Over the past decade we have transformed into a focused leader in health technology.At Philips, our purpose is to improve people’s health and well-being through meaningful innovation. We aim to improve 2.5 billion lives per year by 2030, including 400 million in underserved communities. We see healthcare as a connected whole. Helping people to live healthily and prevent disease. Giving clinicians the tools they need to make a precision diagnosis and deliver personalized treatment. Aiding the patient's recovery at home in the community. All supported by a seamless flow of data.
Philips Recruitment Drive 2025 | Philips Hiring Mechanical Engineer
www.djobbuzz.com
22 Sep 2025
- Company Name
- Philips
- Company Website
- https://www.philips.com/a-w/about.html
- Experience
- 8+ Years
- Job Role
- Design Quality Engineer
- Job Type
-
- Experienced
- Job Location
-
- Pune
- Skills
-
- Good Communication Skill
- Education
-
- BE/BTech
- Branch
-
- Mechanical Engineering
- Job will expire on
- 21 Nov 2025
About Company
Eligibility Criteria
- An Engineering degree in any discipline with at least 8+ years of relevant industry experience.
- Core expertise in Design Quality, Systems Engineering, or Reliability Engineering
- Medical device industry experience is mandatory
- Ability to define detailed systems quality and reliability plans for new medical product developments to ensure those are safe, effective and reliable
- Ability to contribute to Risk Management and lead FMEA activities for new products and assurance that control measures are translated in appropriate critical requirements
- Strong exposure to application of Design Controls; ability to do thorough Design Reviews during new product development to ensure robust designs that further improve patient safety and product quality
- Ability to partner with V&V teams to assure thorough Verification, Validation and Usability testing
- Ability to lead reliability analysis to assess the risks associated with design concepts
- Experience with adequate and accurate review of DHF and DMR documents
- Understanding of global medical device regulations, requirements, and standards, such as 21CFR820, ISO13485, EU MDR, , and ISO 14971
- Experience with working in multidisciplinary teams in a high-tech R&D environment
- You continuously strive for excellence as a way of life and can inspire others to adopt this mentality of prioritizing quality above all else
- You are a self-starter who embraces the change
Job Description
- Ensure appropriate quality plans are made that include all stages of the life cycle of the product and supports Quality Plan design
- Validate key design inputs like usability, reliability, performance, supportability, manufacturability, localizability, safety, security, privacy, serviceability, sustainability, and costs
- Provide effective oversight of the execution of the Quality Plan, any Risk Management activities, and of all design related activities during the product/system lifecycle
- Perform independent technical assessment on product quality performance and post-market product quality analysis.
- Can Lead quality related problem solving and root cause analysis during design and manufacturing
- Uses post-market analytics and statistics to report on product quality performance in the field (provide feedback to manufacturing, suppliers or design teams) and initiates field actions when required.
- Performs independent technical assessment on product quality performance and post-market product quality analysis
- Provide leadership and oversight to ensure Quality Management System Compliance
- Be able to plan, control, and assure product and process quality in accordance with quality principles, which include planning processes, material control, acceptance sampling, and measurement systems
- Ensure the compliance requirements are met during Design review , design verification & Design validation , Design transfer
- Apply and facilitate Design for Quality & Reliability best practices (FMEAs, robust design, V&V, root cause analysis & problem solving)
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