Top Senior Level Biotech Jobs

The Quality Assurance Manager oversees quality assurance activities, provides support to associates, and advises management on improvement efforts to comply with regulatory and quality standards.

As a Backend Software Engineer, you'll design and maintain backend applications, develop APIs, and optimize database systems for a medical device platform, participating in code reviews and mentoring junior team members.

The Director of Commercial FP&A will develop revenue models, lead financial planning for commercial operations, and establish GTN frameworks for a biotech launch.

Lead the configuration and optimization of Workday Advanced Compensation at Revolution Medicines, ensuring effective compensation processes and data integrity while partnering cross-functionally to meet business needs.

The Territory Sales Manager drives agricultural sales, builds client relationships, manages teams, analyzes market trends, and travels extensively for fieldwork.

Lead strategic new business for a SaaS data and analytics platform in the life sciences market, focusing on high-value partnerships with pharma and biotech companies, while shaping the market approach and influencing internal strategies.

The Market Access Director will lead access strategies for Lantheus' products, build relationships with key accounts, and drive brand growth through education and collaboration with health systems and payers.

The Associate Director PSS manages Patient Safety Solutions operations, ensuring project allocation, training, quality service, and regulatory compliance. Responsibilities include staff development, project management, and client interaction, while ensuring timely reporting of adverse events.

The Senior Mobile App UI/UX Designer will create intuitive designs for mobile apps, collaborate with teams, improve user experiences, and maintain design systems.

The role involves overseeing outsourced microbiology testing, ensuring GMP compliance, supporting contamination control strategies, and authoring relevant regulatory documents.