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Tissue Engineering Jobs in Ohio (NOW HIRING)

... tissue, biologic, and medical device products. The Manager, Quality Assurance manages quality ... Minimum of 5 years Quality Engineering/Quality Assurance experience in medical device ...

... tissue, biologic, and medical device products. The Manager, Quality Assurance manages quality ... Minimum of 5 years Quality Engineering/Quality Assurance experience in medical device ...

Domtar is a leading producer of pulp, paper, packaging, tissue and wood products. Through our focus ... Provides electrical engineering primarily for process control and electrical designs, technical ...

Domtar is a leading producer of pulp, paper, packaging, tissue and wood products. Through our focus ... Provides electrical engineering primarily for process control and electrical designs, technical ...

Manufacturing & Engineering Location: Circleville, OH, US, 43113 Date: Jul 28, 2026 The Sofidel Group Sofidel, headquartered in Porcari (Lucca), is a global leader in tissue paper production. With ...

Sr. Engineer, Quality

Vandalia, OH

$83K - $112K/yr

... Human Tissue, Medical Device products) The Sr. Engineer exercises independent judgment in ... Minimum of 5 years in a Quality Engineering/Quality Assurance role for medical device or ...

FTI Defense is seeking a Distinguished AI Software Engineering Lead to serve as both a hands-on ... The Distinguished Engineer will act as the connective tissue between software execution teams ...

The Sofidel Group Sofidel, headquartered in Porcari (Lucca), is a global leader in tissue paper ... On all projects or sub-projects allocated, provide practical project engineering and design ...

Experience within medical device, tissue, biologics or other regulated industry * Experience ... engineering, material handling, and quality areas. * Manage operational KPIs for Safety, Quality ...

Experience within medical device, tissue, biologics or other regulated industry * Experience ... engineering, material handling, and quality areas. * Manage operational KPIs for Safety, Quality ...

Sr. Engineer, Quality

Vandalia, OH

$83K - $112K/yr

... Human Tissue, Medical Device products) The Sr. Engineer exercises independent judgment in ... Minimum of 5 years in a Quality Engineering/Quality Assurance role for medical device or ...

Sr. Engineer, Quality

Vandalia, OH · On-site

$83K - $112K/yr

... Human Tissue, Medical Device products) The Sr. Engineer exercises independent judgment in ... Minimum of 5 years in a Quality Engineering/Quality Assurance role for medical device or ...

Connective Tissue: Serve as the primary operational link bridging Engineering, Product, Design, Data, and go-to-market/customer-facing business teams. * Communication Governance: Author and execute ...

Connective Tissue: Serve as the primary operational link bridging Engineering, Product, Design, Data, and go-to-market/customer-facing business teams. * Communication Governance: Author and execute ...

Showing results 41-60

Tissue Engineering information

See Ohio salary details

$11

$19

$35

How much do tissue engineering jobs pay per hour?

As of Sep 15, 2026, the average hourly pay for tissue engineering in Ohio is $19.97, according to ZipRecruiter salary data. Most workers in this role earn between $16.20 and $20.34 per hour, depending on experience, location, and employer.

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.

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 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 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.

How do you become a tissue engineer?

To become a tissue engineer, you typically need a bachelor's degree in biomedical engineering, bioengineering, or a related field, followed by a master's or Ph.D. for advanced roles. Gaining experience with laboratory techniques, tissue culture, and biomaterials is important, and certifications in relevant skills can enhance job prospects.

What does a tissue engineer do?

A tissue engineer designs and develops biological tissues and organs by combining cells, biomaterials, and engineering principles. They often work in laboratories, using techniques like cell culture and 3D bioprinting, and may require knowledge of biology, materials science, and sterile procedures.

What skills do you need to be a tissue engineer?

Tissue engineers need strong knowledge of biology, materials science, and engineering principles. Skills in laboratory techniques, cell culture, and familiarity with biomedical devices are essential. Additionally, problem-solving abilities, attention to detail, and proficiency with software like CAD or data analysis tools are important for success in this field.
Infographic showing various Tissue Engineering job openings in Ohio as of September 2026, with employment types broken down into 1% Internship, 88% Full Time, 8% Part Time, 2% Contract, and 1% Nights. Highlights an 83% Physical, 4% Hybrid, and 13% Remote job distribution, with an average salary of $41,539 per year, or $20 per hour.

