Cipla
Overview
Position Overview: We are seeking a detail-oriented and motivated Quality Assurance (QA) Inspector to join our 2nd shift packaging operations. This role plays a critical part in ensuring product quality, adherence to cGMP standards, and compliance with internal and regulatory requirements. The QA Inspector will work cross-functionally to conduct quality inspections, support documentation accuracy, and drive continuous improvement efforts on the production floor. Responsibilities
Verify packaging components during dispensing and line clearance processes. Dispense printed packaging materials to packaging lines as needed. Conduct in-process quality checks during batch manufacturing and packaging per batch records. Collect finished product and validation samples as per SOPs and protocols. Perform IPQA testing on packaging lines in alignment with production requirements. Confirm proper cleaning of equipment and areas, and provide line clearance prior to production. Accurately post dispensed materials and sample information into SAP (ERP system) and perform related transactions. Participate in the investigation of deviations, OOS (Out of Specification), OOT (Out of Trend), and other quality events. Complete assigned training and ensure full compliance with company policies, SOPs, and safety standards. Conduct daily quality rounds to verify that shop floor operations remain in a state of GMP compliance. Escalate any discrepancies or issues to QA management in a timely manner. Perform other quality-related duties as assigned by management. Solid knowledge of GMP (Good Manufacturing Practices) and 21 CFR Part 820 regulations. Strong verbal and written communication skills. Proficiency in basic computer applications (Microsoft Word, Excel, PowerPoint). Highly organized, with strong attention to detail and multitasking abilities. Strong mathematical skills and analytical thinking. Self-starter capable of working independently in a fast-paced environment. Physical Requirements
Ability to stand or walk unassisted for at least 75% of an 8-hour shift. Must be able to lift up to 35 lbs. without assistance. Must be able to wear personal protective equipment (PPE) as required. Qualifications
High School Diploma or equivalent (required); strong background in science preferred. 1–2 years of pharmaceutical industry experience, particularly in manufacturing or packaging (preferred). Prior experience in generic pharmaceutical manufacturing/packaging is a plus.
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Position Overview: We are seeking a detail-oriented and motivated Quality Assurance (QA) Inspector to join our 2nd shift packaging operations. This role plays a critical part in ensuring product quality, adherence to cGMP standards, and compliance with internal and regulatory requirements. The QA Inspector will work cross-functionally to conduct quality inspections, support documentation accuracy, and drive continuous improvement efforts on the production floor. Responsibilities
Verify packaging components during dispensing and line clearance processes. Dispense printed packaging materials to packaging lines as needed. Conduct in-process quality checks during batch manufacturing and packaging per batch records. Collect finished product and validation samples as per SOPs and protocols. Perform IPQA testing on packaging lines in alignment with production requirements. Confirm proper cleaning of equipment and areas, and provide line clearance prior to production. Accurately post dispensed materials and sample information into SAP (ERP system) and perform related transactions. Participate in the investigation of deviations, OOS (Out of Specification), OOT (Out of Trend), and other quality events. Complete assigned training and ensure full compliance with company policies, SOPs, and safety standards. Conduct daily quality rounds to verify that shop floor operations remain in a state of GMP compliance. Escalate any discrepancies or issues to QA management in a timely manner. Perform other quality-related duties as assigned by management. Solid knowledge of GMP (Good Manufacturing Practices) and 21 CFR Part 820 regulations. Strong verbal and written communication skills. Proficiency in basic computer applications (Microsoft Word, Excel, PowerPoint). Highly organized, with strong attention to detail and multitasking abilities. Strong mathematical skills and analytical thinking. Self-starter capable of working independently in a fast-paced environment. Physical Requirements
Ability to stand or walk unassisted for at least 75% of an 8-hour shift. Must be able to lift up to 35 lbs. without assistance. Must be able to wear personal protective equipment (PPE) as required. Qualifications
High School Diploma or equivalent (required); strong background in science preferred. 1–2 years of pharmaceutical industry experience, particularly in manufacturing or packaging (preferred). Prior experience in generic pharmaceutical manufacturing/packaging is a plus.
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