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9 дней назад

Manufacturing Associate I/II (Biopharma)

26 - 36$
Формат работы
onsite
Тип работы
fulltime
Грейд
junior/middle
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

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TL;DR
Manufacturing Associate I/II (Biopharma): Manufacturing bulk intermediates and drug substances for biopharmaceutical products with an accent on cGMP compliance, aseptic cleanroom processing, and accurate batch-record documentation. Focus on executing upstream or downstream operations, maintaining manufacturing equipment, and ensuring materials and records are controlled right first time.

Location: Boulder, Colorado, USA; onsite cleanroom work. Schedule: 6:00 AM–6:30 PM on a 2-2-3-day shift schedule.

Salary: Manufacturing Associate I: $26.44–$36.49 per hour; Manufacturing Associate II: $30.29–$41.78 per hour.

Company

hirify.global develops and manufactures biopharmaceutical products and drug substances.

What you will do

  • Manufacture bulk intermediates and drug substances according to approved batch records and quality standards.
  • Perform upstream or downstream processing in a cleanroom while applying aseptic gowning and cleaning procedures.
  • Complete manufacturing records and logbooks at the time of execution in accordance with good documentation practices.
  • Operate and maintain manufacturing equipment according to applicable SOPs.
  • Issue and account for materials used in SPRs, BPRs, and associated forms.
  • Apply cGMP, GLP, and 5S workplace-organization practices to daily operations.

Requirements

  • Manufacturing Associate I: bachelor’s degree in a related scientific or engineering discipline and 0–2 years of related cGMP manufacturing experience; alternatively, a high school diploma and 3–5 years of experience, or equivalent.
  • Manufacturing Associate II: bachelor’s degree in a related scientific or engineering discipline and 2–5 years of related cGMP manufacturing experience; alternatively, a high school diploma and 4–6 years of experience, or equivalent.
  • Ability to work onsite in a cleanroom environment on the specified 2-2-3-day shift schedule.
  • Knowledge of cGMP requirements, good documentation practices, and applicable manufacturing procedures.

Culture & Benefits

  • Full-time employment in a regulated biopharmaceutical manufacturing environment.
  • Work governed by approved procedures, SOPs, current regulations, and right-first-time quality standards.
  • Equal opportunity workplace committed to workforce diversity.

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