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1 день назад

Scientist (Pharmaceutical Analytical Development)

70 000 - 75 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Scientist (Pharmaceutical Analytical Development) (Chromatography/GMP): Developing, validating, and transferring analytical methods for pharmaceutical raw materials, formulations, stability studies, and finished products with an accent on method robustness, regulatory compliance, and experimental design. Focus on solving complex laboratory problems, interpreting analytical data, managing stability testing, and supporting instrument qualification.

Location: Melrose Park, Illinois, United States

Salary: $70,000–$75,000 per year

Company

hirify.global develops and supplies healthcare and pharmaceutical products.

What you will do

  • Conduct analytical development activities, including raw material release, stability testing, formulation testing, and finished product analysis.
  • Develop, validate, verify, and transfer analytical methods to quality control and other testing laboratories.
  • Review and approve validation protocols and reports, data packages, SOPs, and laboratory documentation.
  • Manage stability testing protocols, laboratory logistics, stability summaries, and finished product certificates of analysis.
  • Design and execute experimental programs using chromatography, wet chemistry, and laboratory instruments.
  • Support instrument qualification, identify laboratory problems, and recommend scientifically sound solutions while maintaining GMP-compliant records.

Requirements

  • Bachelor’s degree in Chemistry or a related field and 3+ years of relevant experience.
  • Experience with chromatography methods including HPLC, GC, TLC, and/or ion chromatography, plus wet chemistry and basic laboratory instruments.
  • Ability to design and execute experiments using different laboratory instruments and techniques.
  • Knowledge of statistical analysis, pharmaceutical dosage forms, and concepts for developing novel drug delivery systems.
  • Familiarity with pharmaceutical analytical operations, FDA requirements, and GMP regulations.
  • Effective spoken and written English is required for understanding policies, procedures, training materials, and workplace communications.

Culture & Benefits

  • Full-time, at-will employment.
  • Medical, prescription drug, dental, and vision coverage.
  • 401(k) plan with company contributions.
  • Paid vacation, holidays, personal days, life insurance, disability coverage, employee assistance, and wellness programs.

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