Method Development Scientist

Method Development Scientist

Pharmaceuticals

Location Northumberland

Contract Permanent

Reference

Date Posted

Consultant

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We have an exciting opportunity for an experienced Method Development Scientist at a leading CRO based in Northumberland. The ideal candidate will have proven experience in LCMS/MS assay development for NCEs, with working knowledge in a regulated, GLP bioanalytical laboratory.

Key Responsibilities and Duties:

·   Perform Method Development Scientist duties in the LCMS bioanalytical lab

·   Develop, transfer and pre-validate assessments of assays and analytical methods to support drug analysis

·   Provide technical expertise on troubleshooting and technical investigations of analytical methods

·   Design LCMS/MS protocols for drug optimisation, method development and the processing of analytical runs

·   Prepare and review bioanalytical reports

Ideal Skills and Qualifications:

·   Degree qualified, or equivalent, in a relevant scientific discipline

·   5-10 years’ experience in LCMS/MS development in a regulated bioanalytical and Assay Development laboratory

·   Proven GLP and CRO experience; required

·   Previous experience in communicating with clients on high level science issues as well as remaining strictly confidential

·   Ability to work effectively both in isolation and as part of a team

·   Ability to analyse problems, formulate effective solutions and coordinate tasks simultaneously

If you are interested or have any questions about this role, feel free to contact Sara at CY Partners.


Method Development Scientist

Pharmaceuticals

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