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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 the facility finance function including monthly financial reporting, forecasting, budgeting, internal controls, talent development, pricing guidance, and support for a 5-year strategic plan for a pharmaceutical manufacturing site.

The Senior Financial Analyst will manage budgets, forecasts, and provide financial insights, working closely with leadership and cross-functional teams.

The Senior Manager of Global Reliability Engineering will enhance global standards, manage reliability projects, and support maintenance practices in pharmaceutical manufacturing.

The Production Supervisor oversees daily production tasks, ensures safety and quality metrics are met, and collaborates with various departments to improve workflow and productivity.

Lead development, validation, and execution of analytical methods (HPLC/UPLC/GC/MS/NMR) for drug substances/products under cGMP; perform testing, documentation, client communication, method transfers, data integrity checks, and safety handling of potent compounds while supporting continuous improvement and training.

Lead HR strategy for the site, develop talent pipelines, support leadership in performance management and employee relations, ensuring compliance and engagement.

The Operations Supervisor ensures compliance with GMP and internal quality standards while leading a manufacturing team to achieve production goals.

The QA Specialist ensures compliance with quality standards in manufacturing, investigates discrepancies, tracks complaints, and supports the CAPA program while collaborating with other departments.

Operate and maintain precision machining equipment to fabricate and service softgel encapsulation tooling (dies, wedges, pumps, valves). Review blueprints, perform precision grinding/lapping/coating, assemble components, complete preventative maintenance, and maintain cGMP documentation to ensure production readiness and quality.