Top Biotech Strategic Operations Jobs

Support Quality Systems by executing corrective actions, conducting audits, maintaining documentation, and providing training to ensure compliance with standards.

The US REFS Cluster/Site Head oversees campus operations, ensuring strategic planning, financial management, and facility services meet Novartis standards. Responsibilities include stakeholder management, compliance, and leading a large team for optimal performance.

The Planning Analyst ensures material availability, supports production, optimizes inventory, develops KPIs, and enhances operational efficiency through improved planning processes.

The Manager Site Contracts oversees grant estimates, budget reviews, quality deliverables, internal relationships, process improvements, and mentoring within clinical site contracting at a biopharmaceutical firm.

Oversee GxP computerized systems implementation, compliance, and support for clinical and commercial operations, ensuring adherence to regulatory standards.

The Associate QMS Specialist ensures compliance with cGMP regulations by managing document control, CAPA, audit preparations, and QMS performance metrics.

The Director of Sourcing leads strategic sourcing efforts, manages supplier relationships, negotiates contracts, and promotes cost optimization and sustainability while developing a high-performing team.

The Study Support Specialist assists in designing study events, maintaining communication with clinical teams, and ensuring compliance with protocols in clinical trials.

The Production Control Manager oversees production readiness by managing work orders in ETO/MTO environments, coordinating between departments for material and process flow, and leading a team to drive continuous improvement in manufacturing operations.

The Compliance - Devices Manager oversees device functions for clients, including deployment, inventory management, troubleshooting, and vendor management, ensuring quality and operational efficiency.