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Temp Medical Device Startup Jobs in Texas (NOW HIRING)

Synkriom

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Technical Recruiter -Medical device

Austin, TX · On-site

$40 - $41/hr

Temporary Senior Technical Recruiter At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years ...

Senseye

Design Quality Engineer, SaMD

Austin, TX · On-site

$100K - $125K/yr

We are looking for a Design Quality Engineer for our software medical device (SaMD) who can partner ... Help define pragmatic QMS processes for a fast-moving regulated startup, including software ...

Senseye

Design Quality Engineer, SaMD

Austin, TX

$100K - $125K/yr

We are looking for a Design Quality Engineer for our software medical device (SaMD) who can partner ... Help define pragmatic QMS processes for a fast-moving regulated startup, including software ...

Senseye

Design Quality Engineer, SaMD

Austin, TX · On-site

$100K - $125K/yr

We are looking for a Design Quality Engineer for our software medical device (SaMD) who can partner ... Help define pragmatic QMS processes for a fast-moving regulated startup, including software ...

Aerotek

3rd Shift Mechanical Assembler

Allen, TX

$16/hr

The role offers a clear pathway from temporary to permanent employment, including a pay increase upon conversion, providing stability and growth potential. You gain experience in the medical device ...

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Temp Medical Device Startup information

What are some typical challenges faced by temp employees at a medical device startup, and how can they successfully adapt?

Temp employees at medical device startups often encounter fast-paced environments with evolving priorities and limited onboarding time. They may need to quickly familiarize themselves with complex products, regulatory standards, and cross-functional teams. Successful adaptation involves being proactive in asking questions, embracing flexibility, and staying organized to manage shifting tasks. Building strong communication with permanent staff can also help temp employees integrate smoothly and deliver impactful results.

What is a temp medical device startup?

A Temp Medical Device Startup is a temporary or short-term company focused on developing, testing, or launching new medical devices. These startups often form to rapidly innovate or address specific healthcare needs, sometimes as part of a contract or pilot project. Temporary startups may operate only for the duration of a specific development cycle or clinical trial, after which they may dissolve or be absorbed by a larger company. Working at such a startup typically involves fast-paced, cross-functional teamwork and the opportunity to contribute to cutting-edge healthcare solutions.

What are the key skills and qualifications needed to thrive as a temp at a medical device startup?

To thrive as a Temp at a Medical Device Startup, you need a background in life sciences or engineering, familiarity with regulatory standards, and the ability to rapidly learn new processes. Experience with tools like CAD software, laboratory equipment, or project management systems is often required, along with knowledge of FDA or ISO compliance. Strong problem-solving skills, flexibility, and effective communication help you adapt to the fast-paced and evolving environment of a startup. These competencies are crucial for ensuring product quality, meeting deadlines, and supporting innovation in a highly regulated and competitive field.

What is the difference between Temp Medical Device Startup vs Medical Device Quality Assurance Technician?

AspectTemp Medical Device StartupMedical Device Quality Assurance Technician
CredentialsTypically requires a degree in engineering, biology, or related field; certifications varyRequires a degree in life sciences or engineering; often holds certifications like CQE or ISO auditor
Work EnvironmentFast-paced, dynamic startup setting, often temporary or project-basedStructured environment within established companies, focusing on compliance and quality control
Employer & Industry UsageCommon in early-stage startups developing new medical devicesFound in established medical device companies ensuring product quality and regulatory compliance

While both roles involve working with medical devices, a Temp Medical Device Startup typically focuses on supporting early-stage product development in a dynamic environment. In contrast, a Medical Device Quality Assurance Technician works within established companies to ensure products meet quality standards and regulatory requirements.

What are the most commonly searched types of Medical Device Startup jobs in Texas?

The most popular types of Medical Device Startup jobs in Texas are:

What are popular job titles related to Temp Medical Device Startup jobs in Texas?

For Temp Medical Device Startup jobs in Texas, the most frequently searched job titles are:

What job categories do people searching Temp Medical Device Startup jobs in Texas look for?

The top searched job categories for Temp Medical Device Startup jobs in Texas are:

What cities in Texas are hiring for Temp Medical Device Startup jobs?

Cities in Texas with the most Temp Medical Device Startup job openings:

Temp Medical Device Startup jobs near you
Infographic showing various Temp Medical Device Startup job openings in Texas as of August 2026, with employment types broken down into 64% Full Time, 18% Part Time, 5% Temporary, 9% Contract, and 4% Nights. Highlights an 100% In-person job distribution.

