QC Senior Analyst, Microbiology – AstraZeneca Hiring 2026 | Dublin, Ireland

QC Senior Analyst, Microbiology – AstraZeneca Hiring 2026 | Dublin, Ireland

AstraZeneca Recruitment 2026: AstraZeneca is inviting applications for the position of QC Senior Analyst, Microbiology in Dublin, Ireland. This is an excellent opportunity for experienced pharmaceutical and biopharmaceutical microbiology professionals seeking to advance their careers in Quality Control (QC), sterility assurance, and GMP-regulated laboratory operations.

The QC Senior Analyst, Microbiology position is offered on a 12-month fixed-term contract. The selected candidate will support microbiological quality control activities, environmental monitoring, product release and stability testing, laboratory investigations, and continuous improvement initiatives.

Job Details

• Company: AstraZeneca
• Job Title: QC Senior Analyst, Microbiology
• Job Location: Dublin, Leinster, Ireland
• Job ID: R-261085
• Job Type: 12-month fixed-term contract
• Date Posted: 1 October 2026 (as listed in the supplied vacancy details)
• Application Deadline: 20 October 2026 (check the official vacancy for updates)
• Experience Required: 4–7 years, or an equivalent combination of education and experience
• Qualification: Bachelor’s degree in Microbiology or a biological science, or equivalent experience
• Department: Quality Control – Microbiology

Key Responsibilities

The selected candidate will be responsible for the following activities:

1. Environmental Monitoring: Plan, perform, and trend environmental and facilities monitoring activities to assess contamination risks in cleanrooms, utilities, and controlled areas.
2. Microbiological Testing: Conduct and oversee microbiological testing of pharmaceutical and biopharmaceutical products to support product release and stability programmes.
3. Sterility Assurance: Maintain high standards of sterility assurance and microbiological control in compliance with applicable GMP and GLP requirements.
4. Laboratory Compliance: Ensure adherence to approved Standard Operating Procedures (SOPs), good documentation practices, laboratory safety requirements, and data integrity standards.
5. Laboratory Investigations: Lead or contribute to out-of-specification (OOS), out-of-limit, deviation, and other laboratory investigations using structured problem-solving and root-cause analysis.
6. CAPA Management: Support the implementation of effective Corrective and Preventive Actions (CAPA) within established timelines.
7. Technical Support: Troubleshoot laboratory instruments, microbiological methods, and sample-related issues to minimise repeat testing, deviations, and laboratory downtime.
8. Training and Development: Provide technical guidance to laboratory analysts and contribute to training and retraining programmes.
9. Stability Programmes: Support microbiological testing and stability activities to ensure reliable, timely, and compliant quality decisions.
10. Continuous Improvement: Identify opportunities to improve laboratory workflows, reduce testing cycle times, strengthen data integrity, and improve operational efficiency.
11. Cross-Functional Coordination: Communicate laboratory risks, investigation progress, and emerging quality trends to supervisors and relevant stakeholders.

Educational Qualification and Experience

Candidates applying for this post should meet the following essential requirements:

• Bachelor’s degree in Microbiology or a related biological science, or an equivalent combination of education and experience.
• Approximately 4–7 years of relevant professional experience, as specified in the vacancy.
• Practical experience in microbiological testing of sterile and non-sterile pharmaceutical or biopharmaceutical products.
• Good understanding of microbiology regulations and sterility assurance requirements.
• Experience working in a regulated pharmaceutical Quality Control laboratory.
• Strong attention to detail, analytical thinking, documentation skills, and problem-solving ability.

Desirable Skills

The following skills and experience will be advantageous for this position:

• Working knowledge of cGMP requirements and pharmaceutical QC laboratory operations.
• Familiarity with laboratory equipment used in biopharmaceutical testing.
• Ability to follow approved procedures accurately and consistently.
• Experience in troubleshooting, laboratory investigations, and root-cause analysis.
• Ability to work independently on routine activities while collaborating effectively with the wider team.
• Good communication, technical guidance, and continuous improvement skills.

Why Join AstraZeneca?

AstraZeneca is a global biopharmaceutical company focused on discovering, developing, and delivering innovative medicines. This opportunity offers professionals the chance to contribute to pharmaceutical quality, protect patient safety, and work within a collaborative scientific environment.

The QC Senior Analyst, Microbiology role is particularly suitable for professionals interested in microbiological quality control, sterility assurance, regulatory compliance, and the continuous improvement of pharmaceutical laboratory operations.

How to Apply for AstraZeneca Recruitment 2026

Interested and eligible candidates can review the complete job description and submit their applications through AstraZeneca’s official careers portal.

APPLY NOW

Official Application Link:
https://careers.astrazeneca.com/job/dublin/qc-senior-analyst-microbiology/43991/101443050112

Important: Check the official vacancy for the latest application status, eligibility requirements, and closing date before applying.

Disclaimer: This job information is provided for educational and career-awareness purposes. Pharmaguidances is sharing the opportunity for job seekers; recruitment decisions and applications are handled by AstraZeneca through its official careers website.