Position Title: Technical Service Executive / Associate Work Base: Cheng, Melaka. Duties and Responsibilities: To support smooth operation of validation and qualification activities in plants by providing technical assistance during sampling and inspection activities, follow-up of testing results, compilation of validation and qualification results and outcomes, and assist in preparation of validation and qualification reports.To assist the execution of planned Cleaning Validation activities according to Validation Master Plan. To assist during the coordination of activities with all departments during execution of technology transfer and scale-up, validation and qualifications activities. To provide swab and rinse sampling training to technician from cross-functional department and coordinate the training evaluation by performing recovery studies.To follow-up with Production for production schedules of planned validation and qualification activities.To check and ensure clear labelling of validation and qualification samples to prevent mix-up.To support the compilation of comparative quality evaluation report between current and alternative sources of materials for review by TS Executive and Technical Services Unit Manager.To provide data and documentation supports to Technical Services Engineer I/ Pharmacist I/ Executive I during initiation of change control.To support the training to production shop floor personnel after process validation, cleaning validation and performance qualification activities. To support in operation qualification and performance qualification of new processing and packaging equipment and execute the test run of samples for new packaging components.To participate and contribute during continuous product and process improvement projects and support other types of problem solving activities.To assist in training and supervising the technicians in carrying out their duties during validation sampling.To ensure timely technical support to existing or new projects as assigned from time to time.To inform superior immediately if detect any abnormality, deviation or anomaly condition during the validation and qualification activities. Minimum Requirements: Bachelor Degree in Science, Engineering or Technical related discipline.Fresh graduate with Bachelor Degree in Science and Technical related discipline.Possess learning ability and resourceful to gain the knowledge of cGMP's, pharmaceutical technology and processes, equipment, validation and qualification aspects.Some experiences in one or more of the following areas: Solid dosage manufacturing, Liquids, Creams and Ophthalmic manufacturing and Packaging processes is preferred.Good interpersonal skills to interface with executives, technicians and shop floor personnel.Good communication skills, both written and verbal is preferred.Fresh Graduates are encouraged to apply.