Senior Quality Engineer

What you'll do Lead deviation, CAPA, and root-cause investigations across manufacturing lines.Review and approve batch records, validation protocols, and change controls.Partner with production to embed quality-by-design into daily operations.Support internal and regulatory audits, including FDA and WHO-GMP inspections. What you'll bring ✓Bachelor's in engineering, pharmacy, or life sciences; 5+ years in pharma quality.✓Deep working knowledge of cGMP, ICH, and FDA 21 CFR Parts 210/211.✓Experience leading investigations and authoring CAPAs in a regulated environment.✓Strong data analysis and cross-functional communication skills.