Quality Control Associate I

Target PR Range: 19-22/hr DOE. Responsibilities B shift schedule: 1:00pm – 9:00pm Monday-Friday. Quality control responsibilities: analysis and inspection of products or processes for compliance with specifications and standards. Demonstrate detailed oriented attention in all facets of responsibilities. Perform analytical evaluation or test of products or processes. Demonstrate knowledge of testing methods, product usage, and applicable regulations and standards. Adhere to established policies and procedures. Establish test methodology. Provide technical guidance and training to others on SOPs and quality guidelines. Visually inspect in-process/finished material. Consult with QA personnel or immediate supervisor on clarification of specifications or acceptability of product as required. Refer to procedures manual, sampling charts, blueprints and/or specifications to determine number of samples, specifications to check and method to testing Product Assembly Process Sheets. Obtain samples and use inspection devices and visual inspection to evaluate acceptability of components and finished products. Prepare required inspection reports. Consult supervisor and QA supervisor/technician for clarification of quality issues, defects, workmanship, etc. for direction and corrective action. Record traceability information, production information, cleaning and safety check documentation as required. Observe department’s safety regulations and use personal protective equipment as required. Practice department’s good manufacturing and housekeeping procedures and complete cleaning verification checklists as required. Adhere to plant/Corporate policies/procedures, department safety and environmental regulations, GMPs and ISO 13485 Standards. Report any unusual circumstances to immediate supervisor and perform other miscellaneous duties as assigned. Report machine malfunction to designated individual for action and recommend equipment modifications to improve operation. Monitor machine efficiencies and report any machines not performing to standard to designated individual. Qualifications Applies acquired knowledge and skills to complete standard tasks. Readily learns and applies new information and methods to work in assigned area. Maintains appropriate licenses, training and certifications. Works on routine assignments that require some problem resolution. Works within clearly defined standard operating procedures and/or scientific methods. Adheres to all quality guidelines. Works under moderate degree of supervision. Regular review of output by work lead or supervisor. Refers complex unusual problems to supervisor. HS Diploma, GED or equivalent experience. Preferred 1-2 years experience in related field. #J-18808-Ljbffr Planet Pharma Group