Top Biotech Jobs

Develop numerical kernels, libraries, and applications for a new Scientific Processing Unit, collaborating with hardware architects, and optimizing scientific workloads.

Lead and execute research operations at testing locations, manage field experiments, supervise teams, and ensure data quality and safety compliance.

The Quality Operations Manager oversees quality assurance activities, manages regulatory compliance, coordinates with contract service providers, and leads product quality and operational initiatives throughout the product lifecycle.

Senior C++ Engineer responsible for developing high-performance image processing solutions, leading architecture discussions, and mentoring junior engineers in an Agile environment.

The Senior DevOps Engineer will design and maintain Kubernetes infrastructure, optimize CI/CD pipelines, and improve observability for AI-assisted workflows in healthcare.

Lead QC laboratory automation initiatives, translating business needs into automation strategies and ensuring compliance with GMP regulations. Manage cross-functional projects and collaborate with system owners to integrate automation solutions into QC workflows.

The Cost Accountant at CVRx will manage all cost accounting activities, including monitoring inventory, analyzing variances, supporting month-end processes, and collaborating cross-functionally to improve profitability.

The Director of Compliance will lead compliance initiatives, develop policies, and provide training, ensuring adherence to healthcare regulations within a biotechnology company.

The Manager of Quality Assurance ensures compliance with GMP regulations for CMC development programs, leads QA activities, reviews documentation, and mentors teams.

The Senior Director, Global Privacy leads the privacy governance strategy, ensuring compliance with global privacy laws, overseeing privacy risk management, and guiding senior executives in data use governance.

The Associate Manager oversees centralized monitoring for clinical trials, focusing on risk management, data surveillance, and regulatory compliance while ensuring quality and participant safety.

The Associate Director, Quality Assurance oversees GCP QA operations, conducts audits, supports clinical study activities, and ensures compliance with GCP regulations.

The External Quality Assurance Associate II ensures compliance with regulatory standards in biopharmaceutical production, reviews supporting documentation, and assists in quality improvement initiatives.

Oversees the Client Site Liaison team, ensuring client satisfaction, managing training, resolving issues, and conducting evaluations. Responsible for departmental policies and budget oversight.

The IT Change Manager oversees IT changes ensuring controlled and secure implementation, leads change processes, and collaborates with various teams to improve service stability and quality.

The Associate Project Manager I assists with project planning, implementation, and coordination while learning compliance and good practice standards.