Role Overview - FULL TIME, ONSITE IN COVENTRY. APPLICATIONS FROM HCPC, UK RESIDENTS ONLY
We are seeking an experienced HCPC-registered Laboratory Scientist to play a key role in a growing molecular diagnostics laboratory and support the clinical deployment of a novel endometrial function test.
This is a unique opportunity to join a fast-moving startup at a pivotal stage. You will take ownership of laboratory operations, contribute directly to clinical and regulatory milestones, and help shape the future of the lab as we scale. The role offers significant scope for progression as the company grows.
Key Responsibilities
* Lead day-to-day laboratory operations, ensuring high standards of quality, efficiency, and compliance
* Take a hands-on role in running molecular workflows and troubleshooting where needed.
* Lead and train lab staff.
* Maintain and continuously improve QMS, SOPs, and audit readiness
* Ensure compliance with ISO 15189 and alignment with ISO 13485 standards
* Support clinical validation studies, including multi-site sample coordination and processing
* Collaborate cross-functionally with regulatory and QA teams on validation and documentation
* Oversee LIMS, equipment management, calibration, and sample logistics
Essential Requirements
* HCPC-registered Biomedical Scientist (or equivalent)
* Experience working in an ISO 15189-accredited laboratory
* Strong understanding of laboratory quality systems and audit processes
* Hands‑on experience in molecular diagnostics
* Ability to think flexibly and problem solve
Desirable
* Experience with ISO 13485 or IVD product development
* Exposure to IVDR / UKCA regulatory pathways
* Experience supporting clinical studies or trials
* Familiarity with LIMS systems
* Previous experience in a startup or scaling environment
What We're Looking For
* A highly practical, hands‑on lab leader who enjoys being close to the science
* Someone who thrives in a dynamic, fast‑paced startup environment
* Strong focus on quality, compliance, and continuous improvement
* Comfortable working across research, clinical, and regulatory interfaces
* Highly self‑sufficient and proactive, able to take ownership and deliver without close supervision
* Able to prioritise effectively and make sound decisions in a growing, evolving environment
* Adaptable and excited by the opportunity to build and scale systems
Why Join Us
* Be part of an early‑stage company with real clinical impact
* Work on innovative diagnostic technology at the forefront of women's health
* High level of ownership and visibility from day one
* Significant opportunity for career growth as the company scales
* Collaborative, ambitious, and mission‑driven team
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