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The Manager of Quality Control oversees QC activities, ensures compliance with regulations, leads quality control teams, and manages client interactions regarding testing and quality standards.

Lead all accounting functions (AP, AR, billing, GL, fixed assets, audits), manage and develop the accounting team, deliver month-end close and reconciliations, ensure GAAP compliance, drive ERP (JDE) improvements, collaborate with auditors, and support tax and internal controls in a manufacturing/pharma environment.

Lead QA Associates in providing quality assurance support for cGMP manufacturing operations, ensuring compliance and engaging with cross-functional teams to resolve quality issues.

The Human Resources Manager collaborates with leadership to manage HR strategies, enhance employee engagement, and drive HR excellence in areas like talent management and performance.

The Automation Engineer will maintain and enhance production data collection systems, design electrical schematics, program PLC and HMI platforms, and ensure integration of packaging line systems to improve efficiency.

As a QC Specialist II, you will lead investigations, manage analytical testing, draft technical documents, and ensure compliance in a GMP environment.

Provide high-impact administrative and operational support to the CFO and LIFT leadership (Legal, Finance, IT). Manage complex calendars across time zones, coordinate domestic and international travel using Concur, prepare executive presentations and materials with master-level PowerPoint skills, handle expense reports, schedule meetings and logistics, support special projects, ensure adherence to PCI/cGMP/GCP guidelines, and maintain discretion with confidential information. Travel approximately 20% and work flexible hours as needed.

Lead global sustainable procurement and Scope 3 emissions management. Influence sourcing, run sustainability evaluations, engage suppliers on ESG, implement procurement policies and process excellence, and support reporting, audits, and decarbonization initiatives across the organization.

The Automation Engineer III designs and maintains control systems for biopharmaceutical manufacturing, manages projects, and ensures compliance with GMP standards.

The QA Specialist I - Compliance provides administrative support to the Compliance team, coordinates audits, manages documentation, and ensures compliance during regulatory inspections.