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Biocompatibility Engineer Jobs in Texas (NOW HIRING)

Bachelor's degree in biological or physical sciences, or engineering * Preferred: advanced education in toxicology or microbiology * Minimum 5years ofexperience applying biocompatibility (surgically ...

Systems & Process Engineer

Austin, TX · On-site

$145K - $165K/yr

Master's or foreign equivalent in Chemical Engineering or related field Experience: 2 years of ... Leading development of product characterizations and biocompatibility testing, DOEs, and validation ...

As a Regulatory Engineer at Neuralink, you will be responsible for regulatory affairs activities ... Contribute to cross-functional problem-solving on topics ranging from biocompatibility and ...

Regulatory Engineer

Austin, TX · On-site

$71K - $119K/yr

As a Regulatory Engineer at Neuralink, you will be responsible for regulatory affairs activities ... Contribute to cross-functional problem-solving on topics ranging from biocompatibility and ...

Oversee Microbiological/Biocompatibility efforts in support of NPD/Sustaining Engineering efforts in development and design. * Evaluate microbiological test data and determine product or process ...

Apply Early

Biocompatibility Engineer information

What is the difference between Biocompatibility Engineer vs Materials Scientist?

AspectBiocompatibility EngineerMaterials Scientist
Required CredentialsBachelor's or Master's in biomedical engineering, biology, or related fields; certifications in biocompatibility testingBachelor's or Master's in materials science, chemistry, or engineering; advanced degrees often preferred
Work EnvironmentMedical device companies, research labs, regulatory agenciesResearch institutions, manufacturing, aerospace, automotive industries
Industry UsageDesign and testing of biocompatible medical devices and implantsDevelopment of new materials for various applications, including medical, industrial, and consumer products

While both roles involve materials and testing, a Biocompatibility Engineer specializes in ensuring materials are safe for medical use, focusing on biological interactions. A Materials Scientist has a broader scope, working on developing and analyzing materials across multiple industries. The two roles often collaborate but serve distinct functions within product development and safety assurance.

What is a biocompatibility scientist?

A biocompatibility scientist is a professional who evaluates the safety of medical devices and materials by testing their interactions with biological systems. They often work in laboratories, using assays and standards such as ISO 10993 to assess potential adverse effects and ensure regulatory compliance.

Is there a demand for bioengineers?

There is strong demand for bioengineers, including biocompatibility engineers, due to the growth of the medical device and healthcare industries. These professionals are needed to develop and test biocompatible materials and devices, often requiring knowledge of materials science, biology, and regulatory standards. Job prospects are favorable with opportunities in research, development, and quality assurance roles.

Can a biomedical engineer make 200k?

Biomedical engineers, including biocompatibility engineers, can potentially earn $200,000 or more annually, especially with advanced experience, specialized skills, leadership roles, or working in high-paying industries like medical device manufacturing. Achieving this salary often requires a combination of advanced education, certifications, and years of experience in the field.

What does a Biocompatibility Engineer do?

A Biocompatibility Engineer is responsible for evaluating and ensuring that materials and devices intended for medical use are safe and compatible with biological systems. Their work involves assessing the interactions between medical devices and human tissues to prevent adverse reactions. They conduct laboratory tests, analyze data, and prepare technical documentation to meet regulatory standards. Biocompatibility Engineers play a crucial role in the development and approval of medical devices, working closely with regulatory agencies and product development teams.

What are the key skills and qualifications needed to thrive as a Biocompatibility Engineer, and why are they important?

To thrive as a Biocompatibility Engineer, you need a strong background in biomedical engineering or life sciences, with expertise in toxicology, materials science, and regulatory standards such as ISO 10993. Familiarity with laboratory testing protocols, risk assessment tools, and regulatory submission systems is typically required, and certifications like Certified Biological Safety Professional (CBSP) can be advantageous. Strong analytical thinking, meticulous attention to detail, and effective communication skills help in interpreting data, preparing reports, and collaborating with cross-functional teams. These competencies are crucial for ensuring medical devices are safe for human use and meet global compliance requirements.

What engineers make $500,000?

Senior engineers in specialized fields such as petroleum, aerospace, or software engineering can earn $500,000 or more annually, especially with experience, advanced skills, and bonuses. High-level roles often require advanced degrees, certifications, and leadership responsibilities within their industries.

What are some common challenges faced by Biocompatibility Engineers during the device development process?

