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CSL Plasma

QC Compliance Specialist

Career Insights for Quality Control Analyst

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What they do

A Quality Control Analyst, in the biotech and medical device industries, works in laboratories performing biological, microbiological, and chemical tests on products and materials. Responsible for calibrating equipment, inspecting products, processing and testing materials, and reporting results. May work in other production environments to monitor and improve quality and efficiency in production systems and products.

$73,058 / year median in North Carolina

-11% projected decline

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Job Description

QC Compliance Specialist at CSL Plasma QC Compliance Specialist at CSL Plasma in holly springs, North Carolina Posted in 6 days ago. Job Description Summary Supports the core quality systems including: investigation/deviation management, general CAPA support, incident management, controlled document writing/review, change control support, oversight of vendor work order system Job Description Leads deviation (DR) investigations to adequately identify root cause and implement appropriate corrective and preventative actions (CAPAs) to prevent reoccurrence. Employs standardized root cause analysis, investigation tools and methodologies. Own CAPAs as appropriate. Utilizes Investigation and Deviation systems for owning QC investigations, tracking statuses, leading investigations teams and serve as QC liaison with other department investigation writers to ensure complete and timely resolution. Participates in lean lab operation and continuous improvement programs to eliminate non-value-add activities/maximize efficiency. Provides technical support with assigned area of QC. Provides support with assigned business process systems to support QC. These systems include SAP, LIMS, Data Historian and Trackwise. Responsible for the Work Order Tracking system for tracking and coordinating the initiation, execution and completion of work orders. Complies with policies and procedures in order to maintain compliance with legal regulations, health and safety, and regulatory requirements as written. Responsible for reviewing trends of QC deviations and investigations to identify areas requiring additional action. Maintains departmental metrics and key performance indicators (KPIs) for Senior leadership review. Owns, develops and maintains controlled documents.

Minimum Requirements:

Bachelor's degree and 2+ years' experience or equivalent (minimum). Basic knowledge of cGMP and FDA requirements preferred Knowledge of Laboratory Systems and Investigation/Deviation writing required Excellent organizational, planning and time management skills. Strong oral, written and interpersonal communication skills. Demonstrated technical writing skills. The ability to work effectively in both a team environment and an individual contributor role.