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Tissue Engineering Jobs in Utah (NOW HIRING)

RED CAT HOLDINGS

S&OP Lead

Salt Lake City, UT · On-site

You will serve as the "connective tissue" between Business Development, Finance, Engineering, and Operations. Your goal is to create a single, consensus-based operating plan that balances demand with ...

Trucordia

Enterprise Architect - Vice President

Lindon, UT

$62.25 - $80.25/hr

... tissue across all technical disciplines. Lead Across the Business * Serve as a senior technology ... Ability to read and write code; you don't need to be the lead developer, but you need to be ...

Trucordia

Enterprise Architect - Vice President

Lindon, UT

$62.25 - $80.25/hr

... tissue across all technical disciplines. Lead Across the Business * Serve as a senior technology ... Ability to read and write code; you don't need to be the lead developer, but you need to be ...

Trucordia

Enterprise Architect - Vice President

Lindon, UT · On-site

$62.25 - $80.25/hr

... tissue across all technical disciplines. Lead Across the Business * Serve as a senior technology ... Ability to read and write code; you don't need to be the lead developer, but you need to be ...

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$10

$19

$33

How much do tissue engineering jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for tissue engineering in Utah is $19.12, according to ZipRecruiter salary data. Most workers in this role earn between $15.53 and $19.47 per hour, depending on experience, location, and employer.

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

To thrive as a Tissue Engineer, you need a solid background in biology, biomaterials, and biomedical engineering, typically supported by a relevant degree (such as biomedical engineering or a related field) and laboratory experience. Proficiency in cell culture techniques, bioreactor systems, and analytical tools like microscopy and spectroscopy is essential, and certifications in laboratory safety or Good Laboratory Practice (GLP) can be beneficial. Strong problem-solving abilities, teamwork, and attention to detail set candidates apart in this multidisciplinary field. These skills ensure the successful development of engineered tissues and effective collaboration in advancing regenerative medicine solutions.

What is the difference between Tissue Engineering vs Biomedical Engineer?

AspectTissue EngineeringBiomedical Engineer
Required CredentialsBachelor's or Master's in Bioengineering, Biomedical Engineering, or related fields; often includes specialized tissue engineering courseworkBachelor's or Master's in Biomedical Engineering, Bioengineering, or related fields; broader focus on medical device design and systems
Work EnvironmentResearch labs, tissue manufacturing facilities, biotech companiesHospitals, medical device companies, research institutions
Industry UsageDeveloping artificial tissues, regenerative medicine, organ scaffoldsDesigning medical devices, prosthetics, imaging systems, and healthcare technology

While both roles require a background in bioengineering, Tissue Engineering focuses specifically on creating biological tissues and regenerative solutions, often within research and biotech settings. Biomedical Engineers have a broader scope, working on medical devices, systems, and technology across healthcare environments. Understanding these differences helps professionals choose the right career path or specialization.

What engineering jobs pay $500,000?

In the field of tissue engineering, senior roles such as director or chief scientific officer can reach or exceed $500,000 annually, especially in large biotech or pharmaceutical companies. These positions typically require extensive experience, advanced degrees, and leadership skills, often involving oversight of research teams and strategic planning.

What are some common challenges tissue engineers face when transitioning from academic research to industry roles?

Tissue engineers moving from academia to industry often encounter challenges such as adapting to faster project timelines, working within multidisciplinary teams, and aligning research goals with commercial objectives. In industry, there is a strong emphasis on regulatory compliance, scalability, and product development—areas that may receive less focus in academic settings. Successful candidates typically benefit from strong communication skills, flexibility, and a willingness to learn about manufacturing standards and quality assurance processes.

What is tissue engineering?

Tissue engineering is a multidisciplinary field that combines principles of biology, engineering, and materials science to develop artificial organs, tissues, or biological substitutes that can restore, maintain, or improve tissue function. The goal is to create functional tissues in the lab that can be used to repair or replace damaged or diseased tissues in the body. This often involves using a combination of cells, scaffolds, and biologically active molecules to construct living tissues. Tissue engineering has applications in regenerative medicine, transplantation, and drug testing. The field is rapidly evolving, with ongoing research aimed at creating more complex and functional tissues.

What Are Jobs in Tissue Engineering?

Tissue engineering is a scientific discipline of regenerative medicine in which experts combine structural frameworks known as scaffolds with cells and biological agents to create functional replacement tissues. Jobs in this field include lab technician, research technician, and research bioengineer. As a technician or assistant, your duties involve managing the lab inventory, assisting with quality control and regulatory compliance, maintaining lab equipment, and working hands-on with laboratory test animals like rodents and pigs. As a bioengineer, you develop, lead, and oversee biomedical procedures. Additionally, your responsibilities involve collaborating with peers and writing reports, publications, and patent applications.

