Sr. Design Assurance Engineer (Sustaining)
Job TitleSr.
Design Assurance Engineer (Sustaining)Job DescriptionSr.
Design Assurance Engineer (San Diego based)We're looking for a highly qualified Senior Design Assurance Engineer (sustaining) to join our team within the San Diego site (this role requires the individual to be onsite 3 days per week minimum).
We're looking for someone with experience, drive, and passion to help us continue to provide the highest quality products to our customers.
Our ideal candidate will have extensive experience in design quality engineering, as well as a proven track record of success in the field.
The Senior Design Assurance Engineer will be responsible for leading, supporting and maintaining the design lifecycle of image guided therapy consoles (both hardware and software).
The successful candidate will be a confident problem solver, able to identify potential issues and implement solutions, while ensuring that all products meet the highest quality standards.
This individual will be expected to apply their knowledge of design control principles, statistics, process/systems validation, and quality engineering techniques to positively influence sustaining engineering and remediation projects.
This individual shall also ensure changes to products are developed and manufactured to applicable industry standards, regulatory requirements, and customer requirements.
Your role:
Represent Design Quality Engineering on product/process project teams to ensure product changes (design, supplier, obsolescence) meet pre-defined design input requirements as well as applicable laws and standards (21 CFR 820, ISO 13485, IEC/ISO).
Lead and provide guidance to cross functional teams (Engineering, R&D, Regulatory, Operations, Supplier Quality) to ensure design control requirements are being followed during design verification and validation activities.
Participate in design reviews to ensure all pre-defined requirements have been met.
Lead the risk management process and on-going maintenance of the risk management file (Risk Management Plan, FMEAs, Hazard Analysis, Risk Management Report).
Ability to perform risk assessments for product changes (design, supplier, obsolescence) and update of the risk documentation, as necessary.
Lead the investigation of complex product issues (CAPAs, NCRs, Issue Impact Assessments) and recommend appropriate preventive/corrective actions.
Assess complex product designs (hardware/software-based console systems) and lead/evaluate test protocols/reports to ensure testing is sufficient to meet quality objectives, applicable laws and standards and regulatory requirements.
In addition, ensure the testing demonstrated the ability to meet pre-defined acceptance criteria.
Analyze and investigate returned product (through customer complaints) to determine root cause and recommend preventive actions/measures.
Monitoring/trending of product issues/complaints and initiating appropriate quality planning principles to resolve such issues.
Ability to use quality tools for effective problem solving (5 Why, Pareto, Fish bone, FMEA).
Maintain knowledge of current regulatory requirements, applicable laws, and standards as well as internal quality system requirements.
Represent Philips as appropriate FDA, notified body, internal and external audits.
Mentoring of junior staff that includes training, motivation, and monitoring.
You're the right fit if:
You've acquired 5
years of relevant experience working in a regulated industry with full working knowledge of 21 CFR 820 and ISO 13485 medical device requirements.
Experience with medical device hardware/software systems is required with experience leveraging software as a medical device (SaMD).
Your skills include a strong knowledge of electrical engineering principles with respect to systems, sub-systems, and components.
Ability to thoroughly understand complex hardware systems and understanding of how the system works/operates.
You have a bachelor's degree or higher in either Electrical Engineering (strongly preferred) or Biomedical Engineering.
You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this Office/Remote position.
Strong interpersonal, organizational, and project management skills.
Demonstrated skills in decision making/problem solving and the ability to lead project teams when roadblocks/challenges exist.
Use of statistical analysis techniques and software for basic data interpretation (Minitab preferred).
Use of various tools including microscopes, multimeters, and other inspection equipment.
Proficient in relevant software programs (Microsoft Word, PowerPoint, Excel, and Project).
About PhilipsWe 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 improve the lives of others.
Learn more about our business.
Discover our rich and exciting history.
Learn more about our purpose.
Read more about our employee benefits.
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.
Philips Transparency Details The pay range for this position is $108,472 to $200,256, annually.
The actual base pay offered may vary depending on multiple factors including job-related knowledge/skills, experience, business needs, geographical location, and internal equity.
In addition, other compensation, such as an annual incentive bonus, sales commission or long-term incentives may be offered.
Employees are eligible to participate in our comprehensive Philips Total Rewards benefits program, which includes a generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement and much more.
Details about our benefits can be found here.
At Philips, it is not typical for an individual to be hired at or near the top end of the range for their role and compensation decisions are dependent upon the facts and circumstances of each case.
Additional InformationUS work authorization is a precondition of employment.
The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.
Company relocation benefits will not be provided for this position.
For this position, you must reside in or within commuting distance to San Diego.
#LI-PH1This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates.
Interested candidates are encouraged to apply as soon as possible to ensure consideration.
Philips is an Equal Employment and Opportunity Employer/Disabled/Veteran and maintains a drug-free workplace.
Job SummaryJob number:
517149Date posted :
2024-04-12Profession:
Quality & RegulatoryEmployment type:
Full time.
