Officer

Join Lupin Limited's dynamic Quality division as an Officer within our Validation department based in Pithampur. In this pivotal role, you will take charge of the cleaning validation activities for our API and Formulation facilities. Your responsibilities will encompass comprehensive management and execution of validation protocols supporting our commitment to the highest quality manufacturing standards.

Your core duties will include ensuring rigorous residue cleaning validation processes to maintain contamination-free production environments. You will manage and evaluate nitrosamine and genotoxic cleaning validation activities, essential to safeguarding product safety and regulatory compliance.

In addition, you will perform risk priority number (RPN) calculations to identify and mitigate potential risks effectively. Campaign studies including CEHT/DEHT will fall within your scope, enabling process optimization and validation integrity. The role extends to qualification activities for facilities, equipment, utilities, and HVAC systems, ensuring all operate at validated standards aligned with industry and regulatory requirements.

As the Officer, you will prepare and review validation-related documentation with precision, supporting audit readiness and continuous improvement initiatives. Your efforts will directly contribute to Lupin's mission of delivering safe, efficacious pharmaceutical products to global markets.

We seek an individual with a keen eye for detail, exceptional organizational skills, and the ability to collaborate cross-functionally. Your proactive approach to validation and quality processes will drive success and uphold our high standards.

At Lupin Limited, you will be part of a culture that values innovation, strategic thinking, and continuous development. Join us to advance your career in a challenging and rewarding environment where your expertise makes a meaningful difference.

Applicants should have between 2 to 5 years of relevant experience in pharmaceutical cleaning validation or quality assurance sectors. Experience in executing and managing cleaning validation protocols, facility and equipment qualification, as well as working knowledge of regulatory requirements related to pharmaceutical manufacturing, will be highly valued.