Назад
Company hidden
8 дней назад

(CW) Manufacturing Associate (Temporary/Contract)

Формат работы
onsite
Тип работы
project
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
(CW) Manufacturing Associate (Temporary/Contract) (Biopharmaceutical Manufacturing): Supporting commercial biopharmaceutical manufacturing processes including mammalian cell culture, filtration, chromatography, centrifugation, protein purification, and formulation with an accent on process execution, documentation, and cGMP compliance. Focus on identifying processing issues, supporting optimization initiatives, maintaining quality systems, and working safely on a temporary night-shift schedule.

Location: Novato, California, United States. Temporary night shift from 18:00 to 07:00, Saturday/Sunday through Tuesday.

Company

hirify.global is a biotechnology company developing therapies for rare genetic diseases and operating commercial biopharmaceutical manufacturing capabilities.

What you will do

  • Operate and learn biopharmaceutical manufacturing processes, including mammalian cell culture, depth and tangential flow filtration, chromatography, centrifugation, protein purification, and bulk drug substance formulation.
  • Support process optimization initiatives, identify processing issues, and help implement solutions.
  • Write, review, and improve operational and process documentation.
  • Use quality systems for deviations, CAPAs, change requests, and action or alert reports.
  • Support business projects, department metrics, and systems such as TrackWise and ERP.
  • Work with automation and manufacturing systems including LIMS, MES, and PI.

Requirements

  • Bachelor’s degree in a science-related field or engineering, or an associate degree in science, or a biotechnology certificate with 2+ years of experience in biotech manufacturing or another regulated industry.
  • Knowledge of process theory, equipment operation, and cGMP requirements for commercial operations.
  • Strong verbal and written communication skills.
  • Ability to collaborate, resolve conflicts, identify improvement opportunities, and implement solutions.
  • Ability to perform strenuous repetitive work, use stairs and ladders, make equipment connections, and regularly lift, push, or pull items weighing approximately 25 pounds.
  • Availability for shift-based and off-hours work, including the temporary night shift.

Culture & Benefits

  • Work in a regulated biopharmaceutical manufacturing environment supporting therapies for rare diseases.
  • Work may involve loud equipment and requires personal protective equipment.
  • Schedule includes overnight shifts and weekend work.

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 →