Program Manager, R&D - Selution

Cordis

$111K — $159K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • 8+ years in medical devices industry
  • Prior program or project management experience
  • Bachelor's degree in Engineering or related field
  • Expertise in FDA design controls and documentation standards
  • PMP certification or advanced project management training preferred
  • Experience with cardiovascular or combination product development preferred

Responsibilities

  • Lead and coordinate multi-disciplinary R&D programs from concept to launch
  • Maintain program schedules, risk registers, and milestone tracking
  • Provide regular updates and dashboards to leadership
  • Manage project budgets and ensure alignment with financial targets
  • Ensure compliance with design controls (21 CFR 820) and documentation standards
  • Facilitate collaboration among R&D, Clinical, and Regulatory teams

Benefits

  • Working within the innovative SELUTION™ platform
  • Exposure to cross-functional and multi-disciplinary teams
  • Opportunities for professional development and growth
  • Engagement with high-stakes medical device projects
  • Potential impact on improving patient outcomes through product innovation
Full Job Description
Responsibilities

The R&D Program Manager leads cross-functional project teams to ensure efficient planning, execution, and delivery of product development initiatives within the SELUTION™ platform. The role emphasizes program leadership, risk management, and adherence to regulatory and quality frameworks

Key Responsibilities
  • Lead and coordinate multi-disciplinary R&D programs from concept to launch.
  • Maintain program schedules, risk registers, and milestone tracking.
  • Provide regular updates and dashboards to leadership.
  • Manage project budgets and ensure alignment with financial targets.
  • Ensure compliance with design controls (21 CFR 820) and documentation standards.
  • Facilitate collaboration among R&D, Clinical, and Regulatory teams.


Qualifications

Required Qualifications
  • 8+ years of experience in medical devices.
  • Previous program or project management experience.
  • Bachelor's degree in Engineering or related field.
  • Mastery of FDA design controls and documentation requirements.


Preferred Qualifications
  • PMP certification or advanced project management training.
  • Experience with cardiovascular or combination product development.
  • Previous medical device program or project management experience.


Pay / Compensation
The expected pre-tax pay rate for this position is $111,650 - $159,500 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.

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