BeiGene, Ltd. has proposed to change its name to BeOne Medicines Ltd. The new name is subject to shareholder approval and, once approved, use of the name will be phased in over 2025. There may be instances where “BeiGene” or “BeOne” are used to describe the company during this transition period. 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 incumbent will report to the Director, Distribution & Regional Quality, Europe Commercial Quality Head.
The Qualified Person (QP) Commercial Products, certifying all manufacturing steps up to the finished product level, is responsible for ensuring that each finished medicinal product batch has been manufactured and shipped in accordance with GMP, the terms of the MIA (Manufacturing and Import Authorization), the MA (Marketing Authorization) or made for export as per European Directive 2001/83/EC.
Responsible for batch certification of commercial finished product for the EU and Rest of the World following Annex 16 of EU regulation respectively.
Ideally also qualifies as a Responsible Person GDP taking accountabilities according EU GDP 2013/C 343/01.
Essential Functions of the job:
- Perform EU QP certification for commercial products under BeiGene responsibility.
- Oversight of Quality Management System (QMS) of QP operational responsibilities (EU GMP Annex 16, Annex 21).
- Ensure that all necessary steps have been completed according to the Quality Management System to assure compliance of batches with GMP, the MA and any other legal obligations in the Member State where certification is taking place.
- Maintenance of the Manufacturing and Import Authorization.
- Providing guidance and integration of European and other Health Authority regulations
- Ensuring GMP knowledge of self and others within both the Quality team and other functions are kept up to date.
- Participate in self-inspection activities and external audits as required.
- Support regulatory inspections, audits by clients / partners as required.
- Focusing on the management of authorized activities and the accuracy and quality of records.
- Ensure maintenance of supply to the market.
- Perform GDP activities as required.
- Support Product Complaints related investigation as necessary.
- Authorize recall in collaboration with Recall Committee.
- Support Deviations and Change Controls as necessary.
- Cooperate with all necessary departments to ensure that communication to the authorities is appropriate, coordinated and approved.
Experience and Qualifications:
- Pharmacist/MSc or Scientist recognized by Regulatory Authority to permit Qualified Person (QP) status as per article 49 of Directive 2001/83/EC.
- Solid foundation in QA and understanding of product
- quality requirements through the whole value chain (globally).
- 5+ years pharmaceutical or biotechnology industry experience.
- Pharmacist/MSc or Scientist recognized by Regulatory Authority to permit Qualified Person (QP) status as per article 49 of Directive 2001/83/EC
- Has an understanding of regulatory requirements linked to combination products
- In-depth GMP experience in a quality and manufacturing function.
Core Knowledge and Skill Requirements:
- In-depth knowledge of Quality principles, concepts, industry practices and standards.
- Working Knowledge and experience with EudraLex EU GMP Guidance, 21CFR210, 21CFR211, ICHQ7 as well as international regulations.
- Ability to work independently with scientific/technical personnel.
- Experience with regulatory compliance inspections.
- Apply principles of logical and scientific thinking to a wide range of intellectual and practical problems.
- Must possess good presentation skills to speak effectively before groups; ability to respond.
- Excellent interpersonal skills, including listening, writing, negotiations, facilitations, attention to detail.
- Experienced with working cross-regions Supply Chain, Regulatory, and external service providers
Computer Skills:
- PC literacy required; MSOffice skills (Outlook, Word, Excel, PowerPoint), SAP
- Ability to work on a computer for extended periods of time
Other Qualifications:
- Good Project Management Skill Set
- Clear communication, sense of urgency and sensitive for the needs of the organization.
- Languages: Fluent in Dutch, English (C2), German is a plus
Travel:
- May travel occasionally
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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