മ
Site Engineer / Biomedical Engineer
Dubai, United Arab Emirates · മുഴുവൻ സമയവും
അപേക്ഷിക്കുന്ന ആദ്യയാളാകൂ
- അനുഭവം
- 3–5 വർഷം
- ശമ്പളം
- —
- ഓപ്പണിംഗുകൾ
- 1
- പോസ്റ്റ് ചെയ്തു
- 22 മണിക്കൂർ മുൻപ്
- പ്രവർത്തന രീതി
- ഓഫീസിൽ
- വിദ്യാഭ്യാസം
- ബാച്ചിലേഴ്സ് ഡിഗ്രി
- പുനരാരംഭിക്കുക
- അപേക്ഷിക്കാൻ നിർബന്ധം
നിങ്ങൾ എവിടെ ജോലി ചെയ്യും
ജോലി വിവരണം
Overview
This role involves relocation to Seychelles to support engineering operations at a medical facility. The engineer will manage installation, maintenance, validation, and project oversight of laboratory and cleanroom equipment, ensuring compliance with regulatory standards.
Key Responsibilities
- Oversee installation and commissioning of laboratory instruments and manufacturing systems, ensuring adherence to manufacturer specifications and user needs.
- Develop and execute preventive maintenance plans; conduct inspections, functional tests, troubleshoot equipment issues, and coordinate repairs in collaboration with external vendors.
- Assist in equipment qualification and validation processes including Installation, Operational, and Performance Qualification phases.
- Monitor and maintain cleanroom systems such as HVAC, HEPA filters, pressure, temperature, and humidity controls, gas, vacuum, and water purification systems; contribute to certification activities.
- Ensure dependable operation of utility systems including electrical, UPS, emergency power, fire safety, and medical gas infrastructure.
- Manage engineering projects from planning through execution, including drafting technical specs, vendor evaluation, timeline and budget management, and supervising contractors.
- Maintain compliance with GMP, GTP, ISO, and national regulations; prepare for audits and inspections by maintaining comprehensive engineering documentation and supporting corrective/preventive measures.
- Document and file maintenance, calibration, qualification, validation, service reports, SOPs, and logs in accordance with GMP and document control standards.
Qualifications and Experience
- Bachelor's degree in Biomedical Engineering, Civil Engineering, Project Engineering or related discipline.
- 3 to 5 years of experience in cGMP-regulated environments, preferably within cellular therapy or biotechnology laboratories.
- Hands-on exposure to cleanroom facilities, laboratory equipment management, HVAC systems, building management systems, and project management.
- Preferred certifications: PMP, Network Systems, AutoCAD, and GMP compliance.