Gmp Documentation Specialist, Actris

1 week ago

Singapore Consortium for Clinical Research and Innovation Singapore Full time

**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 GMP Documentation Specialist will support the administrative operations of relevant departments within ACTRIS with the following activities:

- Set up ACTRIS GMP Document physical and online repository.
- Establish records retention and retrieval workflow
- Support ACTRIS as a GMP Librarian to ensure all GMP documentation are securely organised and managed.
- Other GMP documentation tasks assign by Quality managers

**What we are looking for**

**EDUCATION, TRAINING**

Diploma in any discipline.

**ATTRIBUTES**
- Relevant hands on GMP industrial experience in setting up a paper based GMP Documentation repository.
- Proficiency in Microsoft Office and other related software such as Adobe Acrobat, etc.
- Excellent communication skills.
- A team player with good time management, interpersonal and communication skills.

**What you need to know

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