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SCM FDA Analyst

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Date: Feb 15, 2019

Location: Valencia, ES

Company: Celestica International Inc.

Req ID: 37190 
Region: Europe 
Country: Spain 
State/Province: La Pobla De Vallbona 
City:  Valencia 

 

Detailed Description:

 

Incumbents apply knowledge in a Healthtech area of specialization. Work is performed within established professional standards and practices to ensure the supply chain for medical device manufacturing is 100% FDA compliant. Tasks are moderately complex in nature where judgment is required to complete recurring assignments independently and to determine the best methods to follow to complete assignments. Erroneous decisions or failure to achieve results may have a negative impact on the area’s patient safety, operations, schedules, and/or performance goals. Works under general Supervision.

 

 

Key Responsibilities:

 

  • Maintains responsibility for the management of FDA purchasing including meeting customer commits negotiations and agreement with suppliers, meeting quality and delivery requirements.
  • Manages the warehouse and material handling for the FDA business unit, 24x7, while maintaining appropriate level of security.
  • Manages relationship with external carriers, customs brokers and third party warehouses including quality, rate negotiation, performance and alternative providers. Ensures compliance on FDA regulations and laws.
  • Assists with FDA issues related to customs suppliers and material flow.
  • Ensures that all the inbound material is in compliance to all applicable FDA regulations and laws.
  • Oversee design, development, integration and maintenance of SCM systems, tools and processes at the FDA business unit.
  • Develops and execute of FDA inventory management processes including forecasting, analysis, reporting, action plans.
  • Drives continuous improvement to minimize inventory costs and provide necessary management reporting.

 

 

Core Knowledge/Skills/Competencies:

 

  • Knowledge and understanding of supply chain management, distribution methods, and global transportation services and inventory management
  • Working knowledge of FDA and ISO 13485 regulations.
  • Strong knowledge of global business environment and customers' business.
  • Good understanding of IT concepts and integrated business applications
  • Strong knowledge in all areas of import / export, regulatory and logistics management.
  • Ability to communicate effectively, both verbally and in writing, with a wide variety of internal and external customers
  • Ability to effectively lead, manages, train and motivate a diverse group of employees
  • Good negotiation and problem resolution skills.
  • Good communication and presentation skills
  • Very good command of written & spoken English.
  • This position requires a high energy level and a passion for excellence.

      

Typical Experience/Education:

 

  • Bachelor’s degree in related field.
  • 5+ years of relevant experience in the manufacturing industry (Healthtech industry preferred)

 

 

 

COMPANY OVERVIEW:
Celestica (NYSE, TSX: CLS) is a US$5.6 billion global leader in the delivery of end-to-end product lifecycle solutions. Our customers trust us to deliver the most advanced design, engineering and manufacturing expertise for their highly sophisticated and complex products. From advanced medical devices, to highly engineered aviation systems, to next-generation hardware solutions for the Cloud, at Celestica we manage the complexity for our customers and set the bar for quality and reliability in their markets. Our customer portfolio includes leaders in the enterprise computing, communications, aerospace and defense, industrial, smart energy, healthtech and semiconductor markets. Headquartered in Toronto, our global network spans 13 countries with 26,000 employees throughout the Americas, Europe and Asia.


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