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Location:
San Marcos
Category:
Quality Assurance & Control

Workable
Quality Specialist
We are looking for a Quality Specialist to oversee and perform activities necessary to provide confidence that specified Quality and Current Good Manufacturing Practices (cGMP) requirements applicable to materials, operational processes, and company products and services are fulfilled at Enviromedica. The successful candidate will be responsible for overseeing the operation of implemented Quality Systems, and other tasks to support the Quality department. The Quality Specialist must also adhere to all relevant regulatory standards and will report to the Quality Manager.
Enviromedica is a fast-growing natural products innovator, manufacturer and distributor located in North Austin, Texas. We have built out a beautiful facility which includes plenty of natural light, and contemporary design.
Job Duties and Responsibilities
Maintenance of Document Control including maintenance of standard operating procedures (SOPs), quality control methods, master manufacturing records, and controlled forms.
Review and disposition of manufacturing records. This includes, completing the batch release checklist for assurance that all required documents are reviewed and are found to be acceptable for release.
Responsible for ensuring external laboratory testing is conducted on raw materials and products according to specifications.
Perform review of Quality Control analytical documents including raw material analysis report, in-process bulk intermediates and finished products to ensure adherence to required internal specifications.
Perform routine internal audits, identify and implement process improvements.
Provide support for external and vendor audits.
Assist with follow up on deviations (NCEs), CAPAs, and work with manufacturing to ensure they meet target implementation dates.
Provide GMP training for new employees, new or revised documents, processes, or methods, and maintains the employee training records and database.
Support activities for Quality
Prepare and submit reports to the quality manager
Requirements
Associate's Degree in biology, chemistry, or related scientific discipline or a minimum of two (2) years experience in an FDA regulated industry (i.e. nutraceutical / cosmetic / personal care or related bioscience industry)
Bilingual a plus. (English and Spanish)
Excellent written and verbal communications skills.
Ability to easily learn and retain technical information.
Attention to detail and ability to manage multiple priorities.
Ability to understand production flow and evaluate related documentation.
Adapts to changes in the work environment, manages competing demands and is able to deal with frequent change, delays or unexpected events.
Actively promotes and personally observes safety and security procedures, and uses equipment and materials properly.
Ability to work independently.
Computer literacy and experience with MS Office (especially Excel and Word) and database systems.
Benefits
We offer an encompassing benefits package including Medical, Dental, Vision, 401k, PTO and 8 paid Holidays per year.

Austin, TX, USA
Negotiable Salary

Workable
Product Quality Engineer - SaMD
About Us
Senseye is a NeuroTechnology Company in Austin, TX on the cusp of revolutionizing Mental Health. Over the past 6 years we have invested millions of dollars in R&D to build our platform allowing us to measure cognitive activity via the eye through mobile phones. Through multiple iterations and use cases we are now focused on building the world's first Objective Mental Health Diagnostics on top of our core technology. Our first diagnostic is for PTSD and is entering clinical trials now, followed soon by additional indications for Anxiety and Depression. As the world struggles with a mental health crisis, it is not hyperbolic to suggest that an objective diagnostic platform, that gives clinicians a safe and objective accurate approach to identifying and monitoring mental health disease, will redefine how mental health services are provided and will enable access to treatment for hundreds of millions of sufferers. The Senseye platform has the potential to be the technology that drives this change.
Role Description
We are seeking a Product Quality Engineer with strong experience in software and medical device quality systems to join our team. This individual will play a critical role in ensuring that our SaMD products meet regulatory, quality, and customer requirements throughout the product lifecycle—from development through post-market surveillance.
Responsibilities
Partner with Engineering, R&D, Regulatory, and Clinical teams to ensure compliance with ISO 13485, 21 CFR Part 820, IEC 62304, and other applicable standards.
Support design and development activities by developing and reviewing documentation, ensuring design control compliance, and participating in design reviews.
Perform risk management activities per ISO 14971, including creation and maintenance of risk analyses.
Collaborate with development teams on cybersecurity requirements, threat modeling, vulnerability assessments, and post-market monitoring in accordance with FDA, ISO/IEC 27001, and other international standards to ensure product security.
Define and implement non-product software validation strategies in alignment with FDA’s CSA guidance, 21 CFR Part 11 and GAMP 5 principles.
Contribute to the development and continuous improvement of the QMS, with a focus on software-specific quality processes.
Investigate and resolve product quality issues, nonconformances, and CAPAs using root cause analysis techniques.
Lead or support internal and external audits (e.g., FDA, Notified Bodies, ISO registrars).
Participate in supplier qualification and software supplier evaluation processes.
Monitor post-market product performance and contribute to complaint handling and field actions when needed.
Drive quality metrics reporting and trend analysis to support management reviews and continuous improvement initiatives.
Position requires access to Covered Defense Information for which the US Government requires US Citizenship
You'll also need to pass an FBI background check
Senseye maintains a drug free workplace and conducts pre-employment substance abuse testing. Senseye may also conduct substance abuse testing during employment, in accordance with its policies and customer requirements. Employment is subject to successfully completing and passing such tests.
Requirements
Bachelor’s degree in Engineering, Computer Science, Life Sciences, or related technical discipline.
4+ years of experience in medical device quality engineering with 2+years in the SaMD environment (SaMD experience is a must!)
Strong understanding of quality systems and regulatory frameworks, including ISO 13485, ISO 14971, IEC 62304, and 21 CFR Part 820/11.
Experience with design control, risk management, and software validation.
Familiarity with Jira, Confluence, and modern QMS or eQMS tools.
Excellent communication, collaboration, and problem-solving skills.
Extra Points:
Perform agile software development/quality practices
Perform Usability and Human Factor Engineering activities for medical devices
Establish information security against HIPAA, GDPR requirements
The compensation for this role is $97,000 - $121,000 annually.
Benefits
The freedom and trust to define your role as we design, build, and ship our products
Competitive salary and stock option plan
Flexible paid time off (vacation, sick leave, and public holidays)
Flexible schedules
Company health care plan
Medical, dental, and vision insurance
Short and long term disability insurance
Life insurance policy
401k
Commuter benefits for parking, public transit, carshares, etc.
Mothers' room
Fully stocked kitchen
Opportunities for continuing education
Senseye is dedicated to building a community of employees that are diverse, passionate, and engaged. We are committed to equal opportunity regardless of race, color, ancestry, religion, gender, gender identity, parental or pregnancy status, national origin, sexual orientation, age, marital status, disability, or veteran status. When we're safe, healthy, and balanced we can accomplish phenomenal things together.

