Innovative Solutions for Effective Validation and Optimization

Discover cutting-edge solutions with JQCS Consulting. From Validation to Process Optimization, our services are designed to innovate and enhance your business performance for sustained growth.

Understand, Improve, 
Complete & Excel

To become the number one solution provider in the Life Science Sector, by delivering consistently solutions that exceed all expectations while providing the highest quality of work.

Who We Are?

JQCS is a nationally certified Small Business with the NMSDC (National Minority Supplier Diversity Council). We provide a comprehensive range of services tailored to high-volume and highly regulated industries, including biopharma, pharmaceutical, medical device, and combination product manufacturers. Our team excels at assessing existing processes, identifying opportunities for improvement, and implementing innovative solutions to meet specific industry requirements. From initial concept through project delivery, and ongoing support, JQCS is committed to delivering efficient solutions in a timely manner, minimizing disruptions to production schedules.

Our team is comprised of a group of professionals with extensive experience within the biopharma, pharmaceutical, medical device and combination product industries. Educational disciplines may vary, but mostly consist of engineering, chemistry, microbiology, or computer science among others. cGMP is embedded on the company’s culture as well as integrity and professionalism, therefore all work performed by JQCS Consulting, on all projects regardless of size, or industry, are delivered with the highest quality in mind. To exceed client’s expectation is the only way to complete a project correctly.

We offer the full spectrum of services to help your team work better.

C&Q / Validation /
Regulatory / Compliance

  • Commissioning and Qualifications
  • Start-up, Factory Acceptance Tests (FAT)
  • Compliance Services
  • Computerized Systems Validation
  • Document Control
    • Gap & Risk Assessments
    • Engineering Specifications
    • Environmental Monitoring Programs
    • Facilities, Utilities, Manufacturing / Packaging Equipment Qualification
    • FDA Regulations Assessment
    • Functional Requirements Specifications
    • Installation, Operational, Performance Qualification Protocols and Laboratory Systems
    • Process Validation, Process Investigations
    • Quality Assurance / Validation Master Plans Reports
    • Steam In Place (SIP) Validation
    • SOPs, Guidelines, Audits
    • Summary Reports

Cleaning Validation
and Engineering

  • Cleaning Cycle Verification
  • Cleaning Parameters Assessment
  • Cleaning Validation Strategy and Consultation
  • Parts washer Load Configuration Design and Specification
    • Process and Commissioning of cleaning equipment (CIP skid/ parts washers)

Pharmaceutical
Manufacturing Process
Packaging Solutions

  • Capacity Analysis Projects
  • Cleaning In Place Design and Support
  • Cycle time reduction
  • Equipment and systems improvements
    • In Process Testing automation
    • Losses and waste reduction
    • Maximization of productive time
    • Operational Efficiencies Metrics
    • Process / Packaging Optimization and Improvements
    • Six Sigma, DOE and DMAIC solutions Implementation
    • Process / Packaging Process and Product Transfer Validation

Steam in Place (SIP)
Validation and Engineering

  • Autoclave Load Configurations Specification 
  • Clean Steam Generation & Distribution Engineering and Commissioning
  • Contamination Root Cause Investigations/Preventi-on
    • Lethality Testing utilizing Biological Indicators
    • Process Equipment Sterilization and Autoclave
    • Sterilization validation including Temperature Mapping

Contact us

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