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Gxp Quality Systems Jobs (NOW HIRING)

Zevra Therapeutics

Manager, Quality Systems

Boston, MA · On-site

About the role The Manager, Quality Systems is a hands-on, execution-focused role responsible for ... Develop and administer GxP training programs including role-based curricula, on-demand online ...

Merican

GCP Auditor, Quality Assurance

Paramus, NJ · On-site

This position will be focused on ensuring GXP compliance with regulatory authorities, driving and implementing the Company's compliance directives and supporting quality management systems to ensure ...

Parabilis Medicines

OR

Manage Core Quality Management System (QMS) Elements * Document Control ... Manage the lifecycle of GxP documents to ensure compliance with regulations and internal procedures.

kindeva

Quality Systems Specialist

Lexington, KY

Support the development, maintenance, and continuous improvement of quality systems to ensure compliance with current Good Manufacturing Practices (cGMPs), Good Practice (GxP) requirements, 21 CFR ...

kindeva

Quality Systems Specialist

Lexington, KY · On-site

Support the development, maintenance, and continuous improvement of quality systems to ensure compliance with current Good Manufacturing Practices (cGMPs), Good Practice (GxP) requirements, 21 CFR ...

kindeva

Quality Systems Specialist

Lexington, KY

Support the development, maintenance, and continuous improvement of quality systems to ensure compliance with current Good Manufacturing Practices (cGMPs), Good Practice (GxP) requirements, 21 CFR ...

kindeva

Quality Systems Specialist

Lexington, KY · On-site

Support the development, maintenance, and continuous improvement of quality systems to ensure compliance with current Good Manufacturing Practices (cGMPs), Good Practice (GxP) requirements, 21 CFR ...

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How much do gxp quality systems jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for gxp quality systems 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.

How does a GxP Quality Systems professional typically interact with cross-functional teams to ensure compliance?

GxP Quality Systems professionals regularly collaborate with departments such as manufacturing, regulatory affairs, IT, and R&D to ensure that all processes and documentation meet regulatory compliance standards. This often involves leading or participating in audits, facilitating training sessions, and supporting the implementation of corrective and preventive actions (CAPAs). Effective communication and project management skills are crucial, as the role requires coordinating efforts among diverse teams to maintain consistent quality practices across the organization.

What are the key skills and qualifications needed to thrive in GxP Quality Systems, and why are they important?

To thrive in GxP Quality Systems, you need a solid understanding of regulatory compliance (GMP, GLP, GCP), quality management principles, and often a background in life sciences or related fields. Familiarity with electronic quality management systems (eQMS), document control software, and relevant certifications such as Six Sigma or ASQ are commonly required. Strong attention to detail, problem-solving skills, and the ability to communicate effectively across departments are crucial soft skills. These competencies ensure that organizations maintain compliance with industry regulations, minimize risks, and uphold product quality and safety.

What are GxP Quality Systems?

GxP Quality Systems refer to a set of guidelines and regulations that ensure the quality, safety, and integrity of products and processes in the life sciences industry. 'GxP' stands for 'Good Practice' with the 'x' representing different fields such as Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), and Good Clinical Practice (GCP). These systems are designed to maintain compliance with regulatory requirements, prevent errors, and ensure products are consistently produced and controlled to high standards. Implementing GxP Quality Systems helps organizations avoid costly recalls, legal issues, and protects patient safety.
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Gxp Quality Systems jobs near you
Infographic showing various Gxp Quality Systems job openings in the United States as of May 2026, with employment types broken down into 94% Full Time, and 6% Part Time. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $53,326 per year, or $25.6 per hour.
Manager, Document Control and Training

Manager, Document Control and Training

Monte Rosa Therapeutics, Inc

Boston, MA • Remote

$90K - $120K/yr

Full-time

Posted 7 days ago

Job description

The Manager, Document Management and Training is responsible for the oversight of the Document Management and Training Management systems and processes. This includes supporting Quality Metric reporting at QMS Boards and Management Review meetings. This role will also support internal audits (related to document and training management), inspection readiness and regulatory authority inspections. In addition, this role will continuously improve GXP Document and Training processes and lead changes in the organization.



Oversee the strategy, development, and management of GxP Document and Training programs and related documentation, ensuring processes, systems, compliance, and content meet regulations, quality standards and business goals
Develop and implement strategic plans for documentation and training
Subject Matter Expert in electronic learning and document management systems managing user support, system improvements, and data.
Lead system upgrade and changes by partnering with the vendor and users/business on changes needed to support process and systems improvement as well as validation activities.
Oversee and ensure periodic reviews of controlled documents (such as Policy, SOP and Work Instructions) are performed and documented per SOP by working with the GXP business areas
Ensure compliance with legal and regulatory standards for document storage and retention
Oversee company training program partnering with GXP and Non GXP areas, including improving onboarding training experience and process with new employees
Ensure appropriate training requirements are defined in job specific role curriculum/matrix, including gathering training records as requested for audits and regulatory inspections
Oversee, create, implement and manage job specific curriculum/training matrix for GXP functional areas by partnering with GXP Business areas on curriculum training matrix
Assist Quality Management Review for oversight of document revisions, periodic reviews, training assignments, annual curriculum reviews and review metrics performance with this cross functional team
Support inspection readiness activities and regulatory inspections on site and remotely


• Bachelor’s degree in science or related field with 8 - 10+ years of GxP Quality experience in life sciences industry or equivalent experience
• Demonstrated experience in managing pharmaceutical quality systems such as Document Management, Training, Quality Metrics reporting
• Experienced in electronic Quality Management and Training Management Systems
• Excellent communication and time management skills
• Good presentation, verbal and written communication skills
• Ability to project manage and lead cross-functional teams in a fast-paced environment
• Demonstrated experience in leading, managing and improving pharmaceutical quality systems
• Strong leadership, technical, management, problem solving and project management skills
• Ability to quickly understand issues, needs and articulate potential solutions in fast paced environment
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