Manager, Quality Assurance

Vandalia, OH • On-site

Axogen
Biotechnology Research and Development • 201 - 500 employees

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 14 days ago


Job description

Axogen is committed to building and maintaining a strong and gratifying company culture that fosters professional growth. Our hands-on and personal approach makes transitioning to a new job a seamless and enjoyable process. Most benefits are effective on day one!
Axogen is an equal opportunity employer and does not discriminate against applicants on the basis of race, color, creed, religion, ancestry, age, sex, marital status, national origin, disability or veteran status.
Why you'll love working at Axogen:
  • Friendly, open, and fun team culture that values unique perspectives
  • Company-wide dedication to profoundly impacting patients' lives
  • Comprehensive, high-quality benefits package effective on date of hire
  • Educational assistance available for all employees
  • Matching 401(k) retirement plan
  • Paid holidays, including floating holidays, to be used at your discretion
  • Employee Stock Purchase Plan
  • Referral incentive program

Axogen Mission and Business Purpose
Our business purpose is to restore health and improve quality of life by making restoration of peripheral nerve function an expected standard of care. We aim to lead the markets we serve by always requiring the solutions we offer patients and caregivers provide an improved benefit-to-risk profile as compared to existing standards of care. To ensure we deliver improved benefit-to-risk solutions, we will guide and expect the market and design requirement specifications underlying our engineering, business development, and clinical research activities, objectively target advancements in standards of care.
Job Summary of the Manager, Quality Assurance
The Manager, Quality Assurance is responsible for establishing, administering, and maintaining Quality Assurance (QA) processes, systems, and tasks in compliance with current Good Manufacturing Practice (cGMP), current Good Distribution Practice (cGDP), and applicable domestic and international standards for tissue, biologic, and medical device products. The Manager, Quality Assurance manages quality departments at Axogen's facilities, including Processing Centers (DPC or APC) or the Burleson Distribution Center (BDC).
The Manager, Quality Assurance collaborates closely with Operations to provide Quality Assurance (QA) support, ensuring that the organization maintains high standards of compliance and fosters a culture of continuous improvement in manufacturing, processing, systems, testing, and product distribution functions. This role is responsible for developing and executing quality strategies that align with company goals and industry best practices. By working cross-functionally, the Manager, Quality Assurance helps implement scalable processes that support organizational growth and ensure quality standards are met for receiving, storage, processing, shipping, and distribution activities.
Requirements of the Manager, Quality Assurance
  • Bachelor's Degree in Life Science or Engineering discipline and/or a related field.
  • Minimum of 5 years Quality Engineering/Quality Assurance experience in medical device, pharmaceutical, or biotech manufacturing.
  • Minimum 3 years of leading others or project management, direct people management preferred.
  • Experience leading external regulatory audits (e.g., FDA, ISO).
  • Proficiency in Six Sigma or Lean Manufacturing is desirable.
  • Certified Quality Engineer preferred.
  • Travel Requirements are up to 10%
  • Knowledge of current Good Manufacturing Practices (cGMP) and relevant regulatory standards, guidelines, and regulations, both in the US and OUS for tissue, Medical Devices and/or Biologics.
  • Knowledge of statistical sampling and analysis.
  • Knowledge of Root Cause Analysis (RCA) methodologies.
  • Ability to proficiently use MS Office Suite, including Microsoft Smart Sheet, Visio and Project.
  • Excellent communication, interpersonal, and team-building skills.
  • Strong problem-solving skills and the ability to exercise creativity and judgment.
  • Ability to work independently, analyze and work with attention to detail, process and prioritize sensitive complex information and problem solve.

