Senior Bioanalytical LC-MS/MS Analyst — GLP/GCP/GMP Lab

Intertek

Manchester

On-site

GBP 42,000 - 56,000

Full time

18 hours ago
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Benefits offered by this job

Development opportunities worldwide
Client-facing technical work

Job summary

Intertek seeks a Senior Analyst to join its Bioanalytical LC-MS/MS team in Manchester. You will apply quantitative LC-MS/MS experience in a GLP, GCP and GMP environment, preparing, running and processing clinical and non-clinical samples to support pharmaceutical programmes.

You will join a collaborative team, receive structured training, and contribute to method development and validation as you progress to more complex work across a varied client portfolio.

Qualifications

  • Two to three years of hands-on quantitative LC-MS/MS experience in an industry laboratory.
  • Hands-on experience preparing, running and processing samples and interpreting LC-MS/MS data.
  • Experience in, or understanding of, a GxP-regulated laboratory environment and GLP, GCP or GMP principles.
  • Good numeracy and IT skills with the ability to calculate, tabulate and report analytical results.
  • Clear written and verbal communication skills and a collaborative approach to teamwork.
  • Bioanalytical or quantitative pharmacokinetic analysis experience would be advantageous.
  • Method development and validation experience, ideally following ICH M10 guidance.

Responsibilities

  • Prepare, run and process clinical and non-clinical samples using quantitative LC-MS/MS.
  • Perform analytical testing for pharmaceutical and bioanalytical customers in accordance with GLP, GCP and GMP requirements.
  • Extract pharmaceuticals and biopharmaceuticals from biological matrices such as serum, plasma and urine.
  • Generate, interpret and accurately document analytical data and study results.
  • Support quantitative LC-MS/MS method development and validation under supervision.
  • Plan and perform routine analytical work independently once trained and signed off.
  • Ensure studies meet quality standards and regulatory expectations.
  • Prepare technical reports or Certificates of Analysis where required.
  • Learn new techniques and support work in other laboratory areas when needed.
  • Maintain accurate records and comply with safety, COSHH, GMO, SHE and quality systems.

Education

BSc, MSc or PhD in Biology, Chemistry or a related scientific discipline

Job description

Intertek seeks a Senior Analyst to join its Bioanalytical LC-MS/MS team in Manchester. You will apply quantitative LC-MS/MS experience in a GLP, GCP and GMP environment, preparing, running and processing clinical and non-clinical samples to support pharmaceutical programmes.

You will join a collaborative team, receive structured training, and contribute to method development and validation as you progress to more complex work across a varied client portfolio.

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