Dear all,
We would like to remind those interested in applying for the Principal Biochemist (8a) post at Birmingham Children's Hospital that the application deadline is on 30/11/2014.
This is a permanent post within the Inherited Metabolic Disorders laboratory primarily for the interpretation of metabolic investigations (amino acids, organic acids, acylcarnitines etc) and support of these assays (HPLC, GCMS, MSMS etc). Prior experience in these areas is preferred, but full training will be provided as necessary. The post-holder will also be charged with further expanding our test repertoire, and projects for those still working towards full FRCPath will be supported.
The Newborn Screening & Biochemical Genetics department has recently enjoyed significant capital investment in replacement equipment (2x Waters Acquity/Xevo, Agilent HPLC, fluorimeter, spectrophotometer & 2x Biochrom 30+), and also has Agilent GCMS and ABSciex API4000 systems that are only ~5 yrs old.
The clinical scientists work closely with the clinical IMD team (clinicians, dieticians, nurses etc) and, as the regionally commissioned service provider, liaise daily with clinicians and scientists in hospitals across the West Midlands and beyond.
Birmingham is a vibrant city with a wealth of amenities - dull 60's concrete has be razed and replaced: see ichoosebirmingham.com and visitbirmingham.com to find out more.
For further information on the role and the opportunities it presents, please contact Mary Anne Preece (0121 333 9940) [log in to unmask]
NHS jobs reference: 284-SM552-14
___________________________________________
Adam Gerrard PhD FRCPath CSci
Principal Clinical Scientist & Quality Lead
Newborn Screening & Biochemical Genetics
Birmingham Children's Hospital NHS FT
Birmingham B4 6NH (UK)
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