will inherit a functioning compliance programme from the founders and build it into a robust, scalable asset as the company grows.

Rivia is already compliant, this role is about taking ownership, deepening maturity, and ensuring that compliance is both a source of trust and a competitive advantage as the company scales toward 35+ people and expands its client base.

• Owning a function: You want to be the one who carries full accountability, not one voice among many in a large compliance team.
• Working at the edge of biotech and software: The intersection of clinical data platforms, regulatory frameworks, and software validation is where you do your best work.
• Being the trusted expert: You are the person clients and auditors talk to, and you know how to instill confidence in a regulated‑industry audience.
• Building with pragmatism: You understand the balance between a compliance programme built for Rivia’s fast‑moving startup and getting ready to scale for a 500‑person company. You leverage AI to streamline processes and automation.
• Organisation and detail: You balance pragmatism with an eye for detail and efficient organisation.

• Compliance ownership: Take full accountability for Rivia's GCP compliance and required certification including ISO 27001, ISO 9001, and GAMP 5 programme. Maintain, evolve, and defend the certification posture as the product and organisation scale.
• Audit management: Lead all external audits, surveillance reviews, and certification renewals end-to-end. No founder involvement required.
• Client‑facing compliance: Serve as sole point of contact for enterprise vendor questionnaires and client‑initiated audits. Reduce deal friction and accelerate procurement cycles.
• Documentation and records: Own and maintain all compliance documentation, including SOPs, risk registers, validation protocols, and CAPA records, ensuring they reflect and evolve to meet current product and process reality.
• Cross‑functional integration: Embed compliance checkpoints into engineering and product workflows. Translate regulatory requirements into practical tasks that teams can execute without losing pace.
• Training: Design and deliver compliance training to keep staff audit‑ready as the team grows.
• Standards monitoring: Track evolving certification requirements and translate changes into practical implications for the platform and organisation.

• 4+ years of hands‑on experience in quality assurance within a digital, medtech, or pharma environment
• Ownership and strong working knowledge of at least two of: ISO 27001, ISO 9001, GAMP 5 software validation
• Experience implementing and overseeing industry guidance (e.g. GxP, ICH E6 R3) and agency specific regulatory frameworks…