Назад
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16 часов назад

Specialist II, Supply Chain

60 000 - 93 750$
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
Specialist II, Supply Chain (SAP/MRP and Packaging Documentation): Managing packaging documentation changes, new component creation, artwork workflows, and master data for pharmaceutical manufacturing with an accent on SAP, D365, cGMP compliance, and cross-functional coordination. Focus on project-managing change implementation, maintaining validated records and artwork, and resolving complex ERP and material data requirements for product launches.

Location: USA - OH - Blue Ash; onsite at the West Chester supply site. Monday–Friday, 8 hours per day, with periodic access to packaging and production areas and occasional business travel.

Salary: $60,000–$93,750 per year.

Company

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

What you will do

  • Coordinate packaging documentation changes, packaging artwork updates, and Bill of Material change forms.
  • Project-manage changes from initial notification through implementation, coordinating with New Product Introduction, Production, Regulatory Affairs, Quality Assurance, and Planning.
  • Create and maintain Operations Change Management, Veeva, Gazelle, artwork, and job-tracking records.
  • Manage artwork workflows, external artwork resources, approved documentation transfers, and artwork samples.
  • Set up and progress Artwork Order Requests, Technical Labeling Request Forms, and Labeling Request Forms.
  • Serve as the site SAP super user, supporting SAP/D365 transactions, master data, ERP queries, and access requests.

Requirements

  • Experience in packaging operations, production planning, quality assurance, packaging technical services, MRP, or advanced planning systems.
  • Working knowledge of packaging and artwork processes, compliance requirements, and cGMPs.
  • Knowledge of cGMP and FDA regulations related to data management and validation.
  • Detailed knowledge of SAP, MRP, and advanced planning systems used in pharmaceutical production.
  • Strong interpersonal, project management, coordination, analytical, prioritization, and attention-to-detail skills.
  • Must work onsite at the West Chester supply site in a combined office and cGMP manufacturing environment.

Nice to have

  • Bachelor’s degree in a technical or scientific field.
  • 3+ years of experience in packaging documentation, artwork management, supply chain, or a related cGMP-regulated function.
  • Experience with change management systems such as Veeva or TrackWise.
  • Knowledge of inventory control and document management systems.

Culture & Benefits

  • Work in a technology-focused biomanufacturing environment supporting product launches and site initiatives.
  • Benefits include medical, dental, and vision healthcare, life and disability insurance, and family-building support.
  • Paid vacation, holidays, and other leaves of absence.
  • 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.

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