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2 дня назад

Pharmaceutical Manufacturing Technician

Формат работы
onsite
Тип работы
fulltime
Английский
b2
Страна
US
Релокация
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
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TL;DR
Pharmaceutical Manufacturing Technician (GMP/Clinical Manufacturing): Manufacturing clinical trial materials and operating, maintaining, and improving pharmaceutical equipment in an early-phase clinical production environment with an accent on GMP compliance, equipment ownership, and technical documentation. Focus on supporting technology transfer, optimizing processes, analyzing manufacturing data, and ensuring safe, high-quality production.

Location: Bend, Oregon, United States; fully site-based role. Relocation assistance is available for eligible candidates and their families.

Company

hirify.global is a global life sciences company with more than 30 sites across five continents, manufacturing medicines and supporting clinical development.

What you will do

  • Manufacture clinical trial materials in accordance with approved GMP procedures and quality standards.
  • Operate, clean, troubleshoot, and maintain pharmaceutical manufacturing equipment.
  • Own equipment activities across its lifecycle, including qualification and maintenance support.
  • Support technology transfer, process optimization, and continuous improvement projects.
  • Analyze manufacturing data and provide technical insights for project objectives.
  • Prepare GMP procedures, reports, training materials, and other required documentation.

Requirements

  • High school diploma or equivalent with relevant industry experience, or a bachelor’s degree in engineering, science, or a related field.
  • Knowledge of manufacturing equipment and production processes.
  • Strong analytical, problem-solving, organizational, and documentation skills.
  • Ability to work effectively in a collaborative team environment.
  • Commitment to safety, quality, regulatory compliance, and continuous improvement.
  • Pharmaceutical or GMP-regulated manufacturing experience is preferred.

Culture & Benefits

  • Hands-on experience supporting clinical manufacturing and product development.
  • Cross-functional collaboration with manufacturing, engineering, quality, and technical operations.
  • Opportunities to build technical expertise and grow within pharmaceutical manufacturing.
  • Ownership of manufacturing equipment and participation in equipment improvement initiatives.
  • Collaborative and inclusive workplace focused on learning and continuous improvement.
  • Competitive benefits and compensation programs.

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