Radformation creates solutions that detect medical errors and save clinical time for clinicians with a focus in radiation therapy. Using advanced algorithms and optimization techniques, our solutions bring automation to cancer treatments. Currently, many safety checks and planning steps are manually completed. Our goal is to help automate these processes for a more efficient and safer healthcare environment.
Our software focuses on three key areas:
Time savings through automation
Error reduction through automated systems
Increased quality care through advanced algorithms and workflows
We are a fully remote, mission-driven team united by a shared goal: to reduce cancer's global impact and help save more of the 10 million lives it claims each year. Every line of code, every product release, and every conversation with our customers brings us closer to ensuring no patient's treatment quality depends on where they live.
Why This Role Matters
This role will serve as a supervisor within the QARA function, providing oversight and guidance to strengthen communication, alignment, and execution across the team. As Radformation continues to scale, the QARA Operations Lead will coordinate key quality and regulatory deliverables, ensuring they stay aligned with product development timelines. You will work closely with the VP of Regulatory Affairs and cross-functional partners to track progress, support design control activities, and maintain audit-ready documentation across QARA.
Responsibilities Include:
Organize and manage timely completion of QARA tasks, including CAPAs and DHF deliverables
Coordinate due dates, dependencies, and status updates to align QARA work with project schedules
Maintain teamwide deliverable trackers with owners, due dates, and dependencies
Partner with deliverable owners to keep status current and identify risks early
Interface with project leaders, RA, and Quality teams to clarify ownership and escalate risks
Ensure QARA deliverables related to design control release timing are tracked by phase
Coordinate the transition to new DHF/DDS templates during QMSR implementation
Utilize eQMS and ALM systems to ensure deliverables are properly stored and audit-ready
Analyze performance data, tools, and templates to identify operational improvements
Assist with international regulatory submissions and global conformity assessment needs
Coordinate the company-wide CAPA system
Lead CAPA investigations, corrections, corrective actions, preventive actions, and effectiveness checks
Host CAPA CRB meetings and present CAPA content during internal and external audits
Conduct CAPA training as needed
Perform other QARA-related duties as assigned (e.g., validation of QARA applications)
Required Experience:
5+ years of Quality Systems experience and Software as a Medical Device (SaMD) experience
3+ years in a project management or technical leadership role
Experience working in a regulated agile development environment
Expert familiarity with medical device CAPA regulations and requirements
Familiarity with global medical device regulations (QSR/QMSR, MDD/CMDR/MDR)
Strong understanding of ISO 13485, ISO 14971, IEC 62304, GDPR, HIPAA, and related standards
Preferred Experience:
Product development experience
Extensive experience with eQMS and ALM systems
Strong project management skills
Post-market / adverse event evaluation and reporting experience
PMI certification
Who You Are
Clear communicator who works effectively across teams
Highly motivated with strong attention to detail
Adaptable and comfortable managing multiple deliverable-driven projects
Strong ownership mentality and prioritization skills
Committed to improving patient safety and product quality
Analytical, organized, and proactive in identifying risks and opportunities
AI & Hiring Integrity
At Radformation we believe AI can be an incredible tool for innovation, but our hiring process is all about getting to know you--your skills, experience, and unique approach to problem solving. We ask that all interviews and assessments be completed without tools that generate answers in real time. This ensures a fair process for everyone and allows us to see your authentic work.
Benefits & Perks -- What Makes Us RAD
We care about our people as much as we care about our mission. We offer competitive compensation, benefits, and the opportunity to make an impact in the fight against cancer.
Salary range: $140,000-$170,000 USD base
, commensurate with experience and location.
For US teammates (via TriNet):
Health & Wellness
Multiple high-quality medical plan options with substantial employer contributions
Health coverage starting day one
Short- and long-term disability and supplementary life insurance
Financial & Professional Growth
401(k) with immediate employer match
Annual reimbursement for professional memberships
Work-Life Balance & Perks
Self-managed PTO + 10 paid holidays
Monthly internet stipend
Company-issued laptop & home office setup stipend
Fully remote work environment with virtual events and annual retreats
For global teammates (via Deel):
We provide benefits aligned with local standards and regulations, ensuring fairness and equity across regions.
Our Commitment to Diversity
Cancer affects people from every walk of life, and we believe our team should reflect that diversity. Radformation is proud to be an equal opportunity workplace and affirmative action employer. We welcome candidates from all backgrounds and are committed to fostering an inclusive environment for all employees.
Agency & Candidate Safety Notice
Radformation does not accept unsolicited resumes from agencies without a signed agreement in place. All legitimate communication will come from an @radformation.com email address. If you receive outreach from another domain or via unofficial channels, please contact careers@radformation.com.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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