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Senior Scientist

Yourgene Health
Job LocationManchester
EducationNot Mentioned
SalaryCompetitive salary
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypePermanent, full-time

Job Description

Job title: Senior ScientistReports to: Validation Team LeaderLocation: ManchesterContract Type: Full-time, permanentSalary & Benefits: Competitive Salary, Life Assurance, Pension, Private Medical Cover, Share Incentive PlanAbout Yourgene HealthYourgene Health is an international molecular diagnostics group which develops and commercialises genetic products and services. The group works in partnership with global leaders in DNA technology to advance diagnostic science. Yourgene primarily develops, manufactures, and commercialises simple and accurate molecular diagnostic solutions, for reproductive health, precision medicine and now infectious diseases. In addition, Yourgene Genomic Services offers an NIPT and high throughput COVID testing service.Yourgene Health is headquartered in Manchester, UK with offices in Taipei, Singapore, the US and Canada, and is listed on the London Stock Exchanges AIM market under the ticker "YGEN". For more information visit www.yourgene-health.com and follow us on twitter @Yourgene_HealthAbout the role:The Senior Scientist will lead the tactical delivery of IVD (In Vitro Diagnostic) products and services. The Senior Scientist will be an expert in the development and validation of molecular diagnostics and provide scientific expertise and technical leadership on development projects. You will ensures tactical planning is performed effectively and considers problems at a system level. You will support the team to deliver high quality and in a timely fashion. You will design, develops and validates in vitro diagnostic products and services for use in a range of applications.Responsibilities:

  • Provides scientific expertise and technical leadership on projects, as well as planning tactical delivery in functional area
  • Contribute to overall project planning and reporting as well as leading planning and reporting of defined project work-package
  • Lead and participate in activities requiring cross functional collaboration, including leading complex projects
  • Support the resource planning activities of Team Leaders and Project Leaders
  • Provide expertise into the creation, maintenance and improvement of;
  • Overall process SOPs
  • Process flows, standardized plans & reports
  • Ensure planning and reporting of studies and work-packages is accurate and detailed
  • Design effective and efficient studies involving;
  • Accurate, efficient and timely documentation
  • Developing and implementing protocols to show that tests meet acceptance criteria
  • Data generation, ensuring integrity and organized data management
  • Provide accurate, concise and independent data interpretation, factoring in systems-level thinking
  • Determining test parameters, such as output specifications
  • Meeting regulatory or other requirements
  • Lead troubleshooting activities when technical issues arise
    • Team specific responsibilities:
  • Validation: Delivery of validated tests and systems for products and services
  • IVDR: working with the quality and regulatory teams to ensure that our products maintain regulatory compliance during the change over from IVDD to IVDR.
  • Participate in activities outside of own team, such as Innovation, Assay Development, Automation, Validation and Design Transfer, where required
  • Supports the development of external relationships, including through for example, grant applications, KOLs and partners
  • Supports the identification of commercially and technically useful solutions for development
  • Ensure own work meets regulatory & quality requirements (including compliance to SOPs, documentation using lab books, study plans, study reports and integrity of data)
  • Ensure own work and that of junior staff is performed in line with company goals
  • Support and provide guidance to junior staff
    • Consults with:
  • R&D management, Team Leaders and other R&D team members
  • Other Yourgene Health functions; e.g. Quality, Regulatory, Business Development, Legal, Finance, HR, Admin
  • External consultants appointed by Yourgene Health
  • External companies; e.g., potential suppliers, commercial partners, etc.
    • About you:
  • Degree or further degree (or equivalent) in a life science such as molecular biology, biochemistry or genetics
  • Typically 7+ years of relevant experience in molecular diagnostic development
  • Expertise and experience in the development, verification and validation of molecular diagnostic assays in adherence with CE marking and/or design control regulations
  • Hands on experience with a range of molecular based assays and techniques
  • Experienced in data analysis and interpretation.
  • Excellent grasp of experimental design and execution and able to lead and train others
  • Enthusiasm, drive, thoroughness, diligence and a willingness to take personal responsibility to ensure that projects are successful
  • Excellent organisational skills and thrives on working to tight timelines
  • Able to assimilate knowledge from technically detailed scientific sources
  • Can summarize complex scientific data in written form to effectively communicate plans, progress and ideas with Management, Peers or External Audiences
  • Good IT skills, including Microsoft Office suite
    • Yourgene Health is committed to encouraging equality, diversity and inclusion among our workforce. The aim is for our workforce to be truly representative of all sections of society and for each employee to feel respected and able to give their best. Required skills
  • Biotechnology
  • Molecular Biology
  • Molecular Genetics
  • Validation
  • Molecular Diagnostics

    • Keyskills :
    Molecular Biology Validation

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