Jobs at Danaher Corporation

The Principal Regulatory Affairs Specialist develops global market strategies for IVD medical devices, leads regulatory document creation, and ensures compliance with regulatory requirements while mentoring junior associates.

Lead deployment and governance of Danaher Business System (DBS) across North American commercial teams. Coach and certify sales personnel in DBS tools, drive Kaizen/problem-solving funnels, deploy DBS fundamentals and tools, support regional sales leadership with data-driven insights, and manage sustainment and continuous improvement initiatives.

Lead end-to-end third-party risk management across vendor lifecycle, review vendor security evidence and contracts, assess supply-chain and AI vendor risks, ensure consistent scoring and escalation, and support enterprise risk register operations and executive reporting.

The Sr. National Manager, Specialty Markets will create and execute national plans for growth in various medical markets, manage a sales team, and drive strategic initiatives.

The Global EHS Manager leads adherence to EHS programs across global operations, enhances safety practices, and implements compliance policies and procedures.

Drive revenue growth in the San Diego/Southwest territory by building client relationships, prospecting and closing new biotech/pharma/academic/government accounts, supporting cell and gene therapy programs, coordinating with inside sales and technical teams, and maintaining accurate forecasts and CRM pipeline data.

Quota-carrying inside sales role selling research-grade and manufacturing solutions to life sciences customers. Own full sales cycle, generate and qualify leads (including GMP clinical leads), support technical qualification with sales engineering, and drive value-based growth for cell and gene therapy developers.

Lead the global software engineering team at Beckman Coulter Life Sciences, focusing on innovative solutions and compliance in biopharma. Oversee software development lifecycle, aligning technology with business goals, and drive innovation in a regulated environment.

Design, develop, and deploy AI-powered documentation and content management solutions (CCMS) in a regulated life-sciences environment. Improve documentation workflows with NLP, generative AI, translation tools, and automation; lead project planning, execution, and cross-functional coordination.

Support Sales by structuring, analyzing, and executing commercial agreements and quotes across North America. Own end-to-end quote creation and configuration in Salesforce, ensure pricing and financial alignment, validate deal assumptions with cross-functional partners, maintain data quality and governance, and support complex multi-site deals and RFPs while driving process improvements and standardized quoting practices.

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.

The Sr. Product Manager is responsible for driving revenue growth and reducing time to market for new products, collaborating with various teams and analyzing market trends in the genomics sector.

The Principal will lead strategies to win new business, focusing on partnerships with senior hospital executives and the C-suite, while managing high-value client relationships and creating solutions to meet client needs.

Lead global IT business enablement for Manufacturing and Quality, forging partnerships, driving innovation, and ensuring operational excellence through technology.

The Senior Clinical Study Manager oversees clinical trial execution, ensuring compliance with regulations and quality standards while leading study planning and cross-functional collaboration.

The Sr. Clinical Research Associate manages clinical trials, ensuring compliance with FDA standards, develops relationships with stakeholders, and oversees protocol execution and documentation.

The Senior ERP SCM Systems Analyst acts as a bridge between business and IT, leading system improvements and ensuring user needs are met while managing Oracle SCM applications.

The Group IP Paralegal provides operational support including patent and trademark filings, docketing management, and M&A-related IP asset integration.

Lead set-up, initiation, monitoring, and close-out of IVD and medical device clinical trials at external sites. Ensure GCP/FDA compliance, manage site relationships, IRB submissions, TMF maintenance, data quality, investigational product accountability, and contribute to study planning, budgeting, and process improvements. Travel and multi-study management required.