Назад
Company hidden
2 дня 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
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
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, GDP, and audit trails. Focus on verifying sample chain of custody, resolving data discrepancies, and supporting compliant analytical testing in a regulated laboratory.

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

Compensation: USD 26.25–30.00 per hour

Company

Eurofins PSS provides mission-critical analytical testing services for pharmaceutical, medical device, food, cosmetic, and consumer products companies as part of hirify.global’s international laboratory network.

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 Good Documentation Practices.
  • Confirm sample chain of custody and review audit trails for procedural and timing compliance.
  • Collaborate with testing personnel to resolve annotations, discrepancies, and corrections.
  • Support laboratory compliance, continuous improvement, safety walkthroughs, and required training.
  • Cross-train in laboratory testing functions and provide qualified hands-on testing support during periods of increased workload.

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, UV-Vis spectrophotometry, and 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.
  • Authorization to work indefinitely in the United States without sponsorship is required.

Nice to have

  • Experience with ELISA, MCE, and/or iCIEF.

Culture & Benefits

  • Medical, dental, and vision coverage.
  • Employer-sponsored life and disability insurance.
  • 401(k) plan with company match.
  • Vacation days, paid holidays, and additional paid time off.
  • Career development and support within an international life sciences organization.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →