Material Scientist
for section headings: About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. We need to include sections only when posting has real specific content. We have responsibilities content, qualifications content, benefits content, pay content. Also maybe "About the role" could be the introductory paragraphs describing role. "Who we are" and "How we work" could be considered "About the company" but not required headings; we could put them under About the role? Probably better to have About the role section containing the description of role and maybe company overview. But we must not invent sections with placeholder. We'll include About the role (intro + who we are + how we work). Responsibilities (list). Qualifications (list). Benefits (list). Pay (range). No Schedule (not present). Skills maybe part of qualifications; we can combine.
We must use - for any list of duties/requirements/benefits. Use
for prose.
We must not include boilerplate like EEO, accommodation, privacy, export control, data privacy, scam warnings, etc. Remove those.
We must preserve all substantive information; do not invent or summarize away detail. So we need to keep all details from responsibilities, qualifications, benefits, pay, intro paragraphs.
We must not repeat job title as heading. So no heading for "Materials Scientist". Also not put Job ID.
We need to output only HTML fragment, no /, no markdown fences.
Let's extract content.
Intro: "Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions."
Then: "Siemens Healthineers is seeking a Materials Scientist to join our Interventional Oncology (IO) development team. The individual will be a member of our growing embolization product development team that is focused on treating cancers by delivering internal chemical/radiation therapy and occluding the blood supply to tumors. The individual would contribute by leading the materials research and testing aspects of design and development related to new implantable therapy and embolization products. The ideal candidate would be a self-driven individual with a passion for medical device development and a desire to work on products that change people’s lives."
That's role description.
Then "Responsibilities" list: each bullet.
Let's copy responsibilities exactly as given:
- Support design and development of novel chemical and materials-based devices, including chemical (XRD, DSC, leachable, etc), radiation-related, and mechanical (stiffness, sizing, etc) assessments
- Provide material science expertise in glass, ceramic, and polymer-based medical devices
- Lead coordination with external chemical test laboratories to evaluate devices
- Development and execution of complex chemical and mechanical verification protocols involving significant data collection and interpretation, assessment of results, and incorporation of step for continuous design improvements
- Validate analytical and mechanical test methods for design verification and process development
- Create verification reports based on test results
- Contribute to and maintain FDA compliant Design History Files (DHF)
- Execute test processes as they relate to quality system compliance with FDA 510(K), QSR and ISO 13485
- Participate in complaint investigations, and failure analysis of products
- Provide root cause analysis support and drive the implementation of corrective action for process-related issues
- Performs other duties as assigned or required
Note: last bullet has "Performs" maybe typo but keep.
Then "Qualifications & Experience" list:
- BS in Chemical Engineering, Biomedical Engineering, or related filed; MS or PhD preferred
- 3+ years of materials science and testing experience with preference to assessment of medical devices
- Experience in chemical, radiation, and mechanical testing and test method validation of material-based products and devices is preferred
- Experience managing external testing vendor relationships and requirements
- Familiarity with the medical device Regulatory (FDA & MDD) and Quality (QSR & ISO 13485) issues or similarly regulated industry
- Experience in the development of regulated medical devices or combination products is preferred
- Experience with design verification & validation
- Experience working within a company’s Quality System
- Excellent organizational skills and attention to detail
- Strong communication skills, both oral and written
Note "related filed" typo but keep.
Then "Who we are:" paragraph:
"We are a team of more than 72,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision-making and treatment pathways."
Then "How we work:" paragraph:
"When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual’s potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world’s most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably."
Then pay and benefits:
"The Base Pay Range For This Position Is $104,930 - $144,276 Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate. If this is a commission eligible position the commission eligibility will be in accordance with the terms of the Company's plan. Commissions are based on individual performance and/or company performance. The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan. life insurance, long-term and short-term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time."
We need to separate benefits list. The sentence includes list separated by commas and periods. We'll extract each benefit:
- medical insurance
- dental insurance
- vision insurance
- 401(k) retirement plan
- life insurance
- long-term and short-term disability insurance
- paid parking/public transportation
- paid time off
- paid sick and safe time
We need to keep the phrase "subject to applicable eligibility requirements". We'll include that in a
before the list.
Pay section: include the base pay range and factors. Also commission eligibility note. We'll put that in a
maybe.
We must not include boilerplate like EEO, accommodation, privacy, export control, data privacy, scam warnings, recruitment agency note. Remove those.
Now construct HTML.
