QC Analyst

AstraZeneca
Athlone, Leinster, Ireland
Full Time
On Site
Mid
0+
Bachelor Degree
Science & Research Healthcare Life Sciences

Posted 4 days ago

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Excellent 4.7

Job summary

The QC Analyst supports microbiological and chemistry product testing, environmental monitoring, and validation in a biopharmaceutical laboratory. Responsibilities include test execution, data review, investigation, reporting, compliance adherence, and process improvement.

Responsibilities

The QC Analyst will perform analytical testing and environmental monitoring for drug product manufacturing while ensuring compliance with cGMP and GLP standards. They are also responsible for conducting investigations, managing laboratory supplies, and supporting method validation and internal audits.

Qualifications

Chemistry Environmental Monitoring G=LIMS GMP HPLC Laboratory Techniques Microbiology Report Writing Test Method Validation UV

Candidates must hold a BSc (Hons) in biosciences and possess at least 3 years of relevant experience in a QC laboratory environment. Strong technical writing skills, familiarity with gLIMs, and a solid understanding of biopharmaceutical analysis and laboratory safety are required.

English

Company

AstraZeneca

AstraZeneca

linkedin
Pharmaceutical Manufacturing
Location
Athlone, Leinster, Ireland

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Excellent 4.7
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