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Quality System Jobs (NOW HIRING)

Nextern

Quality Systems Manager

Maple Grove, MN · On-site

$120K - $140K/yr

The role is also responsible for the selection, implementation, administration, and monitoring of the Quality Management System ensuring continual compliance of the organization. The role owns the ...

Filtration Group

Quality Systems Manager

Fairburn, GA · On-site

$90 - $120/hr

Lead the execution, maintenance, and improvement of the site's Quality Management System (QMS). * Ensure compliance with ISO standards, customer requirements, and applicable regulatory requirements.

Astemo Ltd

Quality Systems Manager

Monroe, GA · On-site

Responsible for reporting quality system KPI's and status to executive management and ensuring collaboration with cross functional teams to develop improvements and address countermeasures for ...

Nihon Kohden

Quality Systems Manager

Irvine, CA · On-site

$100K - $145K/yr

Manage Nihon Kohden America's Quality Management System (QMS), ensuring ongoing effectiveness and compliance with applicable regulatory requirements, standards, and company policies and procedures.

TTM Technologies

Quality Systems Engineer

Salem, NH · On-site

Communicate quality system performance, compliance concerns, and business risks to leadership. * Develop, review, and maintain quality policies, procedures, standards, and documentation. * Provide ...

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How much do quality system jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for quality system in the United States is $25.64, according to ZipRecruiter salary data. Most workers in this role earn between $22.36 and $28.85 per hour, depending on experience, location, and employer.

What is a quality system?

Quality System jobs involve developing, implementing, and maintaining the processes and standards that ensure a company’s products or services meet regulatory and customer requirements. Professionals in these roles often work with quality management systems (QMS), conduct audits, and ensure compliance with industry regulations like ISO standards. They play a key role in continuous improvement by identifying areas for enhancement and working with other teams to resolve quality-related issues. Quality System jobs are vital across industries such as manufacturing, healthcare, and pharmaceuticals to guarantee product safety, reliability, and effectiveness.

What skills and qualifications are needed to thrive as a quality systems specialist?

To thrive as a Quality Systems Specialist, you need a strong understanding of quality management principles, regulatory standards (such as ISO 9001), and typically a degree in engineering, life sciences, or a related field. Familiarity with quality management software (QMS), document control systems, and relevant certifications like Six Sigma or ASQ are commonly required. Attention to detail, problem-solving abilities, and strong communication skills help ensure compliance and continuous improvement. These skills are essential to maintain product quality, meet regulatory requirements, and support organizational excellence.

What are common challenges faced by professionals working in quality systems, and how can they be addressed?

Professionals in Quality Systems often encounter challenges such as ensuring compliance with evolving regulatory standards, maintaining thorough documentation, and fostering a culture of continuous improvement across departments. Addressing these challenges typically involves staying updated on industry regulations, implementing effective training programs, and utilizing robust digital tools for document management. Additionally, strong communication and collaboration with cross-functional teams are essential to align quality objectives with broader organizational goals.

What is the difference between Quality System vs Quality Assurance?

AspectQuality SystemQuality Assurance
DefinitionFramework of policies, processes, and procedures to ensure quality management across an organization.Part of the quality system focused on preventing defects through planned activities and systematic processes.
FocusOverall quality management and compliancePreventing defects and ensuring product/service quality
CertificationsISO 9001, QS-9000ISO 9001, Six Sigma, CQA
Work EnvironmentCross-departmental, organizational-wideSpecific to quality processes and audits

In summary, a Quality System encompasses the entire framework for managing quality within an organization, including policies and procedures. Quality Assurance is a key component of the Quality System, focusing specifically on preventing defects and ensuring quality through systematic activities.

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What are the most commonly searched types of Quality System jobs?

The most popular types of Quality System jobs are:

What states have the most Quality System jobs?

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Quality System jobs near you
Infographic showing various Quality System job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $53,326 per year, or $25.6 per hour.

