Role Description

This role involves overseeing quality assurance processes and maintaining compliance with relevant standards and regulations within the clinical supply chain. The selected candidate will monitor quality control activities, manage quality assurance documentation, participate in quality audits, and ensure adherence to Good Manufacturing Practice (GMP). Additionally, they will collaborate closely with cross-functional teams to maintain the integrity of quality management systems.

Qualifications

• Proficiency in Quality Control and Quality Assurance processes to ensure compliance with industry regulations and standards
• Knowledge of Quality Management systems and frameworks to oversee and enhance operational processes
• Experience with Good Manufacturing Practice (GMP) principles to ensure product quality and safety
• Competence in conducting Quality Auditing procedures to identify and mitigate risks
• Strong organizational and analytical skills with high attention to detail
• Bachelor's degree in Life Sciences, Quality Management, or a related field
• Previous experience in the clinical trials or pharmaceutical industry is desirable
• Excellent communication skills and ability to work collaboratively in remote teams