Quality Control Raw Material Analyst

As a QC RM Analyst, your role is crucial in ensuring the compliance of raw materials with quality specifications to maintain product safety, efficacy, and regulatory compliance for third-party manufacturing operations. Key Responsibilities: - Conduct routine and non-routine testing of incoming raw materials following SOPs. - Perform physical, chemical, and microbiological tests to verify material quality. - Ensure identification, purity, and conformity of raw materials to specifications. - Record, maintain, and report accurate test results in laboratory documentation systems. - Investigate deviations, non-conformances, and out-of-specification (OOS) results. - Coordinate with procurement, production, and QC teams for timely material release. - Ensure proper calibration, maintenance, and operation of laboratory instruments. - Follow GLP, GMP, and ISO standards strictly. - Support method development, validation, and documentation as required. - Maintain laboratory hygiene, organization, and safety standards. Qualifications: - Bachelors degree in Chemistry, Pharmaceutical Sciences, Biochemistry, or related field. - 3 years of experience in QC raw material testing in the pharmaceutical industry (third-party manufacturing experience is a plus). - Knowledge of QC analytical techniques: HPLC, UV, FTIR, titration, loss on drying, etc. - Familiarity with GLP, GMP, and ISO standards. - Strong analytical, observational, and problem-solving skills. - Attention to detail and ability to follow SOPs accurately. - Good communication and teamwork skills. In the given Job Description, there are no additional details of the company provided.,