The student will gain experience working in a laboratory in a pharmaceutical manufacturing company. Reporting to the QC Team Leader, the role of QC Student requires dedication to the principle of cGMP and adherence to Standard Operating Procedures.
RESPONSIBILITIES:
* To observe GLP/cGMP at all times.
* Testing of all laboratory samples including Raw Materials, Packaging Components, Product Validation, Stability, Environmental, and OH.
* Performance of laboratory tests as per written procedure or as per pharmacopoeia.
* Recording of analytical results accurately.
* Operation, maintenance, and calibration of laboratory instruments.
* To ensure that the laboratory is kept clean, tidy, and safe at all times.
* To report any non-conformance, instrument malfunction, accident, or other abnormal occurrence to immediate superior.
* Ordering, receiving, and controlling laboratory chemicals, reagents, and consumables.
* Receiving and controlling test samples.
* Participate fully in any cross-functional training initiatives.
* Drive and promote the corporate values of Takeda-ism within the workplace.
* Actively foster, in cooperation with other TIL staff, an ethos and culture of safety awareness where safety is accepted as an integral part of the overall business.
* Ensure that Accident Reports/Near Miss Forms are completed in a timely manner after an event.
* Ensure timely completion of all SOP, reading, training, and assessment.
* Other duties as required and directed by the relevant Manager or other Officer appointed by the Board of Directors.
MINIMUM REQUIREMENTS:
* Studying towards a 3rd Level Degree in Science or other relevant course.
* Experience working in a laboratory environment.
* Good organisational, communication, interpersonal, and report writing skills.
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