- Develop and implement quality management systems (QMS) to ensure compliance with industry standards and regulatory requirements.
- Lead cross-functional teams to identify areas for improvement and develop corrective actions to address non-conformities.
- Collaborate with stakeholders to establish quality objectives, metrics, and reporting mechanisms.
- Conduct regular audits and assessments to monitor QMS effectiveness. Job
Requirements:
- 11-15 years of experience in pharmaceutical or life sciences industry with expertise in QMS implementation.
- Strong understanding of Positive Manufacturing Practices (GMPs), Good Laboratory Practices (GLPs), Good Clinical Practice (GCP).
- Proven track record of implementing effective QMS systems that drive continuous improvement.