Responsibilities
- Configure and support Building Management Systems (Rockwell or equivalent) for pharma facilities.
- Perform and document qualification/validation activities (IQ, OQ, PQ) for BMS, HVAC, and utilities systems (e.g., cleanrooms, compressed air, WFI, chilled water).
- Troubleshoot and resolve system or process deviations during commissioning and validation.
- Ensure compliance with FDA 21 CFR Part 11, EU Annex 11, GAMP 5, and cGMP requirements.
- Prepare validation protocols, execute testing, and generate final reports.
- Support incident management and change control processes for validated systems.
- Collaborate with cross-functional teams (engineering, QA, regulatory, and project management) at client sites.
Requirements
- Bachelor's degree in Engineering, Science, or related field.
- Experience in one or more of the following:
Pharma / Biotech / Medical Device industries (validation/qualification role).
HVAC / Utilities / Facilities engineering (with cleanroom or GMP experience).
Automation / Controls engineering (Rockwell, Siemens, Honeywell, or similar BMS/DCS platforms). - Strong knowledge of validation methodology (IQ/OQ/PQ).
- Familiarity with pharma regulations (FDA, EMA, GAMP) is an advantage.
Interested candidates please apply online or send your latest CV to
AlwaysHired Pte Ltd
Reg No: R1549345
EA: 24C2293
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