Director,QMS Process Owner – Global Change Control

BeOne Medicines; Basel; Vor Ort; CHF 120’000 - 180’000; Vollzeit

Zusammenfassung

BeOne Medicines is seeking a Director, QMS Process Owner to oversee and enhance our Quality Management System processes. The role requires extensive experience in quality management within the pharmaceutical industry, ensuring compliance with regulatory standards while fostering a culture of continuous improvement. The ideal candidate will have strong leadership capabilities and a deep understanding of quality management principles, ready to drive significant impacts within a growing organization.

Qualifikationen

• 10+ years of related experience.
• 5+ years of progressive leadership in quality management.
• Proven experience with QMS implementation.

Aufgaben

• Develop, implement, and maintain the Global Change Control process.
• Ensure compliance with ISO 9001 and ISO 13485 standards.
• Conduct root cause analyses and implement CAPAs for process-related issues.

Kenntnisse

Quality Management principles

Regulatory frameworks

Change control management

Analytical thinking

Stakeholder management

Project management

Problem-solving

Communication skills

Ausbildung

Bachelor's degree in life sciences

Advanced degree (preferred)

Jobbeschreibung

Director,QMS Process Owner – Global Change Control

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Director,QMS Process Owner – Global Change Control

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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, 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 Director, 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 the Global Change Control process to ensure compliance with regulatory, customer, and organizational requirements.
• Act as the primary point of contact for questions, issues, and audits related the Global Change Control process.
• Define clear roles, responsibilities, and accountabilities for process execution.
• Ensure process is 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 the process 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.
  
  

Supervisory Responsibilities: NA

Education Required: Bachelor's degree in life sciences, quality management, or related field required. Advanced degree preferred.

Skills And Qualifications

• 10+ years of related experience
• 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

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
  
  

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.

Seniority level

• Seniority level

  Director

Employment type

• Employment type

  Full-time

Job function

• Job function

  Management and Manufacturing

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