Manufacturing Technician II, In-Line Inspector - Sterile Filling

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, In-Line Inspector supports sterile filling inspection operations, working in various Controlled/Non-Classified areas. The Technician operates automated and manual inspection equipment; performs visual, cosmetic, and physical inspection of materials; executes line clearances; and completes batch record entries. The role also supports improvement activities such as 5S, problem-solving, Kaizen events, and manual data collection, all in accordance with cGMPs.

Operations Accountable for the outgoing quality level of inspected product; perform manual visual, cosmetic, and physical inspection of material, promptly escalating concerns to the Lead and Manager/Supervisor. Must obtain and maintain visual inspection qualification. Operate assigned machinery, including servicing automated inspection equipment, monitoring equipment status, reintroducing materials, manually palletizing inspected materials, and assuring a smooth flow of product. Start up equipment, make minor adjustments to machinery, remove jams, and perform minor troubleshooting and assembly/disassembly for cleaning. Use material handling equipment such as motorized and manual pallet jacks and non-motorized lifts. Perform cleaning, housekeeping and line clearance activities for assigned areas as required to maintain a cGMP environment. Apply knowledge of product security controls. Perform work in accordance with SOPs, cGMPs, and OSHA-compliant safety procedures, maintaining familiarity with job-related hazards and controls (PPE, ergonomics, LOTO, human/material/waste/chemical handling, and spill control) and area chemical Safety Data Sheets. Report all discrepancies to the process facilitator. Print SOPs and forms via ECMS. Support lean and process-improvement activities, including 5S, problem-solving, and manual tracking of OEE performance data. Review operational SOPs, forms, and batch records for accuracy, and suggest process improvements while maintaining quality and cGMP compliance. Documentation & Compliance Perform batch record and GMP documentation entries; maintain records and logs as required, including mathematical computation where needed. Perform inventory control, reconciliation, and inventory movements using SAP in a limited role (e.g., moving items between storage locations and goods-issuing to process orders). Training & Development Acquire and maintain all required certifications and qualifications for the assigned work area, including cold room training/access to transfer materials in and out of the cold rooms. Cross-train and support other work areas as needed. Experience & Education Minimum Qualifications Prior experience in a regulated manufacturing environment (e.g., pharmaceutical, biotechnology, medical device, or other GMP-regulated industry) is preferred. Experience in manufacturing, quality, or visual inspection is highly desirable. Ability to effectively read, write, speak, and understand English to accurately interpret and follow Standard Operating Procedures (SOPs), batch records, work instructions, specifications, and other controlled documentation. Basic mathematical proficiency, including the ability to perform routine calculations involving weights, measures, percentages, and unit conversions, while accurately documenting inspection and production data. Ability to follow written procedures and standardized work with minimal supervision while recognizing abnormal conditions and appropriately escalating quality, safety, equipment, or process concerns. Strong