Manager, Laboratory and Production, ACTRIS

4 days ago

Singapore Consortium for Clinical Research and Innovation Singapore Full time

Manager, Laboratory and Production, ACTRIS
Overview
The Consortium for Clinical Research and Innovation, Singapore (CRIS) brings together six national R&D, clinical translation and service programmes to advance clinical research and innovation for Singapore and establish important capabilities for a future-ready healthcare system. The Business Entities under CRIS include:
Singapore Clinical Research Institute (SCRI)
Advanced Cell Therapy and Research Institute, Singapore (ACTRIS)
Cardiovascular Disease National Collaborative Enterprise (CADENCE)
Together, CRIS makes a positive difference to Singapore patients and researchers by ensuring that these clinical research platforms and programmes are at the cutting edge of capability development and innovation. If you are as passionate as we are in clinical trials and research, we want you
ACTRIS
The Advanced Cell Therapy and Research Institute, Singapore (ACTRIS) was established to meet the increasing clinical demand of using cellular therapeutics to treat various life-threatening diseases. ACTRIS' vision is to be the national and regional Centre of Excellence to facilitate discovery, process development and manufacturing of cellular-based therapeutics across the broad spectrum of immunotherapy and regenerative medicine, encompassing both investigational and approval products for the local market. We also provide value-added services such as workforce training, regulatory facilitation, and ancillary material standardization, pertaining to delivery of cellular therapy to patients.
What you will be working on
Oversee production of cell-based therapy products in ACTRIS GMP facility including cell processing, product storage, shipments etc.
Manage all aspects of laboratory operations, which include planning production schedules, resolving operational issues and efficient allocation of manpower and resources.
Develop and implement production-related workflows and processes appropriate for clinical stage and commercial manufacturing.
Ensure compliance to Good Manufacturing Practice (GMP) guidelines and relevant safety requirements.
Oversee qualification and maintenance of equipment and clean rooms within the facility.
Collaborate with other functions to facilitate new product introduction and technology

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