Associate Executive/ Senior Associate (Quality Assurance), Nuclear Medicine &... - #1095365

You will support the department in the management of all Quality Assurance (QA) requirements pertaining to Good Manufacturing Practices (cGMP). Your job duties include:

• Assist in the timely creation, amendment and housekeeping of all QA documents relating to radiopharmaceuticals for both clinical and research procedures
• Assist in the scheduling and preparation of all QA audits
• Daily maintenance of stock checks and equipment inventory and facilities surveillance
• Ensure timely submissions and responses for regulatory requirements
• Assist in data collection and analysis
• Organise meetings

Requirements

• Diploma
• Meticulous and organised
• Proficient in Microsoft Office applications

*This is a 2-year contract role. Renewal is subjected to work performance and availability of post.