Reliability Engineer (Mechanical)

Pfizer Singapore is recruiting permanent employees for manufacturing site expansion of Pfizer Asia Manufacturing Pte Ltd (PAMPL) in Singapore

Why Patients Need You

• Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is vital to making sure customers and patients have the medicines they need, when they need them. Working with our innovative engineering team, you'll help bring medicines to the world even faster by imagining what's possible and taking action.

• Working with Pfizer's dynamic engineering team, you will play a critical part in managing the maintenance and reliability engineering activities involving the redesign, maintenance, and repair of utilities systems, buildings, and production/non-production equipment.
• As a Senior Associate, your knowledge and skills will contribute towards the goals and objectives of the team. Your ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate in managing difficult issues and establishing consensus between teams.
• It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe.

• Perform maintenance and inspection activities on plant equipment according to procedures, good engineering practices and cGMP.

• Lead and execute the predictive maintenance programs, collect data, analyze, generate report and recommend corrective actions/improvements to reduce equipment failures.
• Develop maintenance programs to maintain plant assets. Review and modify the PM/PdM to improve equipment reliability.
• Prepare reports and documentation by collecting, analyzing and summarizing information and trends. Manage the reliability equipment database.
• Establish equipment reliability standards by studying drawings, data sheet and design specifications; verifying specifications with OEM and Engineering staff; writing and updating reliability/inspection procedures.
• Ensure smooth equipment operation by close monitoring of the equipment conditions. Carrying out root cause failure analysis to improve product quality and equipment reliability.
• Lead, coordinate and execute major equipment repair and troubleshooting.
• Confirm and verify equipment performance by designing feasibility inspection and testing methods, testing properties and equipment monitoring parameters.
• Determine acceptability of equipment rework/installation by conducting inspections of reworked equipment and new installation job.
• Support project design, construction and commissioning through active involvement in commissioning activities, discuss equipment improvement and modifications with vendors/Supervisors/Engineers.
• Lead in continuous improvement initiatives, troubleshooting of complex problems and lead in (IRS/QAR) investigations/root cause analysis and write investigation report for approval related to equipment issues.
• Maintain professional and technical knowledge by attending GRP CoP meetings, technical workshops and participating in professional societies.
• Provide training (e.g. OJT) and coaching to colleagues to build-up their competencies.
• AOB

• Safety incident / lost time
• Equipment uptime %
• Critical PM overdue (safety and process critical equipment)

• Diploma or Degree in Engineering related qualifications.
• Minimum 10 years of relevant experiences in pharmaceutical, chemical, or petrochemical industries.
• Knowledge of Reliability Maintenance, Right First Time technique and performance base management.
• Experience in a large, global and complex organization would be an advantage
• Able to handle multiple projects concurrently and possess project management experience
• Able to influence stakeholders or Business Leaders and to build trust throughout the organization
• Demonstrated capability to thrive in a complex and matrix environment
• Experience with Root Cause Failure Analysis, Equipment Criticality Ranking, PM/PdM optimization, and/or Failure Modes and Effects Analysis
• Strong knowledge and understanding of Current Good Manufacturing Practices {part of GxP}
• Excellent oral and written communication skills
• Working knowledge of MS Office
• Fully complete Covid-19 vaccination and could provide official medical certificate

• Relevant pharmaceutical experience