CMMS Engineer

Overview
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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
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