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Medical Device Development Jobs in Austin, TX (NOW HIRING)

Knowledge of regulatory standards relevant to medical device development * Experience with inventory management systems and quality control processes Expected Compensation: The anticipated base ...

Design Quality Engineer, SaMD

Austin, TX · On-site

$100K - $125K/yr

... software medical device (SaMD) who can partner closely with engineering, clinical, regulatory, and product teams to build practical, audit-ready quality processes for SaMD development. Role ...

... software medical device (SaMD) who can partner closely with engineering, clinical, regulatory, and product teams to build practical, audit-ready quality processes for SaMD development. Role ...

Design Quality Engineer, SaMD

Austin, TX · On-site

$100K - $125K/yr

... software medical device (SaMD) who can partner closely with engineering, clinical, regulatory, and product teams to build practical, audit-ready quality processes for SaMD development. Role ...

Prototype & Design Specialist

Austin, TX · On-site

$68K - $114K/yr

Knowledge of regulatory standards relevant to medical device development * Experience with inventory management systems and quality control processes Expected Compensation: The anticipated base ...

... medical device experience preferred) * Experience with prototype inspection or R&D environments is highly desirable * Familiarity with ISO 13485 and quality system documentation Travel Expectations ...

Firmware Engineer

Austin, TX · On-site

$110 - $150/hr

Responsibilities Firmware Development * Design and develop firmware for healthcare and IoT devices ... Support data transmission from medical devices to clinical systems. * Ensure device ...

Showing results 41-60

Medical Device Development information

See Austin, TX salary details

$28.7K

$52.9K

$80.3K

How much do medical device development jobs pay per year?

As of Aug 14, 2026, the average yearly pay for medical device development in Austin, TX is $52,948.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,100.00 and $59,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in medical device development, and why are they important?

To thrive in Medical Device Development, you need expertise in engineering or life sciences, a solid understanding of regulatory requirements, and often an advanced degree such as a master's or Ph.D. in a relevant field. Familiarity with CAD software, prototyping tools, and knowledge of FDA or ISO regulatory standards is typically required. Strong problem-solving abilities, collaboration, and effective communication distinguish top professionals in this field. These skills ensure the development of safe, innovative, and compliant medical devices that meet both user needs and regulatory standards.

What is the difference between Medical Device Development vs Medical Device Quality Assurance?

AspectMedical Device DevelopmentMedical Device Quality Assurance
CredentialsEngineering degrees, certifications like RAPS or regulatory trainingQuality certifications, ISO 13485, regulatory compliance training
Work EnvironmentDesign labs, R&D teams, product development settingsManufacturing sites, quality control labs, compliance departments
Industry UsageDesigning and creating new medical devicesEnsuring devices meet quality and regulatory standards

Medical Device Development focuses on designing and creating new medical devices, involving engineering and product innovation. Medical Device Quality Assurance ensures these devices meet safety, quality, and regulatory standards through testing and compliance processes. Both roles are essential in the medical device industry but serve different functions in the product lifecycle.

What are some common challenges faced by professionals in medical device development, and how can they be addressed?

Professionals in medical device development frequently encounter challenges such as navigating complex regulatory requirements, ensuring product safety and efficacy, and managing cross-functional collaboration between engineering, clinical, and regulatory teams. Addressing these challenges requires staying updated on evolving regulations, fostering open communication among diverse team members, and implementing robust quality control processes. Proactively engaging with regulatory bodies and regularly reviewing project milestones can help streamline development and reduce the risk of costly delays.

What is medical device development?

Medical device development is the process of designing, creating, testing, and bringing medical devices to market. This process involves multiple stages, including concept development, prototyping, preclinical and clinical testing, regulatory approval, and manufacturing. The goal is to ensure that new devices are safe, effective, and meet regulatory standards before they are used by healthcare professionals or patients. Teams in medical device development often include engineers, scientists, regulatory specialists, and quality assurance professionals.

What cities near Austin, TX are hiring for Medical Device Development jobs?

Cities near Austin, TX with the most Medical Device Development job openings:

Infographic showing various Medical Device Development job openings in Austin, TX as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $52,948 per year, or $25.5 per hour.

Director of Business Development, Gene and Cell Therapy

Cincinnati Children's

Burnet, TX • On-site

Full-time

Re-posted 16 days ago


Cincinnati Children's Hospital Medical Center rating

7.3

Company rating: 7.3 out of 10

Based on 150 frontline employees who took The Breakroom Quiz

387th of 1,059 rated hospitals


Job description

The Applied Gene and Cell Therapy Center (AGCTC) is a leading clinical stage center focused on advancing innovative gene and cell therapies from research through clinical translation and manufacturing. AGCTC combines expertise in translational science, process development, analytics, regulatory strategy, and GMP manufacturing to accelerate next-generation therapies for patients with serious diseases. In addition to its research and clinical capabilities, AGCTC provides industry standards CDMO services, supporting process development, tech transfer, GMP manufacturing, analytical development, and quality systems for academic and industry partners. With state-of-the-art infrastructure and a highly collaborative environment, AGCTC offers an exciting opportunity for professionals passionate about shaping the future of advanced therapies. The Director will act as a primary engine for growth at Cincinnati Children's Applied Gene and Cell Therapy Center (AGCTC). This is a high-impact role focused on securing strategic partnerships with biotech and pharmaceutical companies in the Cell and Gene Therapy (CGT) space. You aren't just selling "capacity"; you are selling complex technical solutions, scientific trust, and a roadmap to commercialization for breakthrough therapies (CAR-T, Gene Editing, Viral Vectors, etc.). You will identify market trends, source new clinical-stage assets, and negotiate multi-million-dollar MSAs (Master Service Agreements).

