Analyst I, QC Laboratory Services performing GMP compliant testing in a leading public health company. Supporting raw material testing and product release in a regulated lab environment.
Responsibilities
Perform GMP compliant testing as required for Raw Material testing, In-process, Finished Product Release & Stability, nonclinical/clinical studies
Maintain laboratory documentation and perform preventative maintenance and calibration on laboratory equipment
Participate in execution of investigations, deviations, critical reagent and standard qualifications, validation/verification protocols and reports
Provide training to peers
Receive test samples, maintain accurate laboratory records and inventory
Report results and complete LIMS data entry
Perform peer review of QC data
Adhere to safety requirements and document work consistent with cGMP requirements
Requirements
University degree or technical diploma in chemistry, biology, microbiology, or related field of study
0-2 years directly related experience in a recognized professional or technical/scientific field
Basic knowledge of Microsoft Office - Word, Excel
Basic knowledge of pharmaceutical GMPs
Knowledge of laboratory techniques and safety precautions
WHMIS and biohazard safety awareness
Competent in laboratory safety and generally-accepted lab practice
Ability to work in a fast paced and highly regulated environment
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