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Philips

Makes medical devices and personal health products

Product Quality Engineer

Biomedical Engineering & Medical Devices +1Posted on Nov 5
Full-timeBengaluru, Karnataka, IndiaNo salary listed

About the Job

Requirements

  • A Bachelor's or Master's degree in Mechanical Engineering, Electronics Engineering, Science, or equivalent is required.
  • A minimum of 8–10 years of experience in Quality Engineering, Safety Engineering, R&D Engineering, or equivalent is required.
  • Experience with ISO 14971, 21 CFR 820, ISO 13485, EU MDR, IEC 60601-1, IEC 62366, and IEC 62304 standards is mandatory.

Responsibilities

  • Lead all quality elements of Design Controls and product Design History Files.
  • Drive quality norms associated with design engineering projects.
  • Support integration of Risk Management processes throughout the product lifecycle, from initial development through post-market surveillance, in accordance with Philips processes and global standards.
  • Lead Quality Plan initiatives associated with Risk Management and Quality System integration.
  • Support integration of post-market surveillance processes into Design Controls and Sustaining initiatives by analyzing field performance, identifying trends and risks, and taking actions to eliminate or mitigate adverse post-market issues.
  • Support the Regulatory Affairs department with submissions and respond to submission questions.
  • Lead and support Corrective and Preventive Actions (CAPA) and QMS continuous improvement initiatives.
  • Analyze situations and data using engineering principles and collaboration to identify gaps between project work and QMS.
  • Transfer Quality deliverables for new products and sustaining projects to manufacturing, operations quality, and supplier quality teams.
  • Support internal and external audits.
  • Comply with all applicable regulatory requirements and Philips Quality policies.

Desired Qualifications

  • Six Sigma Green Belt certification.
  • Design Quality Management.
  • Data Analysis and Interpretation.
  • Design for Quality (DFQ).
  • Root Cause Analysis (RCA).
  • CAPA methodologies.
  • Regulatory requirements.
  • Privacy, Safety, and Security Risk Assessment.
  • Technical documentation.
  • Continuous improvement.
  • Product quality and reliability.
  • Product Lifecycle Management (PLM).
  • People Management.
  • Defect Management.
  • Design Verification Planning.
  • Design Validation Planning.
  • Product Test Design.

About the Company

Philips

Makes medical devices and personal health products

Philips makes medical equipment and software for hospitals and care providers, along with personal health products for consumers. Its hospital portfolio spans MRI and CT scanners, ultrasound, image-guided treatment systems and patient monitors, while Sonicare and Avent cover oral health and baby care. Clinical software connects medical images and patient data across care teams, and the company earns revenue from equipment, software, maintenance and consumer product sales. It works with health systems through long-term technology and service partnerships, including solutions for care at home. Founded in 1891, Philips is headquartered in Amsterdam, the Netherlands.

Company size
10,001+
Company stage
IPO
Headquarters
Andover, MN
Founded
1891

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