Назад
Company hidden
9 часов назад

Specialist II, Manufacturing (Dayshift)

29 - 43$
Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Specialist II, Manufacturing (Dayshift) (cGMP pharmaceutical manufacturing): Supporting pharmaceutical manufacturing processes through SAP transactions, production coordination, technical documentation, deviation investigations, and quality audits with an accent on cGMP compliance, documentation control, and operational metrics. Focus on leading process improvements, maintaining audit readiness, and coordinating production activities during a Monday–Friday dayshift.

Location: USA - OH - West Chester; onsite dayshift, Monday–Friday, 8-hour days

Salary: $28.50–$43.00 per hour

Company

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

What you will do

  • Execute SAP transactions and coordinate daily and weekly activities to meet production schedules.
  • Author, revise, approve, review, and audit SOPs, work instructions, master batch records, investigations, line assessments, and corrective actions.
  • Investigate and close manufacturing deviations, CAPAs, and AFCAs while escalating issues outside established procedures.
  • Review batch records and other production documentation for completeness, quality, and cGMP compliance.
  • Lead document-modification training, create training materials, and monitor employee training compliance.
  • Maintain production metrics, OEE data, visual tracking tools, audit readiness, KPI reporting, and process improvement activities.

Requirements

  • Experience with documentation in a cGMP environment and experience in pharmaceutical or other cGMP-regulated manufacturing.
  • Ability to understand, read, write, communicate, and follow instructions in English.
  • Strong attention to detail, accurate recordkeeping, and ability to perform mathematical calculations.
  • Ability to follow cGMP, SOP, safety, sterile-garment, and PPE requirements.
  • Ability to work onsite in West Chester, Ohio, on a Monday–Friday dayshift schedule.
  • Work authorization or visa sponsorship is not available.

Nice to have

  • Production-environment experience.
  • High school, vocational, or bachelor’s degree or equivalent.
  • Experience in LEAN manufacturing and knowledge of cGMP and FDA policies and procedures.

Culture & Benefits

  • Annual cash bonus program and 401(k) plan with company match.
  • Medical, dental, and vision healthcare coverage.
  • Family-building benefits, life and disability insurance, and caregiving support.
  • Paid vacation, paid holidays, and other paid leave.
  • Tuition reimbursement.
  • Cross-functional collaboration with quality, warehouse, procurement, planning, vendors, and the global technology community.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →