Ventura Solutions

Supply Chain Specialist

Ventura Solutions  •  United States (Remote)  •  1 month ago
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Job Description

We are seeking a Supply Chain Specialist that will oversee end-to-end supply chain activities for a drug-device combination product, supporting commercial operations through contract manufacturing partners. This fully remote role is responsible for ensuring uninterrupted supply, managing supplier performance, and coordinating cross-functional activities to support production, product release, and distribution. The position requires strong experience working with external manufacturers and managing complex, regulated supply chains in a virtual environment.

Responsibilities

  • Manage supply planning and execution for device components and finished combination products through contract manufacturers
  • Serve as the primary supply chain liaison with external manufacturing partners to align on production schedules, forecasts, and inventory levels
  • Coordinate remotely with internal stakeholders and external partners to ensure timely production, release, and distribution
  • Monitor supplier performance, capacity, and lead times to ensure continuity of supply
  • Identify supply risks and develop mitigation strategies, including dual sourcing and safety stock planning
  • Support supplier selection, onboarding, and qualification activities
  • Collaborate with Quality, Manufacturing, and Regulatory teams to support product release and ensure compliance
  • Drive continuous improvement initiatives across the supply chain to improve efficiency, cost, and reliability
  • Support change management activities related to suppliers, materials, and manufacturing processes
  • Ensure alignment with GMP requirements, quality agreements, and regulatory expectations

Qualifications

  • Bachelor’s degree in Supply Chain, Engineering, Business, or related field
  • 5-10+ years of supply chain experience in pharmaceutical, medical device, or combination product environments
  • Strong experience managing contract manufacturers and external suppliers in a remote or distributed environment
  • Experience with demand planning, inventory management, and production scheduling
  • Familiarity with GMP requirements and regulated supply chains
  • Experience supporting commercial-stage products preferred
  • Proven ability to work effectively in a remote setting with cross-functional and global teams
  • Strong project management, communication, and problem-solving skills

Location

  • Remote

Employee Type

  • W2 or 1099

About Ventura Solutions

Ventura Solutions is a reputable end-to-end medical device and combination product consulting, staffing, and training firm. With our deep industry expertise spanning medical devices and combination products, coupled with an outstanding talent pool, we stand out as the preferred option for a diverse array of projects. On the consulting side, we integrate seamlessly into your team and manage small to complex Statement of Work (SOW) projects. On the staffing side, we help source, screen, and on-board reputable employees to fill temporary, temp-to-permanent, and permanent job openings. We accelerate product development, keep products compliant, and help build great organizations. For more information, visit us at www.ventura-solutions.com

Equal Opportunity Employer Minorities/Women/Veterans/Disabled

Ventura Solutions

About Ventura Solutions

Ventura Solutions provides End-to-End consulting, staffing, and training services for the Medical Device and Combination Products industry.

We provide consulting, staffing, and training solutions in the following areas:

-Design Controls

-Risk Management

-Verification & Validation

-Design and Development

-Project Management

-Quality

-Regulatory

-Human Factors

-DHF & Quality System Remediation

-Software as a Medical Device (SaMD)

-Statistics

-Clinical Affairs

-Market Access

-Funding

-NIH SBIR Grants

-Start-Ups

Ventura Solutions is your one-stop shop for getting your product to the market or keeping it compliant.

Detailed list of areas of expertise:

Medical Device & Combination Product Consulting

Design Controls, Risk Management, 21 CFR 820.30, ISO 13485, ISO 14971, Design and Development, Systems Engineering, Project Management, Quality Assurance, Human Factors, IEC 62366, Usability, Design Verification, Design Validation, Statistics, Design History File (DHF) Remediation, Software as a Medical Device (SaMD), Manufacturing, Change Control, Regulatory, FDA Q-Sub, Pre-Sub, Breakthrough Device Program (BDP), Investigational Device Exemption (IDE), 510(k), MDR

Medical Device Start-Up & Business Consulting

Co-Development Deals, Licensing Deals, Fundraising, Non-Dilutive Funding, NIH SBIR Funding, Mergers and Acquisitions (M&A), Commercialization, Valuations, Equity Distributions, Board of Directors, Leadership, Organizational Development, Building High Performing Teams, Concept Evaluation & Selection, FDA or EU Regulatory Strategy, Value Proposition

Staffing, Direct Placement, & Executive Recruitment

Medical Device Engineers, Risk Management Engineers, Systems Engineers, Human Factors Engineers, Design Verification & Validation Engineers; Test Method Development Engineers, Materials Engineers, Project Managers; Process Validation Engineers, Process Development Engineers, Quality Engineers, Design Assurance Engineers, Regulatory Affairs Specialists

Industry
Manufacturing & Production
Company Size
11-50 employees
Headquarters
Vernon Hills, IL
Year Founded
2016
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