To support the day-to-day chemistry and physical laboratory activities perform testing on finished products and other non-routine testing such as stability studies, validation studies, developmental prototype and clinical products
Maintain laboratory equipment to ensure they are performing for its intended usage.
To be able to assist and support in basic troubleshooting skills to equipment and process issues
Participate in the laboratory investigation on equipment failure documentation of non-compliance or out-of-spec situations and report to the investigation owner for follow up actions.
Ensure tests assigned are performed in a timely manner in compliance to SOP, cGMP and GLP with a precaution of laboratory safety
Assist in the laboratory administrative work not limited to glassware washing, printing of test results and data entry of test results into given tools and system
Liaise and coordinate with external vendors in carrying out calibration / maintenance of lab equipment when necessary
Perform second person verification of other technician work
Provide basic competency training to new / existing technician to build up practical hands-on experience in accordance to SOP
Closely work with direct supervisor on the requirements of new projects and improvement to achieve annual key performance
Perform and maintain an acceptable level of 5S housekeeping in accordance to the Good Laboratory Practice
Revise and amend the standard operating procedures to reflect the current standards and practice are met
Other adhoc laboratory matters and duties assigned by direct supervisor
Requirements:
Diploma or Degree in Science discipline (e.g. Chemistry, Pharmaceuticals, Chemical Process)
Preferable with at least 2-3 years relevance experience in a laboratory environment
Microsoft Office Applications such as Excel, Word and PowerPoint
Possess ability to operate LC, GC, and UV-Vis Spectrophotometer independently.
Good knowledge in GLP and analytical test methods.
Good Interpersonal and communication skill and possess positive attribute
Self-starter and independent to adopt to the fast-pace laboratory environment
Knowledgeable of applicable cGMP’S, FDA, MDD (93/94/EEC), ISO 9001, EN 46001 and ISO 13485