Brillpharma

Role & responsibilities Assist in vendor management activities including communication, follow-ups, and documentation. Review vendor/CMO quality system documents under guidance. Support in drafting, reviewing, and maintaining Quality/Technical Agreements with vendors/CMOs. Assist in conducting vendor performance evaluations and preparing reports. Help in risk assessments related to vendors, including supply chain mapping and excipient risk. Maintain records and databases for quality parameters, trending, and periodic assessments. Ensure compliance with GMP requirements, internal procedures, and regulatory updates. Support in reviews of assessments related to elemental impurities, excipient risks, and vendor quality. Adhere to Health & Safety (H&S) requirements and company policies. Perform other tasks as assigned by management. Preferred candidate profile Bachelors degree in Pharmacy, Life Sciences, or a related field. Basic knowledge of GMP guidelines and regulatory requirements. Good communication, coordination, and documentation skills. Proficiency in MS Office (Excel, Word, PowerPoint).