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Global Sterility Assurance Systems & Standards Lead

CSL Behring · Kankakee, IL · Full time

Posted Jun 18, 2026 · We last checked this listing on Oct 6, 2026

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Likely interview questions for this role

Written from this job description, not a generic list. Each one notes what the interviewer is really checking.

About your past

Tell me about a major deviation investigation involving sterile filtration that you supported. What was the root cause?

What they are checking: Whether they bring real technical depth to filtration failures and avoid shallow conclusions.

How do you build a sterility assurance culture on the manufacturing floor, beyond procedures?

What they are checking: Whether they understand that aseptic behavior depends on people and habits, not only documents.

Tell me about a time a site leader disagreed with a global standard you were enforcing.

What they are checking: Whether they can hold the line on standards while listening for legitimate local issues.

What would you do

How would you provide sterility assurance oversight to a CMO where you have no direct authority?

What they are checking: Whether they can drive standards at partners through quality agreements, data and relationship.

A media fill fails at one of our sites. What happens next, and what do you look at first?

What they are checking: Whether they know how to respond to an aseptic process simulation failure and assess product impact.

Environmental monitoring shows a slow upward trend in a Grade B area, but no excursions. What would you do?

What they are checking: Whether they act on trends before limits are breached and investigate proactively.

How do you decide which sterility assurance improvements to prioritize across many sites with limited resources?

What they are checking: Whether they rank improvements by contamination risk to patients rather than ease or visibility.

About the work

Walk me through the main elements of a contamination control strategy for a sterile manufacturing site.

What they are checking: Whether they understand Annex 1 expectations and how all the controls fit together into one strategy.

How do you stay current on regulatory and industry trends in sterile manufacturing, and how do you turn that into action for sites?

What they are checking: Whether they gather intelligence and translate it into practical standards rather than just tracking news.

How would you prepare a site for an inspection focused on sterility assurance?

What they are checking: Whether they know what inspectors probe in aseptic operations and how to close gaps ahead of time.

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The full job description

As published by CSL Behring.

Global Sterility Assurance Systems & Standards Lead Reporting to the Head of Global Sterility Assurance, this strategic position sits in the Global Quality Operations organisation. Ensuring the quality, safety and reliable supply of our products’ pipeline is critical. This newly created leadership role executes Sterility Assurance oversight and support to CSL sites and CMOs to ensure that sites operate in compliance to the highest standard regulatory expectations. By driving sterility assurance across partnering functions, this position ensures consistent standards, proactive risk management, and global inspection readiness. Responsibilities: • Provide strategic leadership to the site related to sterility assurance standards, culture and continuous improvement • Perform effective regulatory and business intelligence about sterile manufacturing and Sterility Assurance • Work collaboratively with the global sterility assurance teams to provide a holistic microbial contamination control strategy and improvement plan at the site • Partner closely with the global function leads as well as site leadership team, develop strategies to ensure continuous adherence to regulatory and CSL standards related to sterility assurance governance and drive improvements • Provide expert input to Sterility Assurance related major deviation investigations in the area of sterile filtration, aseptic filling and lyophilization and sterility, media fill and bioburden test fail • Proactively work with sites and global stakeholders on inspection readiness for the sites (before, during and after inspections) • Provide CMOs and filling strategies Sterility Support (CMO selection process, technologies intelligence…) • Provide strong Sterility Assurance background and support on strategic CSL projects (i.e. new filling lines selection and design) • Develop and lead Sterility Assurance Roadmaps for compliance and performance • Ensure appropriate development, implementation and maintenance of sterility assurance standards and processes consistent with global governance, regulatory requirements and industry standards. • Align and facilitate collaboration across Technical Operations, Quality functions, Operations, and R&D, to successfully drive aseptic excellence Qualifications: • Bachelor’s degree in microbiology or biology or life sciences or equivalent relevant field • 8-10 years' experience in pharmaceutical manufacturing industry with direct experience executing quality assurance within a manufacturing and QC microbiology, sterility assurance context • Demonstrated experience in quality assurance and regulation compliance with GxP, FDA, EU and other regulatory agency guidelines • Experience interacting with regulatory authorities including submissions and inspections; knowledge of auditing practices and procedure Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable. 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 .

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