Executive Director, Analytical Science and Characterization Center of Excellence

WuXi Biologics Group; United States; Remote; USD 193,000 - 295,000; Full time

Job summary

A leading biopharmaceutical company seeks an Executive Director for the Analytical Science and Characterization Center of Excellence. This remote role involves strategic planning, team management, and ensuring high-quality technical support for global projects. The ideal candidate will have a Ph.D., over 15 years of experience in biopharmaceutical analysis, and proficiency in mass spectrometry techniques. The anticipated base salary range is $193,000-295,000 annually, with a focus on innovation and compliance in a competitive industry.

Qualifications

• 15+ years of experience in biopharmaceutical analysis, including 8 years in team management.
• Proficient in mass spectrometry and biopharmaceutical physicochemical characterization methods.
• Familiar with biopharmaceutical R&D processes and industry regulations.

Responsibilities

• Develop technology strategies and roadmaps for mass spectrometry and bioactivity Non-GMP development.
• Lead and manage a technical team, optimizing structure for efficiency.
• Oversee analytical support for global projects, ensuring data accuracy and compliance.

Skills

Mass spectrometry techniques (LC-MS, GC-MS)

Biopharmaceutical physicochemical characterization methods

Bioactivity assay development

Team management

R&D process familiarity

Education

Ph.D in Analytical Chemistry, Biochemistry, Biotechnology, Pharmaceutical Sciences

Job description

Executive Director, Analytical Science and Characterization Center of Excellence

United States Posted 2026-02-20

Job Title - Executive Director, Analytical Science and Characterization Center of Excellence

Work Location - Remote

Job Summary- Fully responsible for the strategic planning and operational management of the Mass Spectrometry, Characterization, and Bioactivity Non-GMP Development Center of Excellence. Lead a technical team of approximately 150-200 personnel and establish an integrated analytical technology platform covering bioprocess development through the preclinical stage. By defining technology roadmaps, driving innovative R&D, and optimizing service systems, ensure the center’s technological leadership and industry competitiveness in mass spectrometry analysis, physicochemical characterization, bioactivity assays, and more. Providing efficient, compliant, and high-quality technical support for global projects.

Job Responsibilites

Strategic Planning and Platform Development:

• Develop mid- long term technology strategies and roadmaps for mass spectrometry, characterization, and bioactivity Non-GMP development, defining core technology directions (e.g., high-resolution mass spectrometry applications, complex protein characterization, novel bioactivity assay development). Lead platform technology upgrades and capability expansions;
• Build standardized, modular analytical technology systems; promote cross-technology collaboration and innovation, ensuring the platform meets diverse BU project needs (e.g., monoclonal antibodies, bispecific antibodies, fusion proteins, gene therapy drugs).

Team Management and Talent Development:

• Lead and manage a large technical team (including sub-teams in mass spectrometry analysis, physicochemical characterization, bioactivity assays, method development), optimize organizational structure to maximize people efficiency;
• Establish a top global talent pipeline; lead recruitment, development, and retention of core personnel; design dual career tracks for technical experts and management; build a team with innovative capability and industry vision.

Technical Services and Quality Compliance:

• Oversee provision of full-cycle analytical support for 300+ BU global projects, including but not limited to protein sequence confirmation, structural analysis, post-translational modification characterization, and bioactivity assays; ensure data accuracy, timely reporting, and compliance;
• Establish strict quality control systems; optimize lab workflows and SOPs; lead root cause analysis and improvement of technical deviations and issues to ensure stable service quality.

Technology Innovation and External Collaboration:

• Track cutting-edge global technologies in mass spectrometry, characterization, and bioactivity assays (e.g., AI-assisted analysis, ultra-high-resolution mass spectrometry, automated characterization platforms); lead new technology introduction, validation, and translational application; drive core technology patent portfolio development;
• Build internal and external technical collaboration networks; interface with leading academic institutions, industry partners, and regulatory bodies at home and abroad; participate in industry standard formulation to enhance the influence in global biopharmaceutical analysis.

Resource Coordination and Cross-Department Collaboration:

• Manage center budgets and key resources (instrumentation, consumables, manpower); optimize resource allocation to improve platform operational efficiency;
• Act as a key interface in BU analytical fields, collaborating deeply with R&D, process, quality, clinical departments to solve cross-functional technical challenges and promote achievement of key project milestones.

Qualifications

• Ph.D in Analytical Chemistry, Biochemistry, Biotechnology, Pharmaceutical Sciences, or related fields; strong academic background with biopharmaceutical analysis major is preferred.
• Over 15 years of experience in biopharmaceutical analysis, including at least 8 years team management experience ( hold technical management experience at least 100/team size).
• Proficient in mass spectrometry techniques (LC-MS, GC-MS, etc.), biopharmaceutical physicochemical characterization methods (e.g., SEC-MALS, CE-SDS, DLS), and bioactivity assay development at the non-GMP stage;
• Hands‑on experience in the analysis of monoclonal antibodies and complex protein therapeutics;
• Familiar with the entire biopharmaceutical R&D process (early discovery → process development → pre‑clinical);
• Deep understanding of analytical technical requirements and industry regulations (e.g., ICH, FDA guidelines) at the non-GMP stage ；
• Proficient in biopharmaceutical analysis and relevant regulations; Excellent in biopharmaceutical CMC knowledge ；
• Familiar with biopharmaceutical industry practices and regulatory requirements; possesses digital management mindset;

The anticipated base salary range for this position is $193,000-295,000

WuXi Biologics is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability