Quality Control Analyst

We are hiring Quality Control Analyst.Please let me know if you are interested or anyone who might be interested.Client: Major Pharmaceutical ClientPosition: Quality Control AnalystDuration: 12+ Months ContractLocation: Thousand Oaks CA USA 91320Pay Rate: $40.00-$62.00/ Hr on W2Description:As a QC Analyst II, you will support various activities within the Quality Control department. Key responsibilities include executing analytical method transfers, including raw materials, for use in a cGMP environment. You will be responsible for conducting biological, chemical, and physical analyses on raw materials, in-process samples, drug substance, finished product samples, and other samples collected from manufacturing areas.Essential Duties and Responsibilities:Conduct biological, chemical, and physical analyses on samples including raw materials, initial, in-process, and final products, as well as environmental monitoring samples, in accordance with SOPs and approved protocols Support implementation of new methodologies and introduction of new sample types into existing methods within the QC laboratory Assist in investigations of nonconformances and troubleshoot unexpected results Handle multiple tasks concurrently, including testing and inventory management, in a timely and organized manner Perform review of test data, including adherence to good documentation practices (GDP); may perform release functions in LIMS or other computerized systems Support generation and documentation of validation protocol deliverables Draft and update QC SOPs as required Perform equipment operation, maintenance, and calibrations as required Perform other duties as assigned Qualifications:General understanding and knowledge of: Laboratory functions, test methods, and analytical equipment (e.g., HPLCs, plate readers), processes, and applicable procedures Laboratory safety practices, including handling of hazardous and biohazardous materials Wet chemistry and instrumental analytical methods Operating and basic troubleshooting of laboratory equipment General knowledge of FDA regulations, Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and Good Documentation Practices (GDP) preferred Knowledge of quality and regulatory requirements related to pharmaceutical or biotechnology laboratories is a plus Ability to write detailed investigation reports and apply root cause analysis is a plus Strong team player with the ability to meet deadlines and adapt to changing priorities Effective communication skills with managers, peers, and cross-functional teams Detail-oriented with a focus on accuracy and high-quality work Strong interpersonal skills and ability to work efficiently in a team environment Ability to prioritize multiple tasks and manage time effectively Strong analytical thinking, problem-solving, and decision-making skills Education and/or Experience:High School diploma or equivalent required; Bachelor's degree in Chemistry, Microbiology, Biological Sciences, or a related field strongly preferred Minimum of 2 years of relevant work experience Experience in quality operations within biotechnology, pharmaceutical, or other GMP-regulated environments strongly preferredRegardsVishnu Das Natesandvishnu@radiants.com