16 часов назад
Specialist II, Supply Chain
60 000 - 93 750$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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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