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Validation Engineer H1B Jobs in Texas (NOW HIRING)

AI Engineer

Dallas, TX · On-site

$90 - $120/hr

Strong understanding of prompt engineering, prompt evaluation, and structured output validation ... We are not sponsoring H1B or OPT candidates #J-18808-Ljbffr

Strong understanding of prompt engineering, prompt evaluation, and structured output validation ... We are not sponsoring H1B or OPT candidates* Please complete this brief survey:

Strong understanding of prompt engineering, prompt evaluation, and structured output validation ... We are not sponsoring H1B or OPT candidates*   Please complete this brief survey:

Strong understanding of prompt engineering, prompt evaluation, and structured output validation ... We are not sponsoring H1B or OPT candidates* Please complete this brief survey:

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Validation Engineer H1B information

What is a validation engineer H1B?

Validation Engineers on H1B visas are professionals from abroad who are employed in the United States to ensure that systems, equipment, and processes meet regulatory and quality standards. They typically work in industries such as pharmaceuticals, biotechnology, and manufacturing, performing testing, documentation, and analysis to verify product compliance. The H1B visa allows U.S. employers to temporarily employ foreign workers in specialty occupations that require theoretical or technical expertise, such as validation engineering. These roles often require a bachelor’s degree or higher in engineering or a related field.

What are the key skills and qualifications needed to thrive as a validation engineer?

To thrive as a Validation Engineer, you need a strong background in engineering principles, quality assurance, and regulatory compliance, typically supported by a degree in engineering or a related field. Familiarity with validation tools, statistical analysis software, and knowledge of industry standards such as FDA regulations or ISO guidelines are essential. Strong attention to detail, critical thinking, and effective communication skills help distinguish top performers in this role. These skills are crucial for ensuring products and processes meet rigorous quality and safety standards, reducing risks and maintaining regulatory compliance.

What are some common challenges validation engineers face when working in regulated industries, and how can they prepare for them?

Validation Engineers, especially those in regulated industries like pharmaceuticals or medical devices, often encounter challenges such as evolving regulatory requirements, tight project timelines, and the need for meticulous documentation. To prepare, it's essential to stay updated on industry standards (such as FDA or ISO guidelines), develop strong organizational skills for thorough record-keeping, and collaborate closely with cross-functional teams, including quality assurance and production. Proactively communicating and participating in ongoing training can also help mitigate compliance risks and ensure successful project outcomes.

What is the difference between Validation Engineer H1B vs Quality Assurance Engineer?

AspectValidation Engineer H1BQuality Assurance Engineer
Required CredentialsBachelor's in Engineering or related field, certifications like CSQE or CQE beneficialBachelor's in Engineering, Computer Science, or related field, certifications like CQE or CQA helpful
Work EnvironmentManufacturing, pharmaceutical, or biotech industries focusing on product validationSoftware, manufacturing, or service industries focusing on process and product quality
Employer & Industry UsageCommon in regulated industries requiring validation processesWidespread across industries emphasizing quality standards

Validation Engineers H1B primarily focus on validating products and processes in regulated industries, often requiring specific certifications. Quality Assurance Engineers also ensure product quality but have a broader scope, including process audits and software testing. Both roles share similar credentials but differ in industry focus and specific responsibilities.

What are popular job titles related to Validation Engineer H1B jobs in Texas?

For Validation Engineer H1B jobs in Texas, the most frequently searched job titles are:

What job categories do people searching Validation Engineer H1B jobs in Texas look for?

The top searched job categories for Validation Engineer H1B jobs in Texas are:

What cities in Texas are hiring for Validation Engineer H1B jobs?

Cities in Texas with the most Validation Engineer H1B job openings:

Principal Systems Engineer - Hybrid - San Antonio, TX

Solventum

San Antonio, TX • On-site

$124 - $171/hr

Other

Medical, Dental, Vision, Life, Retirement

This job post has expired today. Applications are no longer accepted.


Solventum rating

8.6

Company rating: 8.6 out of 10

Based on 51 frontline employees who took The Breakroom Quiz

22nd of 545 rated manufacturers


Job description

Thank you for your interest in joining Solventum. Solventum is a new healthcare company with a long legacy of solving big challenges that improve lives and help healthcare professionals perform at their best. At Solventum, people are at the heart of every innovation we pursue. Guided by empathy, insight, and clinical intelligence, we collaborate with the best minds in healthcare to address our customers’ toughest challenges.

