Resident Technical Officer – M&E
2 weeks ago
This is an exceptional opportunity for a highly experienced M&E professional to take on a senior site-based role supervising mechanical and electrical works in pharmaceutical facility construction. You'll play a critical role in ensuring installations meet specifications, regulatory codes, and GMP expectations while coordinating with diverse stakeholders in complex construction environments.
What you'll be doing?- Drawing interpretation: Demonstrate deep understanding of construction drawings and schematics, identifying design conflicts and coordinating resolutions.
- Technical support: Provide expert input for RFIs and constructability reviews, ensuring optimal project outcomes.
- Regulatory compliance: Apply comprehensive knowledge of local codes for fire protection, plumbing, drainage, and chemical handling systems.
- Documentation support: Assist in preparing detailed compliance documentation for FSC and TOP submissions.
- Site supervision: Oversee critical installations to ensure the highest quality standards are met.
- Quality control: Review material deliveries and installation quality for strict conformance with project specifications.
- Testing support: Witness and support various system tests to validate performance.
- Record keeping: Maintain comprehensive project documentation, including site diaries and NCR logs.
- Stakeholder coordination: Attend meetings to resolve technical issues and ensure smooth project execution.
- Quality assurance: Ensure all M&E installations comply with pharmaceutical industry standards and GMP requirements.
- Educational background: Diploma or above in engineering, preferably mechanical or electrical, to provide a solid technical foundation.
- Professional registration: Registered M&E RTO with BCA Singapore to meet regulatory standards.
- Extensive experience: Minimum 15 years of site experience, ideally in pharmaceutical or GMP projects.
- Technical competency: Ability to interpret M&E drawings and handle technical clarifications.
- Regulatory knowledge: Comprehensive understanding of SCDF, PUB, and NEA submission processes.
- Testing expertise: Familiarity with FSC testing and TOP submission procedures.
- Specialized skills: Experience in process/gas piping, high-voltage electrical, or Building Management Systems is valuable.
- Validation support: GMP validation experience, including DQ/IQ/OQ coordination, is preferred.
- Technology proficiency: Ability to use Navisworks or BIM viewers for clash detection is beneficial.
- Collaboration skills: Experience coordinating with diverse stakeholders in construction projects.
Our client offers an attractive remuneration package and other benefits, such as:
- Excellent work-life balance with a 5-day work week
- Generous 14 days of annual leave for personal time
- Additional annual compensation through AWS (Annual Wage Supplement)
- Phone allowance to support professional communication
- Comprehensive medical insurance for your peace of mind
Ready to join this role? Click Apply now to submit your resume and share your availability and expected salary with us
We encourage all passionate professionals interested in pharmaceutical construction and regulatory compliance to apply, regardless of background.
All information received will be kept strictly confidential and will be used only for employment-related purposes.
Jobs DB Singapore Pte Ltd | 24C2640
Oh Zi Yi, Joey | R
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