1

Quality System Coordinator Jobs (NOW HIRING)

OVERVIEW The Quality Systems Coordinator is a member of the Buffalo operations Quality Group and reports directly to the site Quality Manager. The role is primarily responsible for managing all ...

The HRIS Coordinator is responsible to make a compelling difference in the lives of our residents ... Oversees HR technology projects which include ensuring quality, timeliness and proper use of HR ...

The HRIS Coordinator is responsible to make a compelling difference in the lives of our residents ... Oversees HR technology projects which include ensuring quality, timeliness and proper use of HR ...

Maintain the document control system for the SQF program, including SOPs, policies, internal audits ... Communicate Quality performance data and update specifications for co-pack produced products.

Job Summary Assist in the implementation and maintenance of the company's Quality Management System (QMS). Manage customer and vendor return processes, while serving as a key point of contact for ...

next page

Showing results 1-20

Quality System Coordinator information

See salary details

$14

$26

$43

How much do quality system coordinator jobs pay per hour?

As of Jun 12, 2026, the average hourly pay for quality system coordinator in the United States is $26.94, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $31.25 per hour, depending on experience, location, and employer.

What does a quality systems coordinator do?

A quality systems coordinator manages and maintains a company's quality management system, ensuring compliance with industry standards and regulations. They develop, implement, and monitor quality procedures, conduct audits, and collaborate with teams to improve product or service quality. Proficiency with quality tools like ISO standards and audit skills are often required.

What are Quality System Coordinators?

Quality System Coordinators are professionals responsible for managing and maintaining a company's quality management system (QMS). They ensure that processes and procedures comply with industry standards and regulatory requirements, such as ISO 9001. Their duties often include organizing audits, updating documentation, training staff on quality protocols, and identifying opportunities for process improvement. By overseeing these systems, they help organizations achieve and maintain high standards of quality, safety, and efficiency.

What is the highest paying job as a coordinator?

The highest paying coordinator roles are often in specialized fields such as project management, supply chain, or quality assurance, with salaries increasing based on experience, certifications, and industry. For example, a Project Coordinator with PMP certification or a Supply Chain Coordinator in a high-demand industry can earn higher salaries, sometimes exceeding $80,000 annually.

What is the difference between Quality System Coordinator vs Quality Assurance Specialist?

AspectQuality System CoordinatorQuality Assurance Specialist
CertificationsISO 9001 Lead Auditor, CQEISO 9001 Lead Auditor, CQE
Work EnvironmentManufacturing, healthcare, or tech companies focusing on quality management systemsManufacturing, healthcare, or tech companies focusing on product quality testing and compliance
Primary FocusImplementing and maintaining quality management systemsPerforming quality inspections and testing to ensure product standards
Employer UsageUsed in organizations emphasizing quality system complianceUsed in organizations focusing on product quality assurance

The main difference is that a Quality System Coordinator focuses on implementing and maintaining quality management systems, ensuring compliance with standards like ISO 9001. In contrast, a Quality Assurance Specialist primarily conducts inspections and testing to verify product quality. Both roles require similar certifications and work in related environments, but their core responsibilities differ in scope and focus.

What is the role of a quality coordinator?

A quality system coordinator is responsible for developing, implementing, and maintaining quality management systems to ensure products and services meet company standards and regulatory requirements. They conduct audits, analyze data, and collaborate with teams to improve processes, often using tools like ISO standards and quality software. Strong attention to detail and knowledge of quality assurance practices are essential for this role.

What are some common challenges faced by a Quality System Coordinator, and how can they be addressed?

Quality System Coordinators often encounter challenges such as ensuring consistent compliance with evolving regulatory standards and maintaining clear communication across multiple departments. To address these, it’s important to stay updated on industry regulations, proactively conduct internal audits, and facilitate regular training sessions for staff. Building strong cross-functional relationships and utilizing robust documentation systems can greatly help in identifying potential non-conformities early and fostering a culture of continuous improvement.

