Global Sterility Assurance Systems & Standards Specialist

Responsibilities:

Provides 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

Partners closely with the global function leads as well as site leadership team develops strategies to ensure continuous adherence to regulatory and CSL standards related to sterility assurance governance and drive improvements

Provides 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

Plays a proactive role in the investigation of accidents and near misses as well as in the implementation of corrective actions and you are supported by the safety responsible person of your area -> is this one related to EHS Not relevant here in my view

Proactively works with sites and global stakeholders on inspection readiness for the sites (before during and after inspections)

Provides CMOs and filling strategies Sterility Support (CMO selection process technologies intelligence)

Provides strong Sterility Assurance background and support on strategic CSL projects (i.e. new filling lines selection and design)

Develops and leads Sterility Assurance Roadmaps for compliance and performance

Ensures appropriate development implementation and maintenance of sterility assurance standards and processes consistent with global governance regulatory requirements and industry standards.

Qualifications:

Bachelors 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 worlds largest plasma collection networks CSL Plasma. Our parent company CSL headquartered in Melbourne Australia employs 32000 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 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 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 Experience:

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