Sr Associate Clinical Finish Drug Product Global Study Planner Support at Amgen - ScoutJobs - The AI-curated global job board
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Amgen
Posted 3 days ago

Sr Associate Clinical Finish Drug Product Global Study Planner Support

Amgen

Requirements

Bachelor's Degree and 5+ years experience, Master's Degree and 5+ years experience, SAP or similar ERP knowledge, Strong analytical and problem solving skills, Fluency in English, Experience in regulated environments

Skills

SAPERPSupply ChainGMP

About the role

Responsibilities

  • Support the execution of clinical planning processes to ensure finished drug product availability for global clinical trials.
  • Execute production order conversions, stock transfer orders, and clinical planning cycles within the ERP system.
  • Manage labeling job requests and initiate material destruction processes for study close-out activities.
  • Provide operational oversight across supply planning, order management, and material destruction.
  • Partner with Global Study Planners, internal/external labeling facilities, warehouses, and logistics providers.
  • Drive continuous improvement initiatives and root cause analysis to enhance team outcomes and productivity.
  • Maintain compliance with GMP/GDP and regulatory requirements, ensuring all documentation is inspection-ready.

Requirements

  • Bachelor's Degree and 5+ years of experience in supply chain, logistics, planning, or operations.
  • Master's Degree and 5+ years of relevant experience.
  • Hands-on knowledge of SAP or a similar ERP system for material planning and management.
  • Strong analytical and problem-solving skills to drive robust decision-making.
  • Excellent organizational and communication skills with fluency in English (written and oral).
  • Proven ability to work effectively within cross-functional teams in a regulated or structured environment.
  • Experience working with stakeholders across different time zones.

Preferred Qualifications

  • Experience with document workflows in Veeva Vault.
  • Experience in the regulated manufacturing or life sciences industry.
  • Exposure to change initiatives, system implementations, or continuous improvement efforts.
  • APICS or Lean/Six Sigma certification.

About the Company

Amgen is a leading biotechnology company dedicated to unlocking the potential of biology for patients suffering from serious illnesses. By discovering, developing, and manufacturing innovative human therapeutics, Amgen leverages advanced human genetics and biologics expertise to improve health outcomes and dramatically improve people's lives worldwide.

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Sr Associate Clinical Finish Drug Product Global Study Planner Support

Amgen · Hyderabad

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