Director, GTS Quality Systems

Posted 8 Days Ago
Be an Early Applicant
Hopewell, VA, USA
In-Office
173K-233K Annually
Senior level
Biotech
The Role
Leads global technology operations, deployment, support, and lifecycle management for Veeva Quality, QMS, and related GxP systems. Translates Quality requirements into technology roadmaps, configurations, enhancements, projects, and support models. Oversees validation, CSA, compliance, vendors, budgets, service performance, and system operations while managing a team of three. Partners across Quality, GTS, Finance, Procurement, cybersecurity, infrastructure, and vendors to deliver reliable, compliant, and scalable solutions.
Summary Generated by Built In

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; escalate 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 [email protected].

Skills Required

  • Bachelor’s degree in Engineering, Computer Science, or a related technology field and at least 7 years of relevant experience, or a master’s degree and at least 5 years of relevant experience
  • Experience building, configuring, and supporting Quality Assurance and/or Quality Control systems in a pharmaceutical, biotechnology, or life sciences environment
  • Hands-on experience with Veeva Quality applications, including implementation, configuration review, release support, testing coordination, issue resolution, and operational support
  • Experience with Quality Assurance processes including document control, training, deviations, CAPA, change control, complaints, audits, quality risk management, supplier quality, and inspection readiness
  • Strong GTS or IT delivery experience, 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, GxP computer system validation, and Computer Software Assurance principles
  • Experience managing Quality technology projects involving scope, schedule, resources, budgets, risks, dependencies, vendors, stakeholders, and operational readiness
  • Experience with ValGenesis, Inspection Management, AI tools used in pharma, laboratory, manufacturing, training, or other regulated Quality systems
  • Experience supervising, coaching, and developing technology operations or project delivery staff

BeiGene Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about BeiGene and has not been reviewed or approved by BeiGene.

  • Equity Value & Accessibility Equity grants and stock programs are widely available across roles, including RSU grants at hire and opportunities to participate in company equity plans. Total compensation commonly includes equity alongside base pay and incentives.
  • Healthcare Strength Health coverage is described as comprehensive and high quality, with multiple mentions of “top notch” medical benefits. This strength is consistently highlighted as a key component of the package.
  • Retirement Support Retirement offerings include a 401(k) with a competitive employer match. These features contribute to a strong overall compensation bundle.

BeiGene Insights

Am I A Good Fit?
beta
Get Personalized Job Insights.
Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.

The Company
HQ: Cambridge, MA
2,862 Employees
Year Founded: 2010

What We Do

BeiGene is a global biotechnology company that is developing and commercializing innovative and affordable oncology medicines to improve treatment outcomes and access for far more patients worldwide. With a broad portfolio, we are expediting development of our diverse pipeline of novel therapeutics through our internal capabilities and collaborations. We are committed to radically improving access to medicines for far more patients who need them. Our growing global team of more than 8,500 colleagues spans five continents, with administrative offices in Beijing, China; Cambridge, U.S.; and Basel, Switzerland. To learn more about BeiGene, please visit www.beigene.com and follow us on Twitter at @BeiGeneGlobal. See our community guidelines: bit.ly/39o3O6j

Similar Jobs

Zscaler Logo Zscaler

Senior Manager, Enterprise Data Platform

Cloud • Information Technology • Security • Software • Cybersecurity
Easy Apply
Remote or Hybrid
USA
8697 Employees
196K-245K Annually

Shield AI Logo Shield AI

Systems Engineer

Aerospace • Artificial Intelligence • Machine Learning • Robotics • Software
In-Office or Remote
5 Locations
144K-210K Annually

Shield AI Logo Shield AI

Senior Systems Engineer

Aerospace • Artificial Intelligence • Machine Learning • Robotics • Software
In-Office or Remote
5 Locations
144K-210K Annually

inKind Logo inKind

Automation Engineer

eCommerce • Fintech • Food • Mobile • Social Impact
Remote or Hybrid
USA
170 Employees
95K-120K Annually

Similar Companies Hiring

Formation Bio Thumbnail
Artificial Intelligence • Big Data • Healthtech • Biotech • Pharmaceutical
New York, NY
150 Employees
SOPHiA GENETICS Thumbnail
Software • Healthtech • Biotech • Big Data • Artificial Intelligence
Boston, MA
450 Employees
Pfizer Thumbnail
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
New York, NY
121990 Employees

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account