About the role

  • 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
  • Strong organizational and interpersonal skills

Benefits

  • Competitive salaries
  • Flexible work arrangements
  • Extensive benefits package

Job title

Analyst I, QC Laboratory Services

Job type

Experience level

Mid levelSenior

Salary

Not specified

Degree requirement

Bachelor's Degree

Location requirements

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