Project Manager II – PMO & Cross-Functional Delivery

bioMérieux; Hazelwood (MO); On-site; USD 92,000 - 138,000; Full time

Benefits offered by this job

Medical plans

Life and disability insurance

Retirement plan with employer match

Wellness programs

Commuter benefits

Employee Assistance Program

Parental leaves

Job summary

bioMérieux seeks a seasoned Project Manager to lead complex, cross-functional initiatives within a regulated life sciences context. You will own end-to-end delivery, manage scope, budget and risk, and ensure compliance with ISO13485 and FDA/IVDR/CE requirements.

You will mentor junior PMs and drive PMO governance with senior stakeholders. Demonstrated ability to present updates to leadership and coordinate with external vendors is required.

Qualifications

• Bachelor's degree in Engineering, Technology, Life Sciences, Business or PM.
• 5+ years of program/project management experience in PMO or similar.
• Experience in regulated environments (IVD/medical devices/life sciences) with design control, ISO13485, FDA/IVDR/CE knowledge.
• Proven track record in NPD or lifecycle projects from concept to launch.
• Strong presentation of updates to senior leadership using data-driven insights.

Responsibilities

• Develop and manage integrated project plans and schedules.
• Manage scope, risk, budget, and stakeholder expectations.
• Communicate clearly across functional and external teams.
• Ensure compliance with internal and regulatory frameworks.
• Analyze metrics and use data for decision-making.
• Own project lifecycle from initiation to closure.
• Mentor junior PMs and coordinate with PMO.
• Vendor selection and performance management.

Skills

Cross-functional leadership

Data-driven reporting

Risk management

Mentoring

Budgeting

Stakeholder communication

Leadership

PM tools

Education

Bachelor's degree

Tools

MS Project

Jira

Smartsheet

Planisware

Job description

bioMérieux seeks a seasoned Project Manager to lead complex, cross-functional initiatives within a regulated life sciences context. You will own end-to-end delivery, manage scope, budget and risk, and ensure compliance with ISO13485 and FDA/IVDR/CE requirements.

You will mentor junior PMs and drive PMO governance with senior stakeholders. Demonstrated ability to present updates to leadership and coordinate with external vendors is required.