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5 дней назад

Technical Specialist, Large Molecule Bioanalysis

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
UK
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Technical Specialist, Large Molecule Bioanalysis (LBA/GLP/GCP): Developing, validating, troubleshooting, and managing ligand binding assays for PK/TK, ADA, and biomarker studies with an accent on regulatory compliance, data integrity, and assay robustness. Focus on leading complex assay and instrumentation investigations, managing analytical equipment lifecycles, supporting audits and CAPA, and mentoring laboratory scientists.

Location: Onsite in York, UK; Monday–Friday, 9:00 AM–5:00 PM, 37.5 hours per week

Company

hirify.global operates a bioanalytical laboratory supporting regulated and non-regulated studies.

What you will do

  • Act as the technical subject-matter expert for large molecule bioanalysis, including PK/TK, ADA, and biomarker assays.
  • Design, develop, validate, transfer, and support ligand binding assay methods in accordance with regulatory guidance.
  • Lead assay and instrumentation troubleshooting, analytical platform oversight, and equipment lifecycle management.
  • Support computerised system validation, laboratory investigations, deviations, CAPA management, SOP approval, and audit or inspection activities.
  • Mentor and technically train Laboratory Scientists while supporting recruitment, onboarding, resourcing, and performance delivery.
  • Monitor operational and financial metrics, track KPIs, and contribute to laboratory strategy, efficiency, and continuous improvement.

Requirements

  • BSc or equivalent degree or higher in a relevant scientific subject.
  • At least 5 years of experience in a bioanalytical laboratory environment.
  • Experience or strong knowledge of ligand binding assays, large molecule bioanalysis, and analytical platforms such as ELISA and MSD.
  • Ability to work in compliance with GLP, GCP, ICH M10, UK clinical trial legislation, health and safety requirements, and laboratory SOPs.
  • Ability to provide technical leadership, troubleshoot complex scientific or operational issues, and mentor laboratory personnel.

Culture & Benefits

  • Full-time onsite position with a standard Monday–Friday schedule.
  • Work in an inspection-ready laboratory environment focused on quality, compliance, safety, customer focus, and accountability.
  • Opportunity to contribute to scientific excellence, operational strategy, and continuous improvement in bioanalytical studies.
  • Sedentary work requiring prolonged sitting, sustained concentration, independent decision-making, and fine motor skills.

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