Responsibilities of the Manager, Quality Assurance
The specific duties of the Manager, Quality Assurance include but are not limited to:
  • Manages Quality Assurance operations at DPC, APC, or BDC, ensuring compliance with domestic and international quality standards for human tissue, biologic, and medical device products.
  • Establishes, implements, and maintains Axogen's Quality Management Systems (QMS) ensuring alignment with
  • cGMP, cGDP, QSR, ISO13485, MDD, AATB and other applicable standards.
  • Recruits, develops, and manages quality assurance team members, fostering a positive workplace culture and building high-performing team.
  • Provides strategic leadership, coaching, guiding performance development, succession planning, and ensuring alignment with company objectives while achieving goals and maintaining regulatory compliance.
  • Ensures compliance with FDA, ISO, and other relevant regulatory bodies. Acts as the subject matter expert for tissue, medical device, and biologic regulations.
  • Represents Axogen during external audits and inspections. Ensures pre-approval inspection readiness and conducts internal audits and risk assessments.
  • Collaborates with Operations, Finance, and Material Handling teams to ensure Quality Assurance support during GMP activities and to meet product demand and regulatory requirements.
  • Leads quality planning, verification/validation, and continuous improvement activities.
  • Investigates and reduces non-conformances and optimizes inspection processes.
  • Determines quality improvement parameters using improvement methodologies relevant to processing activities.
  • Performs risk assessments, leads investigations to resolve quality issues, and oversees the qualification and validation activities at distribution and processing sites.
  • Trains staff on quality policies and procedures. Facilitates communication regarding changes in facilities, processes, and materials.
  • Prepares quality metrics, reports, and presentations by analyzing data and making recommendations to stakeholders.
  • Leverages analytical skills, tools and best practices to work across business functions to identify opportunities to do things better, eliminate waste, reduce cost, and find workflow efficiencies; prioritizing opportunities that help achieve strategic imperatives.

The specific duties of the Manager, Quality Assurance at APC assigned to own Cleanroom Processing and Laboratory Operations include but are not limited to:
  • Oversight of Avance Starting Material, Drug Substance, and Drug Product Processing processes, including weekly room release, environmental monitoring execution, sample management, gowning for the cleanrooms, process validation, and quarterly dose audits.
  • Serves as the quality assurance subject matter expert for computer systems relating to this area, including but not limited to Tulip, laboratory information management systems, and particle monitoring systems.

The specific duties of the Manager, Quality Assurance at APC assigned to own Drug Product, Facility, and Technical Operations include but are not limited to:
  • Oversight of qualification, maintenance, and calibration activities for equipment, facilities, and utilities; labeling quality review and disposition of drug product, drug product chain of custody, and ancillary systems (including but not limited to: cleaning & sterilization, cleaning solution preparation, and environmental cleaning)
  • Serves as the quality assurance subject matter expert for computer systems relating to these areas, including but not limited to maintenance management systems, cleaning & sterilization systems, building monitoring systems, and security access control systems.

Location
913 Industrial Drive Place, Vandalia, OH 45377
#LI-AC1
Benefits/Compensation
This position is eligible for an annual bonus.
Benefits offered for this position include Health, Dental, Vision, Matching 401K, Paid Time Off, 9 Paid Holidays + 3 Floating Holidays, Dependent Care Flexible Spending Accounts, Medical Flexible Spending Accounts, Tuition Reimbursement, Paid Parental Leave, Paid Caregiver Leave, Basic Life Insurance, Supplemental Life Insurance, Employee Stock Purchase Plan, and Disability Insurance, as described in more detail in summary plan descriptions.
Salary Range
$113,903-$142,378 USD
Company Statements
Axogen follows healthcare system guidelines with respect to credentialing, vaccinations and other employment/compliance related requirements, as well as CDC guidance. Axogen reserves the right to amend its policies from time to time in its sole discretion.
As AI is becoming a common tool throughout the application process, we want to be clear about its appropriate use at Axogen. Using AI to support resume writing, research or interview preparation is perfectly acceptable, provided the content is accurate and genuinely represents your qualifications and skills. For other key parts of your interview process, however, it is important that the ideas, communication, and work you share reflect your own voice, experiences, and thinking. We ask that you participate in our live interviews and complete any assessments without AI assistance unless instructions explicitly indicate otherwise or a specific exception is discussed and approved in advance. This approach ensures fairness, celebrates your individuality, and allows your authentic perspective to shine. Behaviors that do not align with these guidelines may result in disqualification from the hiring process or termination of employment if later discovered. We appreciate your understanding and look forward to learning about the unique contributions only you can bring to Axogen.
No agency solicitation. We kindly request that recruiting agencies, staffing firms, and third-party vendors do not contact us regarding this posting. Unsolicited résumés will not be considered.