Process Associate I - Biotech Manufacturing

Role: Manufacturing Support Technician at Novo Nordisk's bioproduction facility, primarily responsible for supporting downstream manufacturing operations, process documentation, deviations, change control, and process improvements. Responsibilities include training technicians, reviewing and updating SOPs and batch records, investigating deviations via root cause analysis, and ensuring compliance with cGMP standards. The position involves cross-functional collaboration across departments, supporting inspections, and possibly hands-on manufacturing within sterile environments. Requirements: High school diploma with 6+ years relevant manufacturing experience or Bachelor’s in science/engineering with 2+ years; pharmaceutical or biotech experience preferred. Skills include understanding of GMP, manufacturing practices, quality systems, and lean principles; strong analytical, organizational, and communication skills. High-value specifics: sterile bioprocess support, focus on downstream operations, process improvement initiatives, and compliance with health authority inspections. The role is onsite in West Lebanon, NH, with minimal travel and participation in on-call rotations.