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    Deviation Investigator - St Louis, United States - Katalyst Healthcares and Life Sciences

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    Description
    Responsibilities:
    • ssume site level responsibility for all major investigations including items originating from Production, Quality Control, Facilities, etc.
    • Coach and drive root cause analysis (RCA)
    • Facilitate cross functional teams to evaluate causal factors.
    • Provide written documented investigations per the site rubric in an appropriate and timely manner.
    • Ensure adequate CAPAs are put in place to reduce or eliminate recurrence of issues
    • Work without direct guidance and minimal oversight to get results, meet timelines, and improve processes.
    • Effectively communicate with peers and colleagues regarding the status of investigations and offer recommendations based on investigation outcomes.
    • Provide insights based on technical experience and astute judgment as called upon during investigations and daily interpretation of data and results.
    • Perform work with little to no oversight.
    • Perform technical writing of challenging investigations.
    • Provide oversight for technically challenging investigations.
    • Provide client communications and responses.
    • Drive client communications and responses to closure through concurrences.
    • Provide mentorship to deviation management team members.
    • Lead the team in the absence of management.
    • ssign the daily deviation workload in the absence of management.
    • ttending Tier III for deviation updated when needed.
    • Takes ownership of Tier I problem solving and daily accountability.
    • cts proactively to ensure streamlined process operations and promote team collaboration.
    • Promotes a respectful and collaborative work environment.
    Requirements:
    • Bachelor's degree in science required, preferably in a scientific discipline.
    • Minimum of 5-7 years of experience in direct utilization of problem-solving tools (RCA tools including 5-Whys, Tap RooT, Fishbone/6M, Kepnor-Tregoe, Comparative Analysis, etc.) with demonstrated success.
    • t least 7 years of experience working in a regulated environment, preferably in biologics/pharmaceuticals.
    • Preferred experience in either upstream or downstream processing.
    • Experience in Root Cause Analysis and/or LEAN/six sigma experience or Operation Excellence tools.
    • Minimum of 7 years of technical and/or investigative writing with demonstrated proficiency in implementing effective CAPAs based on investigation results.
    • Demonstrated ability to perform intermediate to advanced levels of MS Office functions (Word, PowerPoint, Excel).
    • Equivalent combinations of education, training, and relevant work experience may be considered.
    • Proficiency in technical and/or investigative writing.
    • Excellent verbal and written communication skills.
    • bility to drive functional, technical, and operational excellence.
    • bility to evaluate data and make recommendations based on data analysis.
    • bility to make recommendations based on trends and trend analysis.
    • bility to work in a fast-paced environment with the capability to prioritize effectively to meet timelines.
    • Facilitation skills for groups including staff level employees.
    • Excellent time management and organizational skills to meet deliverables on tight deadlines.
    • Preferred: TrackWise, Root Cause Analysis, Tap RooT.


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