Director - Immunoassay Development

Talentmark

Greater London, Stevenage

On-site

GBP 90,000 - 130,000

Full time

14 days+
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Benefits offered by this job

Share equity options

Job summary

Talentmark is partnering with an innovative early-stage diagnostics company to appoint an Associate Director / Director – Assay Development. You will lead design and development of quantitative immunoassays and drive translation toward commercial release.

Based in Stevenage with the expectation of London relocation, the role is hands-on and leadership oriented, overseeing validation studies, data integrity and collaboration with external experts.

Qualifications

  • PhD in a related biosciences field with industry experience.
  • 5+ years in diagnostics or assay development with hands-on immunoassay experience.
  • Experience translating assays to point-of-care formats and dedicated data integrity.

Responsibilities

  • Lead design and development of quantitative immunoassays.
  • Drive optimisation for sensitivity, precision, reproducibility and stability.
  • Design and execute assay development and validation studies.
  • Maintain robust documentation aligned with regulatory requirements.
  • Establish high standards for data integrity and statistical analysis.
  • Manage external scientific collaborators and advisors.

Skills

Immunoassay development
Leadership
Data analysis
ELISA
Point-of-care formats

Education

PhD in Biochemistry/Analytical Chemistry/Bioengineering/Biomedical Science

Tools

Immunoassay techniques
Lateral flow devices

Job description

Director – Immunoassay Development

On-site/ Hybrid | London/Stevenage | Permanent

Talentmark is working with an innovative, early-stage diagnostics company developing next-generation at-home testing technology.

We are looking for an Associate Director / Director – Assay Development to take ownership of assay development and help shape the company's scientific direction. This is a hands-on leadership role, taking assays from initial design and optimisation through to validation and commercialisation.

The role is currently based in Stevenage, with the longer-term expectation that the company will be London-based. Candidates should therefore be comfortable commuting to Stevenage initially, with longer-term transition to London and hybrid working.

Key Responsibilities
  • Lead the design and development of quantitative immunoassays.
  • Drive optimisation of sensitivity, precision, reproducibility and stability.
  • Design and execute assay development and validation studies.
  • Maintain robust documentation aligned with regulatory and technical-file requirements.
  • Establish high standards for data integrity, experimental rigour and statistical analysis.
  • Manage external scientific collaborators and advisors.
Your Background

You are an experienced immunoassay scientist with a strong industry leadership background in diagnostic assay development, with track record in taking assays through validation towards commercial release.

Essential Experience
  • PhD in Biochemistry, Analytical Chemistry, Bioengineering, Biomedical Science or a related discipline.
  • Industry experience in diagnostics or assay development (5 yrs+)
  • Strong hands‑on expertise in immunoassay development, particularly ELISA, with a good working knowledge of enzymatic assays.
  • Experience translating laboratory immunoassays into point‑of‑care, lateral‑flow, biosensor or microfluidic cartridge formats.
  • Experience with low‑concentration analyte measurement
  • Proven experience developing diagnostic assays through validation and commercial release.
  • Practical experience working with human biological samples (blood, saliva or urine).
Desirable Experience
  • Experience developing steroid or peptide hormone assays.
  • Familiarity with freeze‑drying / lyophilisation for reagent stabilisation.
  • Knowledge IVD technical-file preparation for CE, UKCA or FDA submissions.
  • Experience building or leading a laboratory/science team.
  • Experience working with aptamer technology.
What's on Offer
  • The opportunity to take diagnostic assays from concept through validation and towards market.
  • A senior, hands‑on role within an ambitious early‑stage company.
  • Competitive salary and share equity options scheme.

It is essential that applicants hold entitlement to work in the UK.

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