We'll have:
About the role
Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions. Siemens Healthineers is seeking a Materials Scientist to join our Interventional Oncology (IO) development team. The individual will be a member of our growing embolization product development team that is focused on treating cancers by delivering internal chemical/radiation therapy and occluding the blood supply to tumors. The individual would contribute by leading the materials research and testing aspects of design and development related to new implantable therapy and embolization products. The ideal candidate would be a self-driven individual with a passion for medical device development and a desire to work on products that change people’s lives.
We are a team of more than 72,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision-making and treatment pathways.
When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual’s potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world’s most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably.
Then responsibilities:
Responsibilities
- Support design and development of novel chemical and materials-based devices, including chemical (XRD, DSC, leachable, etc), radiation-related, and mechanical (stiffness, sizing, etc) assessments
- Provide material science expertise in glass, ceramic, and polymer-based medical devices
- Lead coordination with external chemical test laboratories to evaluate devices
- Development and execution of complex chemical and mechanical verification protocols involving significant data collection and interpretation, assessment of results, and incorporation of step for continuous design improvements
- Validate analytical and mechanical test methods for design verification and process development
- Create verification reports based on test results
- Contribute to and maintain FDA compliant Design History Files (DHF)
- Execute test processes as they relate to quality system compliance with FDA 510(K), QSR and ISO 13485
- Participate in complaint investigations, and failure analysis of products
- Provide root cause analysis support and drive the implementation of corrective action for process-related issues
- Performs other duties as assigned or required
Then qualifications:
Qualifications
- BS in Chemical Engineering, Biomedical Engineering, or related filed; MS or PhD preferred
- 3+ years of materials science and testing experience with preference to assessment of medical devices
- Experience in chemical, radiation, and mechanical testing and test method validation of material-based products and devices is preferred
- Experience managing external testing vendor relationships and requirements
- Familiarity with the medical device Regulatory (FDA & MDD) and Quality (QSR & ISO 13485) issues or similarly regulated industry
- Experience in the development of regulated medical devices or combination products is preferred
- Experience with design verification & validation
- Experience working within a company’s Quality System
- Excellent organizational skills and attention to detail
- Strong communication skills, both oral and written
Then benefits:
Benefits
The Company offers the following benefits for this position, subject to applicable eligibility requirements:
- medical insurance
- dental insurance
- vision insurance
- 401(k) retirement plan
- life insurance
- long-term and short-term disability insurance
- paid parking/public transportation
- paid time off
- paid sick and safe time
Then pay:
Pay
The Base Pay Range For This Position Is $104,930 - $144,276. Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate. If this is a commission eligible position the commission eligibility will be in accordance with
for prose. We must not include boilerplate like EEO, accommodation, privacy, export control, data privacy, scam warnings, etc. Remove those. We must preserve all substantive information; do not invent or summarize away detail. So we need to keep all details from responsibilities, qualifications, benefits, pay, intro paragraphs. We must not repeat job title as heading. So no heading for "Materials Scientist". Also not put Job ID. We need to output only HTML fragment, no /, no markdown fences. Let's extract content. Intro: "Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions." Then: "Siemens Healthineers is seeking a Materials Scientist to join our Interventional Oncology (IO) development team. The individual will be a member of our growing embolization product development team that is focused on treating cancers by delivering internal chemical/radiation therapy and occluding the blood supply to tumors. The individual would contribute by leading the materials research and testing aspects of design and development related to new implantable therapy and embolization products. The ideal candidate would be a self-driven individual with a passion for medical device development and a desire to work on products that change people’s lives." That's role description. Then "Responsibilities" list: each bullet. Let's copy responsibilities exactly as given: - Support design and development of novel chemical and materials-based devices, including chemical (XRD, DSC, leachable, etc), radiation-related, and mechanical (stiffness, sizing, etc) assessments - Provide material science expertise in glass, ceramic, and polymer-based medical devices - Lead coordination with external chemical test laboratories to evaluate devices - Development and execution of complex chemical and mechanical verification protocols involving significant data collection and interpretation, assessment of results, and incorporation of step for continuous design improvements - Validate analytical and mechanical test methods for design verification and process development - Create verification reports based on test results - Contribute to and maintain FDA compliant Design History Files (DHF) - Execute test processes as they relate to quality system compliance with FDA 510(K), QSR and ISO 13485 - Participate in complaint investigations, and failure analysis of products - Provide root cause analysis support and drive the implementation of corrective action for process-related issues - Performs other duties as assigned or required Note: last bullet has "Performs" maybe typo but keep. Then "Qualifications & Experience" list: - BS in Chemical Engineering, Biomedical Engineering, or related filed; MS or PhD preferred - 3+ years of materials science and testing experience with preference to assessment of medical devices - Experience in chemical, radiation, and mechanical testing and test method validation of material-based products and devices is preferred - Experience managing external testing vendor relationships and requirements - Familiarity with the medical device Regulatory (FDA & MDD) and Quality (QSR & ISO 13485) issues or similarly regulated industry - Experience in the development of regulated medical devices or combination products is preferred - Experience with design verification & validation - Experience working within a company’s Quality System - Excellent organizational skills and attention to detail - Strong communication skills, both oral and written Note "related filed" typo but keep. Then "Who we are:" paragraph: "We are a team of more than 72,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision-making and treatment pathways." Then "How we work:" paragraph: "When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual’s potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world’s most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably." Then pay and benefits: "The Base Pay Range For This Position Is $104,930 - $144,276 Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate. If this is a commission eligible position the commission eligibility will be in accordance with the terms of the Company's plan. Commissions are based on individual performance and/or company performance. The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan. life insurance, long-term and short-term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time." We need to separate benefits list. The sentence includes list separated by commas and periods. We'll extract each benefit: - medical insurance - dental insurance - vision insurance - 401(k) retirement plan - life insurance - long-term and short-term disability insurance - paid parking/public transportation - paid time off - paid sick and safe time We need to keep the phrase "subject to applicable eligibility requirements". We'll include that in a
before the list. Pay section: include the base pay range and factors. Also commission eligibility note. We'll put that in a
maybe. We must not include boilerplate like EEO, accommodation, privacy, export control, data privacy, scam warnings, recruitment agency note. Remove those. Now construct HTML. We'll have:
About the role
Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions. Siemens Healthineers is seeking a Materials Scientist to join our Interventional Oncology (IO) development team. The individual will be a member of our growing embolization product development team that is focused on treating cancers by delivering internal chemical/radiation therapy and occluding the blood supply to tumors. The individual would contribute by leading the materials research and testing aspects of design and development related to new implantable therapy and embolization products. The ideal candidate would be a self-driven individual with a passion for medical device development and a desire to work on products that change people’s lives.
We are a team of more than 72,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision-making and treatment pathways.
When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual’s potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world’s most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably.
Then responsibilities:Responsibilities
- Support design and development of novel chemical and materials-based devices, including chemical (XRD, DSC, leachable, etc), radiation-related, and mechanical (stiffness, sizing, etc) assessments
- Provide material science expertise in glass, ceramic, and polymer-based medical devices
- Lead coordination with external chemical test laboratories to evaluate devices
- Development and execution of complex chemical and mechanical verification protocols involving significant data collection and interpretation, assessment of results, and incorporation of step for continuous design improvements
- Validate analytical and mechanical test methods for design verification and process development
- Create verification reports based on test results
- Contribute to and maintain FDA compliant Design History Files (DHF)
- Execute test processes as they relate to quality system compliance with FDA 510(K), QSR and ISO 13485
- Participate in complaint investigations, and failure analysis of products
- Provide root cause analysis support and drive the implementation of corrective action for process-related issues
- Performs other duties as assigned or required
Qualifications
- BS in Chemical Engineering, Biomedical Engineering, or related filed; MS or PhD preferred
- 3+ years of materials science and testing experience with preference to assessment of medical devices
- Experience in chemical, radiation, and mechanical testing and test method validation of material-based products and devices is preferred
- Experience managing external testing vendor relationships and requirements
- Familiarity with the medical device Regulatory (FDA & MDD) and Quality (QSR & ISO 13485) issues or similarly regulated industry
- Experience in the development of regulated medical devices or combination products is preferred
- Experience with design verification & validation
- Experience working within a company’s Quality System
- Excellent organizational skills and attention to detail
- Strong communication skills, both oral and written
Benefits
The Company offers the following benefits for this position, subject to applicable eligibility requirements:
- medical insurance
- dental insurance
- vision insurance
- 401(k) retirement plan
- life insurance
- long-term and short-term disability insurance
- paid parking/public transportation
- paid time off
- paid sick and safe time
Pay
The Base Pay Range For This Position Is $104,930 - $144,276. Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate. If this is a commission eligible position the commission eligibility will be in accordance with