Principal Scientist - LC-MS/MS


Dependant on experience

REF: CRP396

Are you an experienced developer and validator of LC-MS methods relating to small molecules? Do you want to join a leading organisation in pharmaceutical testing who’ve been experiencing rapid growth?

Key Information

  • North West
  • 01423 813520
  • Full-time, Permanent
  • 07-08-2020
  • Dependant on experience
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Job Description

We are working with a global contract research organisation to offer a Senior LC-MS/MS method developer the opportunity to join their Pharmaceutical function in Manchester. This vacancy has arisen through the expansion of their workforce across the facility, which has further increased the demand for talented and knowledgeable candidates across their departments.

Your main responsibility will be to act as the subject matter expert for the development and validation of triple quadrupole tandem mass spectrometry methods. Depending on your level of experience, your time spent in the laboratory will vary, with more senior candidates adopting a more client facing role. Excellent communication skills will be vital in this position for leading technical investigations and guiding both colleagues and customers through a variety of projects.

In return, you will receive a highly competitive salary, an impressive range of company benefits and a productive working environment where your personal and career development is championed.

For more information or to apply, please contact Ryan Kennedy on 01423 813520.

Please note that all applicants for this role should be able to prove that they are legally entitled to work in the UK. Network Scientific Recruitment, part of Network Scientific Ltd. is an Employment Business/Agency.

To be considered...

To be considered for this opportunity, you must have extensive experience in developing and validating LC-QQQ methods for small molecule analysis. This experience should have been gain predominantly in a CRO environment and should be accompanied by an exceptional working knowledge of relevant pharmaceutical regulations. Experience with Sciex instrumentation specifically will be viewed as an advantage.

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