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Senior Scientist Molecular

Page Group
Job LocationStirling
EducationNot Mentioned
SalarySalary negotiable
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypePermanent, full-time

Job Description

Role Description

  • You will be responsible for key components in the development of molecular assays for the companies platform, as part of the assay development team, reporting to the R&D Technical Manager.
  • You will have people management and development responsibilities within a project team.
    • Client DetailsCompany OverviewMy client is a MedTech company that are innovating new and adaptable assay platform technologies. They are transforming the In Vitro Diagnostic testing space and are helping to provide more effective, cost-efficient healthcare for everyone. The company is eradicating the need for blood labs. Their affordability means instruments are being shipped to third world countries, helping those in need. They currently have 1000+ people with a plan to be over 20,000 in the next three years. Now is an exciting time for them. They are expanding fast.DescriptionKey Responsibilities
  • Lead the development of significant project activities to ensure robust assay performance such as Amplification Methodologies, On-Board Control Systems, Liquid Controls, Shelf Life Assignment
  • Design and execute appropriate experiments for the purpose of assessing and improving the assay to meet the required performance, stability and cost requirements.
  • Use statistical methods to design and analyse experiments and make the appropriate scientific conclusions and define the next steps required.
  • Ensuring that the developed assay and its components are capable of meeting the required performance, stability and cost requirements for the assay platform.
  • Solve problems encountered during assay development innovatively and independently.
  • Writing and communicating project updates within the organisation.
  • Ensuring Design Control procedures adhere and that reports and procedures are written.
  • Create and maintain quality records for the purpose of assessing and improving assay methodologies and documenting experiments.
  • Ensuring you are trained on all appropriate procedures and training new personnel if and when required.
  • Technically reviewing change controls and peer-reviewing laboratory notebooks.
  • Ensuring you work in conjunction with the quality policy and objectives.
  • Manage and develop scientists and technicians within the team.
  • Lead cross-functional engagement in solving complex problems encountered during product development.
    • ProfileMust have experience
  • Degree Qualified in a relevant scientific discipline.
  • Line management experience.
  • Knowledge and experience working with various isothermal amplification techniques and detailed understanding of PCR and primer design.
  • Experience and understanding of factors which drive assay performance (including sensitivity, range, stability, reproducibility and precision).
  • High level of skills in problem solving and innovation.
  • Knowledge of electrochemical and fluorescent detection and other assay detection architectures.
  • Track record of developing assays within a design controlled framework
  • Ability to write clear and concise protocols for complex assay methodologies.
  • Ability to identify and investigate non-conformances swiftly, and implement robust corrective actions.
  • Experienced in summarizing and communicating project data for senior staff and stakeholders.
  • Ensure laboratory books and other records are completed accurately and timely.
  • Experience of working in a laboratory within GLP + GDP guidelines
  • Computer literate.
  • Experience in Statistical analysis and Design of Experiments.
    • Job OfferCompetitive salary + benifits

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