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Prep Operator II (Biopharmaceutical Manufacturing)

23 - 39$
Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Prep Operator II (Biopharmaceutical Manufacturing): Executing pharmaceutical manufacturing operations using standard operating procedures, batch records, manufacturing control systems, and filtration processes with an accent on GMP compliance, equipment troubleshooting, and continuous improvement. Focus on operating and optimizing centrifugation and membrane filtration processes, investigating deviations, implementing corrective actions, and supporting new product introductions.

Location: On premise in Rocky Mount, North Carolina, United States. 12-hour rotating 2-2-3 shift schedule with day or night shifts required. Relocation support may be available based on eligibility and business needs.

Salary: $23.40–$39.01 per hour, with potential overtime, weekend, holiday, and other shift premiums.

Company

hirify.global develops and manufactures medicines and pharmaceutical products for patients worldwide.

What you will do

  • Execute manufacturing tasks according to standard operating procedures, batch records, and manufacturing control systems.
  • Operate and troubleshoot continuous centrifugation, microfiltration, ultrafiltration, cell disruption, and membrane filtration processes.
  • Identify and resolve non-routine operational problems and support equipment installation, start-up, operation, and troubleshooting.
  • Investigate operational deviations, implement corrective actions, and drive continuous improvement and zero-defect initiatives using Lean tools.
  • Train and provide direction to colleagues while sharing knowledge across work groups.
  • Maintain a safety-oriented, GMP-compliant work environment.

Requirements

  • High school diploma or GED and 4+ years of relevant experience.
  • Experience executing operations in accordance with SOPs, batch records, and manufacturing control systems.
  • Knowledge of filtration and cell-processing operations, Lean tools, and technical and mechanical systems.
  • Strong interpersonal, documentation, problem-solving, analytical, and troubleshooting skills.
  • Ability to work independently and as part of a self-directed shift team in a fast-paced environment.
  • Must have permanent authorization to work in the United States; visa sponsorship is not available now or in the future.

Nice to have

  • Bachelor's degree and experience in a start-up environment.
  • Knowledge of biopharmaceutical manufacturing and process improvement methodologies.
  • Leadership abilities, adaptability, and willingness to learn new technologies and processes.
  • Basic familiarity with AI tools and interest in using them to improve productivity.

Culture & Benefits

  • Work in a controlled-temperature cleanroom environment with required personal protective equipment.
  • Physical work includes standing for 10–12 hours, walking long distances, climbing stairs and ladders, and lifting up to 50 pounds without assistance.
  • Comprehensive benefits including 401(k) matching and retirement contributions.
  • Paid vacation, holidays, personal days, caregiver and medical leave.
  • Medical, prescription drug, dental, and vision coverage.

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