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Laboratory Technician I - Temporary

Req ID #: 225291

Oklahoma City, Oklahoma, USA
This job is located outside of your selected country / language. English (Canada)

About this job

Under direct supervision, the Temporary Laboratory Technician I will perform routine analytical methods as specified in written procedures (e.g., in-house SOPs, client test methods) for quality control, release/stability testing.

Under direct supervision, the Temporary Laboratory Technician I will perform routine analytical methods as specified in written procedures (e.g., in-house SOPs, client test methods) for quality control, release/stability testing.

ESSENTIAL DUTIES AND RESPONSIBILITIES:  
⦁    Independently perform laboratory activities, including but not limited to, reagent preparation, laboratory cleaning, maintenance/monitoring of laboratory equipment, routine testing of client samples, and generation of routine cGMP and R&D reports. 
⦁    Adhere to established processes for laboratory operations and execution of routine testing. 
⦁    Perform routine tests of release and/or stability samples. 
⦁    Demonstrate proficiency in performing different routine tests within the RightSource laboratory. 
⦁    Analyze data and report results of experiments and procedures.
⦁    Competently perform peer review of data.
⦁    Generate analytical data and technical report(s) on-time with respect to internal and client deadlines. 
⦁    Maintain a safe working environment by adhering to company policies and procedures. 
⦁    Actively participate in laboratory operations and maintenance including but not limited to:
⦁    Laboratory cleaning and organization
⦁    Instrumentation and equipment maintenance
⦁    Preparation of common stocks
⦁    Ordering and inventory of materials
⦁    Comply with all pertinent regulatory standards regarding environments, equipment and testing services.
⦁    Make detailed observations and maintain clear, detailed, accurate and timely documentation of all laboratory work.
⦁    Compose high quality documentation including deviation reports and change control documentation under guidance. 
⦁    Follow all SOPs, TRs and cGMP as they relate to specific tasks.
⦁    Maintain up to date training records on all procedures and protocols applicable to work duties.
⦁    Ability to work in a structured and regulated environment.
⦁    Work productively in group situations as well as independently.
⦁    Perform all other related duties as assigned.

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About Charles River

Charles River is an early-stage Contact Research Organization (CRO). Here, we are passionate about our role in improving the quality of people's lives. With 100 sites around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our clients' unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

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