Analytical Scientist

at  Gentronix Ltd

Macclesfield SK10, England, United Kingdom -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate18 Feb, 2025Not Specified06 Feb, 20251 year(s) or aboveAnalytical ChemistryNoNo
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Description:

Are you an analytical scientist with experience in formulation sample analysis looking for your next role in contract research? If so, we’d love to hear from you!
As part of Gentronix’ s success and continued expansion, this is a fantastic opportunity to join our Analytical team. We are looking for a talented individual with HPLC-UV experience to perform the method development, validation and dose formulation analysis phase of our genetic toxicology studies.

ABOUT US

Gentronix is located at Alderley Park in the north-west UK. We are committed to helping our clients develop safer chemicals and medicines, using innovative screening platforms as well as GLP regulatory tests to detect hazard, to understand mode-of-action, and help manage risk.
Comprising a team of over 60 employees with a range of experiences from within the pharmaceutical, agrochemical and CRO industries, our team has extensive expertise in the fields of genetic and skin/ocular toxicology. Our ambition to become the leading provider of predictive and preclinical toxicology products and services across a variety of industry sectors.

Responsibilities:

Reporting to the Principal Scientist, you will be performing method development, validation and sample analysis across a wide range of test items spanning pharma, agrochemical and other chemical industries. You will work closely with colleagues across the business to ensure that client studies are conducted to the highest standards and our excellent customer relationships are maintained.

Specifically, you will:

  • Develop analytical methods and troubleshoot issues as they arise.
  • Be performing validation and test formulation analysis according to GLP.
  • Be reporting analytical work within Gentronix, liaising with study directors and Quality Assurance.
  • Identify and report, out of specifications and deviations from study plan.
  • Performing laboratory investigations and implementing Corrective and Preventative Actions (CAPA).
  • Author and review Standard Operating Procedures.
  • Assist in the calibration and maintenance of analytical laboratory equipment.
  • Coach and support the development of junior team members.
  • Need to maintain an awareness of current scientific and regulatory developments impacting on the conduct and interpretation of analytical studies and all genetic toxicology studies with an analytical component.


REQUIREMENT SUMMARY

Min:1.0Max:2.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

BSc

An hnc (higher national certificate) or a bsc degree in a relevant field of analytical sciences.

Proficient

1

Macclesfield SK10, United Kingdom