Chemveda Formulation Pvt Ltd

As a QA Docscell at our company, your role involves ensuring compliance with cGMP, ICH guidelines, and regulatory requirements. You will be responsible for reviewing and maintaining batch manufacturing records (BMRs), batch packaging records (BPRs), and quality documentation. Additionally, you will conduct in-process checks and line clearance during manufacturing and packaging activities. Your responsibilities will also include participating in internal audits, self-inspections, and external regulatory audits. You will review and assist in the preparation of SOPs, protocols, and reports. In case of deviations, CAPA, change controls, and OOS/OOT results, you will investigate and document them. Furthermore, you will coordinate with cross-functional teams to ensure QA compliance across departments. Qualifications Required: - Preferably a female candidate - Should be stable The company offers the following benefits: - Health insurance - Provident Fund This position is suitable for freshers and requires in-person work at the given location.,