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Lead Configuration Engineer
Quest Global Technologies
posted 1mon ago
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Flexible timing
Key skills for the job
Job Description
You have the opportunity to be part of an exciting team and contribute to the design, development and maintenance of Medical Devices. In this role of Lead Configuration Engineer , you are responsible for product configuration data management and completing appropriate data analysis across the lifecycle of overall system, sub-system and component levels to ensure completeness of data record, customer delivery continuity, and optimum level of products quality for our customers. This requires broad orientation, conceptual skills and a can domentality, keeping abreast with all trends and advancements in technology.
You are responsible for :
- Checking integrity of CAD-E, associated assemblies and CAD-M data
- Transfer to suppliers: Exchanging data with suppliers
- Interface between Philips and supplier for resolving DMR issues
- Consulting on applicable standards, tools and assembly processes
- Managing lifecycle of components, trigger actions for obsolescence risk mitigation
- Complete Installed Base searches and quality analysis
- Suggest process improvements for data integrity including ECR and EOL, data transfer and data storage
- Assist low to frequent users in data transfer and archiving
- Assist in CAD-E tool validation
- Based on specific EOL trigger, create relevant ECR and associated actions
- Creating and maintaining documentation for tools used to support configuration management
- Monitoring all configuration management processes
- Providing the users, support and troubleshooting of issues, with the relevant configuration management software
- Perform the role of Change Admin 1 and 2, for MR Therapy Products (also for overall MR systems in the absence of respective Configuration Designer)
- Conduct DCRB and OCCB meetings for MR Therapy Products (also for overall MR systems in the absence of respective Configuration Designer)
- Gather input from product configuration team in Best for MAXBOM changes in MR Therapy Products
- Review of change notices of Therapy Hardware Team, Supporting the PMO for Where Used analysis of impacted parts etc.
To succeed in this role, you should have the following skills and experience:
- Completed engineering studies at University level; BE/BTech/ME/M-Tech in Mechanical, Electrical, Electronics Engineering or equivalent stream
- 8-12 years of work experience in product configuration management
- Expertise in CAD-E and CAD-M tools for data integrity purposes
- Expert in data storage and transfer tools - e.g. Agile, Windchill SAP-PLM, SAP-IPPe, PDX, ODB++ etc.
- Expert in version control of TPD, CAD-E and non-volatile PL data
- Experience in Transfer of data on PCBAand assemblies to and from relevant suppliers, including Engineering Change and End-of-Life issues
- Experience in Medical Device development and knowledge of IEC 60601 standards will be an added advantage
- Knowledge of Global Medical Quality and Regulatory Standards e.g. IEC, FDA, UL, CE, CSA etc. will be an added advantage
- Disciplined team worker, ability to work independently
- Highly structured and self-organized
- Able to guide and mentor young engineers in the team
- Result oriented team player
- Ability to present and articulate ideas to key stakeholders and leadership team
- Excellent communication skills and Positive can doattitude
- Quality mindset in design and documentation
You have the opportunity to be part of an exciting team and contribute to the design, development and maintenance of Medical Devices. In this role of Lead Configuration Engineer , you are responsible for product configuration data management and completing appropriate data analysis across the lifecycle of overall system, sub-system and component levels to ensure completeness of data record, customer delivery continuity, and optimum level of products quality for our customers. This requires broad orientation, conceptual skills and a can domentality, keeping abreast with all trends and advancements in technology.
You are responsible for :
- Checking integrity of CAD-E, associated assemblies and CAD-M data
- Transfer to suppliers: Exchanging data with suppliers
- Interface between Philips and supplier for resolving DMR issues
- Consulting on applicable standards, tools and assembly processes
- Managing lifecycle of components, trigger actions for obsolescence risk mitigation
- Complete Installed Base searches and quality analysis
- Suggest process improvements for data integrity including ECR and EOL, data transfer and data storage
- Assist low to frequent users in data transfer and archiving
- Assist in CAD-E tool validation
- Based on specific EOL trigger, create relevant ECR and associated actions
- Creating and maintaining documentation for tools used to support configuration management
- Monitoring all configuration management processes
- Providing the users, support and troubleshooting of issues, with the relevant configuration management software
- Perform the role of Change Admin 1 and 2, for MR Therapy Products (also for overall MR systems in the absence of respective Configuration Designer)
- Conduct DCRB and OCCB meetings for MR Therapy Products (also for overall MR systems in the absence of respective Configuration Designer)
- Gather input from product configuration team in Best for MAXBOM changes in MR Therapy Products
- Review of change notices of Therapy Hardware Team, Supporting the PMO for Where Used analysis of impacted parts etc.
Work Experience
To succeed in this role, you should have the following skills and experience:
- Completed engineering studies at University level; BE/BTech/ME/M-Tech in Mechanical, Electrical, Electronics Engineering or equivalent stream
- 8-12 years of work experience in product configuration management
- Expertise in CAD-E and CAD-M tools for data integrity purposes
- Expert in data storage and transfer tools - e.g. Agile, Windchill SAP-PLM, SAP-IPPe, PDX, ODB++ etc.
- Expert in version control of TPD, CAD-E and non-volatile PL data
- Experience in Transfer of data on PCBAand assemblies to and from relevant suppliers, including Engineering Change and End-of-Life issues
- Experience in Medical Device development and knowledge of IEC 60601 standards will be an added advantage
- Knowledge of Global Medical Quality and Regulatory Standards e.g. IEC, FDA, UL, CE, CSA etc. will be an added advantage
- Disciplined team worker, ability to work independently
- Highly structured and self-organized
- Able to guide and mentor young engineers in the team
- Result oriented team player
- Ability to present and articulate ideas to key stakeholders and leadership team
- Excellent communication skills and Positive can doattitude
- Quality mindset in design and documentation
,
Employment Type: Full Time, Permanent
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Flexible timing
Monday to Friday
No travel
Day Shift
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