Ventura Solutions

Quality Control Specialist

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

We are seeking a Quality Control Specialist that will support quality control activities for a drug-device combination product, with a focus on device components and finished product. This role will primarily oversee and review quality control activities performed by a contract manufacturer, ensuring compliance with specifications, GMP requirements, and regulatory standards.

Responsibilities

  • Review batch records, device history records (DHRs), and associated documentation generated by contract manufacturers for accuracy, completeness, and compliance
  • Coordinate and oversee QC testing activities performed by external partners, including device performance and release testing
  • Review test results and certificates of analysis (CoAs) to support product release decisions
  • Ensure all testing and documentation meet established specifications, methods, and GMP requirements
  • Collaborate with contract manufacturers to resolve documentation issues, discrepancies, and data inconsistencies
  • Support investigations related to deviations, nonconformances, and out-of-specification (OOS) results
  • Track and ensure timely completion of QC-related deliverables from external partners
  • Support method validation, method transfer, and specification development activities
  • Maintain accurate and compliant documentation in accordance with data integrity standards
  • Partner with Quality, Manufacturing, and Supply Chain teams to ensure product quality and supply continuity

Qualifications

  • Bachelor’s degree in a scientific or technical discipline
  • 5+ years of QC experience in medical devices or combination products
  • Experience reviewing batch records, DHRs, and QC documentation from external or contract manufacturers
  • Familiarity with device performance testing (e.g., functional testing, dose delivery, spray characterization) preferred
  • Strong understanding of GMP, GDP, and data integrity requirements
  • Experience supporting investigations (deviations, OOS, nonconformances)
  • Ability to work effectively in a remote environment with cross-functional and external teams
  • Strong attention to detail, organization, and communication 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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