Software Quality Engineer

undefined ago • 10 Years + • Quality Assurance

Job Summary

Job Description

This Software Quality Engineer role ensures appropriate software quality plans across all lifecycle stages, supporting design and validating key inputs like usability and reliability. The engineer provides oversight for plan execution, risk management, and design activities, leading quality problem-solving. Responsibilities include using post-market analytics for performance reporting and acting as a business partner to ensure compliance with software quality standards for all project milestones.
Must have:
  • 10+ years of industry experience in PQE
  • Experience (3 to 8 years) in medical industry product development as QE, with SW domain expertise
  • Strong knowledge in QMS 13485, 21 CFR, EU MDR, SW LC 62304, Usability 62366, RMM 14971
  • Experience in guided R&D team
  • Involvement in all design control document reviews and DHF maintenance
  • Experience in guiding R&D team for Defects Handling and tracking defects
  • Experience in handling internal & External audits
  • Good knowledge in CAPA, Regulatory, Verification and Post Market Surveillance
  • B Tech in Computer Science or experience as SW Developer
  • Knowledge of at least one of: ISO 13485, IEC 62304, ISO 14971, IEC 82304, IEC 62366-1, EUMDR, 21CFR
Good to have:
  • Prepared QMS procedures and Templates

Job Details

Job Title

Software Quality Engineer

Job Description

Job title:

Software Quality Engineer

Your role:

  • Ensures that appropriate SW Quality plans are made that include all stages of the software life cycle and supports SW Quality Plan design.
  • Validates key design inputs (i.e. usability, reliability, performance, supportability, manufacturability, localizability, safety, security, privacy, serviceability, sustainability and costs).
  • Provides effective oversight of the execution of the SW Quality Plan and any Risk Management activities, and of all design related activities during the software lifecycle.
  • Can lead quality related problem solving for software.
  • Use post-market analytics and statistics to report on software performance in the field (provide feedback to manufacturing, suppliers or design teams) and initiate field actions as necessary, as required.
  • Act as a business partner, single point of contact (person assigned to project team) responsible to ensure that software design quality related requirements/criteria are completed and meet SW Quality standards for every milestone.

You're the right fit if: (4 x bullets max)

1. Experience- 10+ years of industry experience in PQE

2. Skills:

  • Worked in medical industry product development team (exp of 3 to 8 years) as QE. SW domain is must.
  • Strong knowledge in QMS 13485, 21 CFR, EU MDR, SW LC 62304, Usability 62366, RMM 14971 and experience in guided R&D team.
  • Heavily involved in all design control doc reviews and maintained DHF.
  • Guided R&D team for Defects Handling and tracked defects.
  • Experience in handled internal & External audits
  • Prepared QMS procedures and Templates are additional advantage.
  • Good knowledge in CAPA, Regulatory, Verification and Post Market Surveillance.

3. Education-

Candidate shall be with B Tech in Computer Science (or) experience as SW Developer

4. Anything else-

Must following one the skills

ISO 13485 - Quality management systems for Medical Devices

IEC 62304 - Medical device software — Software life cycle processes

ISO 14971 - Application of risk management to medical devices

IEC 82304 - Health software, Product Safety

IEC 62366-1 - Application of usability engineering to medical devices

EUMDR – European Medical Device Regulation

21CFR – US FDA Medical Regulation

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

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• Discover our rich and exciting history

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• Learn more about our purpose

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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

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About Us

At Philips, we believe that every human matters. As a global health-tech leader, we focus on improving people’s health and wellbeing through meaningful innovation. The people who work here share our passion and are motivated to bring this purpose to life.

For more than 130 years, we have been creating technologies and innovations that improve people's lives and support healthcare practitioners. Headquartered in the Netherlands and operating in more than 100 countries globally, we focus our advanced technology and deep clinical and consumer insights on Precision Diagnosis, Image Guided Therapy, Enterprise Informatics, Monitoring/ Connected Care, Sleep & Respiratory Care and Personal Health.

Together, we deliver better care for more people because we believe that every human matters. That's why we're taking steps to create an environment where we acknowledge and embrace our differences and uniqueness and listen to and value each other's views. When people feel cared for and listened to, they bring their best qualities to work, leading to better collaboration, communication, innovation and success.

It is the policy of Philips to provide equal employment and advancement opportunities to all qualified employees and applicants for employment without regard to race, color, religion, sex, pregnancy/childbirth or related medical conditions, age, ethnic or national origin, sexual orientation, gender identity or expression, physical or mental disability, genetic information, citizenship status, veteran or military status, marital or domestic partner status or any other characteristic protected by law. As an equal opportunity employer, Philips is committed to fostering a culture where all are treated with respect and professionalism.

To ensure reasonable accommodations for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veterans' Readjustment Act of 1974 and Title I of the Americans with Disabilities Act of 1990, applicants that require accommodation in the job application process may contact 888-367-7223, option 5, for assistance.

Philips is an Equal Employment and Opportunity Employer including Disability/Vets and maintains a drug-free workplace.

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About The Company

At Philips, we believe that every human matters. As a global health-tech leader, we focus on improving people’s health and wellbeing through meaningful innovation. The people who work here share our passion and are motivated to bring this purpose to life.For more than 130 years, we have been creating technologies and innovations that improve people's lives and support healthcare practitioners. Headquartered in the Netherlands and operating in more than 100 countries globally, we focus our advanced technology and deep clinical and consumer insights on Precision Diagnosis, Image Guided Therapy, Enterprise Informatics, Monitoring/ Connected Care, Sleep & Respiratory Care and Personal Health.Together, we deliver better care for more people because we believe that every human matters.

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