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Supply Chain Associate

Job in Thousand Oaks, Ventura County, California, 91362, USA
Listing for: The Judge Group
Full Time position
Listed on 2026-08-06
Job specializations:
  • Quality Assurance - QA/QC
  • Supply Chain/Logistics
Salary/Wage Range or Industry Benchmark: 48000 - 60000 USD Yearly USD 48000.00 60000.00 YEAR
Job Description & How to Apply Below

Our client is seeking a detail-oriented Supply Chain Associate to support supply chain, warehouse, manufacturing, and quality operations within a pharmaceutical environment. The ideal candidate will have experience working in GMP/GDP-regulated settings and possess strong documentation, inventory, and quality systems knowledge. This role will support operational activities, continuous improvement initiatives, and compliance-related processes while collaborating cross-functionally with Supply Chain, Quality, Manufacturing, and Warehouse teams.

Key Responsibilities

  • Support daily supply chain, warehouse, and inventory management activities in a GMP/GDP-regulated environment.
  • Maintain compliance with pharmaceutical industry standards, procedures, and quality requirements.
  • Assist with documentation creation, updates, and revisions within CDOCS.
  • Utilize DQMS (Digital Quality Management System) and QMTS (Quality Management Tracking System) to support quality-related activities.
  • Participate in deviation investigations and own minor deviations and CAPA activities as assigned.
  • Support inventory transactions and material movements through ERP systems.
  • Operate Powered Industrial Vehicles (PIVs) safely and effectively when required.
  • Perform weighing and scale-related operations while ensuring accuracy and compliance.
  • Gather operational metrics, prepare reports, and present findings to management.
  • Support continuous improvement and operational excellence initiatives.
  • Collaborate with cross-functional teams to drive process improvements and ensure business objectives are met.
  • Maintain accurate documentation and records in accordance with company policies and regulatory requirements.

Required Qualifications

  • Bachelor's degree or equivalent combination of education and experience.
  • Experience working in a GMP/GDP-regulated environment within Quality, Manufacturing, Dispensing, Warehouse, or Supply Chain Operations.
  • Pharmaceutical or biotechnology industry experience.
  • Experience supporting document revisions and management in CDOCS.
  • Knowledge of DQMS and QMTS, including deviation investigations and CAPA processes.
  • Strong proficiency with Microsoft Office applications, including:
  • Excel
  • Word
  • Power Point
  • Share Point
  • Experience operating Powered Industrial Vehicles (PIVs), such as forklifts or similar equipment.
  • Familiarity with scales, weighing processes, and material handling operations.
  • Experience gathering metrics, preparing reports, and presenting results to management.
  • Experience supporting operational excellence or continuous improvement projects.

Preferred Qualifications

  • Experience working with ERP systems (SAP, Oracle, or similar).
  • Proficiency with Smartsheet and Microsoft Teams.
  • Strong analytical, organizational, and problem-solving skills.
  • Ability to work effectively in a fast-paced manufacturing or warehouse environment.
  • Excellent communication and collaboration skills.
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Position Requirements
10+ Years work experience
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