Top Biotech Jobs in Denver & Boulder, CO

Manage complaint records for SaMD applications, ensure audit readiness, perform trend analysis, and coordinate quality aspects of software releases while collaborating with cross-functional teams.

Manage a multi-state territory to grow laboratory genetic testing sales by expanding menu utilization, acquiring new customers, negotiating contracts, launching new assays, developing demand, delivering presentations, hosting trade shows, maintaining CRM data, and achieving sales targets while residing in the assigned territory.

The Software Engineer will enhance developer experience at Benchling by building production release tooling, improve workflows, and collaborate with teams to scale processes. Responsibilities include developing efficient development tools and championing engineering patterns.

The GRAIL Galleri Consultant role focuses on driving sales growth for the Galleri cancer detection product by engaging healthcare providers and implementing sales strategies.

Lead post-launch lifecycle, adoption, stabilization and continuous optimization of the CFC CRM platform across global markets. Own BAU roadmap, operational governance, integrations, release readiness, value measurement, and cross-functional orchestration with Data, Digital, Compliance, and Markets to ensure CRM delivers sustained commercial value and scalability.

The Sales Director will lead the sales process to close partnerships with research sites, managing all sales activities including discovery and negotiation, while collaborating with Customer Success for onboarding.

Own end-to-end product launch readiness across ecommerce, logistics, supply chain, customer care, finance, marketing, and retail. Track milestones, surface risks, drive cross-functional decisions, measure launch performance and run post-launch retrospectives. Develop repeatable frameworks, playbooks, and operating cadences to improve GTM execution and alignment.

The Senior Director of Quality leads the quality organization, ensuring compliance with FDA and ISO standards, developing quality management systems, and managing quality issues.

The Director, Strategic Accounts will optimize revenue through strategic contracting, manage relationships with health systems, and track contract performance to ensure profitability. Responsibilities include collaboration with sales teams, price management, and providing strategic planning in U.S. markets.

Manage regulatory project planning and execution for clinical trials, ensuring alignment across teams. Drive submissions and optimize regulatory processes.

The Associate Director, Device Development will provide technical leadership in developing biologic/device combination products, oversee manufacturing and regulatory submissions, and collaborate with cross-functional teams.

Manage the end-to-end clinical supply chain for multiple clinical programs, ensuring timely delivery of products while collaborating with various cross-functional teams and maintaining regulatory compliance.

The Group IP Paralegal provides operational support for patent and trademark activities, manages filings and deadlines, and assists in IP asset integrations related to M&A.