Global Medical Sourcing Advisor & Product Launch

Cardinal Health; United States; Sur place; USD 82 000 - 117 000; Plein temps

Avantages offerts par ce poste

Medical coverage

Paid time off

401k plan

HSA

Parental leave

Work-Life resources

Résumé du poste

Cardinal Health is seeking a strategic sourcing advisor for Global Products to coordinate new product introductions from third-party manufacturers and drive cross-functional collaboration. You will partner with Marketing, Sourcing, Engineering, Quality, Regulatory, Operations, Logistics and external suppliers to enable timely product launches that fill portfolio gaps.

The role requires strong sourcing, negotiation, and project management skills, with experience in an FDA-regulated environment

Qualifications

• Bachelor’s degree required; advanced degree a plus.
• Minimum 5+ years in strategic sourcing in medical device/heathcare.
• Experience with FDA-regulated procurement preferred.
• Proven ability to manage global cross-functional programs.

Responsabilités

• Create RFPs and align award recommendations per sourcing process.
• Support a portfolio of projects to fill portfolio/category gaps.
• Improve Private Brand sourcing and new product introduction processes.
• Coordinate cross-functional activities for launching new Private Brand products.

Connaissances

Strategic sourcing

Project management

Cross-functional collaboration

Cost reduction

Analytics

Negotiation

FDA-regulated env

Travel readiness

Formation

Bachelor’s Degree

Outils

Excel

PowerPoint

Word

Tableau

Description du poste

Cardinal Health is seeking a strategic sourcing advisor for Global Products to coordinate new product introductions from third-party manufacturers and drive cross-functional collaboration. You will partner with Marketing, Sourcing, Engineering, Quality, Regulatory, Operations, Logistics and external suppliers to enable timely product launches that fill portfolio gaps.

The role requires strong sourcing, negotiation, and project management skills, with experience in an FDA-regulated environment