Associate Director, Analytical Strategy

CSL Behring; Bern; Sur place; CHF 150 000 - 210 000; Plein temps

Résumé du poste

CSL Behring is seeking two Associate Directors to design and oversee analytical strategies for product development and lifecycle management. You will guide cross-functional teams across regulatory, manufacturing and quality to ensure compliant, innovative analytical approaches for preclinical to commercial stages.

The roles demand doctoral-level expertise in analytical chemistry or related fields, with 8+ years in bioanalysis and a proven record in regulatory submissions and global programs.

Qualifications

• PhD in Analytical Chemistry or related field (or MSc with extensive experience).
• Typically 8+ years in bioanalysis within biotech, pharma, or CRO/CDMO environments.
• Deep expertise in analytical development, product specification testing, characterisation, and data analysis.
• Regulatory requirements and analytical validation standards knowledge.
• Leadership and strategic program experience in global matrix environments.
• Experience supporting regulatory submissions and health authority interactions.
• Excellent communication, able to present complex information to non-scientists.

Responsabilités

• Developing global analytical strategies for assigned products aligned with program and corporate goals.
• Provide scientific and regulatory guidance for analytical plans across all product development and LCM phases.
• Drive innovation in analytical technologies, platforms, and workflows.
• Review analytical study designs, reports, and regulatory documentation.
• Oversee development, validation, characterisation and implementation of analytical methods.
• Ensure high-quality data generation for product development and LCM programs.
• Troubleshoot complex scientific and technical challenges.
• Ensure compliance with global regulatory guidelines and interface with health authorities.
• Lead analytical sections of regulatory submissions (IND/CTA/NDA/BLA/MAA).
• Maintain inspection readiness and quality standards.
• Partner with Manufacturing, Quality, Research, CROs/CDMOs and external vendors.

Connaissances

Analytical chemistry

Leadership

Regulatory knowledge

Bioanalysis

Data analysis

Regulatory submissions

Communication

Formation

PhD in Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, or related field

Description du poste

CSL’s world-class R&D organisation continues to evolve as a biotechnology leader by advancing high-quality science and technology across five therapeutic areas being Immunoglobulins, Haematology, Cardiovascular & Renal, Transplant & Immunology and Vaccines that will make a meaningful difference to the lives of patients with rare and serious diseases.

CSL is now seeking two Associate Director level scientists to design and oversee analytical strategies that support product development and lifecycle management (LCM).

The Associate Director Analytical Strategy ensures the deployment of robust, compliant, and innovative analytical approaches across pre-clinical and clinical development as well as LCM for commercial products.

These are key senior scientific and strategic leadership roles supporting a diverse portfolio of recombinant protein and gene therapy products from early development, through licensure and ongoing commercial operations.

These positions have global reach and could be based at one either of our northern hemisphere sites (Bern, Marburg, King of Prussia or Waltham).

Key Responsibilities

Specific responsibilities for both these roles will include:

• Developing global analytical strategies for assigned products aligned with program and corporate goals

• Provide scientific and regulatory guidance for analytical plans across all product development and LCM phasesDrive innovation in analytical technologies, platforms, and workflows

• Reviewing analytical study designs, reports, and regulatory documentation.

• Oversee development, validation, characterisation and implementation of analytical methods.

• Ensure high-quality data generation for product development and LCM programs.

• Troubleshoot complex scientific and technical challenges.

• Ensure compliance with global regulatory guidelines (FDA, EMA, ICH, GMP) and interface with regulatory agencies, responding to health authority queries.

• Lead analytical sections of regulatory submissions (IND, CTA, NDA, BLA, MAA)

• Maintaining inspection readiness and quality standards.

• Partnering with internal stakeholders across Manufacturing, Quality Control, Quality Assurance, Research and external partners such as CROs/CDMOs, academic collaborators and technology vendors.

Your Profile

• PhD in Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, or related field (or MSc with extensive experience)

• Typically, 8+ years in bioanalysis within biotech, pharma, or CRO/CDMO environments

• Deep expertise in analytical development, product specification testing, characterisation, and data analysis.

• Demonstrated knowledge of regulatory requirements and analytical validation standards.

• Proven leadership and strategic program experience ideally in a global matrix environment.

• Experience supporting regulatory submissions and health authority interactions.

• Excellent communication skills including presenting complex information to non-scientific stakeholders.

• Experience with gene therapy products desirable, but not essential

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 https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/ .

Our Benefits

For more information on CSL benefits visit How CSL Supports Your Well-being | CSL (https://www.cslbenefits.com/csl/candidates) .

You Belong at CSL

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.

To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging

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 https://www.csl.com/accessibility-statement .

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CSL makes all employment decisions without regard to race, color, religion, national origin, ancestry, age, sex, gender, pregnancy, disability, marital status, sexual orientation, gender identity, genetic information, military status, protected veteran status (specifically status as a disabled veteran, recently separated veteran, armed forces service medal veteran, or active duty wartime or campaign badge veteran) or other classification protected by applicable US federal, state or local law. CSL complies with all applicable employment laws, including but not limited to Title VII of the Civil Rights Act of 1964, the Americans with Disabilities Act, the Fair Labor Standards Act, and the Immigration Reform and Control Act. https://www.cslbehring.com/careers/eeo-statement