Top Biotech Jobs

The Chief Operating Officer will lead operational execution and manage delivery teams, drive company-wide operating rhythms, and partner closely with the CEO and leadership team to scale the organization and enhance operational effectiveness.

The Data Manager will own data strategy, management, and governance, ensuring data quality and integration across various scientific datasets whilst collaborating with multiple teams.

The Senior Growth Marketer at Manifold will define and execute solutions-led go-to-market strategies, drive demand through multi-channel campaigns, and collaborate cross-functionally to support solution launches and performance analysis.

The Quality Engineering Manager oversees product quality, manages investigations of quality issues, ensures compliance with global standards, and supports sustaining engineering efforts.

As a Senior Data Engineer, you will design and develop AI-powered data solutions, investigate tools, and collaborate with engineering to enhance Sleuth's platform.

The Enterprise Account Executive will manage key accounts, build relationships, and close new MedTech B2B SaaS deals to meet sales targets.

The Electrical Engineer will manage system-level electrical development, focusing on integration, debugging, and stabilization of hardware and programmable systems, collaborating with cross-functional teams.

The VP of Clinical Affairs will lead clinical research strategies, build relationships with key stakeholders, and ensure compliance with clinical regulations while expanding clinical initiatives globally.

The Electrical Engineer will design and develop PCBs, handle schematics, select components, and coordinate with vendors while ensuring quality and supporting debugging efforts.

The Senior Accountant Lead manages finance and accounting operations, ensuring GAAP compliance, financial reporting, and budgeting in a startup environment.

The Clinical Scientist assists with the conduct of clinical studies, may support or lead studies, and interacts with stakeholders for clinical objectives.

The Clinical Study Specialist organizes reports, schedules meetings, manages study documents, tracks trial progress, and communicates with sites for clinical trials.

The Senior Manager will oversee clinical site engagement, develop relationships with investigational sites, conduct site-level activities, and ensure compliance with protocols and regulatory requirements.

Oversee GMP QA operations, ensuring compliance and quality in batch disposition for clinical and commercial stages. Collaborate with stakeholders, manage resources, and drive continuous improvement in quality processes.

The Associate Director oversees technical quality for cell and genetic therapies, ensuring compliance, risk management, and quality standards throughout product lifecycle stages.

The Associate Director of SC Planning leads transformational SCM projects, develops project plans with stakeholders, manages project timelines, and improves planning processes.