Resilience (resilience.com). Benefits Overview

Performs and coordinates environmental monitoring in classified and non-classified areas up to Grade A at a sterile pharmaceutical manufacturing site. Reviews QC data and documentation for trends and cGMP compliance, schedules sampling workflows, leads investigations and process improvements, and coordinates QC and Operations activities. Trains EM technicians, provides technical guidance, troubleshoots methods, and supports laboratory and manufacturing processes with limited supervision.

Provides advanced quality assurance oversight for pharmaceutical and combination-product manufacturing, including validation, investigations, change controls, technology transfers, audits, batch disposition, CAPAs, risk assessments, and quality systems. Acts as a technical SME, supports regulatory inspections, leads cross-functional quality initiatives, mentors QA staff, and ensures compliance with cGMP and applicable regulatory standards across inspection, assembly, packaging, testing, and product release operations.

Leads process engineering and continuous improvement for automated pharmaceutical manufacturing equipment. Responsibilities include process validation, technology transfer, equipment qualification, change control, deviation investigations, risk management, troubleshooting, SOP and batch record authoring, supplier collaboration, training, and project management in a GMP-regulated environment. This is a rotating night-shift role supporting manufacturing operations, maintenance, and facility improvements.