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Manufacturing Technician II - DAP (Nightshift)

21 - 50$
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
Manufacturing Technician II - DAP (Nightshift) (Biomanufacturing/Packaging): Operating packaging equipment and supporting cGMP manufacturing activities with an accent on equipment setup, in-process inspection, material handling, and batch documentation. Focus on troubleshooting production equipment, maintaining line clearance and cleaning standards, completing accurate records, and supporting process improvement and validation work.

Location: West Chester, Ohio, United States; onsite manufacturing role

Base pay: $21.50–$32.00 per hour

Company

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

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, make minor adjustments, and perform sensor challenges.
  • Complete manual packaging, rework, visual inspections, sampling, minor troubleshooting, and escalation of equipment or product concerns.
  • Move and reconcile materials using pallet jacks, lifts, SAP, and WES.
  • Perform cleaning, housekeeping, line clearance, batch record entries, GMP documentation, and routine calculations.
  • Support safety, lean manufacturing, 5S, equipment qualification, process validation, and daily Tier 0 meetings.

Requirements

  • Prior experience in a regulated manufacturing environment, with 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, including routine weights, measures, and conversions.
  • Ability to read, write, speak, and understand English to interpret SOPs, batch records, and work instructions.
  • Ability to follow written procedures with minimal supervision, identify deviations, and work effectively in a fast-paced production team.
  • Ability to perform non-sedentary work involving climbing, kneeling, repetitive motion, temperature changes, PPE, and exerting up to 100 pounds of force; an eye exam is required during onboarding.

Nice to have

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

Culture & Benefits

  • Work in a controlled manufacturing environment governed by cGMPs, quality procedures, and safety standards.
  • Benefits include medical, dental, and vision coverage, family-building benefits, life and disability insurance, and paid vacation and holidays.
  • Includes a 401(k) plan with company match, annual cash bonus program, tuition reimbursement, and caregiving support.
  • Sponsorship or support for work authorization, including visas, is not available for this position.

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