Executive

As an Executive in the Quality Control (QC) division at Lupin Limited's Pithampur-II facility, you will play a crucial role in ensuring the integrity and efficacy of laboratory and manufacturing processes through comprehensive management and enhancement of Labware 7 LIMS (Laboratory Information Management System) implementations. Your responsibilities include overseeing the creation and maintenance of master data, validating system configurations, and managing calculation protocols to ensure precise and accurate data processing.

You will engage extensively in documentation management, including crafting and reviewing CSV documentation and test scripts to maintain high standards of system testing and quality assurance. Integration of diverse laboratory instruments with the LIMS landscape will be a key focus, ensuring seamless data flow and system interoperability.

Additionally, you will lead troubleshooting efforts and resolutions related to LIMS operational issues, fostering continuous process improvements and minimizing disruptions. You will be responsible for supporting quality assurance initiatives such as QAMS tasks, critical control points (CCP) management, corrective and preventive actions (CAPA), and deviation investigations to uphold stringent compliance with regulatory standards.

This role demands collaboration across interdisciplinary teams to maintain process excellence and drive strategic agility in quality management practices. You will contribute to developing talent and nurturing stakeholder relationships while promoting customer-centric approaches aligned with the company's vision for innovation and operational excellence.

Joining Lupin Limited offers a dynamic work environment committed to quality, safety, and professional growth, positioning you at the forefront of pharmaceutical quality management and LIMS technology advancements.

Applicants should possess a solid background with 8 to 10 years of practical experience in Quality Control environments, combined with proven expertise in LIMS implementation and related QC processes. Experience should include working directly with Labware 7 or equivalent LIMS platforms, accompanied by a thorough understanding of laboratory operations, quality compliance, and system validation principles.

Proficiency in managing deviations, CAPA, and CCP within regulated pharmaceutical environments is essential. Candidates with hands-on involvement in QC analytical methods, instrument integration, and quality documentation preparation will be well-prepared to excel in this role.