AstraZeneca

5 days ago

QC Microbiology Supervisor

✓ Verified Job

Canonical indexed version, validated from employer's careers page.

Source: Company careers pageValidated by: Fursa AI

Last checked: 1 hour agoStatus: Live

Job Summary

Lead a QC Microbiology team responsible for microbiological control of critical utilities, in-process samples, and finished product testing. Coordinate daily priorities to support on-time batch release while embedding cGMP/GLP and data integrity standards. Oversee method and equipment validation/qualification, drive investigations, CAPA, and quality risk assessments, and represent QC during internal and external audits. Improve lab safety, efficiency, and right-first-time performance in an always audit-ready environment.

Location: Ireland

Workplace: Onsite

Employment Type: Full time

Job Function: Quality & Regulatory (Non-Software)

Seniority: Manager level

Key Responsibilities

•Coordinate team work allocation and daily priorities to ensure analysts complete testing on time for manufacturing and batch release.
•Oversee microbiological control testing for critical utilities, in-process samples, and finished product testing (including endotoxin/bioburden and cleaning validation).
•Lead microbiological method and instrument lifecycle activities (validation, verification, and qualification) to ensure regulatory compliance.
•Ensure cGMP/GLP and data integrity through contemporaneous records and technical data reviews.
•Facilitate laboratory and product investigations, drive CAPA effectiveness, and represent QC during internal and external audits while improving lab operations and housekeeping.

Key Requirements

•Lead a team of QC analysts by coordinating daily operations to meet business testing and batch release needs.
•Oversee routine utility testing (endotoxin, bioburden, and cleaning validation) to protect product quality and patient safety.
•Maintain high cGMP and GLP standards with accurate, contemporaneous records and rigorous technical data review.
•Support validation/verification/qualification of microbiological methods and equipment as required.
•Lead and participate QC quality risk assessments and facilitate laboratory/product investigations using structured problem solving and root cause analysis.

Experience:BiopharmaceuticalSterile/aseptic manufacturing

Skills:LeadershipCoachingProblem-solvingTechnical judgmentCross-functional collaboration

Tech Stack:CGMPGLPLIMSElectronic data integrityEndotoxin testingBioburden testingCleaning validationStructured problem solvingRoot cause analysis

Company Brief

AstraZeneca

Global biopharmaceutical company discovering, developing and commercializing prescription medicines across oncology, cardiovascular, renal & metabolism, respiratory, and immunology, focused on innovative therapies and vaccines to improve patient outcomes worldwide.

Industry: Pharmaceuticals

Company Size: Enterprise (1,001+ employees)

Revenue: USD 1B+

Growth: Public Company

Valuation: Public Company (Market Cap in USD)

Funding: IPO / Publicly Listed

Headquarters: Cambridge, United Kingdom

Founded: 1999

Glassdoor: 3.8

Website LinkedIn

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AstraZeneca

5 days ago

QC Microbiology Supervisor

✓ Verified Job

Canonical indexed version, validated from employer's careers page.

Source: Company careers pageValidated by: Fursa AI

Last checked: 1 hour agoStatus: Live

Job Summary

Location: Ireland

Workplace: Onsite

Employment Type: Full time

Job Function: Quality & Regulatory (Non-Software)

Seniority: Manager level

Key Responsibilities

•Coordinate team work allocation and daily priorities to ensure analysts complete testing on time for manufacturing and batch release.
•Oversee microbiological control testing for critical utilities, in-process samples, and finished product testing (including endotoxin/bioburden and cleaning validation).
•Lead microbiological method and instrument lifecycle activities (validation, verification, and qualification) to ensure regulatory compliance.
•Ensure cGMP/GLP and data integrity through contemporaneous records and technical data reviews.
•Facilitate laboratory and product investigations, drive CAPA effectiveness, and represent QC during internal and external audits while improving lab operations and housekeeping.

Key Requirements

•Lead a team of QC analysts by coordinating daily operations to meet business testing and batch release needs.
•Oversee routine utility testing (endotoxin, bioburden, and cleaning validation) to protect product quality and patient safety.
•Maintain high cGMP and GLP standards with accurate, contemporaneous records and rigorous technical data review.
•Support validation/verification/qualification of microbiological methods and equipment as required.
•Lead and participate QC quality risk assessments and facilitate laboratory/product investigations using structured problem solving and root cause analysis.

Experience:BiopharmaceuticalSterile/aseptic manufacturing

Skills:LeadershipCoachingProblem-solvingTechnical judgmentCross-functional collaboration

Tech Stack:CGMPGLPLIMSElectronic data integrityEndotoxin testingBioburden testingCleaning validationStructured problem solvingRoot cause analysis

Company Brief

AstraZeneca

Industry: Pharmaceuticals

Company Size: Enterprise (1,001+ employees)

Revenue: USD 1B+

Growth: Public Company

Valuation: Public Company (Market Cap in USD)

Funding: IPO / Publicly Listed

Headquarters: Cambridge, United Kingdom

Founded: 1999

Glassdoor: 3.8

Website LinkedIn