Scientist – LCMS Analytical

Manchester Source: WhatJobs
See advert for pay

Overview

In this role you apply LCMS/MS to quantitative pharmacokinetic analyses in a GLP/GCP/GMP accredited lab, supporting pharmaceutical and biopharmaceutical projects. You will develop and validate LCMS/MS methods, extract analytes from biological matrices, and generate clear reports for clients. You will work independently within a multidisciplinary team, mentoring junior staff and contributing to regulatory compliance. This role offers variety across PK studies and hands-on lab scientific work aligned with global quality standards.

Pay / Benefits

  • Competitive salary/benefits
  • Global development opportunities
  • Collaborative team environment
  • Equal Opportunity Employer
  • Inclusive workplace
  • Real Living Wage employer

Responsibilities

  • Perform LCMS/MS-based quantitative PK analyses across pharma/biopharma projects
  • Develop and validate LCMS/MS methods per ICH M10 guidelines
  • Extract pharmaceuticals and biopharmaceuticals from biological matrices (serum, plasma, urine)
  • Generate, interpret, and report analytical data and COAs
  • Train and mentor junior scientists
  • Ensure studies meet GLP/GCP/GMP quality standards and regulatory expectations
  • Communicate findings and strategic implications to clients
  • Support business development through technical quote input

Key requirements

  • BSc/MSc/PhD in Biology or Chemistry or related field
  • In-depth LCMS/MS experience with quantitative PK analysis
  • Experience in a GxP regulatory laboratory with GLP/GCP/GMP understanding
  • Specialist method development and validation experience per ICH M10 for LCMS/MS PK
  • Practical knowledge of extraction techniques for small and large molecules from biological matrices
  • Experience training, supervising, and coordinating junior staff
  • Strong data handling, reporting, and regulatory documentation skills
  • Good IT literacy and numeracy
  • Clear written and verbal communication; ability to collaborate cross-functionally
  • Time management and multi-project handling ability
  • Safety and quality systems awareness
  • communication
  • problem-solving
  • teamwork
  • LCMS/MS
  • PK analysis
  • ICH M10 method development and validation

Full job description from WhatJobs. Apply for this role →

Back to all jobs

Help others hire with confidence

Reviews on Trustpilot

Worked with Verifera as a candidate or employer? Your honest review helps the next person trust verified hiring.