Planet Pharma
Clinical Supply Chain Manager - PST Hours
Planet Pharma, California, Missouri, United States, 65018
Clinical Supply Chain Manager - PST Hours
Direct message the job poster from Planet Pharma
CANDIDATES MUST BE COMFORTABLE WORKING PST HOURS
CANDIDATES MAY OCCASIONALLY HAVE EARLY EU MEETINGS (~7:30 AM PST)
Remote
12 Month Contract (May extend or convert to permanent)
$40/hour - $45/hour W2
Top Required Skills/Experience
Completed bachelor's degree, master's degree, or PhD
5+ years of progressive experience in clinical supply chain management, planning, or manufacturing, within a regulated biopharmaceutical environment (experience with GXP guidelines)
Strong working knowledge of SAP (order release, material master data, process work order (PWO) conversions, and SKU management)
Proficiency with Smartsheet, Veeva Vault, and enterprise resource planning tools
Demonstrated ability to manage multiple priorities, triage operational requests, and drive process efficiency
Strong analytical, problem-solving, and data management skills with keen attention to detail
Excellent communication and interpersonal skills to interface effectively across multiple functions
APICS, ISM, or Lean/Six Sigma certification PREFERRED
Operational and Technical Support
Serve as the primary operational support for DSCLs in executing clinical supply chain activities across programs.
Establish and maintain processes for receiving, triaging, and tracking DSCL requests, including:
NPI management for Not for Human Use (NHU) device, packaging activities, and GMP bulk pack Drug Product (DP) workflows.
PWO conversions for bulk clinical DP and NHU device/packaging orders in SAP.
SAP material creation and obsoletion workflows for DSCL-owned SKUs (NHU device, NHU packaging, GMP DP bulk pack).
Coordinate SAP SKU creation and lifecycle management, ensuring data accuracy and compliance with established procedures.
Documentation and Process Control
Manage Clinical product temperature excursion support forms (TE forms) — oversee authorship, routing, and documentation workflows in Veeva Vault.
Centralize and manage shipment requirements updates and transportation lane requests in partnership with Global Distribution.
Support deviation, change control, and CAPA access within site framework, as capacity allows.
Cross-functional Collaboration
Partner with Product Delivery Teams (PDTs), Manufacturing, and Global Supply Chain to ensure end-to-end supply readiness and risk mitigation.
Participate in NPI and cross-functional planning meetings to represent DSCL operational needs.
Contribute to continuous improvement projects, dashboards, and metric tracking to enhance visibility and process efficiency.
Seniority Level
Mid-Senior level
Employment Type
Full-time
Job Function
Science and Supply Chain
Industries
Pharmaceutical Manufacturing
Medical Equipment Manufacturing
Biotechnology Research
#J-18808-Ljbffr
CANDIDATES MUST BE COMFORTABLE WORKING PST HOURS
CANDIDATES MAY OCCASIONALLY HAVE EARLY EU MEETINGS (~7:30 AM PST)
Remote
12 Month Contract (May extend or convert to permanent)
$40/hour - $45/hour W2
Top Required Skills/Experience
Completed bachelor's degree, master's degree, or PhD
5+ years of progressive experience in clinical supply chain management, planning, or manufacturing, within a regulated biopharmaceutical environment (experience with GXP guidelines)
Strong working knowledge of SAP (order release, material master data, process work order (PWO) conversions, and SKU management)
Proficiency with Smartsheet, Veeva Vault, and enterprise resource planning tools
Demonstrated ability to manage multiple priorities, triage operational requests, and drive process efficiency
Strong analytical, problem-solving, and data management skills with keen attention to detail
Excellent communication and interpersonal skills to interface effectively across multiple functions
APICS, ISM, or Lean/Six Sigma certification PREFERRED
Operational and Technical Support
Serve as the primary operational support for DSCLs in executing clinical supply chain activities across programs.
Establish and maintain processes for receiving, triaging, and tracking DSCL requests, including:
NPI management for Not for Human Use (NHU) device, packaging activities, and GMP bulk pack Drug Product (DP) workflows.
PWO conversions for bulk clinical DP and NHU device/packaging orders in SAP.
SAP material creation and obsoletion workflows for DSCL-owned SKUs (NHU device, NHU packaging, GMP DP bulk pack).
Coordinate SAP SKU creation and lifecycle management, ensuring data accuracy and compliance with established procedures.
Documentation and Process Control
Manage Clinical product temperature excursion support forms (TE forms) — oversee authorship, routing, and documentation workflows in Veeva Vault.
Centralize and manage shipment requirements updates and transportation lane requests in partnership with Global Distribution.
Support deviation, change control, and CAPA access within site framework, as capacity allows.
Cross-functional Collaboration
Partner with Product Delivery Teams (PDTs), Manufacturing, and Global Supply Chain to ensure end-to-end supply readiness and risk mitigation.
Participate in NPI and cross-functional planning meetings to represent DSCL operational needs.
Contribute to continuous improvement projects, dashboards, and metric tracking to enhance visibility and process efficiency.
Seniority Level
Mid-Senior level
Employment Type
Full-time
Job Function
Science and Supply Chain
Industries
Pharmaceutical Manufacturing
Medical Equipment Manufacturing
Biotechnology Research
#J-18808-Ljbffr