Senior Medical Laboratory Scientist, NCIS(7774)
5 days ago
Overview
NCIS is establishing a new Stem Cell Therapy Hub (SCTH) as part of expansion of its Specialized Programmes (specifically Cellular Therapy and Haematopoietic Stem Cell Transplant) and to become a Reference Centre of Excellence. We are looking for a Sr Medical Laboratory Scientist, who will be responsible for performing of Cell, Tissue, and Gene Therapy (CTGT) Product manufacturing and interpreting product quality assurance testing results in the department. He/She is also responsible to undertake related laboratory and manufacturing activities to always ensure smooth lab and manufacturing services.
Job Responsibilities
- Perform manufacturing procedures in accordance with cGMP, environmental health and safety guidelines and any other related regulations which could apply.
- Perform routine QC and in-process testing sampling of the CTGT products at various stages throughout manufacturing (e.g. bioburden sampling, water sampling)
- Timely completion of relevant manufacturing batch record and logbooks for the tasks performed and with adherence to Good Documentation Practice (GDP)
- Perform cleaning and upkeep of the equipment and classified area in manufacturing areas as per SOPs
- Report procedure deviations, adverse and out of specification incidents to the supervisor.
- Undertake simple preventative maintenance and calibration of equipment in the facilities to ensure proper working conditions.
- Participate in laboratory administrative work such as filing, processing of deliveries orders and invoices.
- Support new manufacturing and quality control processes under supervision of Manufacturing Lead (IQ, OQ, PQ and PV)
- Support the investigation, change control, and root cause investigations.
- Any other duties as assigned by supervisor.
Requirements
- Bachelor's Degree in Engineering (Chemical / Biomedical), Biotechnology, Life Science or equivalent. Post Graduate Diploma or Professional Degree will be considered an advantage.
- 3 to 5 years of relevant experiences in biopharmaceutical and/or medical device manufacturing industry and prior technical knowledge in batch biopharmaceutical processing will be an advantage.
- Cleanroom with sterile and aseptic processing knowledge and experience
- Good understanding of safe working practices and cGMP
- Highly motivated to work in pharmaceutical industry
- Demonstrated ability to elevate issues effectively and apply appropriate corrections.
- Highly motivated, proactive, and enthusiastic team player with demonstrated history of flexibility
- Ability to work independently, collaborate cross-functionally, and utilize resources efficiently
- Able to provide feedback for operations & elevate concerns as needed.
- Excellent organizational, interpersonal, verbal, and written communication skills.
- Able to work rotating shift
- Good laboratory skills.
- Above average dexterity with good general health and must be able to differentiate colors for work purposes.
- Basic computer literacy.
- Service orientated and customer focused.
Genomics
DNA
Quality Management Systems
Medicine
Telephone Reception
Scientific Writing
Laboratory Medicine
Research and Development
Attention to Details
Publications
Resource Management
DNA sequencing
Board Certified
Genetics
Laboratory
Staff Development
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