JOB RESPONSIBILITIES

Leadership: Build a new business development function from the ground up, including hiring, and talent development.

Market Intelligence & Brand Advocacy:
Competitive Analysis: Stay ahead of the curve on CDMO pricing, capacity trends, and emerging technologies (e.g., closed-system manufacturing, non-viral delivery).
Marketing Collaboration: Provide "voice of the customer" feedback to the marketing team to refine value propositions and sales collateral.

Revenue Generation & Pipeline Management:
Identify & Qualify: Scout the global biotech landscape to identify companies with CGT assets in pre-clinical through Phase III stages.
Deal Execution: Lead the entire sales cycle from initial outreach and RFPs (Request for Proposals) to site visits and works with contract team for the final execution.
Territory Strategy: Develop and execute a regional or global business plan to meet or exceed annual booking targets.

Strategic Relationship Management:
Consultative Selling: Act as a bridge between the client's CMC (Chemistry, Manufacturing, and Controls) needs and our internal technical capabilities.
Strategic Networking: Represent the organization at major industry conferences (e.g., ASGCT, SITC, Ash et al).
Account Growth: Partner with key collaborators to ensure current clients are satisfied and look for opportunities to expand existing programs.

JOB REQUIREMENTS

Bachelor's Degree in a related field.

10+ years related experience primarily in Business Development and/or Value Proposition/Product Development Management. Business development experience is in Gene and Cell Therapy or related life sciences. Strongly prefer 5 years in Business Development or Sales within the CDMO or Life Sciences services sector.

In either Business Development or Sales within the Cell and Gene Therapy, CDMO or a Life Sciences Services Sector, has 5+ years leading teams (direct and cross-functional) in either: medical device/equipment/service company; healthcare consulting; or complex medical center medical device/equipment/service company; healthcare consulting; or complex medical center

A proven track record of closing high-value contracts and building a pipeline from scratch.

Experience leading new product development and launch in a matrix organization. Product development as it relates to the development of strategic partnerships with biotech and pharmaceutical companies in the Cell and Gene Therapy (CGT) space.

Negotiation Skills: Experience navigating complex legal and financial terms in MSAs and Work Orders.

Domain Expertise: A deep understanding of the Cell and Gene Therapy manufacturing lifecycle, including viral vector production, cell processing, and analytical requirements.

Must be able to travel up to 30% of the time. Additional time may be spent traveling internationally.

Advance degree is highly preferred to navigate the complex technical and financial nuances of Cell and Gene Therapy deals.

Annualized Contract Value (ACV) and Total Contract Value (TCV).
Conversion rate from Lead to Signed Proposal.
Accuracy of sales forecasting and CRM (Salesforce) management.

Established network of C-suite and CMC-level contacts within the cell and gene therapy ecosystem.
Ability to build rapport quickly in a highly technical environment.


Primary Location

Burnet Campus


Schedule

Full time


Shift

Day (United States of America)


Department

Applied Gene and Cell Therapy Center


Employee Status

Regular


FTE

1


Weekly Hours

40


*Expected Starting Pay Range

*Annualized pay may vary based on FTE status$126,089.60 - $163,924.80


About Us

At Cincinnati Children's, we come to work with one goal: to make children's health better. We believe in a holistic team approach, both in caring for patients and their families, and in advancing science and discovery. We strive to do better and find energy and inspiration in our shared purpose. If you want to be the best you can be, you can do it at Cincinnati Children's.

Cincinnati Children's is:

  • Recognized by U.S. News & World Report as atop 10 best Children's Hospitals in the nation for more than 15 years

  • Consistently among the top 3 Children's Hospitals for National Institutes of Health (NIH)Funding

  • Recognized as one of America's Best Large Employers (2025), America's Best Employers for New Grads (2025)

  • One of the nation'sAmerica's Most Innovative Companiesas noted by Fortune

  • Consistently certified as great place to work

  • A Leading Disability Employeras noted by theNational Organization on Disability

  • Magnet designated for the fourth consecutive time by theAmerican Nurses Credentialing Center (ANCC)

We Embrace Innovation-Together. We believe in empowering our teams with the tools that help us work smarter and care better. That's why we support the responsible use of artificial intelligence. By encouraging innovation, we're creating space for new ideas, better outcomes, and a stronger future-for all of us.

Comprehensive job description provided upon request.

Cincinnati Children's is proud to be an Equal Opportunity Employer committed to creating an environment of dignity and respect for all our employees, patients, and families. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, genetic information, national origin, sexual orientation, gender identity, disability or protected veteran status. EEO/Veteran/Disability


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About Cincinnati Children's Hospital Medical Center

Sourced by ZipRecruiter

Cincinnati Children's Hospital Medical Center, located in Cincinnati, OH, US, is a premier pediatric hospital renowned for its exceptional clinical services, research programs, and medical education. The healthcare institution, founded in 1883, holds a sterling reputation in the industry, with a mission to improve child health and transform delivery of care through fully integrated, globally recognized research, education and innovation. As one of the oldest and most distinguished pediatric hospitals in the United States, Cincinnati Children's continues to offer a broad range of high-quality, compassionate care to children in the community and around the globe. As a testament to its dedication, it has consistently been ranked among the top three US pediatric hospitals by U.S. News & World Report.

Industry

Hospitals

Company size

10,000+ Employees

Headquarters location

Cincinnati, OH, US

Year founded

1883