Jobs at Danaher Corporation

Designs, develops, implements, maintains, and supports Manufacturing Execution System solutions in a regulated manufacturing environment. The role configures MES, supports ERP and SAP integrations, manages controlled system changes, troubleshoots production-impacting incidents, performs root cause analysis, and drives corrective actions. The engineer collaborates with Manufacturing, Quality, Validation, Engineering, and IT teams to improve production continuity, system reliability, compliance, efficiency, and data integrity.

Designs, develops, configures, implements, maintains, and supports Manufacturing Execution System solutions in a regulated manufacturing environment. The role integrates MES with ERP and SAP platforms, manages controlled system changes, troubleshoots production-impacting incidents, performs root cause analysis, maintains system reliability and compliance, and identifies opportunities to improve manufacturing efficiency, productivity, data integrity, and operational continuity.

The Director of Corporate Communications leads proactive and reactive media relations, develops executive thought leadership platforms, creates press and narrative content, manages reporter relationships, and partners with communications, investor relations, and operating-company leaders. The role strengthens Danaher’s visibility and credibility across business, trade, and national media while translating complex scientific and business topics into compelling external communications.

Executes reagent and buffer manufacturing processes according to production plans, SOPs, quality standards, FDA QSR, GMP, and ISO requirements. Maintains training records, performs laboratory work using GLP, completes work orders on schedule, applies scientific methods, and collaborates cross-functionally to troubleshoot production issues. The role also supports continuous improvement of SOPs and testing using Beckman Coulter diagnostic instruments.

Supports sales and market expansion for immunohistochemistry and pathology imaging products across Southern and Eastern Ontario. Provides pre- and post-sales technical support, equipment installation coordination, demonstrations, customer training, troubleshooting, product evaluations, and instrument optimization. Manages CRM records, forecasting, market analysis, consumables attachment, technical investigations, and customer relationships with pathologists, laboratory managers, technologists, and researchers. The role requires up to 75% travel and a valid driver’s license.

Leads Cepheid’s global trade compliance program across import, export, customs, sanctions, valuation, tariff classification, country of origin, free trade agreements, and export controls. Oversees compliance governance, audits, internal controls, customs broker management, tariff mitigation, and trade planning. Partners with Tax, Finance, Legal, Supply Chain, Procurement, R&D, and Operations. Drives technology, automation, analytics, and data governance initiatives to improve compliance and operational efficiency. This fully remote role supports global operations and requires up to 20% domestic and international travel.

Conduct and document clinical studies for medical devices, including patient screening, venous and arterial procedures, IV placement, vital-sign monitoring, data collection, protocol execution, and adverse-event reporting. Prepare or review study plans, informed consents, IRB submissions, case report forms, and related documentation. Ensure compliance with clinical protocols, Good Clinical Practice, FDA regulations, and medical device research requirements.

Supports software quality, risk management, cybersecurity, verification, validation, and regulatory compliance for medical device software. Reviews requirements, architecture, testing, traceability, risk documentation, and validation records; evaluates software changes and assists with vulnerability assessment and remediation tracking. The role also supports hazard analysis, failure mode assessments, risk control verification, and software development lifecycle deliverables within a regulated medical technology environment.

Lead new product introduction manufacturing activities across multiple locations, including supplier selection, part qualification, process development, process qualification, work instruction creation, bill of materials and print releases, and production readiness. Represent Operations on NPI core teams, mentor team members, lead design changes in regulated environments, and deliver complex projects on schedule and within target costs.

Leads strategic planning and execution for Cytiva’s Filtration business. Responsibilities include defining long-term vision and financial ambition, guiding major strategic decisions, overseeing market intelligence and growth analysis, identifying organic and inorganic opportunities, supporting due diligence, and establishing performance systems for execution. The role partners with senior leaders across Product Management, R&D, Commercial, and Insights, facilitates strategic workshops, and drives cross-functional alignment and market share, profitability, and shareholder value growth.

