QAO Specialist I

Shift: 12 Hour Off ShiftOverview:This is an entry level position into Quality Assurance Operations. Responsibilities include real time production floor monitoring. Real time review of batch records, including critical processing steps, as well as all other ancillary manufacturing and support systems documentation. Assisting with investigating deviations, relevant to area of responsibility. Responsible for supporting continuous improvement on production floor to ensure compliance to cGMPs.

Works under direct supervision.All responsibilities are relative to the specifics of the Value Stream/Department assigned.Responsibilities: Responsible for real-time review of critical in-process steps, review/approval of completed production records, and providing immediate notification to manufacturing personnel (e.g. supervisors/operators) regarding facility/ process /equipment /documentation issues.Real time floor monitoring for process adherence, safety and quality issues, and reporting of any findings through the eQMS or department or Quality escalations as appropriate.Responsible for participating in investigation meetings with responsible department and any required support group(s) to help determine root cause, corrective/preventative actions, and product disposition.On-call for immediate inspections, investigations, and review of possible GMP related issues and ability to provide quality assessment of potential deviation.Execute training/awareness related to investigation and GMP changes to production personnel.Support continuous improvement on production floor to ensure compliance to cGMPs.

As appropriate to area of responsibility, perform Acceptable Quality Level (AQL) assessments.Complies with requirements from CSL Behring's Safety Program, including Health and Safety mandates and OSHA requirements.Provide awareness training on deviations to department personnel.Qualifications:B.A. or B.S. degree preferred in scientific or technical field (e.g., chemistry, biology, physics, engineering, computer science, technical writing).Experience:0-2 years of experience working in a cGMP regulated environment such as the field of quality, manufacturing or engineering field, applying the cGMP rules in everyday activities.

Technical writing experience is preferred.Competencies:Informing - is timely and accurate with information.Peer Relationships - Can quickly find common ground and solveproblems for the good of all, is a team player and cooperative.Self-Knowledge - Seeks feedback, gains insights from mistakes, isopen to criticism.Action Oriented - Enjoys working hard; is energetic for the thingsthat he/she sees as challenging.Written Communications - is able to write clearly in a variety ofcommunication settings and styles, can get messages across.Conflict Management - Steps up to conflicts, seeing them asopportunities, can find common ground.Dealing with Ambiguity - Can effectively cope with change, can shiftgears comfortably, can comfortably handle risk and ambiguity.Learning on the Fly - Open to change, learns quickly when facingnew problems, versatile learner.Must demonstrate competency in verbal and written communication.eQMS knowledge a plus.Working Conditions:Onsite 100% of timeThe expected wage range for this position at hiring is $23.56/hour - $30.29/hour.

Please note this wage range reflects what CSL expects to pay for this position at the listed location as of the time of this posting. Individual base pay for a successful candidate within this range is determined by qualifications, skill level, experience, competencies and other relevant factors. Different qualifications or responsibilities may apply based on local legal and/or educational requirements.

Refer to local job documentation where applicable.