Quality Assurance

As an In-Process Quality Control (IPQC) personnel, your role involves performing in-process checks during manufacturing and packing in order to ensure quality standards are met. You will be responsible for monitoring critical parameters of Tablet, DPI, Liquid Injection & Dry Injection sections, and recording results in real-time as per GMP guidelines. Additionally, you will need to coordinate with production for any process deviations or non-conformities and verify line clearance before the start of manufacturing or packing. Your responsibilities also include maintaining and reviewing batch manufacturing records (BMR) and batch packaging records (BPR) to ensure compliance with ALCOA+ principles (Attributable, Legible, Contemporaneous, Original, Accurate). You will support the preparation and issuance of controlled documents while ensuring proper documentation flow from production to QA. Furthermore, your role involves reviewing existing SOPs and updating them as per regulatory requirements. You will also assist departments in drafting new SOPs to maintain compliance and efficiency within the organization. As an In-Process Quality Control (IPQC) personnel, your role involves performing in-process checks during manufacturing and packing in order to ensure quality standards are met. You will be responsible for monitoring critical parameters of Tablet, DPI, Liquid Injection & Dry Injection sections, and recording results in real-time as per GMP guidelines. Additionally, you will need to coordinate with production for any process deviations or non-conformities and verify line clearance before the start of manufacturing or packing. Your responsibilities also include maintaining and reviewing batch manufacturing records (BMR) and batch packaging records (BPR) to ensure compliance with ALCOA+ principles (Attributable, Legible, Contemporaneous, Original, Accurate). You will support the preparation and issuance of controlled documents while ensuring proper documentation flow from production to QA. Furthermore, your role involves reviewing existing SOPs and updating them as per regulatory requirements. You will also assist departments in drafting new SOPs to maintain compliance and efficiency within the organization.