Responsibilities:
• Responsible for supervising daily activities of laboratory group to ensure compliance with quality and reliability standards
• Supervises the use of chemical tests and various kinds of measuring instruments in accordance with approved methods and standard operating procedures (SOPs)
• Schedules and communicates with appropriate functional groups regarding status of activities and quality testing requirements
• Provides expert review of data, protocols and reports for adherence to cGMPs and good documentation practices
• Communicates aberrant results and leads investigation to determine root cause
• Ensures quality control training and reviews and approves standard operating procedures (SOPs)
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Qualifications:
• Bachelor degree in a relevant scientific discipline (Chemistry, Biology, Biochemistry, etc.)
• Substantial quality control experience in the pharmaceutical/biotech/or other regulated industry
• Leadership/ team management skills
• Direct interaction with regulatory agencies
• Knowledge of current Good Manufacturing Practices (cGMP) principles
• Knowledge of FDA and EMA requirements
Please note this role is on shifts 5 days on and 3 days off
Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.
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CSL Seqirus is committed to attracting and retaining world-class employees who are valued for their contributions to achieving business objectives. Learn more about some of the benefits you can participate in when you join CSL Seqirus.
About CSL Seqirus
CSL Seqirus is part of CSL Limited (ASX: 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. Learn more about CSL Seqirus.
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