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)
• National Health Innovation Centre (NHIC)
• Advanced Cell Therapy and Research Institute, Singapore (ACTRIS)
• Precision Health Research, Singapore (PRECISE)
• Singapore Translational Cancer Consortium (STCC)
• 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 for 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

The QC Laboratory Officer shall perform CTGTP QC related activities in compliance with ACTRIS SOP and relevant GMP and Safety guidelines.

• Perform cell therapy Manufacturing related procedures in compliance with regulatory, GMP and safety guidelines
• Responsible for all aspects of cleanroom activities such as inventory planning, environmental monitoring and facility/equipment sanitisation with a GMP manufacturing setting.
• Ensure proper maintenance and control of manufacturing areas, clean suites and equipment.
• Responsible for accurate and timely documentation of relevant batch records, forms and log sheets for the tasks performed in compliance with GDDP (Good Data and documentation practices).
• Resolve operational issues and escalate when required
• Support non conformance investigations and change controls
• Participate in technology transfer and other cross function projects
• Participate in environmental monitoring, microbiological assessment, materials and/or equipment including developing URS, SOPs and as well as providing training related to laboratory methods and/or equipment
• Assist to check equipment PM/service reports, IOQ document and etc to ensure completeness and GDDP compliance
• Assist SLO review of documents such as, PM IOQ documents, QC test reports and log sheets

What we are looking for









What you need to know

Successful candidate will be offered a 3-year contract, renewable. We regret that only shortlisted candidates will be contacted. For more information about CRIS and the Business Entities, visit our websites below:

• CRIS – https://www.cris.sg
• SCRI – https://www.scri.edu.sg
• NHIC – https://www.nhic.sg
• ACTRIS – https://www.actris.sg
• PRECISE – https://www.npm.sg
• STCC – https://www.stcc.sg
• CADENCE – https://www.cris.sg/our-programmes/cadence/