Senior Scientist, Biomarker Laboratory, Mass Spectrometry, BeOne Medicines USA, Inc., US

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:

We are seeking an accomplished and self-motivated Senior Scientist with deep expertise in mass spectrometry-based bioanalysis to join our Clinical Biomarker laboratory. This role will lead the development, validation, and execution of quantitative and qualitative mass spectrometry assays to support pharmacodynamics study and biomarker research in clinical trials as well as proteomics exploration. The role requires a strong background in bioanalytical chemistry, protein/peptide quantification in biological matrices, deep understanding of relevant regulatory guidance, as well as hands-on experience in mass spectrometry-based biomarker method development, validation and clinical sample analysis.

Essential Functions of the job:

• Build and establish LC-MS/MS workflow and data analysis pipelines
• Lead the design, development and validation of LC-MS/MS assays for target protein, peptides and other biomarker classes in complex biological matrices.
• Design experimental plans and lead execution of clinical sample analysis to generate high-quality and robust biomarker data.
• Serve as subject-matter expert (SME) in mass spectrometry technologies (triple quadrupole, Orbitrap, TOF)
• Collaborate with cross-functional teams including translational science, clinical biomarker scientists, clinical biomarker operations and bioinformatics teams to ensure assay and data alignment with clinical objectives.
• Author and review technical documentation including method validation and clinical sample analysis protocols, reports, and SOPs.
• Ensure quality control, data integrity, and timely delivery of analytical results.
• Maintain accurate lab records and mentor junior scientists.
• Stay current with emerging technologies (HRMS, immunoaffinity-LC-MS, hybrid approaches) and contribute to expanding LC-MS/MS-based biomarker capabilities with an innovative mindset

Supervisory Responsibilities:  

• This role is initially an individual contributor. May supervise lab scientists as the team grows.

Computer Skills:   

Proficiency in general software such as Microsoft Office (Word, Excel, PowerPoint), Outlook, Zoom, Teams as well as task-related systems e.g. Analyst, LIMS, ELN

Other Qualifications:    

• Ph.D. in Analytical Chemistry， Biochemistry， Pharmaceutical Sciences or related field with 3+ years or M.S. with 5+ years of relevant industry experience in a clinical, translational or regulated environment.
• Proven expertise in LC-MS/MS assay development and validation for clinical biomarkers
• Hands-on experience with biological sample preparation (plasma, serum, tissues etc.)
• Demonstrated experience designing and executing clinical biomarker/bioanalytical studies following relevant ICH, FDA, EMA and CDE guidance.
• Strong analytical and problem-solving skills with the ability to think critically.
• Excellent communication, organization and project management skills.
• Experience in lab automation, electronic laboratory notebook (ELN), laboratory information management system (LIMS) and initial lab workflow set-up is a plus.

Travel:  Under 10%

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: $118,000.00 - $158,000.00 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 BeOne Medicines 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. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans’ Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact accommodationsus@beonemed.com.