BeiGeneBE

Senior Director, Regulatory Affairs CMC

BeiGene is an innovative biotechnology company dedicated to developing affordable cancer treatments and improving patient access to advanced therapies globally.

BeiGene

Employee count: 5000+

Salary: 203k-273k USD

United States only

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:
BeiGene is seeking an experienced and instrumental regulatory professional to lead US biologics regulatory CMC team. This individual leads biologics regulatory CMC team based in US, partners with the counter-part based in China and cross-functional stakeholders in developing and executing biologics regulatory CMC strategies, oversees CMC-related regulatory submissions and health authority interactions throughout the product lifecycle. The individual also leads the team to establish or/and optimize biologics regulatory CMC processes. The individual manages direct reports of 10+ and reports to global head of regulatory CMC.

Essential Functions of the job:
• Lead, develop, and optimize the current biologics regulatory CMC team in US.
• Lead or/and oversee the development and implementation of biologics regulatory CMC strategies as well as lead the team authoring and managing CTD CMC sections to ensure on-time and high-quality submissions for investigational, marketing, and post-approval applications.
• Lead or/and oversee the development and implementation of biologics regulatory CMC strategy and execution in the preparation of timely responses to HA CMC questions, pre-meeting packages, and interactions with Heath Authorities.
• Work collaboratively with cross-functional stakeholders and communicate biologics regulatory CMC overarching strategies for alignment,
• Lead or/and oversee biologics CMC change control regulatory CMC impact assessment and ensure right regulatory CMC actions are taken timely.
• Lead or/and oversee regulatory risk assessment, identify key biologics regulatory CMC issues and mitigation activities needed throughout product lifecycle. Escalate the critical issues to senior management timely.
• Lead or/and oversee the establishment or/and optimization of internal regulatory CMC SOP, working instructions, and best practice, etc.
• Ensure proper regulatory CMC assessment and actions are taken when recalls or product complaints arise during product lifecycle.
• Review and approve regulatory CMC submission documents, SOPs/WIs, etc. in regulatory information system (RIM).
• Oversee or lead the assessment regulatory CMC aspects for due diligence projects.
• Lead or participate in external activities/conferences representing the company or the department when needed.

Supervisory Responsibilities:

Manage existing US based biologics regulatory CMC team of 10+ members.

Computer Skills:

Microsoft 360

Other Qualifications:
• Minimum 15 years of relevant pharmaceutical or biopharmaceutical industry experience in innovative drug CMC development, manufacturing, Quality, etc. including minimum 8 years of regulatory CMC experience with a Bachelor's Degree required.
• A proven record of leading Health Authority interactions, CTA, BLA/ submission, and subsequent response to HA queries.
• Demonstrated leadership of managing a team of 10+ people in global working environment is a must-have.
• Educational background in scientific disciplines and expertise in at least one area in pharmaceutical development (upstream, downstream, formulation, analytical, manufacturing, QC, QA, etc.).
• Experience in gene/cell therapy or/and medical device is a plus.
• In-depth knowledge of ICH requirements, global regulatory CMC requirements; Knowledge/experience in Quality Assurance and GMP regulation is a plus.
• Experience in authoring complex technical documents, CTD M2 and M3 sections, and their lifecycle management.
• Excellent oral and written communications skills are a must-have. Multilingual is a plus.
• Excellent interpersonal, communication, and problem-solving skills.
• Strong ability to effectively lead and influence in the collaborative and fast-moving work environment.
• Experience of using Veeva Vault system is a plus.

Travel:

As needed

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
Salary Range: $203,400.00 - $273,400.00 annually

BeOne 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. 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.

About the job

Apply before

Posted on

Job type

Full Time

Experience level

Director
Executive

Salary

Salary: 203k-273k USD

Location requirements

Hiring timezones

United States +/- 0 hours

About BeiGene

Learn more about BeiGene and their company culture.

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BeiGene is a global, science-driven oncology company focused on developing innovative and affordable medicines to improve treatment outcomes and access for patients worldwide. Since its founding in 2010, it has emerged as a leader in the field of biotechnology, primarily concentrating on oncology and hematology. The company is dedicated to enhancing cancer treatment by advancing a diverse portfolio of high-quality therapeutics that address numerous types of cancer, thereby reducing the financial barriers that patients often face.

BeiGene aims to revolutionize the oncology landscape through significant investments in research and development, fostering partnerships with leading healthcare professionals and organizations globally. One of its key philosophies is that cancer has no borders, and the company is committed to breaking barriers to access cancer treatment around the world. With more than 10,000 colleagues across five continents, BeiGene is working tirelessly to make its innovations accessible to all patients, regardless of their geographical location. Their success is reflected in various initiatives, such as collaborations with international health authorities and extensive clinical trial programs aimed at delivering new treatment options rapidly and effectively.

Claim this profileBeiGene logoBE

BeiGene

Company size

5000+ employees

Founded in

2010

Chief executive officer

John V. Oyler

Employees live in

View company profile

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BeiGene hiring Senior Director, Regulatory Affairs CMC • Remote (Work from Home) | Himalayas