Job Description
Our Client, a Medical Device and Healthcare company, is looking for a Quality Engineer I for their Pleasanton, CA location. Responsibilities:
+ Support validation activities — Assist in equipment, process, and software validation (including CSV), troubleshoot discrepancies, and help plan validation efforts using risk‑based approaches.
+ Document quality issues — Prepare, review, and maintain quality control documents, reports, and production records.
+ Participate in CAPA investigations — Support root‑cause analysis and corrective/preventive actions under supervision.
+ Assist with nonconformance management — Help evaluate product defects, deviations, and material review board (MRB) activities.
+ Perform data analysis — Collect and analyze quality metrics to identify trends and improvement opportunities.
+ Support audits and inspections — Prepare documentation and participate in internal audits and external regulatory ins...
+ Support validation activities — Assist in equipment, process, and software validation (including CSV), troubleshoot discrepancies, and help plan validation efforts using risk‑based approaches.
+ Document quality issues — Prepare, review, and maintain quality control documents, reports, and production records.
+ Participate in CAPA investigations — Support root‑cause analysis and corrective/preventive actions under supervision.
+ Assist with nonconformance management — Help evaluate product defects, deviations, and material review board (MRB) activities.
+ Perform data analysis — Collect and analyze quality metrics to identify trends and improvement opportunities.
+ Support audits and inspections — Prepare documentation and participate in internal audits and external regulatory ins...
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