Job Title

Principal Systems Engineer - 3M Health Care is now Solventum

Impact You’ll Make in this Role

As a Principal Systems Engineering, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by:

  • Requirements Engineering: Elicit, document, and manage system-level requirements, ensuring full traceability from user needs to low-level components.
  • System Architecture: Define system boundaries, interfaces, and data flows between subsystems (e.g., embedded software, sensors, and mechanical assemblies).
  • Risk Management: Actively participate in ISO 14971 risk management activities, including Hazard Analysis, DFMEA (Design Failure Mode and Effects Analysis), and Usability.
  • V&V Collaboration: Work with V&V team to execute comprehensive Verification and Validation (V&V) strategies to prove the system meets all design inputs and intended uses.
  • Cross-Functional Synthesis: Act as the technical bridge between Mechanical, Electrical, Software, and Quality teams to resolve design conflicts.
  • Regulatory Documentation: Author and review technical files for global regulatory submissions (FDA 510(k), PMA, or EU MDR).
  • Providing leadership and direction to technical team, guiding them through the stages of requirements definition, design, implementation, and validation to achieve coherent and efficient system architecture.
  • Maintaining a strong operational knowledge of organization’s technologies, products, customers and customers’ needs.
  • Perform technical planning, system design and architecture, evaluate alternatives including cost and risk, and supportability of total system.
  • Developing an in-depth knowledge of product development, manufacturing, engineering, financial, legal, sales and marketing functions and interfaces as required.
  • Managing product documentation through processes.
  • Participating in all reasonable work activities deemed suitable and assigned by management.
  • Conforming to, supporting and enforcing all Company policies and procedures.
Your Skills and Expertise

To set you up for success in this role from day one, Solventum requires (at a minimum) the following qualifications:

  • Bachelor’s degree or higher (completed and verified prior to start) in engineering from an accredited institution AND minimum of seven (7) years combined industry experience in systems engineering and/or product design in a regulated environment
  • High School Diploma/GED (completed and verified prior to start) and eleven (11) years combined industry experience in systems engineering and/or product design in a regulated environment

In addition to the above requirements, the following are also required:

  • Demonstrated understanding and experience in design, development, and testing of embedded, electro‑mechanical medical devices.
  • Experience in a regulated design environment with medical device development, FDA or ISO registered work experience.
  • Experience in GMP certified Manufacturing Processes and UL/IEC Standards.
  • Hands‑on experience in System Engineering with working knowledge of C or C++ embedded systems, IoT Communication, and Cybersecurity risk management.
  • Experience leading system requirements, architecture, integration, and testing through formal design reviews to final verification and validation.
  • Experience facilitating technical working sessions and engineering reviews.
  • Proven experience Identifying, quantifying, and mitigating technical risks.
  • Strong self‑directed execution, problem solving and critical thinking skills.

Additional qualifications that could help you succeed in this role include:

  • Experience with IEC 60601-1
  • Experience with Graphical User Interface development.
  • Experience with wireless communications (Cellular, Bluetooth, WiFi) and/or location services (GPS).
  • Experience driving continuous improvement of processes, tooling, and technical deliverables.
Work location

Hybrid Eligible (Job Duties allow for some remote work but require travel to San Antonio, TX at least 3 days per week).

Travel

May include up to 10% domestic / international.

Relocation Assistance

May be authorized.

Legal and H1B

Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status).

Supporting Your Well‑being

Solventum offers many programs to help you live your best life – both physically and financially. To ensure competitive pay and benefits, Solventum regularly benchmarks with other companies that are comparable in size and scope. Applicable to US Applicants Only:

The expected compensation range for this position is $124,000 - $170,500, which includes base pay plus variable incentive pay, if eligible. This range represents a good faith estimate for this position. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate’s relevant knowledge, training, skills, work location, and/or experience.

In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental & Vision, Health Savings Accounts, Health Care & Dependent Care Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences and Retirement Benefits, etc.).

Additional information is available at: https://www.solventum.com/en-us/home/our-company/careers/#Total-Rewards

Role Responsibilities

Responsibilities of this position include compliance with corporate policies, procedures and security standards while performing assigned duties.

Equal Opportunity Statement

Solventum is a new healthcare company with a long legacy of solving big challenges that improve lives and help healthcare professionals perform at their best. At Solventum, people are at the heart of every innovation we pursue. Guided by empathy, insight, and clinical intelligence, we collaborate with the best minds in healthcare to address our customers’ toughest challenges.

As it was with 3M, at Solventum all qualified applicants will receive consideration for employment without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

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