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Research and Development Specialist 12 month FTC

Adecco
Job LocationYorkshire and Humberside
EducationNot Mentioned
SalarySalary negotiable
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypeContract , full-time

Job Description

Overview:The Research and Development Specialist is responsible for the overall study management of method development, validation and investigational activities, ensuring their effective implementation and completion.Requirements:

  • BSc (or equivalent) or higher in a relevant scientific subject.
  • A minimum of 3 years experience within a laboratory environment preferred.
  • Experience in GCP environments.
  • Clinical Chemistry background required
  • Experience of working in a high throughput laboratory environment
  • Use of analytical instrumentation (Roche systems preferred)
Responsibilities:
  • Develop validation plans, validation summary reports, stability summary reports, correlation plans and correlation summary reports to meet regulatory requirements .Provide supporting information in the evaluation of appropriate testing and/or methodology.Liaise with technical staff on feasibility of testing for new study requirements. Provide pricing as needed to Proposals teams. Selection of appropriate test methods; research / identify suppliers of materials and equipment options for new tests to supportnew opportunities. Facilitate assay development, conduct instrument validations and implement new testing to meet the needs of clinical trials protocols, clients and regulatory requirements. Responsible for assay / panel pre-validation and validation and correlationtesting globally.
  • Perform the investigation and corrective action for assay troubleshooting and proficiency testing failures. Assess the impact of manufacturer / vendor communications and complete associated documentation. Provide study management and direction of laboratoryteams for the implementation of analytical method validations. Provide supportive information for consultation and technical support to clinical trials clients and operational staff. Responsible for communications (meetings, calls audits etc.) with clientsand formulate responses as required.
  • Ensures all methods and validations are done according to all applicable regulatory guidelines, including but not limited to Good Clinical Practice (GCP), Good Laboratory Practice (GLP), Good Clinical Laboratory Practice (GCLP) etc.. Document and ownershipof any quality documentation (Note to File, Quality Event, CAPA, deviation, change control etc.) as appropriate within the required timeframes.
Offer:
  • Flexibility to work 50% from home and 50% on site after the first 2 months
  • Salary based on experience + social benefits.
Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer.By applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explaining how we will use your information is available on our website.

Keyskills :
GCP

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