What You鈥檒l Do
You鈥檒l get to sit at the heart of our system, turning complex user needs and workflows into clear, testable software requirements and architectures that developers can build against with confidence. You鈥檒l join early conversations about what we are building, then help carry those through to validation in real manufacturing environments.
You鈥檒l:
- Shape the system and software architecture for an end-to-end cell therapy manufacturing automation platform, with a strong focus on interfaces, robustness and quality.
- Define, decompose and maintain system and product-level software requirements, giving development teams clear, traceable inputs they can trust.
- Lead structured requirements processes, from capturing user and stakeholder needs through to verification and validation with external partners.
- Identify and communicate key technical risks, trade-offs and interdependencies, helping the wider team make sound, timely decisions.
- Drive the adoption of tools and practices that support regulatory and quality compliance, including requirements management, traceability and change control, to meet and exceed the expectations set by client engineering & quality teams, and industry regulators.
- Develop and maintain technical documentation that keeps system-level designs, requirements and tests aligned across the lifecycle.
- Collaborate with internal and external software development teams to agree designs, test plans and acceptance criteria, and keep everyone aligned on scope and priorities.
- Help plan and sequence agile software feature development over successive phases, from early prototypes through to productised systems in manufacture.
- Work closely with colleagues in software engineering, biology, product, manufacturing and quality to ensure the whole system hangs together in a clean, coherent way.