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2 дня назад

Engineering Technician (Pharmaceutical Manufacturing)

31 - 38$
Формат работы
onsite
Тип работы
fulltime
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
Engineering Technician (Pharmaceutical Manufacturing): Supporting engineering studies, equipment implementation, validation, process improvement, and hands-on sterile pharmaceutical manufacturing with an accent on cGMP compliance, aseptic processing, and equipment qualification. Focus on executing validation studies, troubleshooting manufacturing equipment, preparing sterile products and components, and coordinating with Engineering, Operations, and Quality.

Location: On-site in Charlottesville, Virginia, United States

Salary: $31.35–$38.46 per hour, depending on experience and qualifications

Company

hirify.global is a contract manufacturing organization specializing in small-batch sterile injectable manufacturing, packaging, labeling, laboratory services, and pharmaceutical support from clinical trials through commercial production.

What you will do

  • Execute and report engineering protocols, studies, and validation activities.
  • Evaluate, install, and qualify instrumentation and manufacturing equipment.
  • Select and order parts and components for engineering batches.
  • Set up and prepare sterile pharmaceutical products and components.
  • Support process and product development, manufacturing operations, and Pharmaceutical Operator II duties as needed.
  • Review deviations, change controls, validation protocols, and formal studies while collaborating with Engineering, Operations, Quality, and other departments.

Requirements

  • Technical degree, two-year associate degree, or equivalent industry-related experience.
  • Basic computer proficiency, including Microsoft Word and Excel, with the ability to learn additional software.
  • Professional communication and interpersonal skills.
  • Ability to maintain positive working relationships with coworkers, supervisors, and vendors.
  • Ability to work on-site on a regular basis.

Nice to have

  • Experience in pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.
  • Knowledge of cGMP requirements and validation principles.
  • Experience with manufacturing equipment, engineering projects, or validation activities.
  • Familiarity with aseptic processing and sterile manufacturing operations.
  • Strong mechanical aptitude, troubleshooting skills, and cross-functional collaboration experience.

Culture & Benefits

  • Work in a regulated pharmaceutical manufacturing environment supporting clinical and commercial products.
  • Collaborate across Engineering, Operations, Quality, and other departments.
  • Contribute to custom sterile manufacturing and pharmaceutical support services.
  • Work visa sponsorship is not available.

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