Biocompatibility Engineers often encounter challenges in selecting appropriate materials that meet regulatory standards and ensuring compatibility with biological systems. They must navigate complex testing protocols and documentation requirements to demonstrate safety and effectiveness, which can be time-consuming and require cross-functional collaboration with regulatory, quality, and R&D teams. Additionally, staying updated with evolving international regulations and standards is vital, as non-compliance can delay product approvals and market entry.
What cities in Texas are hiring for Biocompatibility Engineer jobs? Cities in Texas with the most Biocompatibility Engineer job openings:
Biocompatibility Program Manager

Biocompatibility Program Manager

Marmon

Addison, TX • On-site

Full-time

Posted 12 days ago


Marmon Holdings rating

7.7

Company rating: 7.7 out of 10

Based on 15 frontline employees who took The Breakroom Quiz


Job description

Acumed LLC

As a part of the global industrial organization Marmon Holdings-which is backed by Berkshire Hathaway-you'll be doing things that matter, leading at every level, and winning a better way. We're committed to making a positive impact on the world, providing you with diverse learning and working opportunities, and fostering a culture where everyone's empowered to be their best.

Job Scope TheBiocompatibility Program Manageris responsible forestablishingand directing all aspects of the biocompatibility("biocomp")program forAcumed("theCompany").. This individual will ensure all products released and in the fieldare in compliance withcurrent biocompatibility standards for safe use of products inpatients. This individual will work cross functionally with each business unit to ensurebiocompprinciples are appropriately applied to new product development.This individual will ensuretheorganization understandstheimportance ofbiocompprinciples and procedures, provideappropriate training,guidance,andwillreview and approve finalbiocompdocumentation.This individual will manage and report onthestatus ofbiocompinitiatives to management teams, includingtheexecutive teamon a periodic basis. This individualwillwork within a matrixed organization, and may directly manage others on the biocompatibility team.

Duties/Responsibilities

  • Worksindependently andoncross-functionalteamsin a matrixed environment.
  • Communicatestechnical principles related tobiocompeffectivelyandinfluenceskey stakeholders internally and externally.
  • Authors, reviewsand approvesbiocompevaluation plans,test reports,andfinal biocompatibility reports.
  • Responsible for presentingbiocompprogram updatesto large audiences, includingthe Executive Team
  • Usesproject management tools to manage biocompatibility program initiatives.
  • Remainscurrent with biocompatibility standards,testingand regulatory interpretations inthemedical deviceindustry.
  • Createsand trainsothers onwork practices in compliance with applicable ISO and CFR regulations/guidance.
  • Appliesappropriate testingmethods forbiocompevaluations (i.e., cytotoxicity, sensitization, MMP, Irritation, Extractable / Leachable, etc.)
  • Applyappropriatestatisticalprinciples tobiocomptestingandanalysis.
  • Utilizesknowledge ofAcumedproducts andtheirindicationsand method of use to evaluate biological indicators andrisks.
  • Independently manages external vendorsand consultants (i.e.,toxicologist, test houses, etc.)
  • Understandsand utilizesAcumedproject funding processes tomanages all aspects of biocompatibility budget (planning process, budget levels and spend, etc.)
  • Participates as a member of technical review boards for applicable projects/expertise.
  • Interfacesand collaborates with department leaders to influence and helpshapeCompanystrategic initiativesrelated tobiocomp.
  • Supportsnew product development across all business units for biocompatibility compliance.
  • Work withinengineering systems, includingSAP, CAD, Windchillto perform job functions and document results.
  • Follows and works withinAcumed'sDesign Control process and framework.
  • Completes the duties described in the Quality Manual.

Qualifications

  • Bachelor's degree in biological or physical sciences, or engineering
  • Preferred: advanced education in toxicology or microbiology
  • Minimum 5years ofexperience applying biocompatibility (surgically invasive and implantable) principles.
  • Proficiencyin Project Management for organizing and managing deliverables.
  • Ability to multitask and prioritize projects that align with departmental and organizationalobjectives.
  • Strong technical writing, verbal, and interpersonal communication skills
  • Proficiencyof testing methods(bioburden, Cytotoxicity, Irritation, Extractible/Leachable, Sensitization, etc.)
  • Working knowledge of statistical modelsand how to apply to test data for biological evaluations.
  • Proficiencywith ISO-10993, ISO-14971, FDA and EU-MDR regulations and application to biocompatibility evaluations.
  • Familiarity to SAP, Windchill, CAD software

Following receipt of a conditional offer of employment, candidates will be required to complete additional job-related screening processes as permitted or required by applicable law.

We are an equal opportunity employer, and all applicants will be considered for employment without attention to their membership in any protected class. If you require any reasonable accommodation to complete your application or any part of the recruiting process, please email your request to careers@marmon.com, and please be sure to include the title and the location of the position for which you are applying.


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