Top Senior Level Biotech Operations Manager Jobs in Boston, MA

The Associate Director of Global Regulatory Affairs leads global regulatory strategies for neuroscience products, ensuring compliance and guiding teams on complex submissions while managing FDA interactions and project timelines.

The Director of Procurement will develop and execute procurement strategies, manage vendor negotiations, and ensure compliance with industry standards.

The Director of Quality Assurance manages the QA program for Tempus Compass, ensures compliance with GCP and regulatory standards, oversees audits, and collaborates with executive management on quality initiatives.

The Director acts as a strategic digital partner for biotech companies, aligning digital strategies with business needs, overseeing project execution, and facilitating IT governance.

Lead the global quality compliance strategy for radioligand therapies, ensuring GxP adherence and overseeing quality management systems and regulatory inspections.

The Senior Director, CMC Program Lead will oversee CMC development and manufacturing, coordinating across multiple functions to meet program milestones.

The Associate Director leads the US Market Access Field reimbursement team, coordinates internal operations, manages projects, and develops strategies to support market access and reimbursement activities for gene therapy products.

The Senior Associate I, EHS is responsible for environmental compliance, safety programs, and mentoring safety teams at Biogen.

The Associate Director, R&D Quality oversees vendor quality through managing Quality Agreements, vendor metrics, risk audits, and collaboration with stakeholders to ensure compliance and continuous improvement of vendor oversight processes.

Lead GxP quality strategy and operations for development-stage programs, ensuring regulatory compliance and effective quality systems across GCP, GLP, and GMP activities.