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Job description
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.
Worksite address
bradley, IL, 60915, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.