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Quality Systems Consultant Jobs (NOW HIRING)

Apperture Solutions

Systems Consultant

Raleigh, NC · On-site

Strong attention to detail and commitment to quality. * Willingness to travel as needed to support ... Eng, Systems Eng., or other related disciplines. * Minimum of 7 years of experience in large scale ...

Mutual of Omaha

Business Systems Consultant

Omaha, NE · On-site +1

Business Systems Consultant Apply now Job no: 504915 Work type: Full Time Regular Location: Remote ... quality, efficiency, and customer outcomes. * Develop and maintain reports, dashboards, and ...

1 point system

STIBO Systems Consultant

Pleasanton, CA · On-site

Job Title STIBO Systems Consultant Location 5 days onsite in a week - Pleasanton, CA Type of Hire ... This role is critical to ensuring data accuracy, consistency, and quality across the organization ...

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Quality Systems Consultant information

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How much do quality systems consultant jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for quality systems consultant in the United States is $50.76, according to ZipRecruiter salary data. Most workers in this role earn between $36.54 and $67.07 per hour, depending on experience, location, and employer.

How does a Quality Systems Consultant typically collaborate with cross-functional teams to drive process improvements?

Quality Systems Consultants frequently work alongside teams from manufacturing, engineering, regulatory affairs, and quality assurance to assess current processes and identify areas for improvement. They lead workshops, facilitate root cause analyses, and help implement corrective actions to ensure compliance with industry standards. Effective communication and stakeholder management are essential, as consultants must align diverse teams on quality objectives and foster a culture of continuous improvement. Regular meetings and progress reports help keep all parties informed and engaged in the improvement process.

What are the key skills and qualifications needed to thrive as a Quality Systems Consultant?

To thrive as a Quality Systems Consultant, you need in-depth knowledge of quality management systems (such as ISO 9001), auditing practices, and regulatory compliance, often supported by a relevant degree and certifications like Six Sigma or ISO Lead Auditor. Familiarity with quality management software, document control systems, and process mapping tools is commonly required. Strong analytical thinking, problem-solving abilities, and excellent communication skills help you effectively advise clients and drive improvements. These competencies are vital for ensuring organizations meet regulatory standards, optimize processes, and maintain high-quality outcomes.

What is the difference between Quality Systems Consultant vs Quality Assurance Specialist?

AspectQuality Systems ConsultantQuality Assurance Specialist
CertificationsISO 9001 Lead Auditor, CQEASQ CQE, ISO 9001 Lead Auditor
Work EnvironmentConsulting firms, client sites, corporate officesManufacturing, labs, production facilities
Employer & IndustryConsulting companies, manufacturing, healthcareManufacturing, pharmaceuticals, food industry
Primary FocusDeveloping, implementing, and auditing quality systemsPerforming quality inspections, testing, and compliance checks

While both roles focus on quality, a Quality Systems Consultant primarily develops and audits quality management systems across organizations, often working as an external advisor. In contrast, a Quality Assurance Specialist typically performs hands-on testing and inspections within a specific production environment to ensure product quality and compliance.

What does a Quality Systems Consultant do?

A Quality Systems Consultant helps organizations design, implement, and improve quality management systems to meet industry standards and regulatory requirements. They assess existing processes, provide guidance on compliance with frameworks like ISO 9001, and recommend best practices to enhance efficiency and product quality. Consultants also train staff, conduct audits, and help prepare documentation to ensure continuous improvement and successful certification. Their expertise is valuable for organizations aiming to achieve or maintain high-quality standards.
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What job categories do people searching Quality Systems Consultant jobs look for? The top searched job categories for Quality Systems Consultant jobs are:
Quality Systems Consultant jobs near you
Infographic showing various Quality Systems Consultant job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $105,586 per year, or $50.8 per hour.

GMP QC Systems Consultant

Stark Pharma Solutions Inc

Frankford, DE • On-site

Contractor

Posted 17 days ago

Job description

Hi,

My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on GMP QC Systems Consultant position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows

Position: GMP QC Systems Consultant

Location: Frankford, DE (100% Onsite)
Duration: 12+ Month Contract

Job Overview

We are seeking an experienced GMP QC Systems Consultant to support the implementation, integration, and validation of Quality Control laboratory systems in a regulated pharmaceutical environment. The ideal candidate will have strong expertise in GMP laboratory systems, Computer System Validation (CSV/CSA), and cross-functional project execution.

Key Responsibilities

  • Lead implementation and integration of GMP QC laboratory systems.
  • Coordinate system configuration, data migration, deployment, and go-live activities.
  • Manage project timelines, risks, budgets, and stakeholder communications.
  • Support Computer System Validation (CSV/CSA), including IQ/OQ/PQ execution and documentation.
  • Perform risk assessments, testing, and validation activities in compliance with GAMP5 and GxP requirements.
  • Collaborate with QA, IT, laboratory teams, vendors, and business stakeholders to ensure successful project delivery.
  • Ensure compliance with GxP, Data Integrity, and internal quality standards.
  • Prepare project status reports and support release readiness activities.

Required Qualifications

  • 8+ years of experience in Pharmaceutical, Biotechnology, or other GMP-regulated environments.
  • Strong experience implementing and validating QC/Laboratory systems.
  • Hands-on knowledge of CSV, CSA, GAMP5, GxP, IQ/OQ/PQ, and risk-based validation.
  • Experience with system integration, data migration, and cross-functional project coordination.
  • Familiarity with laboratory platforms such as LIMS, SDMS, Empower, LabX, QuantStudio, SoftMax Pro, or similar systems.
  • Excellent communication, documentation, and stakeholder management skills.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.  

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/

Thank you,

Karthik Mutyala

Recruiting Manager

Stark Pharma Solutions Inc

Email: karthik@starkpharma.com

15 Corporate Place S, Suite 350,

Piscataway, New Jersey 08854

www.starkpharma.com