QUALITY INSPECTOR

Quality Inspector Help ensure the quality, safety, and integrity of life-changing medications. We're looking for a Quality Auditor in Rockford, IL to provide hands-on production floor support, verify cGMP compliance, audit manufacturing processes, and drive continuous improvement. This role is ideal for someone who enjoys solving problems, collaborating with operations, and making a measurable impact in a highly regulated pharmaceutical manufacturing environment. Quality Specialist Responsibilities include but are not limited to: Perform production room approvals after product and lot changes Verify first piece inspection to ensure finished goods code, format, and expiration date are correct Ensure equipment is packaged within validated parameters and equipment calibration dates on all process equipment are within required specifications. If not, this individual will contact the appropriate personnel to recalibrate and/or remediate the issue Review batch record to ensure equipment challenges and hourly inspections have been conducted and any non-conformances are addressed appropriately. Conduct periodic checks to confirm hourly inspections are being performed correctly and on track to meet requirements Review sampling pages to ensure samples have been taken, labeled and documented appropriately Audit production room to ensure Cleaning and Use logbooks, Mechanical Set-up logbooks, and Preventive Maintenance logbooks have been completed accurately and timely Confirm package (unit) functionality (perfs, peel, push, seals, etc.)Check to ensure portable equipment has been cleaned and documented correctly on quality form Audit production personnel to ensure the job is performed safely including wearing required personal protective equipment Ensure recovery stations are segregated from product flow Confirm bulk material and components for job are correct and kept covered Review each equipment clean room logbooks for correct clean room, entries are complete, correct and legible Review temperature and humidity data to ensure within acceptable job parameters Document audits using the Quality Auditor checklist listing the room, production job description, and date when the audit was conducted Identify proactively gaps in batch records and to mitigate deviations and documentation errors Participate on improvement teams (i.e. FMEA's, Kaizen, batch record etc.) as needed Support Root Cause Analysis as needed Ensure 5s (Sort, Set in order, Shine, Standardize, Sustain method) Compliance Adhere to cGMP (Current Good Manufacturing Practices), and GCP (Good Clinical Practices) policies, procedures, rules

Work is performed in areas with moderate risk or discomfort that may require special safety precautions, such as -wearing protective clothing or gear for up to 1/4 of the dayWork is primarily performed at a desk and/or in an office environment. for up to 1/4 of the dayWork near moving mechanical parts for 3/4 of the day and upFumes or airborne particles for up to 1/4 of the day The noise level in the work environment is typically moderate Ability to work overtime and/or weekend work