Chemical Engineer

Siemens Healthineers; United States; On-site; USD 73,000 - 100,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k) retirement plan

Life insurance

Disability insurance

Paid parking/public transportation

Paid time off

Paid sick time

Job summary

Siemens Healthineers is seeking a Chemical Engineer to join the interventional oncology (IO) development team. You will help develop implantable therapies and embolization products, work on microsphere applications, and ensure quality and regulatory compliance.

The role requires a BS in Chemical Engineering or related field, and 1+ years in a regulated environment. Expect collaboration across R&D, manufacturing, and QA to deliver medical device solutions.

Qualifications

• BS in Chemical Engineering, Ceramics/Materials Engineering, Biomedical Engineering, or related field.
• 1+ years of engineering experience, preferably in medical device or other regulated industry.
• Knowledge of glass, ceramic, and polymer materials engineering, production, and formulation.
• Knowledge of laboratory techniques for analyzing microsphere properties and chemical composition is preferred.
• Experience working within a company’s Quality System is preferred.
• Experience in the development of regulated medical devices or combination products is preferred.
• Able to define and develop test procedures and to perform design verification.

Responsibilities

• Develop and define glass, ceramic, and polymer microsphere formulations and synthesis methods to meet device needs.
• Develop prototype intravascular devices to demonstrate technical feasibility.
• Understand, operate, and design various thermal spray processes.
• Incorporate homogenization for consistency of batches.
• Utilization of high temperature furnaces.
• Interpretation of material characterization data.
• Transfer knowledge of synthesis processes to manufacturing for ongoing production
• Development and execution of complex test plans involving significant data collection and interpretation, assessment of results, and incorporation of step for continuous design improvements
• Contribute to formal design and instrumentation drawings, analysis plans, and fabrication plans
• Plan and conduct R&D activities to define and develop implantable devices
• Quality assurance testing of devices to ensure conformance to design specifications
• Write technical documentation including process descriptions and test methods
• Contribute to and maintain FDA compliant Design History Files (DHF)
• Execute process improvements 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

Skills

Laboratory techniques

Materials engineering

Quality System knowledge

Test procedures

Design verification

Education

BS in Chemical Engineering

Ceramics/Materials Engineering

Biomedical Engineering

Job description

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 looking for a Chemical Engineer to join our interventional oncology (IO) development team. The individual will be a member of our growing embolics team that is focused on treating cancers by delivery internal chemical/radiation therapy and occluding the blood supply to tumors. The individual would contribute by developing new implantable therapy and embolization products, new applications for existing microspheres, and maintaining our existing microsphere 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 changes people’s lives.

Responsibilities

• Develop and define glass, ceramic, and polymer microsphere formulations and synthesis methods to meet device needs
• Develop prototype intravascular devices to demonstrate technical feasibility
• Understand, operate, and design various thermal spray processes.
• Incorporate homogenization for consistency of batches.
• Utilization of high temperature furnaces.
• Interpretation of material characterization data.
• Transfer knowledge of synthesis processes to manufacturing for ongoing production
• Development and execution of complex test plans involving significant data collection and interpretation, assessment of results, and incorporation of step for continuous design improvements
• Contribute to formal design and instrumentation drawings, analysis plans, and fabrication plans
• Plan and conduct R&D activities to define and develop implantable devices
• Quality assurance testing of devices to ensure conformance to design specifications
• Write technical documentation including process descriptions and test methods
• Contribute to and maintain FDA compliant Design History Files (DHF)
• Execute process improvements 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 & Experience

• BS in Chemical Engineering, Ceramics/Materials Engineering, Biomedical Engineering, or related field
• 1+ years of engineering experience with preference to experience in medical device or other regulated industry
• Knowledge of glass, ceramic, and polymer materials engineering, production, and formulation
• Knowledge of laboratory techniques for analyzing microsphere properties and chemical composition is preferred
• Experience working within a company’s Quality System is preferred
• Experience in the development of regulated medical devices or combination products is preferred
• Able to define and develop test procedures and to perform design verification

Who we are

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.

How we work:

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.

To find out more about Siemens Healthineers businesses, please visit our company page here.

The base pay range for this position is:

$72,860 - $100,188

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.

Equal Employment Opportunity Statement:

Siemens Healthineers is an Equal Opportunity and Affluent Action Employer encouraging diversity in the workplace. All qualified applicants will receive consideration for employment without regard to their race, color, creed, religion, national origin, citizenship status, ancestry, sex, age, physical or mental disability unrelated to ability, marital status, family responsibilities, pregnancy, genetic information, sexual orientation, gender expression, gender identity, transgender, sex stereotyping, order of protection status, protected veteran or military status, or an unfavorable discharge from military service, and other categories protected by federal, state or local law.

EEO is the Law:

Applicants and employees are protected under Federal law from discrimination. To learn more, click here.

Reasonable Accommodations:

Siemens Healthineers is committed to equal employment opportunity. As part of this commitment, we will ensure that persons with disabilities are provided reasonable accommodations.

If you require a reasonable accommodation in completing a job application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please fill out the accommodations form here. If you’re unable to complete the form, you can reach out to our HR People Connect People Contact Center for support at [e-mail]. Please note HR People Connect People Contact Center will not have visibility of your application or interview status.

California Privacy Notice:

California residents have the right to receive additional notices about their personal information. To learn more, click here.

Export Control:

A successful candidate must be able to work with controlled technology in accordance with US export control law. It is Siemens Healthineers’ policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations.

Data Privacy:

We care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. For this reason, we ask you not to send us your CV or resume by email. We ask instead that you create a profile in our talent community where you can upload your CV. Setting up a profile lets us know you are interested in career opportunities with us and makes it easy for us to send you an alert when relevant positions become open. Register here to get started.