Sr CAPA Engineer

What you’d do

Develop and maintain global product transfer processes so quality is met at receiving manufacturing sites. Partner with quality, R&D, and plant teams on new product and site-to-site transfers, ensuring regulatory compliance, quality planning, PFMEA, training, inspection, and validation plans. Found on the employer's careers page on Oct 18, 2026. Apply through the link.

You’ll need

• 6–8 years in Quality, Manufacturing and/or Engineering
• Engineering background
• Medical device, pharma or regulated industry experience
• Design/manufacturing in a GMP environment
• Quality and regulatory compliance knowledge