QA Associate I (Solid Oral Dosage Pharmaceutical Environment) 3454097

QA Associate I (Solid Oral Dosage Pharmaceutical Environment) 3454097 Title: QA Associate I (Biotechnology Industry) 3454097 Location: Kentucky, USA (Open to U.S. Citizens who are local residents of Kentucky) Positions Available: 1 Shift: Sun–Thurs, 10:00 PM – 6:30 AM (Training on 1st shift Mon–Fri, 6:00 AM – 2:30 PM) Position Summary Our client is seeking a QA Associate I to provide essential quality support for the manufacturing of solid oral dosage pharmaceutical products. The QA Associate ensures compliance with cGMP, CFR, and company SOPs through oversight of manufacturing operations, document review, real-time monitoring of production activities, and testing of in-process and finished product samples. This role is critical in maintaining product quality, supporting investigations, and promoting continuous process improvement. Key Responsibilities Review, recommend, and provide feedback on SOPs and batch record revisions . Perform real-time audits of batch records to ensure completeness, accuracy, and compliance with critical process parameters. Conduct room and equipment clearances following cleaning procedures. Perform environmental monitoring via microbial swabbing of equipment and room surfaces. Maintain thorough knowledge of SOPs, cGMP, and CFR guidance applicable to solid oral dosage manufacturing. Conduct routine testing of in-process and finished product samples , including particle size, bulk density, moisture analysis, appearance, and AQL testing. Monitor production areas for compliance with SOP, cGMP, batch record, and safety requirements ; identify and resolve routine errors to prevent deviations. Collaborate cross-functionally to assess potential deviations and assist in investigations when required. Initiate deviation problem reports in TrackWise , providing detailed documentation to support investigations. Manage quality status of WIP and finished goods in physical inventory and JD Edwards system. Assist in investigations by supporting data collection and root cause analysis . Enforce GMP compliance and promote teamwork and effective communication. Provide training and coaching to manufacturing staff as needed. Support process improvements , including training, efficiency projects, and CAPA implementation. Assist in customer complaint investigations by inspecting retains and complaint samples. Required Qualifications Education & Experience: Preferred: Bachelor’s Degree in a related scientific or technical field with 2+ years of relevant experience. Minimum: High School Diploma with 4+ years of relevant experience in a regulated GMP manufacturing environment. Additional certifications such as Lean Six Sigma or ASQ are desirable. Knowledge & Skills: Familiarity with basic laboratory instrumentation . Strong safe work habits and adherence to SOPs. Basic math and computer proficiency . Excellent communication, documentation, and handwriting skills . Ability to follow written and verbal instructions and work with limited supervision. Strong technical problem-solving and decision-making abilities. Good time management and organizational skills. Experienced with continuous improvement techniques . Demonstrates initiative and accountability in completing tasks. Additional Attributes: Ability to enforce and promote GMP compliance . Works effectively in a team-oriented environment . Supports site-wide quality and process improvement initiatives . Note: This opportunity is open only to U.S. citizens who are local residents of Kentucky . #J-18808-Ljbffr ProQuality Network