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Gxp Quality Systems Jobs (NOW HIRING)

Jj

Senior Director, Quality Systems (USA)

Raritan, NJ · On-site

Provide Quality leadership and guidance for strategic system investments, ensuring compliance with applicable GxP, computerized system validation, and quality requirements. * Develop scalable ...

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How much do gxp quality systems jobs pay per hour?

As of Jul 5, 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 June 2026, with employment types broken down into 100% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $53,326 per year, or $25.6 per hour.

Senior Director, Quality Systems (USA)

Jj

Titusville, NJ • On-site

Full-time

Retirement, PTO

Posted 9 days ago

Job description

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Quality

Job Sub Function:

Quality Documentation

Job Category:

People Leader

All Job Posting Locations:

Horsham, Pennsylvania, United States of America, New Brunswick, New Jersey, United States of America, Raritan, New Jersey, United States of America, San Diego, California, United States of America, Titusville, New Jersey, United States of America

Job Description:

Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s).

  • USA Req#: R-084664

  • UK Req#: R-084838

  • Switzerland Req#: R-084835

  • Belgium/Ireland Req#: R-084839

Johnson & Johnson Innovative Medicine Quality & Compliance, Quality Management & Digital team is recruiting for a Senior Director, Quality Systems. This is a global leadership role reporting to the Vice President, Quality Management & Digital, Innovative Medicine Quality & Compliance. The role is responsible for shaping, operating, and continuously improving the Quality Management System technology and operational landscape that enables compliant, efficient, and modern GxP quality processes across Innovative Medicine.

Role Summary

The Senior Director, Quality Systems will provide enterprise leadership for the strategy, roadmap, operation, and sustainment of core QMS systems and enabling platforms. This leader will partner closely with Innovative Medicine Quality & Compliance, Enterprise Quality, IM Digital Quality, JJT, Global Process Owners, and regional stakeholders to ensure QMS systems support business priorities, regulatory expectations, inspection readiness, and continuous improvement.

The role will lead global QMS system strategy, business ownership, system investment planning, and operational services, including support for Transcend, QMS Operations, LMS, EDMS, and related QMS workflows. This leader will also provide strategic direction, people leadership, governance, and stakeholder engagement to advance a scalable, compliant, and digitally enabled QMS ecosystem.

Key Responsibilities

  • Lead the global QMS systems strategy, investment roadmap, and governance model to support current and future Innovative Medicine Quality & Compliance priorities.

  • Oversee planning, execution, sustainment, and continuous improvement of QMS system initiatives and investments.

  • Serve as business owner for core QMS systems and enabling platforms, including LMS, EDMS, QMS workflows, and related operational capabilities.

  • Partner with Global Process Owners, Enterprise Quality, IM Digital Quality, JJT, and regional stakeholders to ensure systems are aligned with process needs, quality architecture, and enterprise priorities.

  • Provide Quality leadership and guidance for strategic system investments, ensuring compliance with applicable GxP, computerized system validation, and quality requirements.

  • Develop scalable operational services and support models that enable consistent, efficient, and compliant QMS operations.

  • Represent IM Quality Systems in enterprise transformation efforts, governance forums, and senior leadership discussions.

  • Lead, develop, and engage a global team, fostering accountability, collaboration, inclusion, and high performance.

  • Monitor internal and external trends in Quality Systems and digital capability to identify opportunities for simplification, standardization, innovation, and value creation.

  • Develop dashboards, metrics, and leadership updates to provide visibility into QMS system performance, investment progress, risks, and opportunities.

Qualifications

  • Bachelor's degree is required.

  • Minimum of 12 years of relevant experience in Quality Systems, Quality Operations, digital quality, program management, transformation leadership, or a related regulated environment.

  • Experience with Quality Management System platforms and solutions supporting GxP processes.

  • Demonstrated experience shaping system roadmaps, leading system investments, and translating business needs into executable plans.

  • Strong understanding of quality systems, regulatory expectations, computerized system validation, and continuous improvement principles.

  • Proven ability to influence, collaborate, and drive alignment across senior leaders, global teams, and matrixed stakeholders.

  • Strong strategic thinking, communication, presentation, analytical, and decision-making skills.

  • Experience leading teams, developing talent, and creating an inclusive, high-performance team environment.

  • Ability to manage multiple priorities and deliver high-quality outcomes in a complex, global organization.

Preferred Qualifications

  • Advanced degree such as M.S., MBA, Ph.D., Pharm.D., or equivalent is preferred.

  • Experience in pharmaceuticals, healthcare, medical technology, or another highly regulated industry.

  • Experience with QMS platforms such as Veeva, TrackWise, ComplianceWire, EDMS, LMS, or similar systems.

  • Experience partnering with digital, technology, process ownership, and quality organizations to deliver enterprise-scale transformation.

  • Experience developing metrics, dashboards, and executive-level updates to support decision-making and governance.

Travel

  • This position may require up to 10% domestic and international travel based on business needs.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center (ra-employeehealthsup@its.jnj.com) or contact AskGS to be directed to your accommodation resource.

Required Skills:

Preferred Skills:

Business Alignment, Compliance Management, Compliance Policies, Developing Others, Inclusive Leadership, ISO 9001, Leadership, Process Improvements, Quality Control (QC), Quality Standards, Quality Systems Documentation, Stakeholder Engagement, Standard Operating Procedure (SOP), Statistical Process Control (SPC), Systems Thinking, Technical Writing

The anticipated base pay range for this position is :

$178,000.00 - $307,050.00

Additional Description for Pay Transparency:

Subject to the terms of their respective plans, employees are eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).
This position is eligible to participate in the Company's long-term incentive program.
Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:
Vacation -120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado -48 hours per calendar year; for employees who reside in the State of Washington -56 hours per calendar year
Holiday pay, including Floating Holidays -13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
Parental Leave - 480 hours within one year of the birth/adoption/foster care of a child
Bereavement Leave - 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
Caregiver Leave - 80 hours in a 52-week rolling period10 days
Volunteer Leave - 32 hours per calendar year
Military Spouse Time-Off - 80 hours per calendar year
For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits

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