Responsible of non-routine testing such as BA9 incoming receiving, Primary BA9 standard qualification, stability studies, validation studies, developmental prototype and clinical, the up-to-date compliance of test method toward the reference standard as well as new product/changes implementation and method transfer activities.
Maintain overall laboratory equipment and apparatus from master list to ensure they are performing for its intended usage and within the calibration validity.
To be able to perform good troubleshooting skills to equipment and process issues
Conduct in laboratory investigation on equipment failure documentation of non-compliance or out-of-spec situations by using 5M 1E, fishbone or 5W 1H to identify the root cause
Assess and develop the risk of all laboratory processes/test methods and take care of the annual review program, and non-conformance investigation report and perform a risk assessment to minimise the risk and severity with implemented controls.
Assist all laboratory related actions such as CAPA are effectively implemented within the given time period
To support in providing laboratory solution to continually improve and lean the laboratory process, minimise cost and reduce laboratory error caused by human factor
To identify and execute laboratory efficiency improvement
To approve test results of all testing data on behalf of the lot release QC manager during his / her absence.
Participate in new / existing analytical method transfer / validation and equipment qualification when needed
Write and develop protocol to support method transfer / validation, compendia method verification and equipment qualification when necessary
Oversee and analyse annual product quality trending review, the lab investigation trending review and ensure that the review is completed within the given timeline. Then initiate and execute projects for the possible efficiency or quality improvement opportunities· Identify, monitor, source and solve for any laboratory gaps needed to be improved and implement in accordance to standards
Responsible in triggering laboratory personnel to learn and build up practical hands-on experience and technical knowledge in accordance to SOP to achieve full competency
Conduct, perform and co-ordinate with multiple requirements of new projects and improvement to achieve annual key performance given by direct supervisor
Supervise and ensure an acceptable level of 5S housekeeping in accordance to the GLP (Good Laboratory Practice) as well as fulfilling the requirements for the safety and EMS (Environmental Management System) aspects.
Revise and amend the standard operating procedures to reflect the current standards and practice are met
Assist in providing new quality standards and analytical test and implement it successfully once it has been approved
Plan, schedule and execute method validation, validation protocol, record and studies during periodic reviews
Other adhoc laboratory matters and duties assigned by direct supervisor
Requirements:
Degree in Science discipline (e.g. Chemistry, Pharmaceuticals, Chemical Process)
Preferable with at least 3-5 years relevance experience in a laboratory environment
Ability to liaise with English and Mandarin counterparts
Strong in Microsoft Office Applications such as Excel, Word and PowerPoint
Possess ability to operate and technically explain LC, GC, and UV-Vis Spectrophotometer independently.
Good knowledge in GLP and analytical test methods.
Strong Interpersonal and communication skill and possess positive attribute
Ability to adopt to the fast-pace and high pressure laboratory environment
Able to make decision on behalf of manager absence and lead the team
Knowledgeable of applicable cGMP’S, FDA, MDD (93/94/EEC), ISO 9001, EN 46001 and ISO 13485