Austin, TX, USA
$97,000/year

Workable
Software Development Engineer in Test (SDET)
Futurex is seeking talented individuals for the position of Software Development Engineer in Test (SDET). This position is on-site at Futurex’s Engineering Campus in Bulverde, 15 miles north of San Antonio, Texas. This position offers an opportunity for passionate, motivated, and driven individuals to join our team of world-class engineers and assist in quality assurance for Futurex's line of innovative, hardware-based cryptographic solutions
In the SDET role, your responsibilities will center on software development and testing. You will ensure the robustness of the company’s automation initiatives before they can be distributed to internal and external clients. You will carry out functional integration testing between the company’s applications, products, and services. Success in this role will be determined by your ability to successfully perform end-to-end testing of automation processes.
Job Responsibilities and Duties:
Assess and understand the flow of code and its interaction with various processes
Document processes and client demands for process improvement
Log, manage, and track user issues and cases
Develop new and extend current testing frameworks
Perform some manual regression testing
Troubleshoot bugs and other issues on desktop and web-based platforms
Test automation builds, execution, and script troubleshooting
Requirements
Job Requirements
Bachelor’s degree in Computer Science, Computer Engineering, or related field
Excellent written and verbal communication skills
Ability to identify risks and errors in applications
Python proficiency
SQL proficiency
Selenium experience
Rest API
Linux/Bash experience
Fundamentals of TCP/IP networking
Strongly preferred:
Jenkins experience
Docker experience
Jenkins, Gitlab and/or other CI pipeline experience
Java Script experience
C++ experience
Knowledge of Micro Service architecture and testing
Kubernetes
MitMproxy experience
Groovy experience
Benefits
Health, dental, vision, life, and short/long-term disability insurance
Paid vacation, holidays, and sick leave
Competitive compensation and opportunities for advancement
Retirement plan with employer contribution match
Scenic corporate campus with amenities including a tennis court, jogging trail, and putting green
Welcoming culture, suited to entrepreneurial, and motivated individuals
Voted as one of the best places to work in San Antonio, 9 years running

Bulverde, TX, USA
Negotiable Salary

Workable
Software Quality Assurance (QA) Tester
This position is for a QA tester. More experienced candidates are encouraged to apply for the SDET position.
Futurex is seeking talented individuals with a passion for testing software for the role of Software Quality Assurance (QA) Tester. This position is on-site at Futurex’s Engineering Campus in Bulverde, 15 miles north of San Antonio, Texas.
This on-site role offers an opportunity for candidates to expand their talents by participating directly in the testing of production software operating on Futurex’s enterprise-grade data encryption hardware. Individual visibility within the team is high, and opportunities for rapid advancement exist. All levels of Futurex QA testers work directly with products using manual testing procedures in a fast-paced, results-oriented environment on products with a rapid time to market.
Qualified candidates possess the ability to test programs and systems based on defined requirements, to prepare test specifications, to write new test cases, to interpret technical information relating to software behaviors, and to communicate effectively. The position involves testing and extending both existing and new applications, as well as documenting methods and procedures.
Responsibilities
Test and troubleshoot software and firmware developed for Futurex’s line of applications and/or cryptographic devices and report conclusions in a clear and concise manner.
Develop new tests that validate new features, verify issue resolution, perform stress tests, and identify security weak points
Consult with team members to develop, understand, and update requirements for product features
Write and maintain testing documentation on subjects including API functionality and software issue creation/resolution
Maintain confidentiality of information being processed, stored, or accessed
Requirements
Requirements
Bachelor’s degree or higher in any field. Computer Science (CS), Computer Information Systems (CIS), Electrical Engineering Technology (EET), or Electronics & Computer Technology (ECT) is preferred.
Comfortable with Linux and Bash (SysV and systemd)
Working knowledge of TCP/IP networking
Strongly Preferred Experience
SQL experience and basic understanding of relational databases
Familiarity with automated and manual software testing tools and frameworks
Intermediate proficiency with Python (version 3 preferred)
Experience with version control software such as Git or Subversion
Benefits
A key role in production-level software projects working directly on cutting-edge encryption technology with a fast time to market
Competitive compensation and opportunities for advancement
Scenic corporate campus with amenities including a tennis court, jogging trail, and putting green
Welcoming, family-style corporate culture uniquely suited to fast-paced, entrepreneurial, and motivated individuals
Health, dental, vision, life, and short/long-term disability insurance
Paid vacation, holidays, and sick leave
Competitive compensation and opportunities for advancement
Retirement plan with employer contribution match
Welcoming, family-style corporate culture uniquely suited to fast-paced, entrepreneurial, and motivated individuals
One of San Antonio’s “Best Places to Work” for nine consecutive years

Bulverde, TX, USA
Negotiable Salary
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