At Edwards Lifesciences, we’re committed to operating with honesty, openness, and fairness. Compliance with the highest levels of integrity is vital to building and maintaining the many trusted relationships that sustain our reputation and credibility. Your dedication to operational excellence will ensure employee business practices meet Edwards’ high ethical standards and continue to enable us to transform patient lives around the world.
The Senior Analyst (ALM) is responsible for sustaining and continuously improving the Application Lifecycle Management (ALM) platform. This role partners with business, quality, engineering, validation, and IT stakeholders to define, implement, and optimize ALM processes that support requirements management, risk management, test management, validation documentation, traceability, workflow governance, reporting, and user adoption in a regulated medical device environment. The ideal candidate combines strong analytical skills, project management awareness, and business acumen with the ability to think broadly across the enterprise.
How you will make an impact:
• System enhancement management: Manages and monitors enhancement request backlog for Application Lifecycle Management (ALM).
• Requirement analysis and management: Act as the primary business analyst and process liaison for the ALM platform by partnering with cross-functional stakeholders to capture business needs and convert them into clear system requirements, functional specifications, workflows, reports, and configuration requests.
• Lead requirements elicitation, analysis, documentation, prioritization, and traceability activities for ALM capabilities, including requirements management, risk management, test management, review and approval workflows, baseline management, and reporting.
• Partner with Quality, R&D, Manufacturing, Software Quality, Validation, IT, and vendor teams to ensure ALM processes align with business requirements, regulatory expectations, and applicable quality system procedures.
• Support configuration design by defining tracker structures, attributes, lifecycle states, approval workflows, role-based access needs, templates, dashboards, and reporting requirements.
• Analyze current-state processes and identify opportunities to streamline, standardize, and optimize ALM workflows, reducing manual effort while improving compliance, usability, and traceability.
• Develop and maintain business process documentation, requirements documents, user stories, test scenarios, training materials, work instructions, job aids, and knowledge base content.
• Ensure defined test strategy and test plans adequately cover the requirements.
• Support user acceptance testing, defect triage, traceability reviews, evidence collection, and validation documentation reviews.
• Facilitate workshops, design sessions, stakeholder reviews, and decision discussions to gain alignment on business process design and system functionality.
• Collaborate with technical teams to troubleshoot system issues, clarify business impacts, support root cause analysis.
• Drive user adoption through training, communication, super-user engagement, best practice sharing, and ongoing support for business users.
• Support governance activities, including change impact assessments, enhancement intake, prioritization, release planning, access reviews, and process compliance monitoring.
• Act as a mentor or knowledge resource for business analysts, project team members, and super-users supporting the ALM platform.
What you'll need (Required):
• Bachelor’s degree in computer science, information systems, engineering, business administration, or a related field with 5 years’ experience or
• Master’s degree, with 3 years’ experience in an analyst, business systems analyst, product owner, or similar role supporting enterprise systems.
What else we look for (Preferred):
• Experience managing small projects
• Experience working in a medical device, life sciences, pharmaceutical, or other regulated industry.
• Ability to adapt to new technology and a rapidly changing environment.
• Ability to interface and manage multiple stakeholders.
• Result Oriented, positive “can-do” mindset with demonstration of appropriate urgency and initiative
• Experience in medical devices, pharma, biotech or healthcare related industries.
• Understanding of business analysis practices, including requirements elicitation, process mapping, stakeholder analysis, gap analysis, and solution documentation.
• Knowledge of SDLC, ALM concepts, Agile practices, requirements traceability, change control, and software validation principles.
• Experience supporting ALM, PLM, EQMS, SDLC, validation, requirements management, test management, or regulated system implementation initiatives.
• Experience drafting presentations and presenting investigation and trend summaries.
• Understanding of regulated system expectations, including 21 CFR Part 11, GxP, computer system validation, audit trails, electronic signatures, and good documentation practices.
• Strong analytical, problem-solving, organizational, and critical thinking skills with attention to detail.
