Director, GTS Quality Systems

BeOne Medicines; Hopewell (NJ); On-site; USD 173,000 - 233,000; Full time

Benefits offered by this job

Medical benefits

Dental benefits

Vision benefits

401(k)

FSA/HSA

Life Insurance

Paid Time Off

Wellness program

Job summary

BeOne Medicines in New Jersey is seeking a Director, Quality Systems to lead technology operations and lifecycle support for enterprise QMS platforms, including Veeva Quality applications.

You will translate QA requirements into technology plans, manage budgets and vendors, and ensure compliant, validated systems across GxP environments. The role reports to Sr. Director Quality Systems and includes overseeing global deployments and ensuring data integrity and inspection readiness.

Qualifications

• Bachelor’s degree in Engineering, Computer Science or related field with 7+ years in QA systems.
• Master’s degree in Engineering, Computer Science or related field with 5+ years in QA systems.
• Experience with QA processes such as document control, training, deviations, CAPA, change control, audits and inspection readiness.

Responsibilities

• Lead deployment and operational support for enterprise QMS platforms, especially Veeva Quality applications.
• Oversee validation, data integrity, and CSA activities across QA systems.
• Coordinate vendor and managed services for quality technology projects.
• Align quality business requirements with technology delivery plans.
• Manage budgets, forecasting, and roadmap execution for Quality tech.
• Ensure systems remain validated and compliant with 21 CFR Part 11.

Skills

Veeva Quality applications

GxP QA processes

Vendor management

Incident & problem management

Education

Bachelor’s degree in Engineering, Computer Science or related technological field

Master’s Degree in Engineering, Computer Science or related technological field

Tools

ValGenesis

Veeva Quality applications

Job description

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.

General Description

• The Director, Quality Systems will report to the Sr. Director, Quality Systems and Validation and serve as a Global Technology Solutions leader responsible for the technology operations, deployment, and lifecycle support of enterprise Quality Management System (QMS) platforms, Veeva Quality applications, other Quality Assurance systems, and related GxP applications.
• This role will be primarily GTS-facing, with accountability for translating Quality business needs and QMS process requirements into technology execution plans, managing application operations, coordinating project delivery, overseeing vendors and managed service partners, and ensuring reliable, compliant, and scalable Quality technology solutions. The individual will work closely with Global Quality, site Quality, business process owners, and GTS functions to support the Quality Systems roadmap, manage budgets and forecasts, prioritize demand, and deliver system enhancements and projects.
• The individual must have hands-on configuration and system administration experience with Veeva Quality applications and a strong working understanding of Quality Assurance processes supported by systems such as document management, training, deviations, CAPA, change control, complaints, audits, risk management, and inspection readiness. The role must bring a strong understanding of the Quality and regulated GxP environment, including data integrity, change control, validation, and CSA expectations.

