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Quality Programs Associate

Company: CSL Plasma
Location: Boca Raton
Posted on: February 18, 2021

Job Description:

With operations in 35+ nations and - 27,000 employees worldwide, CSL is driven to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza. Our therapies are also used in cardiac surgery, organ transplantation and burn treatment.CSL is the parent company of CSL Behring and Seqirus. is a global leader in the protein biotherapeutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions. CSL Behring operates , one of the world's largest collectors of human plasma, which is used to create CSL's therapies. Seqirus is the second largest influenza vaccine company in the world and is a transcontinental partner in pandemic preparedness and a major contributor to the prevention and control of influenza globally.We invite you to take a look at the many career possibilities available around the globe and consider building your promising future at CSL by becoming a member of our team!This position is responsible for collating and analyzing data for reporting Plasma Lookbacks and Biologic Product Deviation Reports (BPDRs) in an accurate and timely manner. A Lookback is the process of identifying and reporting units to a customer that were collected from a donorwho no longer meets applicable donation criteria. A BPDR is a report submitted to the Food & Drug Administration (FDA), to report certain events that mayaffect the safety, purity or potency of plasma.RESPONSIBILITIES1Work with applicable programs, such as LOGIC, eProgesa and Business Objects to generate and report accurateLookbacks.2Track incoming and outgoing notifications to ensure timely processing of Lookbacks and BPDRs per customer andregulatory requirements.3Evaluate Plasma center information to determine appropriate Lookback time period based upon Standard OperatingProcedure (SOP) requirements. Research discrepant and/or missing information to determine the correct course ofaction. Perform Quality Assurance (QA) review of all reports to provide accurate information to customers and theFDA.4Provide guidance to center personnel on whether an event requires a Lookback and/or BPDR.5Communicate with customers, regulatory authorities, other departments, center and laboratory personnel to provideand collect information regarding Lookbacks, BPDRs, and Recall Documentation, as well as to resolve problems.6 Review and evaluate documentation to determine if the event is reportable to the FDA Center for BiologicsEvaluation and Research, (FDA-CBER) based upon defined criteria. Prepare, review and submit BPDRs forConfirmed Viral Marker positive donors, Post Donation Information Reports (PDIRs), Error/Accident Reports, andMedical Device deviations to the FDA.7 Comply with Recall Documentation when requested by FDA Recall Coordinators. Documentation may includecustomer acknowledgment and final disposition of the units reported to the final consignee(s), test results of unitsinvolved, examples of product labels and any additional documentation the FDA might consider relevant to theBPDR8File, fax, scan, copy and submit paperwork and report to centers and customers.9Collaborate with the review and update of department SOPs as needed.10Follow all Standard Operating Procedures (SOPs), company policies and procedures.11Maintain professional image and confidentiality of all company records and information at all times.12Perform other duties, as assigned, to support business needs.JOB SPECIFICATIONSEducation High School diploma or equivalent combination of education, training and experienceExperience Minimum 1 year experience in related industry within a Regulatory Affairs or QA capacity preferred Understand regulatory standards, various local, state and federal laws that apply to the businessand where to find information on standards and interpretations Organizational skills and attention to details to handle multiple tasks, short deadlines, frequentinterruptions, and shifting priorities in support of changing company objectives Establish solid working relationships to interface with and support senior management, third partiesand other positions and circumstances within the organization Strong customer service orientation with flexibility and adaptability to work as a member of the team Intermediate to strong working knowledge of Microsoft Office products Proven ability to work in a fast paced, dynamic environment Learn new processes and quickly engage in assignments to drive for actionWorkingConditions(physical & mental requirements) Ability to make decisions which have significant impact on the department's creditability, operationsand services Ability to formulate complex and comprehensive materials such as authoritative reports of majorscope and impact, etc. and/or to make formal presentations Exercise good judgment to refer decisions to management when decisions fall out of the realm ofestablished guidelines Required to work overtime and extended hours Overnight travel required up to 10% of the time Frequent standing and walking Ability to lift or carry up to 25 lbs. Fast paced environment with frequent interruptionsNote: All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexualorientation, gender identity, disability, veteran status, national origin or other legally protected classifications.Worker Type:EmployeeWorker Sub Type:Regular

Keywords: CSL Plasma, Boca Raton , Quality Programs Associate, Other , Boca Raton, Florida

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