Supply Chain Sr. Associate

Advanced Bio-Logic Solutions CorpThousand Oaks, CA
Remote

About The Position

Join a large biotech pharmaceutical leader’s supply chain team as a Sr Associate focused on transportation qualification and cold chain activities for temperature-sensitive materials. Work cross-functionally to execute, document, and ensure compliance in distribution processes, supporting both study activities and regulatory documentation. This role offers a dynamic environment with opportunities to drive process improvements and ensure product quality.

Requirements

  • 0–3 years’ experience in pharmaceutical, biotech, manufacturing, or regulated industry
  • Understanding of GMP principles (academic or professional exposure)
  • Strong documentation and organizational skills
  • Strong analytical skills with the ability to turn complex information into clear, practical insights
  • Proficiency in Microsoft Excel, Word, and PowerPoint
  • High school/GED + 2 years work experience
  • Associates degree and 6 months work experience
  • Bachelors degree

Nice To Haves

  • Exposure to cold chain, validation, or quality systems
  • Familiarity with deviation, CAPA, and change control processes
  • Experience working in cross-functional teams
  • Familiarity with parcel, transport, and warehousing provider operations
  • Ability to independently interact with various levels and drive tasks to completion
  • Strong negotiation and problem-solving skills

Responsibilities

  • Support execution of transportation qualification studies, including coordination with Thermal Engineering Labs and Sample Management
  • Collect, organize, and analyze temperature monitoring and shipment data
  • Draft qualification protocols and reports; gather, analyze, and interpret data
  • Support deviation investigations, change controls, and CAPA documentation related to transport activities
  • Draft documentation to support Marketing Authorization Applications (MAA) and respond to regulatory inquiries
  • Maintain transportation SOPs and controlled documents in compliance with GMP/GDP requirements
  • Collaborate with Quality and Thermal Engineering teams to interpret data and ensure inspection-ready documentation
  • Track qualification timelines and support cross-functional project coordination
  • Perform shipment performance trending and support risk assessments
  • Manage and support multiple transportation studies at different lifecycle phases
  • Contribute to and drive continuous improvement projects in cross-functional collaboration
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