🎁 Before you apply, rehearse this interview. Create your free WorkMundi account and get an Interview Training on HelpsYouSpeak — no cost, no card. I want my training →
Key Responsibilities - In-Process Quality Assurance (IPQA): - Monitor and ensure compliance during manufacturing and packing operations. - Conduct routine checks and validations to maintain product quality. - Line Clearance Activities: - Perform and document line clearance before batch initiation and between product changes. - Ensure adherence to GMP and prevent cross-contamination. - Batch Manufacturing Record (BMR) & Batch Packing Record (BPR) Review: - Review and verify BMR/BPR for completeness, accuracy, and compliance. - Identify discrepancies and coordinate with production for resolution. - Analytical Quality Assurance (AQA): - Support analytical documentation and ensure lab compliance. - Assist in OOS/OOT investigations and CAPA implementation. - SAP Documentation & Transactions: - Manage quality-related entries and batch release processes in SAP. - Maintain digital traceability and support audits with SAP data. - Injectables Manufacturing Oversight: - Ensure aseptic practices and environmental monitoring in sterile areas. - Support validation and qualification activities for injectable products. Qualifications & Skills - Bachelors/Masters degree in Pharmacy. - Familiarity with GMP, GDP, and regulatory guidelines (e.g., USFDA, EU, WHO). - Robust attention to detail, communication, and problem-solving skills. Interested candidates can mail their resume at recruitment.indore@guficbio.com .