The role involves executing engineering activities, performing validation tasks, technical writing, and ensuring compliance with GMP regulations.

Lead engineering activities for facilities and equipment in a GMP-compliant environment. Oversee projects, manage qualifications, and ensure regulatory compliance.

Lead and manage multiple validation and qualification projects in a GMP-compliant environment, ensuring compliance with regulatory standards and operational efficiency.

The MES Engineer will support manufacturing by improving processes, using POMS and SAP for data analysis, and implementing solutions for GMP compliance.

The Technical Writer will create and revise SOPs and controlled documents, ensuring compliance with cGMP and regulatory standards while supporting engineering teams.