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Senior temperature mapping validation engineer

Dublin
AstraZeneca
Validation engineer
Posted: 27 November
Offer description

Job Summary: The Senior Temperature Mapping Validation Engineer will be accountable for planning, executing, analyzing, and documenting temperature mapping activities across critical and Controlled Temperature Units (CTUs) at the Alexion Manufacturing Dublin facility (ADMF).
This includes the qualification of fridges, freezers, incubators, cold rooms, autoclaves, and steam-in-place (SIP) cycles.
The role ensures temperature mapping qualification and requalification activities comply with regulatory requirements, validation lifecycle management, internal procedures, and industry best practices.
Key Responsibilities:
Lead the planning, execution, and documentation of temperature mapping and requalification studies for GMP-critical equipment.
Ensure compliance with validation lifecycle principles and change control processes.
Lead a team of technicians to ensure validation activities are completed in a timely manner to meet schedule.
Develop and approve temperature mapping protocols, plans, and reports in accordance with site procedures and regulatory requirements such as c GMP, EU, and FDA.
Collaborate with cross‑functional teams including Quality, Engineering, Facilities, Supply Chain, etc.
to ensure timely completion of validation activities.
Support investigations and deviations related to temperature excursions or environmental monitoring.
Analyze data, process trends, validation outcomes, and recommend appropriate corrective actions.
Participate in audits and inspections, providing subject‑matter expertise on temperature mapping qualification.
You will need to have:
Bachelor's degree in Engineering, Science, or related discipline.
Minimum 5 years of experience in temperature mapping or validation within a GMP‑regulated environment.
Strong knowledge of temperature mapping equipment, loggers, calibration, and data analysis tools.
Ability to keep work pace and meet deadlines; good organization and planning skills.
Strong knowledge of regulatory requirements (EU GMP Annex 1, Annex 15, FDA, ICH Q9/Q10).
Excellent communication, organizational, and project‑management skills.
Preferred Skills:
Technical degree in Engineering/Life Sciences or greater preferred.
Date Posted 24-Nov-2025 Closing Date 23-Dec-2025
Our mission is to build an inclusive and equitable environment.
We want people to feel they belong at Astra Zeneca and Alexion, starting with our recruitment process.
We welcome and consider applications from all qualified candidates, regardless of characteristics.
We offer reasonable adjustments/accommodations to help all candidates to perform at their best.
If you have a need for any adjustments/accommodations, please complete the section in the application form.
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