Leads finance operations for IDT and Aldevron manufacturing, connecting operational performance to financial outcomes. Responsibilities include product and standard costing, cost accounting, COGS, variance analysis, inventory valuation, profitability, forecasting, capital deployment, capacity planning, ERP implementation, KPI reporting, and transformation. Partners with Operations, Supply Chain, Quality, Engineering, Commercial, and executive leadership while building and developing a high-performing Operations Finance team.

Drives territory revenue, market share, and histology instrument placements through strategic account planning, pipeline management, forecasting, customer relationship development, and competitive selling. Partners with Applications, Service, and Commercial teams on demonstrations, evaluations, installations, and onboarding. Requires frequent overnight travel, territory management, capital equipment or complex sales experience, CRM proficiency, and strong organizational skills.

Drives complex, multi-departmental sales of molecular diagnostic tests and instruments to hospitals across Quebec. Builds relationships with laboratory, pharmacy, infection control, nursing, emergency, risk management, and physician stakeholders; generates demand, increases market share and revenue, improves margins, and reduces customer attrition. Uses Salesforce CRM to manage accounts and sales opportunities. Requires bilingual French and English communication, healthcare sales experience, vendor credentialing eligibility, a valid driver’s license, and travel up to 75%.

Manage customer accounts and drive revenue growth for Leica Biosystems products across an assigned Polish territory. Develop account plans, identify opportunities, conduct consultative sales activities, manage tenders and negotiations, close deals, maintain customer relationships, and use CRM tools for forecasting and pipeline management. The role requires extensive travel, medical-industry account management experience, fluent English, and a valid driver's license.

Provides advanced remote and occasional on-site technical support for molecular diagnostic instruments and assay systems. Troubleshoots hardware, software, configuration, connectivity, peripherals, system logs, and LIS/middleware interfaces; performs root cause analysis and data-driven investigations; prioritizes critical issues affecting uptime and patient outcomes. Documents cases, contributes to knowledge resources, mentors colleagues, and supports training. The role requires medical device or diagnostic instrumentation experience and approximately 2–3 years of relevant healthcare or biomedical experience.

Supports product and supplier quality activities, including inspections, investigations, validation, KPI monitoring, CAPA, QMS documentation, audits, regulatory compliance, nonconformity management, and supplier qualification and improvement. The role is on-site in Pasir Gudang and involves office, laboratory, and manufacturing work, including testing, audits, computer use, and lifting up to 50 pounds.

Leads regulatory and quality operations for medical devices, supporting compliance, market access, tenders, and commercial success. Oversees EUDAMED, UDI frameworks, regulatory records, QMS processes, CAPA, change control, deviations, audit readiness, and compliant documentation. Partners with commercial, contracts, and cross-functional teams to interpret requirements, identify gaps, and implement solutions. Requires extensive EU medical device regulatory and quality experience, including EU MDR, CE marking, ISO 13485, and people or matrix leadership.

Leads software and systems development projects using Scaled Agile practices, coordinating release trains and multidisciplinary teams across software, firmware, hardware, instruments, and third-party components. Manages integration, validation, commercial readiness, risks, technical trade-offs, project metrics, and stakeholder communications for concurrent device development programs.

Supports accounting and financial reporting through financial analysis, journal entries, account reconciliations, accruals, and month-end and quarter-end close activities. Analyzes general ledger accounts and financial results, identifies variances and errors, supports internal and external audits, and maintains documentation for internal controls and SOX compliance.

Leads the SAP technical platform team and roadmap across S/4HANA, BTP, Basis, ABAP, Fiori, integrations, security, automation, and DevOps. Oversees platform operations, governance, release management, compliance, monitoring, vendors, incident response, and continuous improvement. Partners with enterprise applications, architecture, infrastructure, cybersecurity, compliance, and business teams to deliver secure, stable, scalable SAP services and transformation initiatives.