Line Inspector, Quality Assurance

Title: Line Inspector, Quality Assurance Date: Sep 25, 2026 Location: Sun Pharma Canada Inc. Company: Sun Pharma Canada Inc. Driven by a bold pursuit of science and fueled by an unwavering commitment to patients, Sun Pharma is a leading global pharmaceutical company, providing high-quality medicines trusted by healthcare professionals and patients. As part of our mission to Reach People and Touch Lives, we deliver Innovative Medicines, Generics and Consumer Healthcare products that improve the lives of millions of people. With a broadly diversified portfolio of products that span multiple therapeutic areas, we improve access to effective, affordable treatments that promote better health and well-being. Reaching People. Touching Lives. Job purpose The main responsibility of this position is to perform regular QA inspection checks during the day to day packaging and compounding operations at Sun Pharma Canada Inc. This activity would include routine line inspections for GMP requirements, bulk and documentation to ensure first time quality is built into the finished product to meet SPCI and government agency cGMP requirements. Duties and responsibilities Perform routine line clearances/inspections on the packaging lines. Provide Line Clearance certification and re-certification to production floor Ensure routine compliance of day to day activities on the compounding and packaging areas; working with operations personnel to achieve compliance. Monitor packaging and compounding to ensure that batch documentation requirements and SOPs are being followed. Review the required paperwork for accuracy and compliance on line and upon completion of the activity. Initiate incident reports and perform initial floor investigations and impact assessments to ascertain product quality impact as required. Coordinate and cooperate with investigation team to complete investigations in timely manner. Collect representative samples for testing and retention, and ensure all relevant paperwork is complete. Submit samples/re-samples to laboratory in a timely fashion to meet business needs. Maintain sample and retention records program. Communicating discrepancies to QA Manager or other departments where required. Work effectively with operation personnel to build in quality up front in the process. Prepare and update written procedures (SOPs/Forms/WIs) in areas of responsibility. Automate job functions to achieve continuous increase in productivity. Issuance, monitoring, review and archival of Production Logbook review, Perform Real time review of PWOs and related documents (paper documents as well as /electronically) Review MFs (paper / MES), release bulk to packaging, enter and verify CPPs data as applicable Perform QA review for Magnehelic gauges, Pest control and Temperature monitoring in the GMP areas and prepare quarterly EM reports Perform routine inspection of GMP areas and provide coaching to improve compliance and GMP behavior Provide continuous support to packaging line, assess issues in GMP manner and provide real time solutions Initiate change control as required Initiate incident reports related to production areas, as required Provide floor support to investigation team and perform QA review of event reports, as required Oversee temperature monitoring systems for GMP areas; TempTale procurement, configuration, installation and monthly data downloading and trending. Initiate Product Hold / Reject notification requests Record GMP observations on production floors on shift basis and communicate as required Update databases as required related to Quality Operations i.e. MF tracker, correction tracker for RFT, line clearance certification / decertification tracker etc.. Review and approve exceptions in electronic batch system. Provide one on one coaching to packaging support staff i.e. mechanics to improve RFT and good documentation practices Share GMP ideas/ thoughts and provide feedback to production floor during kick off meeting/weekly/mont…

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