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Contract Medical Device Testing Jobs in Texas (NOW HIRING)

For years, Abbott's medical device businesses have offered technologies that are faster, more ... We're seeking a Contract Development Analyst to join our team supporting the Structural Heart (SH ...

For years, Abbott's medical device businesses have offered technologies that are faster, more ... We're seeking a Contract Development Analyst to join our team supporting theStructural Heart (SH ...

For years, Abbott's medical device businesses have offered technologies that are faster, more ... We're seeking a Contract Development Analyst to join our team supporting theStructural Heart (SH ...

... a Contract Research, Development, Testing, and Consulting Organization (CRO) supporting pharmaceutical, biotechnology, and medical device companies across the drug development lifecycle. We are ...

... a Contract Research, Development, Testing, and Consulting Organization (CRO) supporting pharmaceutical, biotechnology, and medical device companies across the drug development lifecycle. We are ...

... a Contract Research, Development, Testing, and Consulting Organization (CRO) supporting pharmaceutical, biotechnology, and medical device companies across the drug development lifecycle. We are ...

For years, Abbott's medical device businesses have offered technologies that are faster, more ... Clinical Contract Associatepositionwith Sylmar, CA, Santa Clara, CA, Plano, TXor Maple Grove, MN as ...

For years, Abbott's medical device businesses have offered technologies that are faster, more ... Clinical Contract Associatepositionwith Sylmar, CA, Santa Clara, CA, Plano, TXor Maple Grove, MN as ...

Strong background in medical device product development, including design, testing, and ... Experience with contract manufacturer development and working relationships. * Experience with ...

Strong background in medical device product development, including design, testing, and ... Experience with contract manufacturer development and working relationships. * Experience with ...

Strong background in medical device product development, including design, testing, and ... Experience with contract manufacturer development and working relationships. * Experience with ...

Sales Executive

Prosper, TX · On-site

$60K - $130K/yr

... device testing, and innovation. We collaborate with hospitals, surgeons, academic centers, and medical device companies across the U.S. and internationally. Position MedTech Sales Executive / Sales ...

Showing results 41-60

Contract Medical Device Testing information

What is the difference between Contract Medical Device Testing vs Medical Device Quality Assurance Specialist?

AspectContract Medical Device TestingMedical Device Quality Assurance Specialist
CredentialsTypically requires technical testing certifications, knowledge of testing standardsRequires quality management system certifications, ISO 13485 knowledge
Work EnvironmentLaboratories, testing facilities, controlled environmentsManufacturing sites, quality departments, regulatory offices
Employer & Industry UsageContract testing labs, CROs, medical device companiesMedical device manufacturers, regulatory agencies

Contract Medical Device Testing focuses on performing specific tests to ensure device safety and compliance, often in labs or testing facilities. Medical Device Quality Assurance Specialists oversee quality systems, compliance, and regulatory adherence within manufacturing or corporate settings. While both roles require knowledge of industry standards, testing professionals concentrate on technical testing, whereas QA specialists focus on quality management and regulatory processes.

What are the most commonly searched types of Medical Device Testing jobs in Texas? The most popular types of Medical Device Testing jobs in Texas are:

Manager, Chemical & Materials Testing

Siemens Healthineers

Austin, TX

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 21 days ago


Siemens Healthineers rating

8.4

Company rating: 8.4 out of 10

Based on 89 frontline employees who took The Breakroom Quiz

98th of 487 rated machine equipment manufacturers


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.

Varian Medical Systems, a Siemens Healthineers company is seeking a Test Engineering Manager 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 testing aspects of design and development related to new implantable therapy and embolization products, as well as managing a team of laboratory technicians. 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.


Siemens Healthineers is seeking a Manager; Chemical & Mechanical Testing 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 testing aspects of design and development related to new implantable therapy and embolization products, as well as managing a team of laboratory technicians. 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.

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
  • 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
  • Lead the R&D team of chemical & mechanical laboratory technicians including hiring, performance management, and training
  • Manage technician resources within and across projects to reach program goals
  • Provide technical leadership and guidance to the project team
  • Mentortechniciansin best practices
  • 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 & Experience

  • BS in Chemical Engineering, Biomedical Engineering, or related filed; MS or PhD preferred
  • 5+ years of test engineering experience with preference to assessment of medical devices
  • 3+ years of laboratory or engineering management experience with preference to experience in medical device or other regulated industry
  • 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
  • Experience in project resource allocation
  • Familiarity with the medical device Regulatory (FDA & MDD) and Quality (QSR & ISO 13485) issues or similarly regulated industry
  • Experience in the development of regulatedmedical devicesor 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

#LS-OS1

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:

$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.

Equal Employment Opportunity Statement: Siemens Healthineers is an Equal Opportunity and Affirmative 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 peopleconnectvendorsnam.func@siemens-healthineers.com. 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.

Beware of Job Scams: Please beware of potentially fraudulent job postings or suspicious recruiting activity by persons that are currently posing as Siemens Healthineers recruiters/employees. These scammers may attempt to collect your confidential personal or financial information. If you are concerned that an offer of employment with Siemens Healthineers might be a scam or that the recruiter is not legitimate, please verify by searching for the posting on the Siemens Healthineers career site.

To all recruitment agencies: Siemens Healthineers does not accept agency resumes. Please do not forward resumes to our jobs alias, employees, or any other company location. Siemens Healthineers is not responsible for any fees related to unsolicited resumes.


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