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The Accounting Analyst II manages finance support including invoice processing, reconciliations, payroll, compliance with SOX, and reporting using JD Edwards ERP.

Supports project managers in coordinating customer and internal pharmaceutical development and manufacturing projects. Tracks project plans, tasks, risks, timelines, invoicing, forecasts, meetings, action items, communications, technical information, customer visits, status reports, and project logistics throughout the project lifecycle. Coordinates lower-complexity projects and workstreams under project management oversight while maintaining accurate project metrics and escalating issues.

Manages customer development and manufacturing projects across their full lifecycle, coordinating technical teams, timelines, budgets, documentation, issue escalation, incident closure, and customer communications. Tracks project progress, ensures deliverables meet requirements, supports customer relationships, and reports status and risks to management. The role is fully onsite, Monday through Friday, in Chelsea, Massachusetts.

Coordinates site-wide training programs covering onboarding, GMP, safety, quality, compliance, and workforce development. Facilitates orientation and group learning, develops instructional materials with subject matter experts, administers ComplianceWire and training records, monitors completion, produces compliance metrics, and evaluates training effectiveness. Partners with Production, Quality, Engineering, Safety, and HR to address training needs and improve employee capability, quality performance, and operational efficiency in a regulated manufacturing environment.

Supervise regional operations across pre-production, pre-distribution, and master data departments. Lead daily priority discussions, coordinate teams and sites across functions and time zones, manage regional deliverables, and support continuous improvement initiatives. The role requires operational leadership, compliance focus, strong organization, and prior supervisory or team leadership experience in clinical trial materials, supply chain, master data, or related operations.

The Senior Program Manager will lead complex client projects in Process Development and GMP Manufacturing, manage client contracts, and ensure project objectives are met.

The Automation Engineer supports manufacturing systems, troubleshoots automation issues, ensures compliance with regulations, and documents technical operations in a GMP environment.

Manage enterprise-wide sales incentive programs, administer compensation operations (target setting, credit rules, payouts), build reports/dashboards, analyze plan effectiveness and ROI, ensure compliance, partner with Sales and Finance on forecasting, accruals, and territory/headcount updates.

The role focuses on ensuring the compliance and effectiveness of Supplier and Material Quality Assurance programs, conducting audits, managing documentation, and collaborating on quality agreements. Training and oversight of quality systems are also involved.

Lead strategy, design, implementation, and administration of enterprise sales incentive programs and systems. Oversee plan design, target setting, calculations, payouts, reporting, compliance, and ROI analysis. Partner with Sales, Finance, and HR, implement compensation tools, build a team, and provide executive insights to drive sales performance and align pay with corporate goals.