Quality Control Analyst

Client: Major Pharmaceutical Client Position: Quality Control Analyst Duration: 12+ Months Contract Pay Rate: $40.00-$43.00/ Hr on W2 Description Primary duties of this position will focus on daily laboratory operations and execution of testing to support manufacturing operations. Testing may include, but is not limited to: Drug substance and drug product samples Manufacturing samples Stability samples Raw materials Various protocol studies using established test methods The assays performed range from routine analytical testing such as pH and enzyme concentration to more complex assays including: SDS Silver Gels PCR DNA analysis Enzyme activity assays This position is expected to maintain operational and GMP readiness of the QC laboratory areas. In addition, the individual will participate in complex projects, operational excellence initiatives, and quality system activities. Experience with the following is preferred: A280 SOLO A280 Compedia methods: pH Osmolality (OSMO) Appearance Enzyme activity assays DNA analysis PCR Free Thiol testing Responsibilities Testing Execution (80%) Execute routine and non-routine QC testing to support manufacturing operations. Perform laboratory testing according to approved methods and procedures. Accurately document and report testing results. QC Operations Support (10%) Perform data review and trending. Support Operational Excellence (OE) and 5S initiatives. Maintain laboratory equipment and reagents. Prepare reagents. Maintain laboratory housekeeping. Provide support to other QC groups as needed. Compliance & Quality Systems (10%) Support compliance activities. Assist with SOP revisions. Provide input to quality systems. Maintain GMP compliance and laboratory documentation. Education & Experience Required Bachelor's degree in Biology, Biochemistry, Chemistry, Molecular Biology, Biotechnology, or a related scientific discipline. 1+ years of relevant laboratory experience. Preferred Experience working in a GMP-regulated environment. Knowledge of quality systems and laboratory compliance requirements. Required Skills Strong scientific understanding and analytical skills. Critical thinking and problem-solving abilities. Familiarity with laboratory documentation practices. Working knowledge of: Microsoft Office LIMS SAP TrackWise EDMS Understanding of GMP compliance. Problem Solving & Work Environment Solve routine laboratory problems following established procedures and policies. Analyze laboratory data using standard practices. Work independently on assignments of limited scope and complexity. Build effective working relationships with supervisors and team members. Collaborate with cross-functional laboratory and manufacturing teams. #J-18808-Ljbffr