Software Quality Engineer
Software Quality Engineer
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Job Description
Job Title
Software Quality EngineerJob 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.
Youre 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 QMSCFR 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 systemsfor 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
IECApplication 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 companys facilities.
Field roles are most effectively done outside of the companys 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 wont 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 about our purpose.
If youre 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.
Employment Type
Full-Time