Estimated Salary: $20 to $28 per hour based on qualifications.
Design Assurance Engineer (Sustaining)Job DescriptionSr.
Design Assurance Engineer (San Diego based)We're looking for a highly qualified Senior Design Assurance Engineer (sustaining) to join our team within the San Diego site (this role requires the individual to be onsite 3 days per week minimum).
We're looking for someone with experience, drive, and passion to help us continue to provide the highest quality products to our customers.
Our ideal candidate will have extensive experience in design quality engineering, as well as a proven track record of success in the field.
The Senior Design Assurance Engineer will be responsible for leading, supporting and maintaining the design lifecycle of image guided therapy consoles (both hardware and software).
The successful candidate will be a confident problem solver, able to identify potential issues and implement solutions, while ensuring that all products meet the highest quality standards.
This individual will be expected to apply their knowledge of design control principles, statistics, process/systems validation, and quality engineering techniques to positively influence sustaining engineering and remediation projects.
This individual shall also ensure changes to products are developed and manufactured to applicable industry standards, regulatory requirements, and customer requirements.
Your role:
Represent Design Quality Engineering on product/process project teams to ensure product changes (design, supplier, obsolescence) meet pre-defined design input requirements as well as applicable laws and standards (21 CFR 820, ISO 13485, IEC/ISO).
Lead and provide guidance to cross functional teams (Engineering, R&D, Regulatory, Operations, Supplier Quality) to ensure design control requirements are being followed during design verification and validation activities.
Participate in design reviews to ensure all pre-defined requirements have been met.
Lead the risk management process and on-going maintenance of the risk management file (Risk Management Plan, FMEAs, Hazard Analysis, Risk Management Report).
Ability to perform risk assessments for product changes (design, supplier, obsolescence) and update of the risk documentation, as necessary.
Lead the investigation of complex product issues (CAPAs, NCRs, Issue Impact Assessments) and recommend appropriate preventive/corrective actions.
Assess complex product designs (hardware/software-based console systems) and lead/evaluate test protocols/reports to ensure testing is sufficient to meet quality objectives, applicable laws and standards and regulatory requirements.
In addition, ensure the testing demonstrated the ability to meet pre-defined acceptance criteria.
Analyze and investigate returned product (through customer complaints) to determine root cause and recommend preventive actions/measures.
Monitoring/trending of product issues/complaints and initiating appropriate quality planning principles to resolve such issues.
Ability to use quality tools for effective problem solving (5 Why, Pareto, Fish bone, FMEA).
Maintain knowledge of current regulatory requirements, applicable laws, and standards as well as internal quality system requirements.
Represent Philips as appropriate FDA, notified body, internal and external audits.
Mentoring of junior staff that includes training, motivation, and monitoring.
You're the right fit if:
You've acquired 5
years of relevant experience working in a regulated industry with full working knowledge of 21 CFR 820 and ISO 13485 medical device requirements.
Experience with medical device hardware/software systems is required with experience leveraging software as a medical device (SaMD).
Your skills include a strong knowledge of electrical engineering principles with respect to systems, sub-systems, and components.
Ability to thoroughly understand complex hardware systems and understanding of how the system works/operates.
You have a bachelor's degree or higher in either Electrical Engineering (strongly preferred) or Biomedical Engineering.
You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this Office/Remote position.
Strong interpersonal, organizational, and project management skills.
Demonstrated skills in decision making/problem solving and the ability to lead project teams when roadblocks/challenges exist.
Use of statistical analysis techniques and software for basic data interpretation (Minitab preferred).
Use of various tools including microscopes, multimeters, and other inspection equipment.
Proficient in relevant software programs (Microsoft Word, PowerPoint, Excel, and Project).
About PhilipsWe 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 improve the lives of others.
Learn more about our business.
Discover our rich and exciting history.
Learn more about our purpose.
Read more about our employee benefits.
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.
Philips Transparency Details The pay range for this position is $108,472 to $200,256, annually.
The actual base pay offered may vary depending on multiple factors including job-related knowledge/skills, experience, business needs, geographical location, and internal equity.
In addition, other compensation, such as an annual incentive bonus, sales commission or long-term incentives may be offered.
Employees are eligible to participate in our comprehensive Philips Total Rewards benefits program, which includes a generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement and much more.
Details about our benefits can be found here.
At Philips, it is not typical for an individual to be hired at or near the top end of the range for their role and compensation decisions are dependent upon the facts and circumstances of each case.
Additional InformationUS work authorization is a precondition of employment.
The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.
Company relocation benefits will not be provided for this position.
For this position, you must reside in or within commuting distance to San Diego.
#LI-PH1This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates.
Interested candidates are encouraged to apply as soon as possible to ensure consideration.
Philips is an Equal Employment and Opportunity Employer/Disabled/Veteran and maintains a drug-free workplace.
Job SummaryJob number:
517149Date posted :
2024-04-12Profession:
Quality & RegulatoryEmployment type:
Full time.
Estimated Salary: $20 to $28 per hour based on qualifications.
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