Responsibilities:
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Under general direction, provides support on Quality systems to ensure compliance with company standards and GMP regulatory guidelines
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Develops, maintains and improves GMP-related quality control systems including standard operating procedures (SOPs)
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Participates in project teams to provide review and approval of project Validation documentation according to applicable approval matrix or procedures
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Supports quality systems related to Validation, LIMS, Calibration, Document Management, Deviation Management, CAPA, Change Control, and Enterprise Learning Management
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Writes and manages validation plans, ensuring appropriate, timely validation/revalidation is maintained
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Conducts internal audits and assists with 3rd party quality audit; plans and implements continuous improvement projects
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Supports GxP health authority inspections by serving as subject matter expert for computerized systems topics
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Provides guidance on quality and regulatory requirements to project teams, internal stakeholders and other teams on GxP compliance relating to computerized systems
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Collaborates to resolve technical issues, provide quality training and communicate best practices
Qualifications:
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Bachelor degree in Engineering or a relevant scientific discipline (Chemistry, Biology, Microbiology, IT etc.) or equivalent experience
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5+ years' quality systems experience in pharmaceutical manufacturing/cGMP regulated environment
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Knowledge of current Good Manufacturing Practices (cGMP)
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Knowledge of FDA and EMA requirements
Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.
About CSL Seqirus
CSL Seqirus is part of CSL. As one of the largest influenza vaccine providers in the world, CSL Seqirus is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness. With state-of-the-art production facilities in the U.S., the U.K. and Australia, CSL Seqirus utilizes egg, cell and adjuvant technologies to offer a broad portfolio of differentiated influenza vaccines in more than 20 countries around the world.
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.
Watch our ‘On the Front Line’ video to learn more about CSL Seqirus
Manager, QA IT in Maidenhead employer: Seqirus UK Limited
CSL Seqirus is an exceptional employer, offering a dynamic work environment that prioritises inclusion and belonging, fostering a culture of curiosity and empathy. Employees benefit from comprehensive support for their well-being, alongside opportunities for professional growth within the highly regulated pharmaceutical industry. Located in the EMEA region, this role not only contributes to global health through innovative vaccine solutions but also allows for meaningful engagement with diverse stakeholders, making it a rewarding place to advance your career.
