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Job ID :
52943BR
Location :
United Kingdom - East Grinstead
:
Job Description

When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals.

Job Description: To report to the R&D Manager and co-ordinate with the R&D Project Leader for designated R&D work, such as Drug Development and R&D Projects.

Responsibilities:

•Drug development: Carry out all aspects of manual/autoread drug developments to include customer conferences, correspondence and specific requirements, batch records, wet and dry plate manufacture, MIC and bioassay testing, solution stability and IVDD, result analysis, internal and customer reporting, documentation updates and methods for production implementation.

•Data collection and algorithm development: Carry out all aspects of a data collection to include plate manufacture and software, dry vs. wet testing, culture collection monitoring, liaising with the R&D Data Analyst on agreement rates, specimen data and well difference reports as well as internal and customer reporting together with algorithm implementation.

•Validation/verification projects: Manage projects within R&D from writing protocols, carrying out risk assessments, planning with time/4-box and Gantt charts, organising project and management team meetings, scheduling with other departments, testing, result analysis, reporting and organising final QA/all department sign-off.

•Updating protocols and SOPs, ensuring general laboratory equipment weekly and monthly maintenance.

Minimum Qualifications:

•Competent in the use of the MS Office suite

•High attention to detail

•Ability to communicate openly with colleagues and customers

•Work flexibly to ensure deadlines are met

•A levels to include a science subject and relevant laboratory experience

Preferred Qualifications:

•Degree level qualification or equivalent

•Experience in cGMP or GMP environment



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