Job Description

Job Title
Mechanical Designer- QPL

#STET
#HIC
#LIPHILIN
Job title:

Mechanical Designer - QPL (Quality Project Lead)
:
You are a part of A high-impact, global organization " Sustaining Engineering Team" (STET) within Philips and will be working closely with R&D team of "Intense Pulsed Light Therapy" (IPL) Business. STET has been established as an entrepreneurial organization that focuses on fast paced, high-quality portfolio transfers within the Philips global supply base to mitigate risk & maximize profitability. As a senior member within this team, the transfer leader is responsible for driving technical excellence within said projects to ensure first-time-right quality.
In this role,
The Quality Engineer is accountable for quality oversight of system, hardware and risk management throughout the product life cycle. The Quality Engineer provides independent oversight of the design input process, design V&V activities, design transfer and product realization, and performance in the field to ensure that all design requirements are effectively met. The Quality Engineer also provides analytics to the Business on the efficacy and efficiency of the design and product realization processes• Ensures that appropriate quality, reliability- and Post Market Surveillance (PMS) plans are made and include all stages of the product life cycle Supports Quality Plan design for hardware and Software design and ensure they meet quality and compliance standards for every planned milestone.
• Validates key design inputs like usability, reliability, performance, supportability, manufacturability, localizability, safety, security, privacy, serviceability, sustainability and costs
• Provides effective oversight of the execution of the quality, reliability, PMS Plans, any Risk Management activities, and all of design related activities during the product/system lifecycle
• Performs independent technical assessment on product quality performance and post-market product quality analysis to lead quality related problem solving and root cause analysis during design and manufacturing and initiates field actions when required
• Supports stakeholders during the execution of quality system- and product audits and inspections.


Your role:
To succeed in this role, you should have the following skills and experience• B.E. in Mechanical / Electrical / Electronic Engineering / MS in engineering preferred / Equivalent Degree
• 8 - 15 or more years of experience form Medical Devices / Personal Health
• Working Knowledge of global medical device regulations, requirements, and standards, such as 21 CFR Parts 803, 806, and 820, ISO13485, and ISO9001.
• Independently Produces and completes Quality Engineering Documents.
• Responsible for Performing timely, quality engineering tasks like : Assessing Quality Plans, product designs & reviewing tea and other performance data, analyses market feedback, lead root cause analysis and Quality problem solving
• Responsible for following major deliverables:
+ Post Market Surveillance plan / Periodic Quality review report
+ Safety Risk Management plan / matrix / report
+ Product reliability status
+ Hazardous substance management (risk management + declaration)
+ Bio compatibility assessment
+ Substance dispensation request (waiver)
+ Product Design Release
• Hands on experience on DOORS
• Hands on experience with Windchill & releases management
• Working with multiple stakeholders to align and ensure timely delivery and release in the Windchill
• Working knowledge of Microsoft Project, Excel, Power Point, and Word required
• Good team player
• Strong English written and verbal communication skills required


Note : Job location is Philips office at Pune (Baner) and expected to be working from Philips office.
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If you're interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion here.