QC Analyst
About this position
The QC Analyst will be responsible for maintaining laboratory areas, equipment, and facilities in a clean and operational state. They will also support chemical and physical analyses on samples from pharmaceutical manufacturing operations.
Responsibilities
• Maintain Laboratory area, equipment, facilities in a clean, orderly and operational state.
• Monitor that all reagents, reference standard are always available and ensure all reagents and reference standards are valid to use and stored according to requirement.
• Perform verification or calibration of instruments/ equipment.
• Support chemical and physical analyses on samples from all areas of our pharmaceutical manufacturing operations and support in providing data for annual product review.
• Develop good working practices/guidelines to work as tools to assist staff in the use of quality system Standard Operating Procedures.
• Manage review and approval of Building Management System Alarms.
• Lead the Continuous Improvement (CI) process for the Integrated Manufacturing Excellence (IMEx) within the Drug Product unit, identify and conduct continual improvement project.
• Consult with managers in various groups to coordinate and implement decisions made regarding compliance practices.
• Build trusted relationship with customers, colleagues in team, cross functions.
• Contribute to the completion of complex projects, manage own time to meet agreed targets and develop plans for work activities on own projects within a team.
Requirements
• Vocational High School Degree (Medicinal/Analytical)
• Good working knowledge of common laboratory databases
• Knowledge of regulatory compliance requirements for Pharmaceutical manufacturing
• Good analytical thinking and high-level integrity
• Able to work well either as an individual or as a team member
• Excellent interpersonal and communication skills