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Job description
Keystone Industries in Gibbstown, NJ seeks a Quality Engineer/Consultant for an approximately six‑month, on‑site engagement. The role requires 5–10 years in regulated pharma/manufacturing, aseptic processing experience, and strong QA/QC and regulatory knowledge.
The consultant will work in a GMP environment, support audits, lead CAPA and MRB activities, and collaborate with engineers on validation and process improvements. Compensation is hourly and flexible for highly qualified candidates.
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.