Quality Auditor

Overview Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are VRT Pharma. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of VRT Pharma. Summary Of Objective This position is responsible for providing the direction, organization, alignment, monitoring and cGMP compliance to ensure the successful, cost effective, timely and safe processing of customer orders. The position audits production room documentation, sampling requirements, reviews equipment challenges and that hourly in-process inspections have been performed within compliance. The Quality Auditor performs real-time batch record review during batch processing in order to drive improvements into our Right First Time (RFT) metrics. They are also responsible for leading and realizing continuous quality and process improvements on the production floor by mentoring, coaching, and training their operational counterparts. Responsibilities Perform production line clearance inspections after product and lot changes. Evaluate equipment high-risk areas to drive line clearance excellence. Verify first & last piece inspections to ensure finished goods code, format, and expiration date are correct. Ensure equipment is packaged within validated parameters. Ensure equipment calibration dates are current and that all process equipment are within required specifications. Perform in-line review of batch record (MPI) to ensure equipment challenges and hourly inspections have been conducted and any non-conformances are addressed appropriately. Confirm that hourly inspections are on track to be met according to the applicable sample size. Review product sampling pages to ensure samples have been taken, labelled, and documented appropriately. Perform product quarantine of impacted materials including accumulation totals, confirming segregation and negative issuing of effected product and/or materials. Review Cleaning and Use logbooks, Mechanical Set-up logbooks, and Preventive Maintenance logbooks for completeness, accuracy, and legibility. Confirm package (unit) functionality (perforation, peel, push, seals, etc.). Ensure portable equipment has been cleaned and documented correctly. Review and confirm PPE attire aligns with batch record instructions. Ensure recovery stations are segregated from product flow. Confirm bulk material and components for production orders are correct, documented and ‘checked by’ via second signature. Confirm temperature and humidity data is within acceptable job parameters. Proactively identify gaps in batch records to mitigate deviations and documentation errors. Support Root Cause Analysis as needed. Write quality event notifications for issues encountered within operations. Ensure 5s Compliance is followed during packaging. This position may require overtime and/or weekend work. Must have knowledge of and adherence to all cGMP, and GCP policies, procedures and rules. May perform duties of a Quality Coordinator. May perform duties of Label Technician. Perform other duties as assigned by Manager/Supervisor. Shift and Special Demands Shift is Friday-Sunday 8:00am-8:00pm. Stationary Position: Under a 1/4 of the day. Move, Traverse: 3/4 of the day and up. Operate, activate, use, prepare, inspect, or place: From 1/2 to 3/4 of the day. Ascend/Descend or Work Atop: Up to 1/4 of the day. Position self (to) or Move (about or to): From 1/2 to 3/4 of the day. Communicate or exchange information: 3/4 of the day and up. Detect, distinguish, or determine: 3/4 of the day and up. On an average day, the individual can expect to move and/or transport up to 10 pounds less than 1/4 of the day. This position may have the following special vision requirements: Close Vision, Distance Vision, Color Vision, Peripheral Vision, Depth Perception, Ability to focus. Work Environment The following are some environmental conditions that one may be exposed to on a daily basis and for various lengths of time: Work is performed in areas with moderate risk or discomfort that may require special safety precautions, such as wearing protective clothing or gear for 1/4 to 1/2 of the day. Work is primarily performed at a desk and/or in an office environment. For up to 1/4 of the day. Work near moving mechanical parts for 1/4 to 1/2 of the day. Extreme cold (non-weather) for up to 1/4 of the day. Required Qualifications High School Diploma or GED and/or 1-3 months related experience and/or training. Basic Mathematical Skills Intermediate Computer Skills: Ability to perform more complex computer tasks and has knowledge of various computer programs. Full Professional Proficiency: Ability to speak, read, and write fluently and accurately on all levels pertinent to professional needs. High reasoning: Ability to define problems, collect data, establish facts, and draw valid conclusions. Be able to interpret an extensive variety of technical instructions in math or diagram form and deal with several abstract/concrete variables. High attention to detail. Must be able to address and identify operational discrepancies. Preferred 1-5 years performing quality task within a cGMP environment. Ability to follow instructions and respond to management direction. Ability to work independently and/or part of a team. Ability to display excellent time management skills. Equal Opportunity Employer/Disabled/Veterans Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future Equal Employment Opportunity (EEO) Statement: VRT Pharma is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. #J-18808-Ljbffr