Validation Lead

Role summary

Written by MyIslandJob from the job title and employer. See the employer's page for the full description.

The Validation Lead is expected to plan, coordinate and oversee validation activities for pharmaceutical manufacturing systems, equipment, processes, facilities and, where applicable, computerized systems. The role typically covers validation strategy, protocols, risk assessments, execution, deviation investigations, change controls and final reports in accordance with GMP, Novartis standards and local regulations. Candidates should have a degree in engineering, pharmacy, life sciences or a related discipline, with substantial experience in pharmaceutical validation, quality systems or manufacturing support. Strong knowledge of GMP, qualification practices, documentation and audit readiness is required. The successful candidate should be analytical, organized and confident working with cross-functional teams, contractors and regulators, while also demonstrating leadership, communication and problem-solving skills.

About the employer

Novartis is a global medicines company headquartered in Switzerland and focused on discovering, developing and delivering innovative treatments. Its work spans areas such as cardiovascular, renal and metabolic diseases, immunology, neuroscience, oncology and hematology. The company combines scientific research, advanced manufacturing, digital technologies and data-driven approaches to address significant healthcare needs. Novartis operates across many countries and employs professionals in research, clinical development, manufacturing, quality, regulatory affairs, commercial operations and corporate functions. In Malaysia, its activities may include pharmaceutical supply, commercial operations, medical engagement and support for regional business functions. Employees generally work in an environment shaped by strong regulatory expectations, international collaboration and a focus on patient outcomes, integrity and continuous improvement.