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Salary
$25k – $103k per year (Estimated)
Location
In office (Basel)
Seniority
Junior · 2+ years exp
Employment
Full-Time
Overview
Company
Impact
Profile match
BeOne Medicines is a global biotechnology company headquartered in Basel, Switzerland, and founded in 2010. The firm focuses on the discovery, development, and commercialization of innovative molecularly targeted and immuno-oncology drugs for treating various types of cancer. It maintains a significant presence across North America, Europe, and Asia-Pacific, operating large-scale manufacturing facilities and an extensive internal clinical research organization.

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 Quality Assurance Specialist, Commercial, executes Work Center Team (WCT) activities for externally manufactured commercial APIs, drug products, and finished goods. This role is responsible for batch record review, batch disposition, quality system execution, and regulatory activities that enable compliant, risk-based, and timely commercial product release across the global commercial supply network.

Essential Functions of the job:

  • Support multiple commercial products and CMOs while managing competing priorities in a fast-paced environment.

  • Perform batch record review and data verification for commercial APIs, drug products and finished goods manufactured at CMOs, in accordance with approved procedures.

  • Prioritize and execute batch review activities to support commercial supply commitments and product availability.

  • Perform batch disposition activities, including compilation, verification, and documentation of quality information supporting commercial product release.

  • Escalate quality or compliance observations identified during batch review in accordance with established procedures.

  • Initiate and manage quality system records (e.g., deviations, CAPAs) within the electronic Quality Management System (eQMS), including lifecycle tracking through closure.

  • Perform data verification and document completeness checks to support inspections, audits and regulatory requests.

  • Support regulatory request management, including document retrieval, archival and readiness for repeat requests.

  • Maintain trackers and metrics related to batch record review, record status and WCT deliverables.

  • Author, revise and maintain internal quality documents (i.e., SOPs, work instructions) as assigned.

  • Collaborate with CMO Managers and cross-functional stakeholders to support batch disposition, issue resolution and commercial supply continuity.

  • Perform other WCT responsibilities as assigned.

Education

  • Bachelor’s degree in scientific discipline or equivalent combination of education and 2+ years of work experience.

Required Experience

  • Experience in the pharmaceutical or biotechnology industry

  • Experience working in a GMP-regulated Quality function

  • Commercial Quality Assurance experience preferred

  • Previous experience navigating external manufacturing models would be an advantage

Knowledge, Skills, and Abilities

  • Strong understanding of GMP principles and pharmaceutical quality systems.

  • Working knowledge of pharmaceutical GMP requirements, including ICH Q7, ICH Q9, ICH Q10, 21 CFR Parts 210/211, EU GMP, and applicable global regulations.

  • Ability to support risk-based quality activities and quality system execution in accordance with established procedures and governance.

  • Ability to work independently in a regulated environment and manage competing priorities.

  • Strong analytical, problem-solving and organizational skills.

  • Excellent written, verbal and interpersonal communication skills.

  • High attention to detail and ability to collaborate cross-functionally.

Computer Skills

  • Proficiency in Microsoft Office applications (Outlook, Word, Excel, PowerPoint, Teams)

  • Experience with electronic Quality Management Systems (eQMS) required

Travel

  • Approximately 5 - 10% travel may be required

Salary Range Switzerland: 86,600.00 CHF - 108,200.00 CHF

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.

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