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Senior Quality Associate – Global Pathogen Safety at CSL, EMEA

Senior Quality Associate – Global Pathogen Safety at CSL in EMEA. Full-time. Apply with swipeandhired.

Innovative and committed to patients worldwide.

CSL Behring is a global biotechnology leader, driven by its promise to save lives. At our site in Bern, our employees develop and manufacture life-saving therapies for people with serious and rare diseases around the world.
For our Global Pathogen Safety (GPS) organization in Bern, we are looking for an experienced quality professional to join us as

Senior Quality Associate – Global Pathogen Safety (100%) (m/f/d)

In this role, you will provide Quality Assurance oversight for our Global Pathogen Safety laboratories and help ensure that laboratory and research activities are conducted in accordance with applicable quality and regulatory requirements. You will work closely with laboratory teams, study personnel and other stakeholders to maintain and continuously improve our quality systems, support inspection readiness and foster a strong and proactive quality culture.

Your primary focus will be on compliance with the OECD Principles of Good Laboratory Practice (GLP), GCLP (ISO/IEC 17025) and CSL's Good Research Laboratory Practice (GRLP) standards. Depending on business needs, you may also provide quality oversight for nonclinical development activities within Research EU and support biosecurity and biosafety compliance at the Bern site.

Responsibilities

Provide Quality Assurance oversight for Global Pathogen Safety laboratory activities and ensure compliance with applicable GLP, GCLP/ISO 17025, GRLP and internal CSL requirements.
Establish, maintain and continuously improve quality procedures, standards and systems in collaboration with laboratory teams and other stakeholders.
Review study plans, protocols and reports for GLP compliance and prepare Quality Assurance statements for final study reports.
Plan and conduct process, facility, study and document inspections in accordance with GLP and GRLP requirements, document findings and follow up on resulting actions.
Communicate inspection results and quality-related observations to Facility Management, Study Directors, Principal Investigators and other relevant stakeholders.
Support inspection readiness and participate in or host regulatory inspections, providing guidance and support for responses and resulting quality actions.
Support the internal audit and inspection program and contribute to the timely and compliant implementation of corrective and preventive actions (CAPAs).
Act as a Quality Assurance partner for laboratory teams and other functions, providing guidance on quality systems, compliance requirements and continuous improvement opportunities.
Support biosecurity and biosafety compliance for CSL operations in Bern in accordance with applicable global, regional and local requirements, as required.
Collaborate with colleagues across the global laboratory network to support harmonized quality standards, processes and continuous improvement initiatives.
Depending on business needs, provide Quality Assurance oversight for nonclinical development activities within Research EU.

Qualifications

Bachelor's degree in Biology, Microbiology, Life Sciences or another relevant scientific discipline.
At least 3 years of professional experience in Quality Assurance, R&D, laboratory operations or another relevant regulated environment.
Practical knowledge and understanding of the OECD Principles of Good Laboratory Practice (GLP) and their application within laboratory or research environments.
Experience with Quality Management Systems and the implementation, maintenance or continuous improvement of quality processes.
Experience in R&D Quality Assurance, process development or similarly regulated laboratory environments is highly desirable.
Knowledge of microbiology, pathogen safety, biological containment and/or applicable biosafety and biosecurity requirements is an advantage.
Experience with laboratory inspections, audits, CAPAs or regulatory inspections is highly desirable.
Strong planning and organizational skills with the ability to manage multiple priorities independently.
Strong communication and stakeholder management skills, with the ability to communicate quality and compliance requirements clearly across different functions and levels of the organization.
Sound judgment, analytical thinking and confident decision-making skills combined with a pragmatic and solution-oriented approach.
Proactive mindset and commitment to continuous improvement, collaboration and a strong quality culture.
Very good German and English language skills, both written and spoken, are required.

About this position

As a Senior Quality Associate within Global Pathogen Safety , you will work at the interface of science, laboratory operations and Quality Assurance.
The position combines hands-on quality oversight with inspections, quality systems, regulatory compliance and cross-functional collaboration, giving you exposure to a broad range of laboratory and research activities.
You will collaborate with stakeholders in Bern as well as colleagues across our global network and have the opportunity to contribute to the continuous development and harmonization of quality processes within Global Pathogen Safety.
Your work will directly support robust scientific practices, regulatory compliance and the consistent application of CSL quality standards.

Interested in this opportunity? We look forward to receiving your application. Please submit your CV, employment references and degree certificates together as one file.

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 .

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 .