For our global Technical Operations Organization, we are currently looking for a
Director, Analytical Strategy
The Director, Analytical Strategy is a senior scientific and strategic leadership role responsible for designing and overseeing analytical strategies that support drug discovery, development, and regulatory approval. This position ensures robust, compliant, and innovative analytical approaches across preclinical, clinical programs and LCM.
Key Responsibilities
Strategic Leadership
Develop and lead the global analytical strategy aligned with program and corporate goals
Provide scientific and regulatory guidance for analytical plans across all development phases (discovery post-marketing)
Drive innovation in analytical technologies, platforms, and workflows
Represent analytical function in cross-functional governance and decision-making forums
Scientific Oversight
Oversee development, validation, and implementation of analytical methods (e.g., LC-MS/MS, ligand binding assays, biomarkers, immunogenicity)
Ensure high-quality data generation for PK, PD, biomarker, and immunogenicity studies
Review and approve analytical study designs, reports, and regulatory documentation
Troubleshoot complex scientific and technical challenges
Regulatory & Compliance
Ensure compliance with global regulatory guidelines (FDA, EMA, ICH, GLP, GCP)
Lead analytical sections of regulatory submissions (IND, CTA, NDA, BLA, MAA)
Interface with regulatory agencies and respond to health authority queries
Maintain inspection readiness and quality standards
Cross-Functional Collaboration
Partner with Clinical Pharmacology, DMPK, Toxicology, Biomarkers, and Clinical Operations
Support translational strategy and dose selection decisions
Manage external CROs, academic collaborators, and technology vendors
Leadership & Management
Lead and mentor analytical scientists and project leaders
Manage budgets, timelines, and resource allocation
Build and scale analytical capabilities and infrastructure
Your experience
PhD in analytical Chemistry, Pharmaceutical Sciences, Biochemistry, or related field (or MSc with extensive experience)
Typically, 12–15+ years in bioanalysis within biotech, pharma, or CRO environments
Deep expertise in LC-MS/MS, ligand binding assays, biomarkers, and immunogenicity testing
Strong knowledge of regulatory requirements and analytical validation standards
Proven leadership and strategic program experience
Experience supporting regulatory submissions and health authority interactions
Are you interested? We are looking forward to receiving your online application.
About CSL Behring
CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.
CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.
To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit and CSL Plasma at
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At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.
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Equal Opportunity Employer
CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit
Full Time