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QC Analyst

Posted: 03/10/2024

Supervisor: QC Supervisor



· 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



· Bachelors in Science related field required; Chemistry preferred

· Will consider: Associates in Chemistry and 2 years’ experience in lab setting.

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