Do you want to work with a company that tackles fascinating problems and find solutions to complex challenges? Seqirus has an exciting opportunity to join our expanding team in Holly Springs, NC. With an advanced manufacturing facility and expertise in influenza science we are one of the world leaders in the production of the influenza vaccine. We operate as one integrated global company, drawing together expert staff from different countries to collaborate. Together, we're working on the front line to protect communities from seasonal influenza and global pandemic threats. When you join Seqirus, you join a team dedicated to making a difference in people's lives. It's a feeling of possibility, creativity, and purpose that inspires us every day.

• Function as primary FLQA and Quality Management System (QMS) subject matter expert to assigned area(s) of responsibility within manufacturing, laboratories, utilities, maintenance and/or logistics
• Perform the quality oversight and approval of Deviations, CAPAs, and Change Controls in close collaboration with Record Owners throughout the process. Ensures the investigation, identification of root cause, the development of CAPAs, and the technical accuracy and comprehensive scope of change controls within assigned area(s) of oversight.
• Monitor and tracks on-time closure of assigned QMS records.
• Active participate in cross-functional suite team meetings and provide FLQA support of suite team projects
• Provide on-the-floor walkthroughs and coaching to manufacturing staff to embed a quality mindset, build compliance knowledge and sustain a strong quality culture
• Bring adherence to and continuous improvement of the quality systems within assigned area(s) of oversight
• Support the development, revision and implementation of SOPs, protocols, and other GMP documents.
• Helps deliver the Deviation, CAPA, and Change Control Annual Product Quality Review (APQR) sub-reports
• Lead continuous improvement projects and may provide quality support to site capital projects and/or global quality system improvement projects
• Ensure inspection readiness in assigned area of support via performing routine quality walkthroughs, monitoring quality system adherence, and direct involvement in Site Self Inspections
• Be the QA SME for internal and external audits
• Must be proficient in the use of computerized systems including but not limited to: TrackWise, Veeva QMS and QDocs, GLIMS, SAP, CMMS
• Support greater FLQA organization including shop floor quality operations also including QA reviews of batch records and other GMP records at the site.
• Acquires and maintains knowledge of current local and international regulatory requirements/trends to ensure that expert advice and appropriate technical support on all quality/compliance related matters are provided to the site.

• Bachelors degree in a relevant scientific discipline (Pharmacy, Chemistry, Biology, Biochemistry) preferred or equivalent experience in biotech or pharmaceutical industry
• 3+ years' GMP experience in the pharmaceutical/biotech industry - cGMPs, FDA requirements, and Quality Systems
• 2+ years technical understanding of the production processes used in pharmaceutical parenteral drug product manufacturing
• Previous experience directly working in vaccine manufacturing operations and/or QC laboratories and/or previous experience in ownership and/or approval of GMP deviations, CAPAs, and change controls
• Previous experience in root cause analysis and risk management, including working experience of root cause analysis tools such as Fishbone/5Why
• Examples of ownership and/or approval of GMP deviations, CAPAs, and change controls