Quality Engineer (GMP/Pharma Manufacturing)

Dice is the leading career destination for tech experts at every stage of their careers. Our client, Brillfy Technology, is seeking the following. Apply via Dice today!Role: GMP Quality Assurance Engineer / Quality Systems EngineerLocation: Phillipsburg, NJ (Onsite M-F)Duration: 18 Months Contract-to-HireClient: AvantorInterview Process: 15-min Teams + 2-hour onsite interviewJob Description:The ideal candidate will have experience in pharmaceutical, biotech, or chemical manufacturing environments and strong knowledge of cGMP and ISO standards.Required Skills:5+ years of Quality Engineering / Quality Assurance experience Experience in pharmaceutical, biotechnology, chemical, or GMP manufacturing environments Strong knowledge of cGMP, ISO 9000, FDA regulations, CAPA, audits, validation Experience handling customer complaints and investigations Background in Quality Systems and compliance programs Bachelor’s degree in chemistry or related Science field Excellent communication and analytical skills Preferred Skills:Experience with ICHQ7, IPEC guidelines Stability, SPC, validation experience Internal/supplier audit experience GMP/GDP training experience Responsibilities:Lead quality assurance and compliance programs Manage CAPA and complaint investigations Support GMP, ISO, regulatory, customer, and internal audits Perform validation and statistical evaluations Drive quality improvements and corrective actions Collaborate with operations, suppliers, and customers Ensure ongoing compliance with FDA and ISO standards Work Environment:Manufacturing facility environment PPE required in designated areas Occasional domestic travel