Quality System Scientific Specialist Tier III

Nephron Pharmaceuticals

West Columbia, SC • On-site

Full-time

Re-posted 3 days ago

Job description

Job Purpose:
The purpose of the Quality Systems Scientific Specialist (Tier III) is to responsible for ensuring data integrity, compliance, and adherence to established quality standards. This role involves analyzing reports, and identifying discrepancies or inconsistencies, and escalating issues accordingly. Contribute to continuous improvement of processes and products by identifying trends all while adhering to regulatory standards and company policies.
Essential Duties and Responsibilities:
• Responsible for ensuring compliance with all State and Federal regulatory bodies as it pertains to the completion of Annual Product Reviews (APR) for all Nephron Pharmaceuticals Corporation (Nephron) and Nephron 503B Outsourcing Facility (503B) drug products.
• Responsible for performing Quality Assurance reviews of Microbiology and Chemistry documents for final Quality Approval. This includes review of method validation protocols and summary reports, Media Fills, environmental monitoring performances qualifications, drug supply chain security act, and other related documentation provided to the Quality Systems Scientific Team.
• Review and approval of protocols and summary reports for Process Development (PD) studies, stability studies, validation studies, and additional documentation as requested.
• Review and approve initiations and final reports of laboratory investigations for Chemistry and/ or Microbiology related events.
• Stay abreast of current FDA requirements and ensure compliance by familiarity with important department Standard Operating Procedures (SOPs) and routine observance of procedures being performed.
• Report any quality related issues to Quality Systems Scientific Manager or Quality Systems Director.
• Assist in other activities (as needed) for Quality Assurance Management.
Supplemental Functions:
  • Copying, filing, and scanning of documents.
  • Performs other similar duties as required.

Requirements
Job Specifications and Qualifications:
• Bachelor's degree preferred with 1-2 years of pharmaceutical experience in Quality Systems or relevant area preferred.
• 1-3 years of experience with MS Word, Excel, and PowerPoint preferred.
• 1-2 years project management and coordinator experience preferred.
Knowledge & Skills:
• Written and Oral communication skills.
• Pharmaceutical experience with equipment, instrumentation, production, maintenance, and engineering preferred.
• Experience in Root Cause Analysis and technical writing skills required.
• Team Player, must be able to interact within the company with all departments.
• Experience in Root Cause Analysis and technical writing skills required.
• Specific expertise, skills and knowledge within quality assurance gained through education and experience.
• A board perspective that aligns decisions to organizational objectives and long-term consequences of day-to-day activities.
• The ability to take strategic objectives and accept accountability to drive results through effective actions.
• The ability and willingness to change direction and focus to meet shifting organizational and business demands.
• The ability to set clear targets and use performance measures to assess risk and opportunities in order to effectively manage the assets of the business. The ability to create and contribute that values people, encourages trust, teamwork, and open communication, and provides participation, learning, feedback and recognition.
• The ability to effectively manage one self, demonstrates integrity, be productive under pressure, and achieve development goals.
• The ability to take strategic objectives and accept accountability, motivate and influence others, thinks globally, and leverages diversity.
• The ability to manage a multitude of resources and to be accurate and current with data and information.
• Position requires lifting (up to 40lbs), vision (20/20), standing (10%), sitting (40%), walking (50%), talking, typing and hearing.
• Salary range: Based on experience
• Hours of work: Monday thru Friday on an 8-hour shift, or as needed based on company demand.
Education/Experience:
  • Bachelor's degree in a scientific discipline or 1-2 years of related experience in the pharmaceutical industry, preferred.
  • 1-3 years of experience with MS Word, Excel, and PowerPoint preferred.
  • 1-2 years project management and coordinator experience preferred.

Working Conditions / Physical Requirements:
  • This position requires bending, typing, lifting (up to 40 lbs.), standing, sitting and walking throughout the facility.

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