Manufacturing Technician II - DAP

A career at Resilience is more than just a job – it’s an opportunity to change the future. Resilience is a technology-focused biomanufacturing company that’s changing the way medicine is made . We’re building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need.   For more information, please visit www.resilience.com The Manufacturing Technician II reports to a Supervisor/Manager, Manufacturing and performs a variety of manufacturing tasks in Controlled/Non-Classified areas in accordance with cGMPs, supporting Packaging operations. Responsibilities include operating packaging equipment, performing in-process monitoring, line clearances, cosmetic inspection, cleaning, and completing batch record entries.

Operations Perform the duties of operating assigned machinery: service machines with materials, monitor equipment status, reintroduce materials, manually palletize finished materials, and ensure smooth product flow. Start-up machinery including equipment setup, recipe selection, data entry on SCADA and HMI; make minor adjustments and perform critical sensor challenges. Perform manual packaging tasks as required including hand packaging and rework of in-process and finished material. Operate light material handling equipment (motorized and manual pallet jacks, non-motorized lifts) to safely move, store, or deliver material. Perform visual quality inspection and sampling of in-process materials; promptly escalate concerns to Lead and Management as needed. Perform minor troubleshooting including clearing minor jams and identifying equipment defects; escalating to the Lead and Management as needed. Perform inventory control and reconciliation activities using SAP and WES. Perform cleaning, housekeeping, and line clearance activities for assigned areas to maintain a cGMP environment. Documentation & Compliance Perform batch record and GMP documentation entries; perform mathematical computations as required. Follow job-related safety procedures including PPEs, LOTO, ergonomics, and material/chemical/waste handling, spill controls and human safety. Support lean activities and process improvement work including 5S, problem-solving, and manual data collection. Execute protocols as required as part of equipment qualification and process validation work. Training & Development Provide flexible support to other areas of the Manufacturing Team as needed. Acquire and maintain all required certifications and qualifications for the assigned work area. Attend and actively participate in daily Tier 0 meetings. Experience & Education Minimum Qualifications Prior experience in a regulated manufacturing environment. Working knowledge of product security controls and material handling equipment. Demonstrated documentation and data entry skills, including accurate completion of batch records and logbooks. Basic mathematical skills, including the ability to perform routine calculations (e.g., weights, measures, conversions). Ability to effectively read, write, speak, and understand English to interpret SOPs, batch records, and work instructions. Ability to follow written procedures and work instructions with minimal supervision, escalating issues as needed. Basic problem-solving skills and the ability to identify deviations or inconsistencies in processes or documentation. Ability to work effectively as part of a team in a fast-paced production environment.

High school graduate, vocational school graduate, or equivalent. 1+ years of experience in a pharmaceutical, biotechnology, or cGMP-regulated manufacturing environment. Experience working in a lean manufacturing environment. Working knowledge of cGMP principles, including documentation practices, safety procedures, and compliance expectations. Experience working in a lean manufacturing environment. Working knowledge of Microsoft