The Senior Global Applications Specialist – Science & Industrial provides advanced technical and applications expertise supporting ASP sterilization systems across the global Science & Industrial segment.
This role serves as a senior technical authority for global field service teams, regulated customers, and cross-functional partners by delivering expert-level troubleshooting, application guidance, and service readiness support. The position plays a critical role in resolving complex system challenges, supporting new product introductions, maintaining validated system performance in regulated environments, and ensuring consistent global service capability.
The role operates at the intersection of engineering, field service, quality, and product development, providing technical leadership that supports system reliability, regulatory compliance, and customer success.
This position requires domestic and international travel, including periodic visits to ASP headquarters in Irvine, CA.
Key Responsibilities
Technical Leadership & Applications Expertise
Provide senior-level technical and scientific expertise supporting ASP sterilization systems used within science and industrial environments.
Serve as the global technical escalation point for complex system issues affecting hardware, software, networking, and integrated system performance.
Monitor platform performance trends and identify emerging technical risks or recurring field issues.
Provide authoritative technical guidance to ensure consistent troubleshooting methodologies and resolution strategies across global service teams.
Customer Engagement & Field Support
Support high-visibility customer situations requiring deep technical and applications expertise.
Partner with regulated customers—including medical device manufacturers, laboratories, and testing organizations—to ensure compliant system operation and optimal application performance.
Provide onsite technical support globally when required to address complex system investigations, escalations, or critical customer needs.
Act as a trusted technical advisor to internal stakeholders and external customers during complex technical situations.
Technical Risk Management & System Reliability
Independently assess and manage technical risks associated with sterilization platforms and their deployment within regulated environments.
Provide clear technical accountability for decisions impacting system reliability, regulatory compliance, and operational safety.
Lead investigations into significant technical issues, system failures, or safety-related events.
Support the development of corrective and preventive actions to improve system reliability and mitigate future risk.
Advanced Troubleshooting & Root Cause Analysis
Lead complex technical investigations involving system failures, out-of-box issues, or field non-conformances.
Conduct structured root cause analysis using data-driven methodologies to identify underlying system or process issues.
Develop and recommend scientifically sound corrective actions to resolve recurring technical challenges.
Collaborate with engineering, quality, and product development teams to implement long-term solutions.
New Product Development & Launch Readiness
Collaborate cross-functionally with engineering, product management, quality, and service teams during new product development activities.
Provide field-informed insights to ensure new products are designed for serviceability, reliability, and real-world application workflows.
Support global product launch readiness through the development of service documentation, troubleshooting strategies, and training materials.
Participate in product verification, validation, and qualification activities within regulated or controlled environments.
Service Workflow & Operational Excellence
Leverage extensive field service experience to influence global service workflows, troubleshooting processes, and operational best practices.
Partner with regional service leaders to drive continuous improvement initiatives that enhance service efficiency and customer experience.
Support global service readiness planning and proactive issue resolution initiatives.
Promote knowledge sharing and best practices across the global service organization.
Compliance, Standards & Quality
Ensure platform processes and service activities remain aligned with global regulatory expectations and relevant ISO sterilization standards.
Support system validation and qualification activities while ensuring systems operate within a validated state in regulated environments.
Author and review critical technical documentation including:
* Standard Operating Procedures (SOPs)
* Validation protocols
* Investigation reports
* Technical bulletins
* Service documentation
Provide technical input supporting CAPA investigations, regulatory compliance initiatives, and quality system improvements.
Technical Mentorship & Knowledge Development
Provide mentorship and technical guidance to service engineers and technical specialists across the global organization.
Support the development of training materials and knowledge transfer initiatives to strengthen global troubleshooting capability.
Foster collaboration and knowledge exchange across engineering, service, and quality teams.
Required Qualifications
Bachelor’s degree in Engineering, or a related technical discipline.
Extensive field service experience with complex technical systems in GMP and/or ISO13485 regulated industries.
Demonstrated expertise supporting ASP sterilization equipment or comparable sterilization or laboratory systems.
Strong understanding of global service workflows, escalation processes, and lifecycle service support.
Proven ability to work effectively within global cross-functional teams and influence outcomes without direct authority.
Experience supporting new product development, product launch, and service readiness initiatives.
Demonstrated experience supporting system validation and qualification activities in regulated or controlled environments and quality systems.
Advanced critical thinking and analytical skills with the ability to diagnose and resolve highly complex system issues.
Working knowledge of relevant ISO sterilization standards and industry regulatory frameworks.
Excellent communication, interpersonal, and stakeholder engagement skills.
Ability and willingness to travel domestically and internationally, including periodic business travel to Irvine, CA.
Preferred Qualifications
Experience working within global organizations with matrix reporting structures.
Project management experience or formal certification.
Expertise in structured problem-solving methodologies such as root cause analysis, CAPA, or reliability engineering approaches.
Experience contributing to technical training or mentoring within technical service organizations.
Language Qualifications
Fluent in English - oral and written
Fortive Corporation Overview
Fortive's essential technology makes the world safer and more productive. We accelerate transformation in high-impact fields like workplace safety, build environments, and healthcare.
We are a global industrial technology innovator with a startup spirit. Our forward-looking companies lead the way in healthcare sterilization, industrial safety, predictive maintenance, and other mission-critical solutions. We're a force for progress, working alongside our customers and partners to solve challenges on a global scale, from workplace safety in the most demanding conditions to advanced technologies that help providers focus on exceptional patient care.
We are a diverse team 10,000 strong, united by a dynamic, inclusive culture and energized by limitless learning and growth. We use the proven Fortive Business System (FBS) to accelerate our positive impact.
At Fortive, we believe in you. We believe in your potential—your ability to learn, grow, and make a difference.
At Fortive, we believe in us. We believe in the power of people working together to solve problems no one could solve alone.
At Fortive, we believe in growth. We're honest about what's working and what isn't, and we never stop improving and innovating.
Fortive: For you, for us, for growth.
About Advanced Sterilization Products
ASP is a leading global provider of innovative sterilization and disinfection solutions, and a pioneer of low-temperature hydrogen peroxide sterilization technology.ASP’s mission is to protect patients during their most critical moments. We support healthcare facilities in the fight to protect patients against hospital acquired infections, which are a leading cause of morbidity and mortality. ASP’s products, which are sold globally, include the STERRAD system for sterilizing instruments and the EVOTECH and ENDOCLENS systems for endoscope reprocessing and cleaning.
We Are an Equal Opportunity Employer. Fortive Corporation and all Fortive Companies are proud to be equal opportunity employers. We value and encourage diversity and solicit applications from all qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity or expression, or other characteristics protected by law. Fortive and all Fortive Companies are also committed to providing reasonable accommodations for applicants with disabilities. Individuals who need a reasonable accommodation because of a disability for any part of the employment application process, please contact us at applyassistance@fortive.com.
Bonus or Equity
This position is also eligible for bonus as part of the total compensation package.
Pay Range
The salary range for this position (in local currency) is 116,600.00 - 216,900.00