Responsibilities
- Plan and execute temperature mapping studies for cold rooms, warehouses, freezers, incubators, and stability chambers.
- Perform Commissioning, Qualification, and Validation (CQV) for equipment and facilities.
- Prepare and review validation protocols (IQ / OQ / PQ), reports, and related GMP documentation.
- Ensure mapping equipment is properly calibrated and maintained.
- Support troubleshooting, deviation management, and CAPA related to environmental control systems.
- Coordinate with engineering, QA, and facility teams.
- Ensure all validation activities comply with GxP and regulatory requirements.
Requirements
Degree in Engineering, Pharmaceutical, Life Sciences, or related field.Hands‑on experience in temperature mapping for pharma / GMP environments is a prefered.Familiar with CQV practices, validation lifecycle, and qualification protocols.Understanding of HVAC, cold chain, and environmental monitoring systems is a plus.Strong documentation and GMP compliance awareness.Interested candidates please apply online or send your latest CV to
AlwaysHired Pte Ltd
Reg No : R
EA : 24C2293
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