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Associate Director of R&D Quality Systems, Strategy, and Excellence (Strategy & Innovation)

extra holidays - extra parental leave
Remote: 
Full Remote
Contract: 
Salary: 
134 - 184K yearly
Experience: 
Senior (5-10 years)
Work from: 

Offer summary

Qualifications:

Bachelor's degree with 8+ years experience, Master’s degree with 6+ years experience, PhD/MD/PharmD with 4+ years experience, Expert knowledge of GCP, FDA, EMA, ICH requirements, Expertise in data analytics and risk management.

Key responsabilities:

  • Lead and execute risk-based quality strategy
  • Implement change management strategies for quality improvements
  • Develop strong cross-functional partnerships
  • Modernize and streamline RD Quality Management System
  • Ensure compliance with industry standards and best practices
BeiGene logo
BeiGene Biotech: Biology + Technology XLarge http://www.beigene.com/
5001 - 10000 Employees
See more BeiGene offers

Job description

BeiGene 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 Associate Director of R&D Quality Systems, Strategy, and Excellence (Strategy & Innovation) is responsible for leading initiatives that advance a proactive, data-driven quality culture across the organization. This role focuses on leveraging quality metrics, trends, and data insights to implement risk-based strategies that improve quality outcomes and enhance decision-making processes. The Associate Director will drive cultural change and system modernization, ensuring that quality management systems (QMS) evolve across R&D to meet industry standards and future needs. A key focus will be on strategic alignment, collaborating cross-functionally and cross-GxP to ensure that R&D Quality Management Systems (QMS) are optimized for both compliance and innovation. This role is pivotal in fostering a forward-thinking quality culture and integrating data-driven insights into all aspects of quality management and operations.

The position is responsible for ensuring that BeiGene’s research, development, and pharmacovigilance activities comply with all relevant regulatory requirements, internal standards, and industry best practices. This individual will lead a proactive approach to quality assurance, quality by design, data integrity, and continuous improvement across the entire R&D Quality function while maintaining a fit-for-purpose QMS. The Associate Director will lead a team of quality professional and oversee R&D Quality Systems, Strategy, and Excellence activities.

Essential Functions of the Job:

Manage and oversee R&D Quality activities which include, but are not limited to:

  • Lead the development and execution of a data-driven, risk-based quality strategy, using real-time data and analytics to identify risks, anticipate quality challenges, and proactively prevent quality events.
  • Leverage quality metrics and data from across the organization to inform strategic decisions, improving both operational efficiency and regulatory compliance. Help drive implementation of Risk Based Quality Management and Quality by Design principles.
  • Champion a proactive quality culture, fostering an environment where quality is integrated into every facet of the organization’s processes and systems.
  • Implement change management strategies to advance quality practices, enabling the organization to shift from reactive quality control to proactive quality assurance.
  • Engage leadership and teams at all levels to drive cultural change, reinforcing the importance of quality as a core business value.
  • Align the organization’s quality goals with broader strategic objectives, ensuring that quality initiatives support overall business goals.
  • Work with executive and senior leadership to establish quality as a key driver of innovation, operational excellence, and business success.
  • Provide thought leadership and guidance on the evolving landscape of quality management, ensuring the organization stays ahead of industry trends and regulatory requirements.
  • Build and maintain strong cross-functional partnerships across GxP areas (GCP, GMP, GVP) to ensure alignment in quality practices and systems.
  • Collaborate closely with teams in R&D, Regulatory, Clinical Operations, and IT to ensure that data-driven quality initiatives are integrated into all aspects of the development lifecycle.
  • Lead efforts to modernize the R&D Quality Management System (QMS), ensuring it is fit for purpose, scalable, and adaptable to emerging industry trends and regulatory changes.
  • Implement tools and technologies to streamline quality processes, reduce complexity, and enhance transparency across the R&D QMS.
  • Facilitate discussions on quality trends, risk areas, and opportunities for improvement, ensuring that leadership is equipped to make informed decisions.
  • Continuously monitor industry trends and regulatory changes, ensuring that the organization’s quality strategy is forward-thinking and adaptable to the evolving landscape.
  • Translate global quality themes into actionable initiatives, ensuring that R&D and broader organizational efforts remain competitive and compliant.
  • Represent the organization in industry forums and collaborative efforts, ensuring that the company is at the forefront of quality innovation and modernization.
  • Engage with external partners and regulatory bodies to influence industry standards and adopt best practices in proactive, data-driven quality management.
  • Establish strong partnerships with key business stakeholders, including Clinical Operations, Clinical Development, Regulatory Affairs, Data Management, Biostats, GPS, RBQM, etc.
  • Support the inspection readiness activities and participate in managing regulatory health authority inspections as needed Collaborate with cross-functional departments (e.g., Clinical Operations, Regulatory, Pharmacovigilance, and Laboratory teams) to align quality strategies and enhance compliance across the organization.
  • Drive continuous improvement initiatives and manage quality system infrastructure to support global R&D quality processes.

Additional Qualifications:

  • Expert knowledge of GCP, FDA, EMA and ICH requirements.
  • Bachelor's degree with 8+ years, Master’s degree with 6+ years, or PhD/MD/PharmD with 4+ years of R&D quality assurance experience.
  • Expertise in data analytics, risk management, and quality metrics tracking.
  • Strong leadership skills with the ability to drive cross-functional and cross-GxP collaboration.
  • Excellent communication and change management skills, with the ability to influence and inspire at all levels.

Supervisory Responsibilities:  

This position may include managing staff: coaching and mentoring of junior staff with training/orientation/qualification and development plan for new Quality staff when required.

BeiGene Global Competencies

When we exhibit our values of Patients First, Collaborative Spirit, Bold Ingenuity and Driving Excellence, 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: $134,400.00 - $184,400.00 annually

BeiGene 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 BeiGene 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 and we value diversity. BeiGene 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.

Required profile

Experience

Level of experience: Senior (5-10 years)
Industry :
Biotech: Biology + Technology
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Coaching
  • Communication
  • Leadership
  • Collaboration
  • Entrepreneurship
  • Analytical Thinking
  • Mentorship

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