9 дней назад
Manufacturing Associate I/II (Biopharma)
26 - 36$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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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