Posted:1 month ago|
Platform:
Work from Office
Full Time
Lead Engineering & Utilities for sterile injectable formulation and filling operations.
Manage cleanroom facility, equipment & utility design, qualification, and lifecycle management.
Oversee Black & clean utilities WFI, Purified Water, Clean Steam, Compressed Air, HVAC, AHU, HEPA, LAF/RABS/Isolators.
Implement robust preventive, predictive & breakdown maintenance programs.
Ensure process automation SCADA, PLC, BMS, MES, and digital monitoring systems.
Preparation & managing of CAPEX & OPEX for Engineering Section.
Lead equipment qualification & process validation (IQ/OQ/PQ) and documentation.
Maintain regulatory compliance USFDA, EMA, MHRA, WHO, PIC/S, etc.
Ensure audit readiness – support inspections, manage observations & CAPA closures/compliance.
Manage QMS documentation – change controls, deviations, CAPA.
Collaborate cross-functionally with QA, Production, EHS, Regulatory, R&D teams.
Hands on experience in SAP.
Ensure sterility assurance & contamination control strategy compliance.
Lead safety & EHS programs – incident prevention, risk assessments (HAZOP, FMEA).
Drive continuous improvement initiatives – Lean, TPM, Kaizen, 5S.
Build, coach & lead a high-performing engineering team; define training & succession plans.
Manage vendor development & contractor performance – ensure GMP & safety compliance.
Reduce equipment downtime, optimize OEE, and improve plant reliability.
Ensure zero critical observations during audits related to engineering activities.
Sterile/Injectable facility operations & maintenance
Clean utilities (WFI/PW/Clean Steam/Compressed Air)
Equipment qualification, validation & documentation
Process automation (SCADA, PLC, BMS, MES)
Regulatory compliance (USFDA, EMA, WHO, PIC/S)
CAPEX/OPEX project planning & execution
QMS, SOP & change control management
Audit readiness & inspection handling
Team leadership & cross-functional collaboration
Safety & EHS compliance
Continuous improvement (Lean, TPM, 5S)
MJ Biopharm
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