Назад
Company hidden
обновлено 2 дня назад

GMP Laboratory Technician - Evening Shift (Biotechnology)

Формат работы
onsite
Тип работы
fulltime
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 Laboratory Technician - Evening Shift (Biotechnology): Performing GMP laboratory testing and supporting mammalian and microbial fermentation and purification processes for clinical and toxicology supplies with an accent on bioreactors, filtration, chromatography, and analytical methods. Focus on executing regulated laboratory operations, evaluating data, maintaining equipment, and documenting results in compliance with GMP and data integrity requirements.

Location: Onsite in St. Louis, Missouri, USA; candidates should live within a commutable distance of Chesterfield, Missouri. Evening shift, Monday–Friday, 3:30 PM–12:00 AM, with overtime as needed.

Company

An international life sciences company providing analytical testing, laboratory, pharmaceutical, food, environmental, cosmetic, genomics, and contract research services through a global network of laboratories.

What you will do

  • Set up, execute, and evaluate GMP manufacturing unit operations, including seed trains, bioreactors, fermentation, centrifugation, filtration, chromatography, UF/DF, conjugation, and lyophilization.
  • Perform routine analytical, compendial, and general laboratory testing using pH, appearance, UV-Vis spectroscopy, and other applicable methods.
  • Complete aseptic sampling, CIP/SIP, parts washing, sample preparation, documentation, work order generation, and data entry.
  • Operate, maintain, and conduct routine checks of laboratory instruments and equipment.
  • Review analytical data for accuracy, completeness, and compliance, and support laboratory investigations.
  • Collaborate with laboratory, manufacturing, and cross-functional teams to meet testing timelines and maintain laboratory operations.

Requirements

  • Associate’s degree or BS/BA in Biotechnology, Microbiology, Cell Biology, Chemical Engineering, Biochemistry, or an equivalent field.
  • 0–2+ years of experience in a laboratory or manufacturing environment, preferably in bioprocessing or the chemical process industry.
  • Authorization to work indefinitely in the United States without restriction or sponsorship.
  • Knowledge of GMP, safety, quality, regulatory, SOP, test method, specification, and data integrity requirements.
  • Strong oral and written communication, teamwork, and Microsoft Office skills, especially Microsoft Word and Excel.
  • Ability to lift 40 lbs and stand for an 8-hour shift.

Nice to have

  • Experience in a biological pilot plant or commercial manufacturing setting.
  • Knowledge of fermentation and downstream processing techniques.

Culture & Benefits

  • Full-time employment with comprehensive medical, dental, and vision coverage.
  • Life and disability insurance.
  • 401(k) plan with company match.
  • Paid vacation and holidays.
  • Yearly goal-based bonus and eligibility for merit-based increases.
  • Collaborative work within a diverse, cross-functional laboratory and manufacturing environment.

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 →