Director of Clinical Science and Applied Research

Motif Neurotech

Houston, TX • On-site, Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted yesterday

Job description

What is Motif?
Motif is a medical device startup based in Houston, Texas. We are designing and developing minimally invasive electronic solutions for serious mental health conditions. Powered by our patent-pending methods for wireless power and data transmission, our goal is to create the smallest implantable brain stimulator to treat people with mental health disorders.
We are an early-stage startup with funding from venture capital firms, grants, and private angel and founder investments.
Motif's technology stack consists of a small implant that is wirelessly powered via magnetic fields from an external wearable transmitter, configured and controlled from a programming interface. It delivers novel stimulation therapy to cortical targets and will evolve to record biomarkers of symptoms, disease state, and therapy response.
Where are we going?
We are currently completing the development of our first minimally invasive neural stimulation system and preparing for future versions with additional functionality based on our platform technology.
About the Job
We are seeking a cross-functional strategic leader to oversee clinical evidence generation and external research partnerships. If you have a passion for translating early-stage neurotechnology into therapies that reach patients, apply now to be part of our dedicated team. Lead the clinical roadmap from early feasibility through reimbursement while shaping the scientific narrative for a new class of psychiatric therapy.
Job Location: Remote with occasional visits to Motif Headquarters in Houston, Texas
Does this sound like you?
  • Do you believe openness and honesty are key to team success?
  • Do you enjoy learning and are curious about how and why things work?
  • Do you like challenging the conventional way of doing things to find efficiencies and new ways of working?

If yes to the above, then come work with Motif! We are highly dedicated people with a passion for neurotechnology, clinical product development, and putting the patient first. We are looking for people with the same energy who will thrive in a high growth - high autonomy environment.
In this role, you will:
  • Develop and own the clinical roadmap
    • Define the end-to-end evidence generation strategy from early feasibility studies through to successful reimbursement decisions
    • Integrate regulatory and reimbursement requirements into study design to ensure clinical data supports both approval and coverage
    • Partner with leadership to align the clinical roadmap with company strategy, financing milestones, and product development timelines
  • Oversee clinical development projects and grants
    • Provide oversight of active clinical studies, ensuring programs are delivered on time, on budget, and to protocol
    • Identify, secure, and manage non-dilutive funding sources, including federal grants and foundation support for evidence development (clinical and preclinical) programs
    • Oversee grant-funded programs end-to-end, including reporting, milestone tracking, and renewals
  • Represent the company externally and build the scientific community
    • Represent the company at scientific and medical meetings, presenting data and shaping the clinical narrative for our platform
    • Build and maintain peer-level relationships with key opinion leaders in psychiatry, neuromodulation, and related fields
    • Establish and manage external research partnerships with academic investigators and clinical collaborators
  • This is not an exhaustive list of duties and you may be asked to perform different tasks if your role within or the objectives of the organization changes.

To be considered, you will need:
  • 10+ years of experience in clinical development within the medical device, pharmaceutical, or biotech industry, with progressive leadership responsibility
  • Demonstrated experience leading clinical studies from protocol design through execution, including at least one study that supported a regulatory submission or market approval
  • Experience directly managing clinical, scientific, or medical affairs teams, and a track record of representing an organization at scientific meetings
  • To be able to travel to Houston, TX for onsite meetings (approximately ~4-5 times per year) and to other scientific conferences and/or clinical meetings

It is a bonus if you have:
  • Experience in active implantable medical devices, neuromodulation, or neurostimulation therapies
  • Clinical or research background in psychiatry, depression, or related mental health indications
  • Advanced degree (MD, PhD, or equivalent) and a record of peer-reviewed publications or successful grant applications

Work Authorization Notice
Motif Neurotech hires only individuals who are authorized to work in the United States. At this time, visa sponsorship is not offered for this role.
Benefits*
  • Medical, dental, and vision insurance for you and your dependents
  • Participation in our 401k plan
  • Unlimited PTO
  • The chance to work with an incredible group of people working towards a common goal for a better future

We envision a world where everyone with a mental health disorder can get well and stay well, regardless of who you are, where you live, or how much money you make, and we are excited to build that future with you.
Let's use our powers for good.
Motif Neurotech is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, disability status, or any other protected class status.
*for regular full-time, exempt, salaried US employees

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