More about Tissue Engineering jobs
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What cities in Utah are hiring for Tissue Engineering jobs? Cities in Utah with the most Tissue Engineering job openings:
Tissue Engineering jobs near you
VP of Regulatory Affairs & Quality Assurance

VP of Regulatory Affairs & Quality Assurance

Sintx Technologies Inc

Salt Lake City, UT

$144K - $190K/yr

Other

Posted 10 days ago

Job description

Description

Company Overview

SINTX Technologies, Inc. is an advanced ceramics and biomaterials company focused on developing, manufacturing, and commercializing next-generation medical device solutions. SINTX is one of a small number of global manufacturers capable of producing ceramic biomaterials for implantable applications, with a platform centered on silicon nitride (SiN) and the next evolution into SiN/PEEK composite manufacturing and patient-specific solutions.


Position Summary

SINTX Technologies is seeking an experienced VP of Regulatory Affairs & Quality Assurance to lead global regulatory strategy and quality system execution across its expanding silicon nitride (SiN) and SiN/PEEK biomaterial platforms. This role will be critical in supporting 3D-printed patient-specific implants, antipathogenic wound-management and soft-tissue technologies, and the commercial launch and lifecycle management of the SINERGY SiN/PEEK biomaterial.

The successful candidate will provide hands-on leadership across FDA regulatory submissions, quality system compliance, partner enablement, and post-market surveillance, while helping position SINTX as a best-in-class biomaterials platform company capable of supporting both internal products and external licensing opportunities.

Requirements

Regulatory Affairs Leadership

Develop and execute U.S. and international regulatory strategies for:

Conventional and Additively Manufactured implants for traditional and Patient-specific applications using SiN biomaterials (including 520b)

Silicon nitride-based wound management, suture, and soft-tissue applications

Biomaterial platforms intended for internal use and third-party licensing

Lead and manage FDA submissions, including:

520b, 510(k)s, De Novo requests, IDEs, PMAs (as applicable), 

Q-Submissions 

Serve as the primary regulatory interface with the FDA and international regulatory bodies.

Evaluate regulatory risks and timelines for new indications and changes to materials, processes, and designs.


Quality Systems & Compliance

Own and continuously improve SINTX's Quality Management System (QMS) in compliance with:

21 CFR Part 820 (QSR)

ISO 13485

ISO 14971 (Risk Management)

Applicable ASTM and additive manufacturing standards

Oversee: 

Design, Process and Document controls

Supplier qualification and audits

CAPA, complaints, nonconformance, and change control

Internal and external audits (FDA, notified bodies, partners)

Ensure quality readiness to support scalable manufacturing, clinical use, and partner commercialization.


Product Launch & Lifecycle Management

Provide regulatory and quality leadership for the launch and expansion of SINERGY SiN/PEEK biomaterial, including:

Intended use expansion

New form factors

Manufacturing scale-up - process validation and risk mitigation

Support post-market surveillance, vigilance reporting, and lifecycle regulatory maintenance.

Collaborate with R&D and manufacturing to ensure regulatory alignment during material innovation and process optimization.

Support implementation and maintenance of Lean Six Sigma methods for process control and waste minimization


Platform & Licensing Support

Enable regulatory and quality frameworks that support licensing, co-development, and supply agreements with third-party partners.

Support due diligence and regulatory documentation for strategic transactions.

Help define regulatory positioning for silicon nitride's antipathogenic claims and mechanisms of action, in collaboration with clinical and scientific teams.


Cross-Functional Leadership

Act as a strategic advisor to executive leadership on regulatory and quality matters.

Coordinate external consultants, testing labs, and notified bodies.

Support investor, partner, and board communications related to regulatory milestones and risk posture.


Qualifications & Experience

Required

Bachelor's degree in Engineering, Life Sciences, or related field (Master's preferred).

10+ years of progressive experience in Regulatory Affairs and Quality within orthopedic medical devices or biomaterials.

Direct experience with FDA submissions & PMS (520b, 510(k), De Novo, IDE, PMA).

Strong working knowledge of QSR, ISO 13485, and risk management standards.

Experience supporting manufacturing, supplier quality, and audits.  


Highly Preferred

Experience with:

Additive manufacturing / 3D-printed medical devices

Patient-specific and custom medical devices

Biomaterials platforms or materials-science-driven technologies

Familiarity with:

Antimicrobial or antipathogenic technologies

Licensing or partner-driven commercialization models

Prior experience interacting directly with the FDA in Q-Subs and  audits.

Experience with and advanced certification in Lean Six Sigma methodologies  


Core Competencies

Strategic yet hands-on leadership

Strong regulatory judgment and risk assessment

Ability to operate effectively in a growth-stage, platform-driven company

Clear communicator with executives, regulators, and partners

Comfortable balancing innovation speed with compliance rigor


Compensation:

$180,000 - $225,000 base + Bonus + RSU

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