Supervisor: QC Supervisor
Duties:
· Performs routine sampling, analysis and documentation of pharmaceutical samples – raw materials, intermediates, drug products, package materials*
· Accurately weighs samples and prepares volumetric solutions*
· Performs analytical tests: titration, conductivity, pH, residuals on ignition, specific gravity, loss on drying, etc.*
· Generates experimental data according to written SOP, protocol, method, or work instructions*
· Follows guidelines when recording data*
· Accurately calculates and reports results*
· Accurately maintains laboratory data and logs*
· Maintains, calibrates and cleans laboratory equipment*
· Cleans glassware*
· Accurately labels samples and chemicals*
· Collaborates in cross-functional teams*
· Follows all Aurora Pharmaceutical policies, procedures, regulations and the employee handbook. *
· Follows designated work schedule. *
· Assumes additional responsibilities as requested. *
· Accepts and acts upon supervisory directions. *
· Supports supervisor’s role. *
· Demonstrates flexibility, i.e., willingly takes on new tasks. *
(*denotes essential job functions)
Knowledge, Skills & Abilities:
· Prefer candidates with interest and background in pharmaceutical testing, sampling and regulations
· Basic knowledge of analytical chemistry and laboratory concepts and techniques
· Basic knowledge of computer applications
Education:
· Bachelors in Science related field required; Chemistry preferred
· Will consider: Associates in Chemistry and 2 years’ experience in lab setting.
