CMMS Engineer (1 year contract) - D22 Jurong, Jurong Island, Tuas, SG

Roles & Responsibilities

About No deviation

At No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to impactful projects and drive innovation.

We believe that great things happen when Empathy, Integrity, and Transparency guide our actions. That's why we foster a culture of collaboration, inclusion, and continuous development – empowering our team members to grow personally and professionally.

Position Overview

We are seeking an experienced CMMS Engineer to support the deployment of a Computerized Maintenance Management System (CMMS) at our client's site. This role is project-focused and will involve working closely with engineering, maintenance, IT, and compliance teams to design, configure, validate, and implement the CMMS in alignment with operational and regulatory requirements.

Key Responsibilities

• Support the setup and configuration of CMMS modules, including asset register, work order management, preventive and predictive maintenance, calibration, and spare parts inventory.
• Support integration with related systems such as ERP (SAP / Oracle), Building Management System (BMS), SCADA, QMS, and LIMS.
• Develop and manage master data (equipment hierarchy, spare parts catalog, preventive maintenance plans).
• Oversee data migration activities, ensuring completeness and accuracy of historical maintenance and calibration records.
• Contribute to system documentation including User Requirement Specifications (URS), Functional Specifications (FS), and Design Specifications (DS).
• Support Computer System Validation (CSV) activities including IQ, OQ, and PQ.
• Ensure the CMMS deployment complies with relevant industry standards and regulations (e.g., GMP, FDA 21 CFR Part 11, ISO 55000).
• Maintain audit-ready documentation throughout the deployment project.
• Work closely with cross-functional stakeholders to capture requirements and align CMMS configuration with business processes.
• Track deployment milestones, risks, and deliverables to ensure on-time and within-scope delivery.
• Provide regular updates to project leadership on progress and issues.

Required Qualifications

Why join us?

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Pharmaceutical Industry

Maintenance Management

Preventive Maintenance

FDA

Predictive Maintenance

ISO

GMP

SCADA

SAP

Data Migration

Computer System Validation

Reliability Engineering

LIMS

Medical Devices

Calibration

Work Order