赛诺菲
Reliability & Methods Engineer
Reliability & Methods Engineer
发布于 大约 13 小时前普通员工/个人贡献者
Singapore, Singapore
高级经验
全职员工
仅现场办公
本科
生产制造
FMEA
RCM
TPM
MTBF
CAPA
cGMP
HAZOP
Root Cause Analysis
Sap Cmms
AI 估算 · 25k–40k
Singapore pharmaceutical engineering role with 5+ years experience; market rate for similar roles ranges SGD 5k-8k/month, conver
职位详情
关于这个职位
This role is a Reliability & Methods Engineer at Sanofi's Singapore manufacturing site, part of the Modulus program. You will be responsible for improving the reliability, sustainability, and maintainability of GMP and non-GMP systems through FMECA, predictive maintenance, root cause analysis, and continuous improvement. You will support new plant start-up, maintenance strategy development, and compliance audits in a pharmaceutical manufacturing environment.
最低要求
Bachelor's Degree in Engineering or related technical discipline from an accredited institution.
Minimum 5 years of experience in maintenance management and reliability engineering in plant operations or engineering environments.
Experience with reliability engineering tools such as FMEA, RCM, MTBF, Life-Cycle Costing, Pareto, and Root Cause Failure Analysis.
工作职责
Develop and maintain FMECA as a knowledge platform for plant-specific risk assessment and reliability-enhancing activities.
Perform periodic analysis on equipment databases to determine improvement priorities.
Originate and develop analytical methods for determining reliability of components, equipment, and processes.
Manage Predictive Maintenance (PDM) programs such as vibration analysis, infrared thermography, motor circuit analysis, ultrasonics, and related technologies.
Interpret predictive maintenance data outputs and prioritize corrective actions.
Review, monitor, and ensure compliance with engineering design requirements, standards, specifications, and local regulatory codes.
Routinely audit operational performance and regulatory compliance of highly complex equipment and systems.
Support maintenance excellence initiatives to improve system reliability, maintainability, and performance.
Support project procurement activities including vendor and subcontractor management, RFQs, tender review, and technical/commercial bid analysis.
Apply and implement Total Productive Maintenance (TPM) principles.
Ensure all maintenance activities are properly documented to demonstrate compliance with regulatory requirements (e.g. cGMP).
Implement measures to maintain data integrity, including secure maintenance data storage and audit trail controls.
Support contract and change management activities.
Support planning and execution of scheduled maintenance activities.
Ensure assigned CAPA, deviation, CCR, and DCR tasks are managed and resolved in a timely manner.
Lead improvement actions and projects to modify, improve, or replace equipment identified as “bad actors”.
Perform work within budget and schedule parameters.
Perform root cause investigations for repetitive problems and equipment failures.
Prepare for audits through self-assessments and mock audits.
Serve as a subject matter expert (SME) during audits for maintenance and equipment-related matters.
Facilitate on-site startup and training activities as required.
Support and participate in commissioning and qualification (C&Q) of related systems.
Participate in activities related to HAZOP, HAZID, FMEA, SOP, CMMS, maintenance procedures, and regulatory compliance requirements.
Prepare and support C&Q documentation including URS, DR, FCCA, and SIA.
Participate in system startup, shakedown, pre-startup checks, and commissioning.
Review and update operational support documents such as SOPs, PM plans, and training matrices.
Coordinate with manufacturing and maintenance planning teams to establish maintenance plans with minimal production impact.
Collaborate across functions to investigate repetitive failures and implement corrective actions.
Utilize quality systems to ensure compliance with regulatory requirements.
Comply with Sanofi Safety Program requirements, including Health & Safety regulations and OSHA standards.
Lead or support cross-functional engineering initiatives to improve operational reliability and efficiency.
优先资格
Experience in pharmaceutical manufacturing and/or petrochemical plant operations is preferred.
Certification as a reliability professional is preferred.
Familiarity with SAP Computerized Maintenance Management Systems (CMMS) is advantageous.
Certification in calibration or related technical fields is desirable.
AI 洞察
优缺点分析
优点
- Work on cutting-edge modular pharmaceutical manufacturing under the Modulus program, gaining exposure to innovative technologies.
- Join a top global pharmaceutical company with strong investment in R&D and career development.
- Gain deep expertise in reliability engineering within a regulated industry, highly valued in pharmaceutical and biotech sectors.
- High level of responsibility for plant uptime and compliance
- pressure to resolve issues quickly.
- Requires extensive knowledge of both engineering and regulatory standards
- steep learning curve for newcomers to pharma.
