Jobs at Danaher Corporation

Leads U.S., Canadian, European, and global trade compliance operations, including import/export regulatory compliance, customs classification, export controls, restricted-party screening, tariff mitigation, duty savings, and country-of-origin determinations. The role develops policies, SOPs, internal controls, and process improvements while partnering with Supply Chain, Logistics, R&D, Quality, and other stakeholders. Travel of approximately 20–30% is required, including visits to San Jose and other locations.

Lead biopharma market development by translating complex scientific workflows into scalable commercial use cases. Engage senior scientific stakeholders, define demand-generation strategy, shape early-stage opportunities, build repeatable workflows, and influence cross-functional commercial priorities to drive adoption and growth.

The Equipment Engineer leads installation, qualification, validation, maintenance, troubleshooting, and optimization of manufacturing and laboratory equipment used for oligonucleotide production. Responsibilities include developing SOPs and maintenance programs, managing calibration and asset systems, coordinating field service activities, resolving equipment issues, and driving continuous improvement to enhance uptime, reliability, throughput, and compliance. The role is on-site in a laboratory and manufacturing environment and supports technology transfer and production scale-up.

Serves as the primary on-site Quality representative for Sunnyvale, supporting San Diego as needed. Oversees Quality Management System compliance, ISO 13485 requirements, audits, inspections, quality metrics, and continuous improvement. Partners with Operations, Supply Chain, Engineering, Facilities, and R&D to implement quality requirements and manages processes including CAPA, nonconformance, change control, and risk management.

Leads product innovation for new molecular diagnostic products by translating customer and business needs into prioritized roadmaps, business cases, market requirements, and product definitions. Leads cross-functional product development teams, manages market and product requirements, assesses risks and tradeoffs, and collaborates with project management, portfolio management, R&D, quality, regulatory, and clinical affairs. The role requires extensive medical or diagnostic industry experience and up to 25% travel.

Leads enterprise Total Rewards transformation, operating model improvements, governance frameworks, and cross-functional initiatives spanning compensation, benefits, executive compensation, mobility, recognition, wellness, and HR M&A. Partners with HR, Finance, Legal, HR Technology, and service delivery stakeholders to execute scalable solutions. Provides strategic compensation consulting, analytics, planning support, and program administration for corporate functions.

Lead product strategy, roadmap, and P&L for BioMek and Echo automation platforms and enterprise automation solutions. Drive customer and market insights, define modular architecture and integration standards (APIs, data models, telemetry), manage commercial outcomes, and oversee the Access Solutions Group delivering large-scale integrated automation deployments. Build and lead product management and solutions teams to enable AI-ready, connected laboratory workflows while ensuring regulatory compliance and scalable execution.

Designs, programs, tests, troubleshoots, and supports PLC-based automation, HMI, and machine vision systems for high-volume manufacturing. Responsibilities include system integration, commissioning, equipment upgrades, validation, production troubleshooting, controls standards, electrical and code reviews, control panel integration, and technical documentation. The role collaborates cross-functionally to ensure reliable and compliant equipment performance.

Leads global operational and manufacturing technology programs across Cepheid sites, improving reliability, cybersecurity, compliance, scalability, and operational effectiveness. Manages cross-functional initiatives involving OT infrastructure, industrial networks, computerized systems, modernization, and continuous improvement. Establishes governance, plans, metrics, risk strategies, and executive communications while translating manufacturing needs into technical solutions and coordinating with Operations, Engineering, Quality, IT, and Cybersecurity.

The Sr. Technical Product Manager will lead multi-team efforts in delivering software capabilities, manage product scope, and enhance requirements processes using AI while ensuring compliance in regulated medical environments.

Conduct bench experiments advancing nucleic acid biochemistry and develop and characterize genomics products. Design experiments, analyze results, support NGS products, present findings, collaborate cross-functionally, lead complex projects, provide scientific and customer support, and manage external research collaborations.

Provides confidential, autonomous support to the VP of Human Resources and leadership team. Responsibilities include managing complex calendars, travel, expenses, budgets, purchase orders, meetings, events, communications, and administrative processes. Coordinates HR initiatives and executive-sponsored programs by managing project plans, tracking milestones, documenting actions, escalating risks, and ensuring timely delivery. The role is onsite in Sunnyvale, California, with domestic and international travel as needed.

Leads Western US key account management and sales teams to achieve revenue, market share, and profitability goals. Responsibilities include sales planning, forecasting, performance management, customer relationship development, industry event representation, coaching, onboarding, leadership development, quote approvals, cross-functional collaboration, and participation in product development and continuous improvement initiatives. The role requires extensive travel throughout the territory and focuses on life sciences, biotechnology, pharmaceutical, academic, government, and contract laboratory customers.

Develop and maintain embedded firmware for STM32 and Cortex-A53 boards used in molecular diagnostic systems. Lead real-time, bare-metal, RTOS, and interrupt-driven programming; control assay temperature precisely; develop new hardware capabilities; and serve as a subject matter expert diagnosing complex edge-case accuracy issues across cross-functional teams. The role is primarily on-site, with occasional local travel to manufacturing sites.

Leads mechanical design and development for advanced imaging and optomechanical systems. Responsibilities include designing precision mounts, flexures, autofocus modules, motion-control systems, and stable structures; integrating and testing systems; applying GD&T, simulation, FMEA, DoE, and manufacturability principles; and guiding products from concept through prototype, verification, commercialization, and production support.

Architect and develop scalable, event-driven backend services, APIs, orchestration systems, and data-context management solutions for AI agents supporting laboratory workflows. Integrate cloud infrastructure, scientific instruments, and software systems while establishing data contracts, integration standards, observability, security, and resilience. Prototype emerging AI technologies and mature successful solutions for regulated production environments. The role requires extensive distributed systems experience and supports R&D software teams in San Jose or Indianapolis.

Provide strategic legal support for global commercial operations in life sciences. Draft, review, and negotiate complex commercial agreements; advise on compliance, data privacy, and commercial initiatives; support M&A, cross-functional projects, and litigation as needed; improve legal operations and templates while partnering with business and legal teams.

Provide global legal and compliance support for life‑sciences diagnostics: draft, negotiate, and advise on complex commercial agreements; manage litigation, investigations, and regulatory matters; support IP and corporate governance; develop training, playbooks, and AI-enabled legal process improvements; partner with business leaders and external counsel.

Lead cross-functional innovation projects for next-generation oligonucleotide synthesis platforms. Drive project delivery, portfolio visibility, KPIs, and DBS adoption. Remove barriers, manage risk, and coordinate scientific, engineering, and operations partners. On-site in Sunnyvale with up to 20% travel. Mandarin and English bilingual communication required.

Manage and grow assigned global semiconductor customer accounts by implementing account strategies, driving orders and shipments, coordinating cross-functional resources, maintaining customer profiles/SWOTs, monitoring competitors, and identifying unmet needs and new product opportunities. Achieve growth targets within allocated SG&A and support commercial negotiations.