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Reliability Engineer

10.00 to 12.00 Years   Pune   11 Jan, 2021
Philips
Job LocationPune
EducationNot Mentioned
SalaryNot Disclosed
IndustryMedical / Healthcare
Functional AreaGeneral / Other Software
EmploymentTypeFull-time

Job Description

nullIn this role, you have the opportunity toIn this role, you can run projects as a part of Global Procurement Team and have a visible impact on finding the best way to meet the challenges of sourcing, markets and global competition.Perform reliability testing for range of products and the components in such a way that all the realized products options and features; are verified and validated. You are responsible for identifying test protocols, methods and equipment for sub-system and component levels. You will ensure that the design is consistent with the system requirements.Perform Supplier Quality activities related to purchased part qualification with suppliers, supplier quality issue resolution and ensuring appropriate incoming material inspection strategies. Partner with Product Development and Manufacturing to adequately define Critical to Quality (CTQs) purchased parts. Plan, execute, and manage quality activities with suppliers, setting a high standard and fast response expectation so quality issues are prevented or minimized. Lead with best practices to enable our organization to provide high quality medical products to our customers.You are responsible for

  • Creating reliability test specification/acceptance criteria from Requirements.
  • Creating of reliability test fixture & automations
  • Preparation of System integration plan/report, System verification plan/report
  • Independently Produces and completes Supplier Quality Engineering related activities and documentation.
  • Completes Qualification of materials and components (including spare parts), development/ improvement of supplier processes for CtQs, supplier process control plans; ensuring that the supplied part meets specifications, and the control limits/tolerances for CtQ parameters are met.
  • Qualifies and sustains sub-processes of suppliers, including performing process validations for critical supplier processes impacting part quality.
  • Ensures that the components/products at the supplier (including spare parts and services) are released according agreed specification and quality requirements (MQA/APQP / PPAP), and SQ audit results.
  • Executes SCAR management, effective and timely closure and Review/risk assessment of QNs and their escalation to SCARs where needed.
You are a part ofEngineering & Procurement cross-functional team responsible for R&D knowledge transfer, localisation, global transfer projects in Idea to Market (I2M), Market to order (M2O) and Order to customer (O2C). KPI s include new part development, BOM savings, reverse engineering, value engineering projects, global product & parts transfers, part of extended team of design authority, new cost savings ideas supporting procurement processesTo succeed in this role, you should have the following skills and experience
  • 10+ years of working experience in the related field.
  • Bachelor or master s degree in Electronics, Computer Communication or other relevant discipline.
  • Working experience of Mechatronics, Electrical & Electronics, Electromechanical components
  • Competencies and skills:
  • Good understanding of Reliability Concepts and Testing like HALT and HAST.
  • Excellent interpersonal and communication skills.
  • Familiar with New Product Development, Engg Change Management, Defect Management processes, Risk management and Traceability matrix
  • Experience in root cause analysis, corrective and preventive action methods.
  • Expertise/experience in problem solving with quality tools such as: 6-sigma / 8-D / CAPA / FMEA/ 5WHY etc.
  • Good knowledge of production/quality development and control methods; CtQ definition, DfSS, SPC, APQP, FMEA, Control Plans, etc.)
  • Working knowledge of appropriate global medical device regulations, requirements and standards such as 21 CFR Parts 803, 806, and 820, ISO13485, ISO14971, European Medical Device Directive (93/42/EEC), Canadian Medical Devices Regulation (SOR/98-282), Japanese MHLW Ordinance 169, and ISO 9001 is preferred
In return, we offer you
  • A rewarding career in Philips with attractive package. `
  • Extensive set of tools to drive your career, such as a personal development budget, free training and coaching
  • Attractive collective health insurance package
  • Opportunity to buy Philips shares and products with discount
Why should you join Philips Working at Philips is more than a job. It s a calling to create a healthier society through meaningful work, focused on improving 2.5 billion lives a year by delivering innovative solutions across the health continuum. Our people experience a variety of unexpected moments when their lives and careers come together in meaningful ways. Learn more by watching this video.To find out more about what it s like working for Philips at a personal level, visit the Working at Philips page on our career website, where you can read stories from our employee blog. Once there,you can also learn about our recruitment process, or find answers to some of the frequently asked questions.#LI-PHILIN,

Keyskills :
reliabilityfmeamechanicalsafetycommissioningcorrectivepreventive actionroot cause analysisnew product developmentmedical device directiveservice center operationssupplier quality engineering

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