Quality Control Analyst

Quality Control Analyst Job Summary The Quality Control Analyst is responsible for the timely analysis of samples, ensuring accurate test results, and maintaining compliance with quality systems and regulatory standards. This role supports production quality, documentation, and continuous improvement within the quality department. Responsibilities Perform timely analysis of samples under test and provide accurate results. Coordinate with external partners for quality-related issues and clarifications. Conduct sampling and analysis of raw materials, intermediates, and finished goods. Ensure compliance with approved test reports and analytical testing requirements. Assist the team in implementation and maintenance of ISO standards. Perform calibration, standard preparation, standardization, and related documentation. Operate and maintain analytical instruments such as HPLC, GC, and perform wet chemistry analysis. Submit timely reports to SAP for result recording. Complete and update all relevant quality documents accurately. Support zero-accident objectives in quality operations. Meet batch-wise timelines, quantity, and quality targets. Train and supervise operators working in the quality department. Monitor and control waste generated during quality operations. Participate as a member of the emergency response team and guide team members during emergencies. Maintain

ISO 9001, ISO/IEC

17025, SAP, and other quality systems within the department. Maintain analytical records and log sheets in compliance with GMP and ISO guidelines. Requirements High school diploma or equivalent education. 1 2 years of experience in quality, including exposure to cGMP, ISO, and regulatory audits. Knowledge of quality control in fine chemicals and pharmaceutical environments. Experience working under cGMP conditions. Summary Qualification High school diploma or equivalent. 1 2 years of quality control experience in regulated environments. Familiarity with ISO 9001 and

ISO/IEC 17025

standards. Experience with GMP-compliant documentation and audits. Skill Proficiency in HPLC, GC, and wet chemistry techniques. Knowledge of calibration, standard preparation, and standardization. Ability to maintain accurate analytical records and documentation. Understanding of cGMP, ISO, and quality management systems. Willingness to learn and adapt to new procedures. Team-oriented with the ability to train and supervise others. Good verbal and written communication skills. Strong attention to detail and adherence to safety practices. Wollborg Michelson Recruiting is an Equal Opportunity Employer and prohibits discrimination of any kind. We ensure job offers are made based of one s employment experience, skills, and qualifications, regardless of race, gender, ethnic origin, or any other classification protected by law. All applicants must furnish proper identification to prove their legal right to work in the US upon a job offer. We participate in E-Verify to confirm one s right to work in the US. Wollborg Michelson Recruiting does not provide sponsorship for an employment-based visa status.