• Excellent written and verbal communication skills, including the ability to communicate with technical and non-technical audiences.
• Strong facilitation skills with the ability to lead workshops, drive decisions, and build alignment across cross-functional teams.
• Ability to manage competing priorities, work independently with minimal supervision, and deliver high-quality documentation in a fast-paced environment.
• Proficiency with Microsoft Office tools, including Word, Excel, PowerPoint, Teams, and SharePoint.
Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
For California (CA), the base pay range for this position is $81,000 to $116,000 (highly experienced). The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.
Skills Required
- Bachelor’s degree in computer science, information systems, engineering, business administration, or a related field, plus 5 years of experience
- Master’s degree plus 3 years of experience in an analyst, business systems analyst, product owner, or similar role supporting enterprise systems
- Experience managing small projects
- Experience in medical device, life sciences, pharmaceutical, biotech, healthcare, or another regulated industry
- Understanding of business analysis practices, including requirements elicitation, process mapping, stakeholder analysis, gap analysis, and solution documentation
- Knowledge of SDLC, ALM concepts, Agile practices, requirements traceability, change control, and software validation principles
- Experience supporting ALM, PLM, EQMS, SDLC, validation, requirements management, test management, or regulated system implementation initiatives
- Experience drafting presentations and presenting investigation and trend summaries
- Understanding of 21 CFR Part 11, GxP, computer system validation, audit trails, electronic signatures, and good documentation practices
- Strong analytical, problem-solving, organizational, and critical thinking skills with attention to detail
- Excellent written and verbal communication skills for technical and non-technical audiences
- Strong facilitation skills, including leading workshops, driving decisions, and building cross-functional alignment
- Ability to manage competing priorities, work independently, and deliver high-quality documentation in a fast-paced environment
- Proficiency with Microsoft Word, Excel, PowerPoint, Teams, and SharePoint
- Ability to adapt to new technology and changing environments
Edwards Lifesciences Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Edwards Lifesciences and has not been reviewed or approved by Edwards Lifesciences.
-
Healthcare Strength — Health coverage is considered strong, with multiple plan choices, HSA options, and fertility support, and the company highlights holistic well‑being programs.
-
Retirement Support — A company 401(k) match and well‑regarded retirement offerings add clear long‑term value to total compensation.
-
Equity Value & Accessibility — An Employee Stock Purchase Plan with a discount and look‑back feature makes equity ownership accessible and enhances the total rewards package.
Edwards Lifesciences Insights
What We Do
Edwards Lifesciences (NYSE: EW), is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. We thrive on discovery and expanding the boundaries of medical technology, serving patients in 100+ countries, with the help of our employees in areas including Clinical Affairs, Quality Engineering, Research & Development, Regulatory Affairs, Sales & Marketing, corporate functions and more. Our roots date back to 1958 when Miles Lowell Edwards, a retired engineer with a background in hydraulics and fuel pump operations, set out to build the first artificial heart. Edwards believed the heart could be mechanized and was encouraged by Dr. Albert Starr to focus on developing an artificial heart valve. After just two years, the first Starr-Edwards mitral valve was developed and successfully placed in a patient. This innovation spawned Edwards Laboratories. Miles’ fascination with healing the heart and helping patients with heart disease stemmed from his own experience with rheumatic fever as a teenager and continues to fuel our patient-first culture today. Today, we are as passionate about providing innovative solutions for people fighting cardiovascular disease as we have ever been. It's our Credo. It takes integrity, collaboration, innovation, and focus. We are leaders in the design and manufacture of tissue replacement heart valves and repair products as well as advanced hemodynamic monitoring. We partner with physicians to innovate products designed to help patients live longer, healthier, and more productive lives. Our work is both rewarding and a privilege. The importance of what we do defines our approach. We work together to create an environment where ideas can flourish and we provide our people with the resources, expertise and support to bring those ideas to life. For our legal terms and trademarks, please visit: https://www.edwards.com/legal/legal-terms









