GRA CMC Scientist

CSL; Bern; On-site; CHF 140,000 - 190,000; Full time

Job summary

CSL Behring is seeking a GRA CMC Scientist to lead global CMC regulatory activities across product development, clinical submissions, registrations and lifecycle management. You will shape global strategies, ensure compliant submissions, and partner with technical and regulatory teams worldwide.

The role covers both strategic and operational CMC tasks, including content maintenance of regulatory dossiers, technical authoring, and timely responses to Health Authority questions, ensuring

Qualifications

• University degree in natural sciences; Regulatory Affairs degree advantageous.
• Minimum of 3 years' biotech/pharma experience, with at least 1 year in Regulatory Affairs.
• Solid knowledge of natural sciences with focus on biological medicinal products.
• Basic knowledge of regulatory framework in key regions (US, EU, Japan, CH, Australia).

Responsibilities

• Drive global CMC strategies for clinical trial applications, new product licenses, and post-approval changes.
• Assess CMC, facility/equipment, and plasma-related changes and manage regulatory submissions with regional teams.
• Serve as primary regulatory liaison with technical experts; support GMP inspections and inspection readiness.
• Interpret regulatory guidelines; prepare impact assessments and contribute to process improvements.
• Provide technical guidance to the organization.

Skills

Excellent communication

Project management

Planning

Problem solving

Presentation skills

Team player

Microsoft Office

Fluent in English

Local language

Education

BS/BA/MS or equivalent

Regulatory Affairs degree advantageous

3+ years biotech/pharma, 1+ year Regulatory Affairs

Biological medicinal products knowledge

Regulatory frameworks knowledge (US/EU/Japan/CH/AUS)

Job description

We are looking for a GRA CMC Scientist to lead strategic and operational CMC regulatory activities across product development, clinical submissions, registrations, and lifecycle management. In this role, you will shape global CMC regulatory strategy, ensure compliant execution of submissions and changes, and partner with technical and regulatory teams worldwide.

Key Responsibilities:

• Drive global CMC strategies for clinical trial applications, new product licenses, and post-approval changes.
• Assess CMC, facility/equipment, and plasma-related changes and manage regulatory submissions in coordination with regional teams.
• Serve asprimaryregulatory liaison with technical experts; support GMP inspections and inspection readiness.
• Interpret regulatory guidelines and requirements; prepare impact assessments and contribute to process improvements.
• Providetechnical guidance to Providetechnical guidance to the organization

Responsible for operational CMC regulatory activities related to the assigned products and/or intermediates, including as applicable:

• Maintenance of the content of relevant parts of the regulatory dossiers.
• Preparation, revision and review of Module 2.3, Module 3, required facility and equipment information and related documents for new product registrations (e.g.MAAs, BLAs) and life cycle submissions according to agreed timelines and taking regional regulatory requirements into account. This may include technical authoring of dossier narratives and other regulatory CMC documentation.
• Timely provision ofhigh-qualityresponses to CMC related Health Authority questions.
• Compilation and review of CMC information for CTAs, INDs and other regulatory submissions related to product development (e.g.CMC documentation for Scientific Advice Meetings, Briefing Books, IBs).
• Provision or support oftimelyand compliant regulatory assessments as well as efficient execution of CMC changes.
• Preparation and review of CMC related information and documentationrequiredfor tenders, PSURs, DSURs, CCDS/productinformationand promotional materials.
• Regulatory contribution to annual product quality reviews and risk assessments.

Responsible for strategic CMC regulatory activities related to the assigned products and/or intermediates, including as applicable:

• Is a permanent member of the Regulatory Affairs Strategy Team(s) and/or of relevant CMC Regulatory Sub-Team(s).
• MayrepresentGlobal Regulatory Affairs in Project Teams for CMC projects.
• Is responsible fordevelopment and implementation of global CMC regulatory strategies for product development, clinical trial applications, new license applications, productchangesand relevant CMC projects with a view to reach approvals in the most efficient way while ensuring compliance with global regulatory requirements.
• Is the primary GRA contact point interfacing with relevant technical expert departments for project planning purposes,compilationand updates of technical documentation and for addressing CMC regulatoryquestions.
• Evaluates the available technical and scientific CMC information for compliance with regulatory requirements, performs gapanalysisand proposes solutions and strategies to remediate risks.
• Supports scheduling and prioritization of CMC related submissions.

Qualification

• University degree in natural sciences (BS/BA/MS or equivalent), a degree in Regulatory Affairs isadvantageous.
• Minimum of 3 years' experience in the biotech or pharmaceutical industry, with at least 1 year in Regulatory Affairs.
• Sound knowledge in natural sciences with a focus on biological medicinal products.
• Basic knowledge of the regulatory framework in at least one key region (US, EU, Japan, CH, Australia).

Competencies

• Excellent communication, project management, planning, problemsolvingand presentation skills.
• Strong teamplayer with a demonstrated ability to develop constructive and effective relationships with peers and management.
• Strong organizational and follow-up skills, as well as attention to detail.
• Ability to work with minimal supervision based on sound technical and analytical judgment.
• Flexibility to work in a global cross-cultural work environment.
• Microsoft Office skills.
• Fluent in English and local language.

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 https://www.csl.com/How CSL Supports Your Well-being | CSL.

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.