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9 дней назад

Manufacturing Technician II - DAP (Nights) (Biomanufacturing)

21 - 32$
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
Manufacturing Technician II - DAP (Nights) (Biomanufacturing): Operating packaging equipment and supporting device assembly in a cGMP manufacturing environment with an accent on equipment setup, in-process inspection, documentation, and material handling. Focus on troubleshooting production equipment, completing batch records, maintaining line clearance and cleaning standards, and supporting process improvement activities.

Location: Blue Ash, Ohio, USA; onsite night shift

Salary: $21.50–$32.00 per hour

Company

hirify.global is a technology-focused biomanufacturing company developing sustainable, end-to-end manufacturing solutions for medicine production.

What you will do

  • Operate packaging machinery, load materials, monitor equipment status, manage product flow, and manually palletize finished materials.
  • Set up equipment, select recipes, enter data in SCADA and HMI systems, adjust equipment, and perform sensor challenges.
  • Complete manual packaging, rework, visual inspections, sampling, minor troubleshooting, and escalation of equipment or quality concerns.
  • Move and reconcile materials using pallet jacks, lifts, SAP, and WES.
  • Perform cleaning, housekeeping, line clearance, batch record documentation, and GMP data entry.
  • Support lean activities, equipment qualification, process validation, daily Tier 0 meetings, and other manufacturing areas.

Requirements

  • Prior experience in a regulated manufacturing environment.
  • Working knowledge of product security controls and material-handling equipment.
  • Accurate documentation and data-entry skills, including batch records and logbooks.
  • Basic mathematical and problem-solving skills, with the ability to identify process or documentation inconsistencies.
  • Ability to read, write, speak, and understand English to interpret SOPs, batch records, and work instructions.
  • Ability to follow procedures with minimal supervision and work effectively in a fast-paced production team.

Nice to have

  • High school, vocational school, or equivalent education.
  • At least one year of pharmaceutical, biotechnology, or cGMP-regulated manufacturing experience.
  • Experience with lean manufacturing, cGMP principles, Microsoft applications, SAP, or Veeva Vault.

Culture & Benefits

  • Full-time 12-hour 2/2/3 night-shift schedule, subject to operational changes and overtime requirements.
  • Work in controlled and non-classified manufacturing areas under cGMP, quality, safety, PPE, and LOTO requirements.
  • Physical work may include climbing, kneeling, repetitive motion, temperature changes, and exerting up to 100 pounds of force.
  • Benefits include healthcare, dental and vision coverage, 401(k) with company match, paid vacation and holidays, paid leave, life and disability insurance, tuition reimbursement, and caregiving support.
  • Occupational health screening, vaccination or testing, PPE use, and an onboarding eye exam are required.
  • Sponsorship or support for work authorization, including visas, is not available.

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