Developing and Implementing Quality Management Systems (QMS): this includes creating and updating procedures, processes, and documentation to meet quality standards.
Monitoring and Analyzing Quality Data: tracking quality metrics, identifying trends, and pinpointing areas for improvement.
Prepare and submit periodic reports on the performance of the quality management system to company management
Working with Cross-Functional Teams: collaborate with other departments (e.g., production, engineering, procurement) to resolve quality issues and improve processes.
Investigating Quality Issues: analyzing root causes of quality problems and developing corrective and preventative action plans.
Quality System Governance: fostering a culture of quality and ongoing improvement throughout the site.

Degree in scientific subjects (Chemistry, Pharmaceutical Chemistry and Technology, Engineering)
At least 5 years of experience in manufacturing sites within the pharmaceutical and biopharmaceutical sector, specifically in Quality Assurance, Production, and Process Technology departments
Excellent knowledge of pharmaceutical guidelines (EU and FDA regulations)
Specialized expertise in GMP compliance improvement processes
Fluent English (both written and spoken)

Senior Quality & Compliance System Specialist

Key skills