Lab Ops Specialist 1

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.

**This is a 5 month fixed term contract**

**Responsibilities**:
**Sample Collection & Logistics**
- Acts as the liaison between Charles River Singapore and client(s) for sample collection and courier services.
- Receives and inspects incoming test samples against accompanying documents and resolves discrepancies prior to accepting the sample in accordance with SOPs
- Processing samples for laboratory testing

**Management of Test Reports**
- Coordinates and manages test reports logistics
- Ensure integrity and completeness of final test reports and issue the reports to the relevant clients in both hardcopy (Mail out) and softcopy formats
- Maintain and archive test reports for the laboratory

**Database Management**
- Updates and maintains the samples and incoming material databases, and other relevant database

**Procurement (Laboratory)**
- Raising Purchase Request and send Purchase Order to supplier for confirmation order
- Process Purchase Order and Delivery Order for payment.

**Inventory**
- Receives and inspect incoming inventory materials against Delivery Order and resolves any discrepancies prior to accepting the material in accordance with Standard Operating Procedure.
- Inventory management

**General Responsibilities**:

- Maintain appropriate records and documentation of activities to facilitate continuous compliance to ISO/IEC 17025, cGMP, Company local & global SOPs and data integrity principles and requirements.
- Maintains proper records and documentation of activities in compliance with Good Documentation Practices and Data Integrity requirements
- Undertakes any other duties or responsibilities, at the request of your supervisor that may be required within reason and the remit of the role.

**Requirements**:

- Minimum Higher Nitec in Biotechnology or Biochemical Technology
- Working experience in cGMP or ISO 17025 regulated environment preferred
- Preferably 2 years working experience in advantage, will consider entry level / fresh graduate
- Meticulous, self-starter and motivator
- Good command of English

**About Charles River**
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

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