Key Responsibilities

• Perform analytical testing of drug products, finished goods, and materials following approved procedures and standards

• Document laboratory activities and results accurately in line with Good Manufacturing Practice requirements

• Manage sample storage, tracking, and handling to ensure integrity and compliance

• Conduct stability testing and maintain proper documentation of stability studies

• Investigate and report technical complaints, adverse events, and quality issues within 24 hours

• Ensure full adherence to Standard Operating Procedures and regulatory guidelines at all times

• Support audit and inspection readiness through consistent compliance and documentation practices

• Monitor deadlines and ensure timely completion of all testing and reporting activities

• Identify and implement process improvements to enhance efficiency and reduce operational costs

• Collaborate with cross-functional teams to maintain quality standards and resolve issues effectively

Essential Requirements

• Degree in Chemistry, Pharmacy, or a related scientific field

• Experience in quality control within a pharmaceutical or regulated manufacturing environment

• Knowledge of Good Manufacturing Practice and quality standards

• Hands-on experience with analytical laboratory techniques and equipment

• Ability to follow Standard Operating Procedures with high attention to detail

• Strong problem-solving skills and ability to manage competing priorities

• Intermediate level of English, with good reading and writing skills

Desirable Requirements

• Experience with stability testing and lifecycle management of pharmaceutical products

• Familiarity with audit and inspection processes within regulated environments

Commitment to Diversity and Inclusion:
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve