Vision
To be a world leading research centre for clinical imaging.
Mission
To provide a shared national resource in human imaging for translational research by fostering collaboration between scientists and clinicians.
1. Supporting Quality Assurance Operations by:
1) Daily issuance of Batch Manufacturing Records
2) Issuance of SOPs, protocols, log books
3) Maintaining and improving overall document management system
3) Managing training system
4) Preparation of training materials
5) Assisting in the release of investigational radiopharmaceuticals
6) Assisting in validation management activities
2. Improving Quality Management System procedures required for GMP/GCP/IS09001 compliance for investigational radiopharmaceutical manufacturing and MR/PET imaging of human subjects
Qualifications
Dynamic, positive, firm and open attitude
- Dynamic, positive, firm and open attitude
- Ideally 1 year and above experience in applying GMP or GCP or ISO 9001 in a pharma, health care, or life science environment
- Excellent in communication and empowering
- Well organised
- Self-starter with process orientated and strategic thinking
- Intention to detail
- Wiling to accept exposure of low radiation levels during radiopharmaceuticals
- Occassionally gown up to enter the clean rooms
- Minimum qualification Bachelor Degree preferably in Chemistry, Pharmacy or Life Sciences
- Handling and Project Management
- Strong demonstration on execution.
Schedule
: Full-time - Fixed Term (Contract)