Quality Control Analyst (Temporary Position)

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