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4 дня назад

Biomanufacturing Associate I - Production Support

Формат работы
onsite
Тип работы
fulltime
Грейд
junior
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
Biomanufacturing Associate I - Production Support (Biomanufacturing/cGMP): Supporting tissue-engineering and biomanufacturing operations through equipment operation, material handling, sterilization, and production preparation with an accent on aseptic technique, inventory control, and Good Documentation Practices. Focus on troubleshooting equipment and process deviations, maintaining GMP records, and supporting continuous 24/7 manufacturing operations.

Location: 100% onsite at the Research Triangle Park (RTP), North Carolina, United States; flexible shifts, 24/7 operations, and on-call support may be required.

Company

hirify.global is a publicly traded biotechnology and pharmaceutical company developing therapies for rare diseases and technologies for manufacturing transplantable organs.

What you will do

  • Operate bioprocess equipment and perform production-support activities in compliance with cGMP, OSHA, and company procedures.
  • Monitor, restock, rotate, and request supplies and materials for JIT warehouse inventory.
  • Prepare single-use assemblies, media, buffers, surgical pans, instruments, and other materials according to SOPs.
  • Perform autoclave and parts-wash runs and support scaffold production, recellularization, and cell-production activities.
  • Coordinate preventative maintenance and calibration activities, including vendor access and scheduling in the Blue Mountain RAM system.
  • Record data in batch records, logbooks, and system documentation; troubleshoot basic equipment issues and draft process deviation reports.

Requirements

  • Bachelor’s degree in biology, biotechnology, biomedical engineering, or a related scientific discipline.
  • Proven proficiency in aseptic technique and strong attention to detail.
  • Strong computer skills and proficiency with Microsoft Office or equivalent software.
  • Ability to work independently and collaboratively with manufacturing teams.
  • Excellent verbal and written communication skills and adherence to Good Documentation Practices.
  • Ability to work flexible shifts supporting 24/7 operations and on-call coverage.

Nice to have

  • At least one year of cGMP biomanufacturing, R&D, or laboratory operations experience.

Culture & Benefits

  • Hands-on experience in a startup, new GMP manufacturing facility focused on tissue engineering and biomanufacturing.
  • Medical, dental, vision, and prescription coverage for eligible employees.
  • Employee wellness resources, 401(k), and ESPP savings plans.
  • Paid time off, paid parental leave, and disability benefits.
  • Mission-driven work addressing rare diseases and the shortage of transplantable organs.

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