What are the key skills and qualifications needed to thrive as a Quality System Coordinator, and why are they important?

To thrive as a Quality System Coordinator, you need a solid understanding of quality management systems (such as ISO 9001), process improvement, and data analysis, often supported by a relevant bachelor’s degree. Familiarity with document control software, audit management tools, and quality-related certifications like Six Sigma or ISO internal auditor certification is typically required. Excellent organizational skills, attention to detail, and strong communication abilities make someone stand out in this role. These skills ensure the effective implementation and continuous improvement of quality systems, which are vital for maintaining compliance and driving organizational excellence.

What does a quality coordinator do?

A quality coordinator is responsible for developing, implementing, and maintaining quality management systems to ensure products and services meet company standards and regulatory requirements. They conduct audits, analyze data, and collaborate with teams to improve processes, often using tools like ISO standards and quality software. Strong attention to detail and knowledge of quality assurance practices are essential for this role.
More about Quality System Coordinator jobs
What cities are hiring for Quality System Coordinator jobs? Cities with the most Quality System Coordinator job openings:
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 Coordinator jobs? States with the most job openings for Quality System Coordinator jobs include:
Quality Systems Coordinator

Quality Systems Coordinator

Catalent Pharma Solutions

Manassas, VA • On-site

Full-time

Life, PTO

Posted 8 days ago


Catalent rating

7.7

Company rating: 7.7 out of 10

Based on 50 frontline employees who took The Breakroom Quiz

45th of 71 rated pharmaceutical


Job description

Quality Systems Coordinator

Position Summary

  • Work Schedule: M-F 8am-4:30pm

  • 100% based on-site in Manassas, VA

Our Manassas, Virginia site is a part of the Consumer Health division and provides expanded capabilities in soft chews and lozenges. With extensive development and manufacturing expertise and a wide range of flavors, ingredients, and colors available, we can work with complex formulations to help create engaging new products consumers will love.

The Quality Coordinator will play a critical role in supporting the Quality function
by ensuring compliance with cGMP, SOPs, and regulatory requirements within
the Consumer Health facility.

The Role

  • Assist in leading and coordinating the resolution and completion of Deviations, CAPAs, and batch record backlogs, collaborating with functional teams or assignees to drive timely completion.

  • Partner with cross-functional teams to propose and implement process improvements for better visibility, accountability, and sustainability of quality systems, with the goal of avoiding future backlogs.

  • Support the management and tracking of Deviations, CAPAs, Batch Records, Change Controls, and related quality records to ensure timely follow-up and effectiveness.

  • Support preparation for internal and external audits and inspections and 24/7 inspection readiness.

  • Coordinate training activities, ensuring personnel are trained on relevant SOPs, policies, and quality procedures.

  • Assist in building a culture of quality awareness, accountability, and adherence to procedures across functions.

  • Assist in establishing process to maintain accurate training records and escalate gaps to management.

  • Other duties assigned.

The Candidate

  • HS Diploma or GED required.

  • Bachelor's degree in a scientific or technical discipline preferred (e.g., Chemistry, Biology, Quality, Engineering). Equivalent experience considered.

  • 2+ years of experience in a GMP-regulated manufacturing or consumer health/OTC environment.

  • Strong knowledge of quality systems (Deviations, CAPA, Change Control, Training, Documentation, Batch Records).

  • Experience supporting raw material specifications, SOP management, and training materials development preferred.

  • Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook); ability to create reports, trackers, and presentations. Power BI skill is preferred.

  • Strong communication and interpersonal skills; able to work collaboratively across departments and with external vendors.

  • Demonstrated ability to bring structure and accountability in environments requiring process discipline.

Why You Should Join Catalent

  • Spearhead exciting and innovative projects

  • Fast-paced, dynamic environment

  • High visibility to members at all levels of the organization

  • 152 hours of PTO + 8 paid holidays

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.


What Catalent employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


Catalent logo

About Catalent

Sourced by ZipRecruiter

Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Somerset, NJ, US

Year founded

2007

Social media