Essential Functions Of The Job

• Lead GTS delivery, deployment, and operational support for enterprise QMS platforms and other Quality Assurance systems, with emphasis on Veeva Quality applications and related integrations.
• Manage application operations across QMS and QA technology platforms, including incident and problem management, enhancement intake, configuration oversight, release coordination, service performance, operational metrics, user support, and lifecycle planning.
• Experience leading enterprise QMS deployments, enhancements, application support, and project delivery for Quality Assurance systems in a pharmaceutical, biotechnology, or life sciences environment is required. Hands-on experience with Veeva Quality applications is required, including practical involvement in implementation, configuration review, release support, testing coordination, issue resolution, and operational support.
• Translate Quality Assurance business requirements, QMS process needs, and compliance expectations into practical technology plans, Veeva configuration and enhancement approaches, delivery commitments, system changes, and support models in partnership with Quality stakeholders and GTS functions.
• Strong GTS or IT delivery experience is required, including service management, vendor management, release coordination, budget management, demand management, roadmap support, and cross-functional technology delivery. Working knowledge of 21 CFR Part 11, data integrity expectations, GxP computer system validation, and Computer Software Assurance principles is required, with emphasis on applying approved procedures and maintaining validated systems rather than designing enterprise validation strategy.
• Experience with Quality platforms such as Validation Management System (ValGenesis), Inspection Management, AI tools used in pharma, laboratory, manufacturing, training and/or other regulated Quality systems is preferred.
• Manage delivery of Quality technology projects and initiatives, including scope, schedule, resources, budget, risks, dependencies, vendor performance, stakeholder communication, and operational readiness.
• Provide hands-on leadership for Veeva Quality deployment activities, including requirements clarification, solution design input, configuration review, data and integration considerations, testing coordination, defect resolution, release readiness, and post-go-live stabilization.
• Support deployment and enhancement of QA systems supporting document control, training, deviations, CAPA, change control, complaints, audits, quality risk management, supplier quality, inspection readiness, and related Quality processes.
• Demonstrated ability to work across GTS, Quality, site stakeholders, Procurement, Finance, and vendors to deliver reliable, compliant, and business-aligned technology solutions.
• Support creation, maintenance, and execution of the Quality Systems roadmap by partnering with Quality and GTS leadership to consolidate demand, assess technical feasibility, estimate effort and cost, sequence priorities, and convert roadmap items into executable delivery plans.
• Manage department and project budgets, including supporting forecasting, annual planning input, purchase requisitions, purchase orders, vendor spend oversight, accrual support, and routine financial reporting to leadership.
• Partner with GTS architecture, infrastructure, cybersecurity, data, integration, service management, procurement, finance, and external vendors to deliver and support Quality technology solutions.
• Ensure Quality systems remain in a validated and compliant state by following approved SOPs, change control, release management, validation, CSA, data integrity, access management, and system lifecycle procedures.
• Coordinate and support validation and CSA deliverables for system changes and projects, including planning input, documentation coordination, testing evidence review, deviation support, release readiness, and operational handover.
• Maintain strong working knowledge of Quality business processes, GxP expectations, inspection readiness, and regulated system operations to ensure technology decisions appropriately support the Quality organization.
• Monitor technology service trends, compliance risks, project status, resource constraints, and vendor performance; elevate issues and recommend practical improvements to strengthen operational reliability and business value.
• Provide clear communication to Quality and GTS leadership regarding project delivery, operational performance, roadmap progress, budget status, risks, tradeoffs, and decisions required.

Supervisory Responsibilities

• Will have direct supervisory responsibility for approximately three direct reports supporting Quality technology operations, application support, and project delivery.
• Provide coaching, performance management, workload prioritization, and professional development for team members in a GTS operating model.
• Establish clear team priorities, operating rhythms, service expectations, project assignments, and accountability for technology operations, system lifecycle activities, and delivery commitments.
• Promote collaboration across GTS functions, Quality business stakeholders, site teams, vendors, managed service partners, and shared service functions to resolve issues and deliver business outcomes.
• Maintain strong communication, technical writing, stakeholder management, financial management, and presentation skills appropriate for cross‑functional technology and Quality leadership forums.

Education Required

• Bachelor’s degree in Engineering, Computer Science or related technological field and minimum 7 years of relevant work experience in building, configuring, and supporting Quality Assurance and/or Quality Control systems, or
• Master’s Degree in Engineering, Computer Science or related technological field and minimum 5 years of relevant work experience in building, configuring, and supporting Quality Assurance and/or Quality Control systems.

Other Qualifications

• Experience with QA business processes such as document control, training, deviations, CAPA, change control, complaints, audits, quality risk management, supplier quality, and inspection readiness is required.

Travel

• Periodic domestic and international travel Less than 20%

Global Competencies

When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.

• Fosters Teamwork
• Provides and Solicits Honest and Actionable Feedback
• Self-Awareness
• Acts Inclusively
• Demonstrates Initiative
• Entrepreneurial Mindset
• Continuous Learning
• Embraces Change
• Results‑Oriented
• Analytical Thinking/Data Analysis
• Financial Excellence
• Communicates with Clarity

Salary Range: $172,500.00 - $232,500.00 annually

BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.

We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans’ Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact [e-mail].