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Production Scheduler/Purchasing Manager
Job in
Gastonia, Gaston County, North Carolina, 28054, USA
Listed on 2026-02-12
Listing for:
medtechrec
Full Time
position Listed on 2026-02-12
Job specializations:
-
Manufacturing / Production
Operations Engineer, Quality Engineering
Job Description & How to Apply Below
About the job Production Scheduler / Purchasing Manager Overview
Our client, a leading medical device manufacturer, is seeking a Production Scheduler / Process & Material Planner to join their operations team. This position plays a key role in coordinating materials, processes, and production workflows to ensure manufacturing efficiency and compliance with ISO 13485 and FDA 21 CFR 820 standards. The ideal candidate will be detail-oriented, proactive, and capable of managing multiple priorities with minimal supervision.
Responsibilities- Create and maintain engineering master data and work orders, including accurate cycle times for machining operations.
- Schedule, print, and release work orders while ensuring accuracy across all production documentation.
- Monitor inventory levels and plan vendor-managed inventory to align with production demands.
- Collaborate with Engineering and Methods teams to develop and maintain supporting documentation such as models, drawings, and inspection reports.
- Update part revisions and work orders in the Visual ERP system according to Engineering Change Orders (ECOs).
- Review production schedules and confirm material availability and quality approval.
- Evaluate and manage suppliers based on cost, quality, reliability, and service performance.
- Investigate non-conforming materials and coordinate corrective actions with suppliers and quality teams.
- 3+ years of experience in material planning, production scheduling, or process-related roles (or an equivalent combination of education and experience).
- Proficiency in Visual ERP and strong understanding of work order and process creation.
- Skilled in Microsoft Office (Excel, Word, Outlook) and Solid Works
. - Working knowledge of ISO 13485 and FDA 21 CFR 820 quality system requirements.
- Excellent problem-solving, prioritization, and analytical skills.
- Ability to work independently and manage multiple projects within tight timelines.
- Strong communication and collaboration skills.
- High school diploma or GED required.
- Additional certifications or training in manufacturing, process planning, or ERP systems preferred.
- Eye protection, hearing protection, and non-slip footwear in designated areas.
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