Senior Associate – Supply Chain Transformation
Location: Remote – U.S. (fully remote; collaborate across global time zones)
Employment Type: Full-Time, Contingent Worker (Contract, W2)
Compensation: $35–$40 per hour (based on experience)

Summary of the Role
Join a large biotech pharmaceutical leader as a Senior Associate supporting Supply Chain Transformation with a focus on the Plan to Stock domain. You’ll map current/future-state processes for a new ERP implementation, drive GMP-compliant documentation and technical writing, and partner with cross-functional SMEs to enable smooth adoption across global operations.

Key Responsibilities

• ERP & Process Enablement

  • Develop a deep understanding of current and future supply chain/manufacturing flows tied to ERP changes

  • Create, revise, and organize procedures/work instructions that align with new system processes

  • Contribute to project workshops, testing activities, and readiness assessments

• Documentation Governance (GMP)

  • Manage and maintain GMP-compliant documentation for regulated operations

  • Ensure accuracy, usability, and inspection readiness of all controlled documents

• Cross-Functional Collaboration

  • Partner with business process owners and functional SMEs to align processes and enable knowledge transfer

  • Support study/functional stakeholders to resolve documentation/process issues

Required Experience & Skills

• 3+ years of experience in supply chain, manufacturing, or process improvement in a regulated industry (biotech/pharma preferred)

• Proven GMP documentation and technical writing experience

• Exposure to ERP systems (SAP or Oracle) and large-scale system transitions

• Strong organization, detail orientation, and communication skills in a fully remote, cross-functional setting

Preferred Qualifications

• Prior experience on ERP implementations or major systems transitions

• Familiarity with the Plan to Stock process domain

• Bachelor’s degree in Supply Chain, Life Sciences, Engineering, or related field

• Continuous improvement mindset; adaptable and organized

Key Competencies

• Documentation excellence (clarity, compliance, control)

• Process mapping and change readiness

• Collaboration and stakeholder communication across time zones

• Detail orientation, organization, and follow-through

Top 3 Must Have Skills

1. Supply chain/manufacturing experience (3+ years) in biotech/pharma

2. GMP documentation & technical writing

3. ERP exposure (SAP/Oracle), especially in Plan to Stock
    

"This posting is for Contingent Worker, not an FTE"