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Senior Medical Laboratory Scientist, NCIS
2 weeks ago
Senior Medical Laboratory Scientist, NCIS
Job ID: 7774
Job Function: Allied Health
Institution: National University Hospital
Overview
NCIS is establishing a new Stem Cell Therapy Hub (SCTH) as part of the 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 Cell, Tissue, and Gene Therapy (CTGT) Product manufacturing and interpreting product quality assurance testing results in the department. He/She is also responsible for undertaking related laboratory and manufacturing activities to 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.
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 records and logbooks for the tasks performed, adhering to Good Documentation Practice (GDP).
Perform cleaning and upkeep of the equipment and classified areas in manufacturing as per SOPs.
Report procedure deviations, adverse events, and out of specification incidents to the supervisor.
Undertake simple preventative maintenance and calibration of equipment to ensure proper working conditions.
Participate in laboratory administrative work such as filing and processing delivery orders and invoices.
Support new manufacturing and quality control processes under the supervision of Manufacturing Lead (IQ, OQ, PQ, and PV).
Support investigations, 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 experience in the biopharmaceutical and/or medical device manufacturing industry; prior technical knowledge in batch biopharmaceutical processing is an advantage.
Knowledge and experience in cleanroom sterile and aseptic processing.
Good understanding of safe working practices and cGMP.
Highly motivated to work in the pharmaceutical industry.
Demonstrated ability to elevate issues effectively and apply appropriate corrections.
Proactive and enthusiastic team player with a demonstrated history of flexibility.
Ability to work independently, collaborate cross-functionally, and utilize resources efficiently.
Able to provide feedback for operations and elevate concerns as needed.
Excellent organizational, interpersonal, verbal, and written communication skills.
Able to work rotating shifts.
Good laboratory skills.
Above average dexterity with good general health and must be able to differentiate colors for work purposes.
Basic computer literacy.
Service-oriented and customer-focused.
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