Senior Program Analyst (United States)
Overview
When you join the team at Cordis, you become part of an inspiring mission to save lives, impacting millions of people and broadening access to life-saving cardiovascular and endovascular technology. As a global leader for over 60 years, we are dedicated to being the heart of innovation to transform cardiovascular care. At Cordis, we’re teammates, not just employees. We embrace an empowered and one-team culture where teammates are inspired to unleash their full potential. With diverse teams on a global scale, we believe the richness of our experiences and backgrounds enhances the careers of our teammates, the service to our customers, and ultimately, the lives of our patients. If you love a challenge and are ready to have a direct, transformative and positive impact on the lives of millions, then Cordis is just the place for you. We are the people behind the people who keep saving lives.
Responsibilities
The Senior Program Analyst supports the planning, execution, and monitoring of key organic and inorganic programs. This role provides data-driven insights, maintains program schedules, works collaboratively across functions and ensures timely communication of project performance to leadership and cross-functional teams.
Key Responsibilities
Define and drive alignment of project goals and milestones with cross-functional partners. Define and drive success metrics and leading indicators for program. Drive program execution by planning, tracking deliverables, timelines, and dependencies. Develop and maintain program dashboards, performance metrics, and risk registers. Conduct data analysis and reporting to support strategic decision-making. Prepare executive-level presentations and reports summarizing program status. Identify process improvement opportunities and recommend solutions. Facilitate communication between internal and external stakeholders. Support budgeting, forecasting, and resource allocation processes. Ensure program data accuracy and maintain version control of key project documents.
Qualifications
Required Qualifications: Bachelor’s degree in engineering, business, or related field. 5+ years of experience in program coordination, business analysis, or data management. Proficiency with MS Office, Smartsheet, and project management software. Strong analytical, communication, and organizational skills. Preferred Qualifications: Experience in medical devices or regulated manufacturing industries. Familiarity with design control, CAPA, or risk management principles. PMP certification or similar project management credential. Key Competencies Strong attention to detail and analytical thinking. Effective communication and reporting abilities. Ability to manage multiple priorities under tight deadlines. Cross-functional collaboration and problem-solving mindset. Proactive, organized, and adaptable. Working Conditions Office-based work environment. May require occasional travel for meetings or conferences. Pay / Compensation The expected pre-tax pay rate for this position is $89,000 – $119,000 per year. Actual pay may fluctuate outside of the listed range depending on skills, education, experience, job-related knowledge and location. US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa.