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Astrix Inc

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.

$69,465 / year median in New York

-13% projected decline

Explore Career

Job Description

Pay Rate Low:
35 |
Pay Rate High:
50 Our client is seeking an experienced QC Analyst to support laboratory investigations, root cause analysis, and CAPA activities within a cGMP-regulated environment. This is a great opportunity for a quality-focused professional looking to take ownership of critical investigations and work closely with cross-functional teams. Responsibilities Lead and document QC and OOS investigations from initiation through closure. Conduct root cause analysis using 6M, 5 Why, and Fishbone methodologies. Identify CAPAs and support corrective actions to prevent recurring issues. Collaborate with QC, QA, customers, and cross-functional teams to meet investigation deadlines and quality commitments. Ensure investigations comply with cGMPs, SOPs, and global quality standards . Track laboratory metrics and identify opportunities to reduce analyst errors, equipment failures, and testing issues. Provide investigation updates to management and support critical laboratory investigations. Qualifications Bachelor's degree in Chemistry or a related scientific discipline with 6+ years of QC laboratory experience, or an equivalent combination of education and experience. Experience with investigations, root cause analysis, investigation writing, and CAPA identification . Strong knowledge of cGMP requirements and laboratory quality practices. Excellent problem-solving, documentation, and communication skills. INDBH #LI-BH1