
Pharmaceutical Site Technical Lead
6 days ago
This is a site-based position that requires strong understanding of Mechanical and Electrical design drawings, regulatory compliance, and coordination with design teams to ensure installation meets specification, code, and GMP expectations.
- Key Responsibilities:
- Familiarity with construction drawings, schematics, SLDs, and layout plans. Interpretation & Design Coordination involves identifying design conflicts or issues on-site and coordinating with designers for resolution, support RFIs and constructability reviews with the design team.
- Regulatory Compliance & Submission Support includes familiarity with local codes such as SCDF (Fire Protection/FSSD submissions), PUB (Plumbing, condensate, chilled water drainage), NEA (Exhaust systems, chemical handling). Preparation of compliance documentation and test plans for FSC and TOP submissions is also required.
- Site Supervision & Quality Control involves supervision of key installations including HVAC, fire protection, process piping, electrical, and control systems. Review of material deliveries, installation quality, and documentation to ensure conformance is essential.
- Coordination & Documentation includes maintenance of daily site diary, photo records, NCR logs, and rectification tracking. Attendance at coordination meetings with contractors, designers, and client to resolve technical issues is necessary.
Requirements:
- Diploma or above in engineering disciplines, preferably mechanical or electrical. Registered M&E RTO with BCA Singapore is mandatory.
- Minimum 15 years of site experience, preferably in pharmaceutical or GMP projects.
- Capability of reading and interpreting M&E drawings; experience in technical clarifications (RFI) is a plus.
- Familiarity with SCDF, PUB, NEA submission and approval processes is required.
- Familiarity with FSC testing, TOP submission flow, and common system testing requirements.
Preferred Qualifications:
- Experience in process/gas piping, high-voltage electrical, or BMS is an advantage.
- GMP validation support experience (e.g., DQ/IQ/OQ coordination) is preferred.
- Ability to use Navisworks or BIM viewers to assist in clash checking is a plus.
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