Director QMS Process Owner Training and Document Management

Reposted 4 Days Ago
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Hiring Remotely in US
Remote
165K-225K Annually
Senior level
Biotech
The Role
The QMS Process Owner is responsible for overseeing the effectiveness, compliance, and continuous improvement of Quality Management System processes. Key functions include developing and maintaining QMS processes, ensuring compliance with regulatory and organizational requirements, conducting performance monitoring, and leading process improvement initiatives. The role also involves training employees and representing the process area during audits.
Summary Generated by Built In

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 QMS Process Owner is responsible for overseeing and ensuring the effectiveness, compliance, and continuous improvement of the Quality Management System processes. This role involves designing, implementing, and maintaining QMS processes in alignment with organizational goals, regulatory requirements, and industry standards. The QMS Process Owner serves as the subject matter expert and point of accountability for their assigned QMS processes, driving a culture of quality and continuous improvement across the organization.

Essential Functions of the job:

  • Develop, implement, and maintain GxP Training and GxP Documentation management processes to ensure compliance with regulatory, customer, and organizational requirements.
  • Define and implement GxP training strategy for the organization assuring effective and efficient GxP personnel qualification.
  • Represent Global Quality at the Enterprise Learning and Development Council
  • Act as the primary point of contact for questions, issues, and audits related to the assigned QMS processes.
  • Define clear roles, responsibilities, and accountabilities for process execution.
  • Ensure processes are compliant with applicable standards (e.g., ISO 9001, ISO 13485, ICH Q10) and regulations (e.g., FDA, EMA).
  • Maintain documentation, including procedures, templates, and work instructions, to support the QMS processes.
  • Monitor process performance using key performance indicators (KPIs) and other metrics.
  • Identify opportunities for process optimization and lead improvement initiatives.
  • Conduct root cause analyses and implement corrective and preventive actions (CAPAs) for process-related issues.
  • Develop and deliver training for employees involved in the assigned processes.
  • Provide guidance and support to ensure proper execution of QMS processes by stakeholders.
  • Establish and lead user communities for the assigned process to collaborate with cross-functional teams to integrate quality processes into business operations.
  • Ensure effective communication of process changes and updates to relevant stakeholders.
  • Represent the process area during audits, inspections, and management reviews
  • Perform other responsibilities as assigned.

Skills and Qualifications:   

  • Advanced degree in life sciences, quality management, or related field
  • 5+ years of progressive leadership experience in quality management within a regulated industry (pharmaceutical, biotechnology, or medical devices).
  • Proven experience with QMS implementation and process ownership.
  • Deep understanding of quality management principles, regulatory frameworks, and industry standards (e.g., ISO 13485, ICH Q10).
  • Expertise in managing core QMS processes such as CAPA, change control, and deviation management.
  • Excellent communication, negotiation, and stakeholder management skills.
  • Strong analytical and problem-solving skills.
  • Proficient in data analysis, project management, and quality improvement methodologies (e.g., Lean, Six Sigma).
  • Ability to communicate complex information clearly and effectively across business functions

Travel:  up to 20% internationally

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: $164,600.00 - $224,600.00 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.

Top Skills

Capa
Change Control
Data Analysis
Deviation Management
Ich Q10
Iso 13485
Project Management
Quality Improvement Methodologies
Quality Management
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The Company
HQ: Cambridge, MA
2,862 Employees
On-site Workplace
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

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