Senior Quality Assurance Specialist
hace 1 semana
The Senior Quality Assurance Specialist will play a pivotal role in ensuring compliance with local and international regulatory requirements. As a key member of the Novartis team, this individual will be responsible for implementing and maintaining quality management systems, evaluating and approving GMP service providers, and ensuring the quality and business continuity of products marketed in the region.
Key Responsibilities- Develop and implement quality plans, monitor progress, and report to senior management
- Evaluate and approve GMP service providers, ensuring they meet regulatory standards
- Collaborate with cross-functional teams to ensure quality and regulatory compliance throughout the product lifecycle
- Maintain knowledge of local and international regulations, industry trends, and best practices
- Conduct audits and assessments to identify areas for improvement and develop corrective action plans
- Bachelor's degree in pharmaceutical sciences or a related field
- Minimum 1 year experience in quality assurance or regulatory affairs in the pharmaceutical industry
- Knowledge of good manufacturing practices (GMP), good storage and distribution practices (GSDP), and quality systems
- Excellent communication, leadership, and problem-solving skills
- Ability to work in a fast-paced environment and prioritize multiple tasks
At Novartis, we're dedicated to improving people's lives through innovative science. We believe in empowering our employees to drive change and make a meaningful impact. If you're passionate about quality, compliance, and regulatory affairs, and want to join a dynamic team that shares your values, then this could be the perfect opportunity for you.
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