The Client
Our client is a leading global pharmaceutical company specializing in the development, manufacturing, and marketing of generic and specialty medications. They aim to enhance patient access to effective treatments across multiple therapeutic areas. They are dedicated to innovation and sustainability in the healthcare sector. Would you like to join a dynamic team that is shaping the future of healthcare?
Role Description:
As a Quality Monitoring Coordinator , you will lead a team of operators, specialists, and technicians, ensuring strict compliance with quality standards, including GMP guidelines, safety regulations, and SOPs. This role requires flexibility for 24/7 shifts.
Key Responsibilities:
-Collaborate with Shift Managers to coordinate personnel and production.
-Adjust automated workflows and monitor production activities.
-Approve production based on PMS and analysis results.
-Enforce compliance with quality and safety regulations.
-Identify and report deviations, halting operations if necessary.
-Lead and support operators and technicians effectively.
-Monitor and evaluate documentation and batch reports.
-Manage Maintenance and Utilities reporting.
-Record deviations and incidents in Trackwize.
-Propose enhancements based on feedback and collaboration.
Requirements:
-HBO level or equivalent, preferably in Pharmacy, Chemical Technology, or a related field.
-Familiarity with pharmaceutical processes (septic and aseptic) and production control systems.
-Knowledge of quality assurance systems, Lean Six Sigma, and Operational Excellence.
-Previous experience in a coordinating role within a production organization, demonstrating strong leadership and communication skills.
-Proficiency in English and Dutch (spoken and written), with excellent planning, organizational, and analytical abilities, as well as a results-oriented mindset.
-Willingness to work in shifts 24/7

Additional Information
Apply to our vacancy for more details. Looking forward to chatting with you!
 

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