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1 день назад

Associate Analytical Scientist (Analytical Chemistry)

69 036 - 89 570$
Формат работы
onsite
Тип работы
fulltime
Грейд
junior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

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TL;DR
Associate Analytical Scientist (Analytical Chemistry): Performing routine analytical testing and data verification for process R&D and pharmaceutical production in cGMP-compliant laboratories with an accent on raw material release, in-process testing, release testing, and analytical method validation. Focus on developing and transferring HPLC and GC methods, maintaining instruments, troubleshooting analytical issues, and preparing technical documentation for regulatory filings.

Location: On-site in San Diego, California, United States

Anticipated salary range: $69,036–$89,570 per year

Company

hirify.global is a contract development and manufacturing organization providing process development, R&D, GLP toxicology lots, and GMP small-molecule manufacturing services for the biopharmaceutical industry.

What you will do

  • Perform routine analytical testing and data verification for process R&D and production.
  • Conduct raw material release, in-process, and drug substance release testing under cGMP guidelines.
  • Perform qualitative and quantitative assays using wet chemistry and analytical instrumentation.
  • Execute HPLC and GC method validation and transfer experiments, including protocols and reports.
  • Support analytical method development, stress studies, stability-indicating methods, IPC methods, and residual solvent methods.
  • Maintain and troubleshoot instruments and author SOPs, protocols, technical reports, specifications, and regulatory filing sections.

Requirements

  • Master’s degree in analytical chemistry or a related field; no work experience required, or a bachelor’s degree with 1–2 years of relevant experience.
  • Experience with analytical techniques, method development, and method validation.
  • Required experience with high-pressure chromatography systems and related software.
  • Ability to work under cGMP, safety, and quality standards and maintain accurate records.
  • Ability to work independently and collaboratively, manage multiple tasks, and switch shifts as needed.
  • Availability to work holidays, weekends, or overtime when required.

Nice to have

  • Hands-on experience with HPLC, GC, LCMS, dissolution, and GCMS.
  • Experience with capillary electrophoresis and electronic laboratory notebook programs.
  • Experience using Microsoft Office and standard statistical analysis tools.

Culture & Benefits

  • Work in cGMP-compliant analytical and R&D laboratories.
  • Use state-of-the-art analytical tools and laboratory systems.
  • Follow structured safety, quality, and regulatory procedures.
  • Perform work requiring PPE, extended standing or walking, variable noise exposure, color identification, and repetitive motions.

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