Demo

Program Analyst

Cordis
Irvine, CA Full Time
POSTED ON 4/14/2026
AVAILABLE BEFORE 5/10/2026
Overview

Selution, in partnership with Cordis, specializes in the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery disease. Our mission is to revolutionize healthcare by creating next-generation solutions that address unmet and critical medical needs.

Responsibilities

The Program Analyst supports the execution of R&D programs by managing project data, tracking milestones, and assisting in the preparation of reports and presentations. This role provides analytical and administrative support to ensure projects stay on schedule, within scope, and aligned with business objectives.

Key Responsibilities


  • Track and maintain project timelines, milestones, and deliverables using program management tools.
  • Collect, analyze, and summarize program data for leadership reporting.
  • Assist with the preparation of technical and project documentation including dashboards, status reports, and risk registers.
  • Collaborate with cross-functional teams to ensure alignment between technical activities and program objectives.
  • Support budget tracking, resource planning, and vendor coordination.
  • Maintain accurate project documentation and version control.
  • Identify project risks and assist in the development of mitigation strategies.
  • Provide support during program audits and reviews.
  • Facilitate communication between project stakeholders to ensure timely resolution of issues.


Key Competencies


  • Strong attention to detail and data accuracy.
  • Excellent written and verbal communication.
  • Ability to work cross-functionally in a fast-paced environment.
  • Proactive, solution-oriented mindset.


Qualifications

Required Experience:


  • Bachelor’s degree in Engineering, Business, or related field.
  • 3 years of experience in program coordination, data analysis, or project management.
  • Experience working in highly-regulated environment, ideally medical device, is highly preferred.
  • Strong organizational and analytical skills.
  • Proficient in Microsoft Excel, PowerPoint, and project tracking tools (e.g., Smartsheet, MS Project).


Preferred Experience:


  • Experience in a medical device or regulated manufacturing environment.
  • Familiarity with FDA and ISO documentation requirements.


Working Conditions


  • Office-based position with occasional manufacturing floor interface.
  • May require occasional extended hours during critical project phases.


Pay / Compensation

The expected pre-tax pay rate for this position is $78,650 – $105,600 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.

Cordis is proud to be an equal opportunity employer and is committed to providing equal opportunity for all teammates and applicants. At Cordis, our teammates all bring different strengths, experiences, and backgrounds, who share a passion for improving people's lives. Diversity not only includes race and gender identity, but also age, disability status, veteran status, sexual orientation, religion, and many other parts of one’s identity. All our teammates’ points of view are key to our success, and we believe inclusion is everyone's responsibility. Together, we strive to create and maintain working and learning environments that are inclusive, equitable and welcoming.

Salary : $78,650 - $105,600

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