Supply Chain Manager

Advanced Bio-Logic Solutions CorpThousand Oaks, CA
16dRemote

About The Position

Join a big biopharma leader as a Supply Chain Serialization Manager, responsible for ensuring robust performance and compliance of serialization systems and processes. This role supports cross-functional traceability projects and continuous improvement initiatives leveraging innovative SAP technologies. You'll be instrumental in the deployment and evolution of serialization and Track & Trace programs in a regulated environment.

Requirements

  • Proven experience with SAP ATTP, SAP ICH, and S/4 Hana or similar supply chain/traceability systems
  • Demonstrated success in GMP-regulated environments
  • Strong background supporting cross-functional teams in technical projects

Nice To Haves

  • Relevant experience in biopharmaceutical operations or supply chain
  • Experience in manufacturing, engineering, or operations roles
  • Hands-on S/4HANA and SAP ICH use in a regulated environment
  • Familiarity with Serialization and Global Track & Trace regulations (such as US DSCSA, EU FMD)
  • Knowledge of GS1 standards and guidelines (e.g., EPCIS)
  • Ability to manage multiple projects concurrently
  • Strong communication and cross-functional collaboration skills

Responsibilities

  • Support cross-functional Track & Trace projects from initiation through completion
  • Contribute to implementation of S/4 Hana and SAP Information Collaboration Hub (ICH)
  • Leverage innovative technologies to enhance organizational value, decision-making, and patient experience
  • Transform existing business models to improve performance and operations
  • Ensure compliance with regulatory requirements related to serialization and traceability
  • Maintain procedures and support ongoing compliance with serialization regulations
  • Provide expertise in GMP documentation and process adherence
  • Collaborate across teams to resolve project challenges and ensure timely execution
  • Support key serialization and traceability projects
  • Assist in GMP document creation and project management
  • Provide reporting
  • Resolve issues
  • Ensure compliance with relevant guidelines and regulations
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