Manufacturing Quality Manager (PFMEA)

Vision RT is a fast-growing MedTech company transforming radiation therapy for cancer patients by helping make it more accurate, effective, and comfortable. The company is the inventor of, and a market leader in, Surface Guided Radiation Therapy (SGRT). This technology uses advanced 3D cameras to track surface data, providing enhanced guidance across every step of the radiotherapy workflow.

Vision RT’s SGRT solutions are in 24 out of the 25 “Best Hospitals for Cancer,” as tracked by US News & World Report.

The company is recognized as one of Britain’s fastest-growing private tech companies, as featured in the 2025 Sunday Times 100 Tech list. Vision RT is also a recipient of the 2026 King’s Award for Enterprise, our fifth in 10 years. It is the UK’s most prestigious accolade for business excellence.

With around 300 employees globally and offices in the UK, Poland, and the USA, Vision RT operates independently as part of the Danish company William Demant Invest A/S, one of the world’s largest investors in healthcare companies. Employees benefit from the security and reach of being part of a large global enterprise, combined with the agility and innovation of a startup.

Vision RT is a company with strong values, a clear mission, and a bright future. It is an exciting and rewarding organization in which to work.

About the role

We are seeking a PFMEA/ Quality Lead who is responsible for ensuring robust, compliant, and risk based process control across all manufacturing and engineering change activities. The role leads PFMEA (Process Failure Mode & Effects Analysis) processes, ensures documentation meets regulatory and internal standards, collaborates with cross functional teams, oversees change control evidence, validation of production processes, and drives continuous improvement in operational quality.

Key Responsibilities

• Lead, facilitate, and maintain PFMEA activities for new and existing manufacturing processes. Maintain high standards of communication with stakeholders and ensure timely delivery of PFMEA activities.
• Ensure PFMEAs comply with ISO 14971, ISO 13485, FDA 21 CFR Part 820, and internal QMS/ risk-management procedures.
• Validate process changes by reviewing evidence, guiding teams, and writing high quality technical reports to support change orders and support process readiness and product launch activities.
• Support development and maintenance of Control Plans, Process Flow Diagrams, and Work Instructions.
• Approve the Device Master Record revisions and ensure documentation accuracy.
• Support internal and supplier quality audits and support regulatory inspections.
• Review and implement engineering, design, and documentation changes impacting production.
• Maintain and improve QMS procedures and ensure regulatory alignment.
• Partner with Manufacturing Engineering to define and validate process controls using statistical tools (MSA, SPC, capability studies).
• Drive improvements to reduce variation and strengthen process capability.
• Contribute to root‑cause investigations risk-based decision-making and CAPA activities.
• Provide line management, coaching, and development for quality personnel in the production environment.
• Guide cross functional teams in gathering correct and supporting evidence for PFMEA and change orders and quality best practices.
• Coordinate with manufacturing teams to ensure quality standards are met through all stages of production.
• Perform additional reasonable duties aligned with role scope and organisational needs.

Skills & Experience Required

• Proven experience in PFMEA leadership within a regulated manufacturing environment; medical devices preferred.

Desirable Skills & Experience

• Experience within Class IIa, IIb or Class III (EU) medical devices.
• Lean Six Sigma Green Belt or higher.
• Knowledge of DFMEA and its interaction with PFMEA.