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Supply Chain Sr. Associate

Louisville, KY
Description:
Note:
  • This position will be 100% ONSITE in the Louisville (LDC) office. 
  • Potential remote work on Fridays (contingent on business needs). 
  • All candidates must be local to Louisville and have the ability to work onsite. 
  • EW will be working standard business hours from 8 AM-5 PM ET.

The type of qualities/characteristics the hiring manager is looking for in candidates to work best with the team:
  • Strong communication and presentation skills (verbal & written).
  • GMP knowledge and understanding of pharmaceutical regulations with an understanding of Quality and regulatory requirements
  • Problem solver with high sense of responsibility to achieve results

Candidate Non Negotiables:
  • Inability to work onsite in Louisville, KY.
  • Poor writing/communication skills.
  • Must have experience in a Healthcare environment.

Job Description:
  • Under minimal direction of Supply Chain Manager, manages the following responsibilities:
  • Executes implementation of cold chain and transportation process requirements as defined by  strategy
  • Support daily transport operation for assigned areas on LDC site
  • Collects, processes and reports outs data and KPI related to cold chain, transportation and vendor performance
  • Supports transportation and cold chain for LDC
  • Supports root cause analysis and performance analysis and risk assessment, helps support action plans to improve or mitigate risk with departments involved.
  • Supports the development and maintains departmental SOPs and other controlled documents on transportation management
  • Owns quality records related to TSP activities – Deviations/Corrective Actions
  • Manages other projects as assigned

Basic Qualifications
  • Bachelor’s degree
  • OR
  • Associate’s degree and 4 years of experience
  • OR
  • High school diploma / GED and 6 years of experience

Top 3 Must Have Skill Sets:       
  • Problem solver with high sense of responsibility to achieve results.
  • Strong communication and presentation skills (verbal & written).
  • GMP knowledge and understanding of pharmaceutical regulations with an understanding of Quality and regulatory requirements.

Day to Day Responsibilities:
  • Own and support Quality Records (e.g. Deviations, CAPA), Processes and Procedures.
  • Manage track and trace process of small parcel shipments
  • Assist with cross functional special supply chain improvement projects.

PAY RATE : $40/Hr on W2.

"This posting is for Contingent Worker, not an FTE"

 

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