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9 часов назад

GMP Analytical Chemistry Data Reviewer

26 - 30$
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
GMP Analytical Chemistry Data Reviewer (GMP/Analytical Chemistry): Reviewing GMP laboratory data and documentation for compliance with procedures, data integrity standards, and regulatory requirements with an accent on HPLC/UPLC, UV-Vis spectrophotometry, and Good Documentation Practices. Focus on verifying audit trails, sample chain of custody, quantitative liquid chromatography data, and resolving documentation discrepancies in a regulated laboratory environment.

Location: Rensselaer, New York, USA; candidates must live within commuting distance. Full-time, Monday–Friday, first shift from 8:00 a.m. to 4:30 p.m.

Salary: $26.25–$30.00 per hour

Company

hirify.global Scientific is an international life sciences company providing analytical testing services through a global network of laboratories and teams serving pharmaceutical, medical device, food, cosmetic, and consumer products industries.

What you will do

  • Review GMP laboratory data and documentation for compliance with approved procedures, data integrity standards, and regulatory requirements.
  • Verify logbook and documentation entries for accuracy, completeness, and adherence to Good Documentation Practices.
  • Confirm sample chain of custody and review audit trails throughout the testing lifecycle.
  • Collaborate with laboratory personnel to resolve annotations, discrepancies, and corrections.
  • Support cross-training and provide qualified hands-on laboratory testing assistance during increased workload periods.
  • Conduct laboratory safety and compliance walkthroughs and document observations.

Requirements

  • Bachelor’s degree in Chemistry, Life Sciences, or a related scientific field.
  • At least 2 years of cGMP experience in a regulated laboratory environment.
  • Direct experience reviewing GMP data in an industrial setting.
  • Hands-on experience with HPLC/UPLC and UV-Vis spectrophotometry, including quantitative liquid chromatography data.
  • Ability to meet physical requirements including lifting 25 lbs., prolonged standing or walking, pushing and pulling equipment, and bending or reaching.
  • Must be authorized to work in the United States indefinitely without sponsorship.

Nice to have

  • Experience with ELISA, MCE, or iCIEF.

Culture & Benefits

  • Medical insurance options, dental coverage, and vision coverage.
  • Employer-sponsored life and disability insurance.
  • 401(k) plan with company matching.
  • Paid vacation, holidays, and additional paid time off.
  • Required safety, procedural, and refresher training with opportunities for cross-training.

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