- On-site role in Tuas industrial area, may involve shift work or on-call duties for critical failures.
- This role is ideal for an experienced reliability engineer with a background in manufacturing or pharmaceuticals who enjoys problem-solving, data analysis, and working in a highly regulated environment.
缺点 / 挑战
暂无明显挑战项
角色解读
- Progress to Senior Reliability Engineer or Reliability Manager leading a team of engineers.
- Transition into plant engineering manager or maintenance director roles with broader plant operations responsibility.
- Specialize in advanced reliability analytics or asset management across multiple sites within Sanofi.
- Develop and implement reliability strategies using FMECA and predictive maintenance technologies for GMP and non-GMP systems.
- Lead root cause investigations for equipment failures and drive continuous improvement projects.
- Support new plant start-up by participating in commissioning, qualification, and HAZOP activities.
- Coordinate with cross-functional teams to ensure maintenance plans align with production needs and regulatory compliance.
- Strong knowledge of reliability engineering tools: FMEA, RCM, MTBF, Life-Cycle Costing, Pareto Analysis, Root Cause Failure Analysis.
- Proficiency in predictive maintenance techniques (vibration analysis, thermography, motor circuit analysis, ultrasonics).
- Understanding of cGMP, FDA, EMA, HSA regulations and safety standards.
- Experience with SAP CMMS and maintenance management systems.
申请策略
- Tailor your resume to explicitly mention reliability engineering methodologies and results achieved.
- Research Sanofi's Modulus program and be prepared to discuss how your experience aligns with its modular, agile manufacturing vision.
- Emphasize hands-on experience with FMECA, FMEA, RCM, and predictive maintenance programs.
- Highlight any work in pharmaceutical, biotech, or chemical plants showing compliance with cGMP and regulatory audits.
- Quantify achievements: reduced downtime, increased equipment reliability, cost savings from reliability improvements.
- Demonstrate familiarity with SAP CMMS and other maintenance software.
- Obtain a Certified Reliability Engineer (CRE) or similar certification if not already held.
- Deepen knowledge of pharmaceutical regulations (FDA, EMA, HSA) through online courses or training.
面试指南
- Use the STAR method (Situation, Task, Action, Result) for behavioral questions.
- For technical questions, demonstrate systematic thinking: problem definition, analysis, solution implementation, and monitoring.
- Describe a time when you used FMECA to improve equipment reliability. What was the outcome?
- How do you prioritize maintenance activities when multiple critical failures occur simultaneously?
- Walk me through your approach to a root cause analysis for a recurring equipment breakdown.
- How do you ensure compliance with cGMP in maintenance documentation and activities?
- Explain how you have used predictive maintenance technologies to prevent failures.
- Review basic reliability engineering concepts and be ready to discuss specific tools (FMEA, RCM, MTBF).
职位点评
68
综合评分
Strong career development in pharmaceutical reliability engineering, with good compensation but demanding on-site presence and compliance pressure.
更适合这类人
This role is best for candidates who prioritize technical growth and career advancement in a stable industry, and are willing to accept on-site work with limited flexibility.
表现最好
成长发展
相对薄弱
工作生活
薪资福利75
成长发展85
工作生活40
使命价值70
薪资福利
75中等
The role offers competitive salary for Singapore's engineering market, plus benefits from a large multinational like Sanofi (bonus, health insurance, etc.). However, the salary range is not disclosed, so signal is '未披露'.
薪资信号未披露（AI估算：25K-40K/月）
成长发展
85较高
The role provides strong growth in reliability engineering within a cutting-edge pharmaceutical manufacturing program. Opportunities to learn new technologies (predictive maintenance, modular design) and potential for certification. Clear promotion path to senior roles.
技术前沿主流现代技术
技术栈FMECA、Predictive Maintenance、FMEA、RCM、SAP CMMS、TPM
成长机会certification as a reliability professional is preferred、Pursue Progress、Discover Extraordinary
业务类型cost_center
工作生活
40较低
Based in Tuas industrial area, Singapore; requires on-site presence. No mention of flexible work or WLB. Overtime may be required during plant startups or emergencies.
工作模式仅现场办公
办公地点工厂/生产基地
加班情况未提及（无法判断）
使命价值
70中等
Working at Sanofi contributes to improving people's health through pharmaceutical manufacturing. The role is part of an innovative program (Modulus) that aims to transform manufacturing. However, the direct social impact is indirect.
行业发展稳定成熟行业
社会影响正向社会影响力较高
使命信号improve people's lives、chase the miracles of science
创新程度积极采用新技术
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