Supply Chain Senior Specialist, Site Scheduling

Scorpion Therapeutics; Boston (MA); Hybrid; USD 120,000 - 170,000; Full time

Job summary

Scorpion Therapeutics in Boston is seeking a Senior Scheduler / Site Planning role to manage site scheduling processes and align manufacturing schedules across teams.

You will coordinate across schedulers and stakeholders, resolve conflicts, and provide visibility into milestones, assumptions, and changes. The role requires 6+ years in cGMP biotech/pharma planning and strong ERP, data management, and MS Office/Teams proficiency. Hybrid or on-site work; no travel.

Qualifications

• Bachelor's degree in Supply Chain, Manufacturing Operations, or related field.
• 6+ years in site planning, production scheduling, or supply chain in cGMP biotech/pharma.
• Strong understanding of cross-functional planning, manufacturing execution, ERP systems, and master data management.

Responsibilities

• Coordinate across schedulers and stakeholders to ensure a single, accurate plan.
• Identify and resolve schedule conflicts and dependencies.
• Provide visibility into key milestones, assumptions, and changes.
• Oversee RTMS support, system updates, data quality, and issue escalation.
• Manage scheduling communications and daily operations.

Skills

Cross-functional planning

Manufacturing execution

ERP systems

Master data management

MS Office & Teams

Education

Bachelor's Degree in Supply Chain or related field

Tools

MS Office

Teams

Job description

Role

Support Vertex Cell and Genetic Therapies by managing site scheduling processes and maintaining manufacturing schedule alignment.

Responsibilities

• coordinate across schedulers and stakeholders to ensure a single, accurate plan;
• identify and resolve schedule conflicts and dependencies;
• provide visibility into key milestones, assumptions, and changes;
• oversee RTMS support, system updates, data quality, and issue escalation;
• manage scheduling communications and daily operations.

Requirements

• Bachelor's Degree in Supply Chain, Manufacturing Operations, or related field;
• 6+ years of experience in site planning, production scheduling, or supply chain within cGMP biotech/pharma environments;
• strong understanding of cross-functional planning, manufacturing execution, ERP systems, and master data management;
• proficiency with MS Office and Teams.

Preferred

• experience managing contractor support and workflow coordination.

High-Value

• cGMP regulated biotech/pharma manufacturing, cell and gene therapy context, supply chain and scheduling focus, hybrid or onsite work setup, no travel specified.