5 Cmms jobs in Singapore

• Well Established Company

• Salary: $3500 - $500 + 300 Allowance

• Working hour: 8.30am – 5.30pm (Monday - Friday)

• Working Location: Islandwide

• Variable bonus + Excellent Wellfare

Job Scope:

• Plan and perform maintenance for equipment and facilities.
• Diagnose and fix technical issues (mechanical, electrical, electronic).
• Implement preventive/predictive maintenance programs.
• Collaborate with production, quality, and safety teams.
• Maintain maintenance records and reports.
• Support installation and upgrades of systems.
• Identify and implement process and cost improvements.

Requirement:

• Diploma in IT Engineering, Civil Engineering, Architecture, or related field
• 2–3 years of experience in maintenance or technical roles in manufacturing/industrial settings

Candidates are encouraged to apply this position via Apply Now button with the following information in the resume:

• Work experiences and job responsibilities
• Current and Expected salary
• Reason for leaving
• Date of availability
• Education background

We regret that only shortlisted candidates will be contacted.

YEOW CHANG FU (R )

EA Recruitment Pte Ltd

EA License No: 21C0492

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
Bachelors Degree in Engineering, Information Systems, or a related discipline.
6 to 8 years of relevant experience in
CMMS implementation, deployment, or maintenance engineering .
Hands-on experience with CMMS tools such as
SAP PM, IBM Maximo, Blue Mountain RAM, Infor EAM, or equivalent .
Strong knowledge of preventive/predictive maintenance, asset lifecycle management, and reliability engineering.
Proven experience with
Computer System Validation (CSV)
in regulated industries (e.g., pharma, biotech, medical devices) is highly preferred.
Familiarity with
GMP, FDA 21 CFR Part 11, ISO standards
and audit requirements.
Excellent problem-solving, analytical, and stakeholder management skills.
Strong communication skills with the ability to train and support end-users.
Why join us?
Comprehensive Health & Wellness Coverage: Receive robust medical and dental coverage to support your health needs.
Professional Development Opportunities: Access continuous learning programs and resources for career growth within the company.
Inclusive Culture: Work in an environment where innovation, collaboration, and diverse perspectives are encouraged and celebrated.
Shape the Future: Make a real difference in the pharmaceutical industry while advancing your career.
#J-18808-Ljbffr

Overview
Join to apply for the
CMMS Engineer (1 year contract)
role at
No deviation .
No deviation
is 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 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
Bachelors Degree in Engineering, Information Systems, or a related discipline.
6 to 8 years of relevant experience in CMMS implementation, deployment, or maintenance engineering.
Hands-on experience with CMMS tools such as SAP PM, IBM Maximo, Blue Mountain RAM, Infor EAM, or equivalent.
Strong knowledge of preventive/predictive maintenance, asset lifecycle management, and reliability engineering.
Proven experience with Computer System Validation (CSV) in regulated industries (e.g., pharma, biotech, medical devices) is highly preferred.
Familiarity with GMP, FDA 21 CFR Part 11, ISO standards and audit requirements.
Excellent problem-solving, analytical, and stakeholder management skills.
Strong communication skills with the ability to train and support end-users.
Why join us?
Comprehensive Health & Wellness Coverage: Receive robust medical and dental coverage to support your health needs.
Professional Development Opportunities: Access continuous learning programs and resources for career growth within the company.
Inclusive Culture: Work in an environment where innovation, collaboration, and diverse perspectives are encouraged and celebrated.
Shape the Future: Make a real difference in the pharmaceutical industry while advancing your career.
How To Apply
Are you ready to play a key role in shaping the future of pharmaceutical solutions? If you're passionate about making an impact, we want you on our team!
Please submit your resume, outlining your qualifications and experience relevant to the role, here.
Job Details
Seniority level: Not Applicable
Employment type: Contract
Job function: Engineering and Information Technology
Industries: Pharmaceutical Manufacturing
#J-18808-Ljbffr

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

• Bachelors Degree in Engineering, Information Systems, or a related discipline.
• 6 to 8 years of relevant experience in CMMS implementation, deployment, or maintenance engineering .
• Hands-on experience with CMMS tools such as SAP PM, IBM Maximo, Blue Mountain RAM, Infor EAM, or equivalent .
• Strong knowledge of preventive/predictive maintenance, asset lifecycle management, and reliability engineering.
• Proven experience with Computer System Validation (CSV) in regulated industries (e.g., pharma, biotech, medical devices) is highly preferred.
• Familiarity with GMP, FDA 21 CFR Part 11, ISO standards and audit requirements.
• Excellent problem-solving, analytical, and stakeholder management skills.
• Strong communication skills with the ability to train and support end-users.

Why join us?

• Comprehensive Health & Wellness Coverage: Receive robust medical and dental coverage to support your health needs.
• Professional Development Opportunities: Access continuous learning programs and resources for career growth within the company.
• Inclusive Culture: Work in an environment where innovation, collaboration, and diverse perspectives are encouraged and celebrated.
• Shape the Future: Make a real difference in the pharmaceutical industry while advancing your career.