Lead Scientist
Dyddiad hysbysebu: | 09 Gorffennaf 2025 |
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Cyflog: | £45,000 i £65,000 bob blwyddyn |
Oriau: | Llawn Amser |
Dyddiad cau: | 08 Awst 2025 |
Lleoliad: | Bath, Somerset, BA1 1SS |
Cwmni: | ProTech Recruitment Ltd |
Math o swydd: | Parhaol |
Cyfeirnod swydd: | 57297_1752064989 |
Crynodeb
An established and growing company within the medical diagnostics industry is seeking a Lead Scientist to join their UK-based research and development team. This role involves leading the technical development of innovative molecular diagnostic products in a highly regulated environment.
The successful candidate will play a key role in developing next-generation point-of-care diagnostic assays, leading a small team of scientists, and managing projects from concept through to design transfer.
Key Responsibilities-
Lead technical development for multiple R&D projects across the organisation.
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Line-manage a team of 2-3 assay development scientists.
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Design and execute complex experimental plans and review data for accuracy and quality.
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Develop technical strategies for assay optimisation using DOE and robust design principles.
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Act as a subject matter expert in experimental design and statistical analysis.
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Create and maintain technical documentation compliant with regulatory and quality standards (e.g., ISO 13485, ISO 14971).
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Ensure all activities meet internal quality and compliance requirements.
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Produce technical reports and contribute to product design decisions.
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Promote high standards of laboratory practice and scientific rigor.
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BSc with 7+ years or MSc/PhD with 5+ years of experience in molecular diagnostics or IVD development.
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Industrial experience developing NAAT-based assays (e.g., PCR, LAMP).
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Strong understanding of Design Control within a regulated framework (ISO 13485).
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Experience with risk management activities (ISO 14971).
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Proficiency in analysing and interpreting complex datasets.
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Track record in technical project management within a laboratory-based environment.
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Excellent communication and leadership skills.
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Advanced knowledge of Design of Experiments (DOE) and robust design principles.
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Experience with Minitab, JMP, MATLAB, Python, R, or similar tools.
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Lean Six Sigma certification or equivalent.
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Prior experience with design verification, validation, and design transfer.
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Experience working within Quality Management Systems in a regulated diagnostics environment.