A rapidly growing biotechnology company is seeking an Assay Development Scientist to drive the end-to-end development of single-molecule assay kits for pharmaceutical research applications. This is a hands-on, cross-functional position bridging product design and manufacturing — ideal for a scientist who combines technical depth with practical experience in developing robust, scalable assay products.
You’ll convert product specifications into validated, manufacturable kits optimized for advanced single-molecule detection platforms. The remit spans feasibility assessment, experimental design, optimization, validation, and technology transfer, ensuring each product meets rigorous scientific and operational standards.
Key Responsibilities
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Translate product specifications into experimental objectives and development plans.
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Assess assay feasibility, component compatibility, and manufacturability within single-molecule workflows.
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Develop and optimize fluorescence-based assays (e.g. smFRET, FCS, FCCS).
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Design and execute analytical validation studies for sensitivity, precision, and reproducibility.
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Define and implement quality control criteria and documentation for manufacturing transfer.
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Collaborate closely with Manufacturing, Quality, and Product Management to ensure seamless scale-up.
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Provide technical data and support for pharmaceutical customer applications.
Essential Skills and Experience
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PhD (or equivalent industry experience) in Biophysics, Biochemistry, Chemistry, or a related discipline.
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Proven track record in assay development, optimization, and validation for industrial or pharmaceutical use.
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Experience translating research assays into reproducible kit formats.
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Strong experimental design and quantitative analytical skills.
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Excellent documentation and communication abilities.
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Proven success managing cross-functional development projects.
Preferred
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Hands-on experience with single-molecule fluorescence techniques (smFRET, FCS, FCCS).
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Expertise in biochemical assay development for proteins, nucleic acids, or complex molecular systems.
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Familiarity with pharmaceutical assay development, kinetics, or screening.
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Exposure to design-for-manufacture, GLP, or ISO 13485-aligned frameworks.
The Offer
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Competitive salary
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Share options
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4% employer pension contribution
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26 days annual leave
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On-site, collaborative R&D environment
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Opportunity to shape a new generation of high-performance molecular assays for the pharmaceutical industry
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Consultant
Lexie Farrar
Lexie primarily focuses on Precision Medicine, OMICS and CGT tools within the US and Europe. Lexie joined Jackson Hogg at the beginning of May 2024 with 4 years of experience in life science recruitment. She has worked with a variety of businesses in this area ranging from early stage startups to 5000+ people global organisations; on cross-functional roles from R&D to Sales.
Managing Consultant - Science
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