Senior Project Manager, IVD & Medical Devices — Remote

Meridian Bioscience International Limited; Northern (KY); Hybrid; USD 120,000 - 160,000; Full time

Job summary

Meridian Bioscience International Limited seeks a Senior Project Manager to lead cross-functional, FDA‑ regulated in vitro diagnostic product development from concept to launch. You will manage scope, schedule, risks, budgets and ensure design controls compliance with R&D, Regulatory, QA and external partners.

The role collaborates across clinical, regulatory and manufacturing teams to drive timely decisions and milestones, with travel as needed.

Qualifications

• Bachelor’s degree in science, engineering or business administration or related field required; advanced degree preferred.
• At least 7 years of project management experience leading cross‑functional product development projects.
• Direct experience with FDA-regulated IVD product development and launch in the U.S. market is expected.

Responsibilities

• Define project scope, goals, deliverables and governance for complex product development projects.
• Develop integrated project plans with critical path, dependencies and resources; communicate plans to team and leadership.
• Drive ownership, identify risks/issues and recommend changes to meet objectives.
• Track performance: schedule, milestones, risks, resources and budget; provide status and escalations.
• Lead cross-functional teams and external partners to ensure on-time delivery and launch readiness.

Skills

Project management

Cross-functional leadership

Risk management

Communication

Problem solving

Education

Bachelor’s degree in science/engineering/business administration

Advanced degree preferred

Job description

Meridian Bioscience International Limited seeks a Senior Project Manager to lead cross-functional, FDA‑ regulated in vitro diagnostic product development from concept to launch. You will manage scope, schedule, risks, budgets and ensure design controls compliance with R&D, Regulatory, QA and external partners.

The role collaborates across clinical, regulatory and manufacturing teams to drive timely decisions and milestones, with travel as needed.