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Product Manager
Mount Olive, NJ
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Director, Global Sourcing & Product Development Location:
On-Site (Budd Lake, NJ / Parsippany, NJ)
Position Type:
Full-Time, Direct-Hire Target Compensation:
$150,000 - $175,000
Base Salary Industry:
Medical Supplies & Healthcare Solutions Seniority Level:
Director (Hands-on Leadership / Individual Contributor) About the Role We are seeking a commercially minded, hands-on Director of Global Sourcing & Product Development to lead global supply chain initiatives and drive innovative new product development in advanced healthcare solutions. This role serves as a key bridge between global manufacturing partners and internal cross-functional commercial teams. The ideal candidate brings deep expertise in sourcing medical consumables, devices, and personal protective equipment (PPE), along with a track record of executing successful product launches from ideation to delivery.
Analyze global market dynamics, manufacturing landscapes, raw material trends, and geopolitical factors to align supply strategies with corporate goals.
Supplier Selection & Development:
Identify, evaluate, and qualify primary, secondary, and tertiary manufacturing partners across global regions.
Commercial Negotiation:
Lead competitive pricing and contract negotiations, securing favorable terms while maintaining rigorous manufacturing quality and efficiency standards.
Performance Tracking:
Build and maintain supplier relationship management frameworks to monitor manufacturing metrics, cost competitiveness, quality, and on-time delivery.
Global Travel:
Travel internationally to conduct factory visits, perform supplier audits, and participate in industry conferences. New Product Development (NPD)
Product Strategy & Launch:
Partner with executive leadership to plan and execute global NPD initiatives across targeted medical supplies, consumables, and devices.
Clinical & Technical Evaluation:
Build clinical and in-use expertise to evaluate product design, regulatory requirements, and competitive positioning.
Product Lifecycle Ownership:
Oversee product design validation, sample testing, and clinical performance standards directly with manufacturing sites and sales teams.
Specifications & Compliance:
Maintain technical documentation, material specifications, and quality test records to ensure strict regulatory compliance.
Cross-Functional Collaboration:
Partner closely with R D, Quality, Regulatory, Operations, Marketing, and Sales teams to support seamless commercial rollouts and internal product training.
Required Qualifications & Experience Education:
Bachelor's degree in Business, Supply Chain, Engineering, or a related technical discipline required.
Experience:
7+ years of progressive experience in global sourcing, product design, and medical product launches.