For nearly 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

QUALIFICATIONS:

• Diploma / Higher NITEC / ITE or any related field.
• Preferred minimum 1 years of working experience in cGMP or ISO17025 regulated laboratory.
• Meticulous, self-starter and motivator.
• Good command of English
• Good technical understanding and judgment.
• Good interpersonal and communication skills
• Team player with ability to work in cross functional teams as well as independently depending on the requirement of task in hand

• Performs all laboratory functions as tasked with high degree of accuracy and strict adherence to Company’s quality requirements.
• Maintains proper records that are compliant with good documentation practices (GDP) and data integrity requirements, for all testing and test-related activities (e.g. raw data sheets, usage logbooks, and all other records).
• To prepare media and other materials used for test services, including washing of glassware and depyrogenation
• To perform Environment monitoring as required
• To perform QC of media and lab consumables as required
• Receives and inspects incoming test samples against accompanying documents and resolves discrepancies prior to accepting the sample in accordance with SOPs.
• Receives and inspect incoming inventory materials against Delivery Order and resolves any discrepancies prior to accepting the material in accordance with SOP.
• Generates reports for all tests performed in an accurate and timely manner, ensuring that targets are met for accuracy and turnaround time.