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Chemical Development Trace Analysis Scientist (LC-MS)

Формат работы
onsite
Тип работы
fulltime
Английский
b2
Страна
UK
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Текст:
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TL;DR
Chemical Development Trace Analysis Scientist (LC-MS): Developing, optimizing, and validating advanced trace-analysis methods for small molecules in pharmaceutical raw materials, intermediates, and drug substances with an accent on LC-MS, Orbitrap, and parts-per-billion impurity analysis. Focus on investigating mutagenic impurities and nitrosamines, interpreting complex scientific data, and producing GMP-compliant analytical documentation.

Location: Macclesfield, UK; based at a client pharmaceutical facility

Company

International life sciences and analytical testing organization providing pharmaceutical and other industry testing services, including on-site insourcing solutions.

What you will do

  • Develop, optimize, and validate advanced trace-analysis methods using LC-MS and Orbitrap technologies.
  • Detect and quantify trace-level small molecules in raw materials, intermediates, and drug substances.
  • Support the assessment of mutagenic impurities, nitrosamines, and other trace analytes at parts-per-billion levels.
  • Conduct complex analytical investigations, interpret scientific data, and troubleshoot instrumentation issues.
  • Provide technical expertise to project teams, advise stakeholders, and contribute to trace-analysis capability development.
  • Author and review analytical testing plans, method development reports, and validation protocols.

Requirements

  • Degree or higher qualification in Chemistry, Analytical Chemistry, or a related scientific discipline.
  • Strong foundation in organic chemistry and analytical science, with pharmaceutical analytical experience in a development laboratory.
  • Hands-on experience with LC-MS/MS, GC-MS/MS, GC-HRMS, and LC-HRMS.
  • Knowledge of drug development processes and analysis of raw materials, intermediates, and drug substances.
  • Understanding of GMP requirements and experience with electronic systems and Microsoft Office.
  • Strong problem-solving, documentation, data-management, communication, and collaboration skills.

Nice to have

  • Experience with NMR, IC, or ICP-MS.

Culture & Benefits

  • Permanent full-time employment with a flexible 36.5-hour Monday-to-Friday week.
  • Reward and recognition scheme, increasing holiday entitlement, and long-service awards.
  • Health Cash Plan, life assurance at four times annual salary, and company pension plan after three months.
  • Employee Assistance Programme, volunteering days, free on-site parking, and Perkbox discounts.
  • Access to worldwide career opportunities and a focus on technical excellence, continuous improvement, and professional development.

Hiring process

  • Assessment centre or staged interview process, depending on the role requirements.

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