Jobs / India / Philips North America LLC
Product Quality Engineer
Philips North America LLC · 🌍 Bangalore
Sponsorship verdict
No sponsorship evidence yet
No government record and no wording either way. Not a refusal — ask the recruiter.
- No government sponsor record hereNo government sponsor record covers this employer in this country.
- The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
- Can’t check pay against the visa rulesWe don’t have visa salary rules for this country yet.
- Last confirmed live 2 days agoWhen a source last listed this job as open.
A verdict summarises public evidence; it is not legal advice and never a guarantee — the employer and the immigration authority decide. Sign in to factor in where you can already work.
Or apply yourself on the official page →
Why not apply?
No register record and no sponsorship wording in the posting. Worth asking the employer before investing significant time.
SponsorApply flags time-wasters so your applications go where they can land. These come from the posting's own wording — read the original listing to confirm. See better-fit alternatives →
Sponsor Radar — Philips North America LLC
No government sponsor record covers this employer in this country.
Past sponsorship or register membership never guarantees sponsorship for this vacancy or for you. Full Sponsor Radar for Philips North America LLC →
About the role
Job Title Product Quality Engineer Job Description Job Title : Product Quality Engineer The Product Quality Engineer will support design controls and quality management associated with the development, transfer and sustaining initiatives for the medical devices. You are responsible for • 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 through analysis of field • performance, identification of trends and risks, and actions to eliminate or mitigate adverse post market issues. • Support the Regulatory Affairs department for submissions and respond to submission questions. • Lead and support Corrective and Preventive Actions (CAPA) and QMS continuous improvement initiatives. • Analyze situations/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 and operations quality and supplier quality teams. • Support internal and external audits. • Acts in full compliance to all applicable regulatory requirements and Philips Quality policies. • Your role: • Lead all quality elements of Design Controls and product Design History Files. • Lead Quality Plan initiatives associated with Risk Management and Quality System integration. • Analyze situations/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 and operations quality and supplier quality teams Minimum required Education: Bachelor's / Master's Degree in Mechanical Engineering, Electronics Engineering, Science or equivalent. Minimum required Experience: Minimum 8-10 years of experience with Bachelor's/Master's in areas such as Quality Engineering, Safety Engineering, R&D Engineering or equivalent. Preferred Certification: Six Sigma Green Belt Preferred Skills: • Design Quality Management • Experience in ISO 14971, 21 CR 820, ISO 13485, EU MDR, IEC 60601-1, IEC 62366, and IEC 62304 standards - Mandatory • Data Analysis & 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 How we work together We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations. Indicate if this role is an office/field/onsite role. About Philips We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others. • Learn more about our business . • Discover our rich and exciting history . • Learn more abo