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Vlsi Design Verification Engineer Jobs in Florida

Sr. FPGA Engineer

Melbourne, FL · On-site

$120K - $154K/yr

Sr. FPGA Engineer Melbourne, FL - Onsite Visa: Open Experience level: 5 to 10 yrs Exp Client ... design verification. * Prototype evaluation, design-to-cost tradeoffs, design reviews ...

Graphics Software Content Engineer

Orlando, FL · On-site

$130K - $161K/yr

Architectural validation and design verification knowledge Knowledge of hardware architecture and ... Excellent C/C++ programming skills. Knowledge of key graphics rendering algorithms. Relevant ...

Typically requires a degree in Science, Technology, Engineering or Mathematics (STEM) and a minimum of 8 years of prior relevant experience * FPGA or ASIC design and/or verification * Integration and ...

Associate, Electrical Engineer Job Code: 43220 Job Location: Palm Bay, FL Job Schedule: 9/80 ... Design and modify tests to verify the operational state of various L3Harris products and ...

Associate, Electrical Engineer Job Code: 43219 Job Location: Palm Bay, FL Job Schedule: 9/80 ... Design and modify tests to verify the operational state of various L3Harris products and ...

Associate, Electrical Engineer Job Code: 43218 Job Location: Palm Bay, FL Job Schedule: 9/80 ... Design and modify tests to verify the operational state of various L3Harris products and ...

Senior Electrical Engineer

Melbourne, FL · On-site

$99K - $129K/yr

Support verification, validation, manufacturing troubleshooting, and design-for-manufacturability ... Mentor junior engineers and serve as a technical subject matter expert (SME) on complex electrical ...

Showing results 41-60

Vlsi Design Verification Engineer information

See Florida salary details

$78.8K

$111.5K

$124.8K

How much do vlsi design verification engineer jobs pay per year?

As of Sep 1, 2026, the average yearly pay for vlsi design verification engineer in Florida is $111,458.00, according to ZipRecruiter salary data. Most workers in this role earn between $101,600.00 and $124,000.00 per year, depending on experience, location, and employer.

What is a VLSI design verification engineer?

A VLSI Design Verification Engineer is a specialist responsible for ensuring that integrated circuits (ICs) and systems-on-chip (SoCs) meet their design specifications before manufacturing. They use various verification methodologies, such as simulation, formal verification, and hardware emulation, to identify and fix functional errors in digital designs. Their role is critical in the semiconductor industry to ensure product quality, reduce costly re-spins, and speed up time-to-market. They often work closely with design engineers, using tools like SystemVerilog, UVM, and other verification frameworks.

What are the key skills and qualifications needed to thrive as a VLSI design verification engineer?

To thrive as a VLSI Design Verification Engineer, you need a solid background in digital logic design, computer architecture, and verification methodologies, typically supported by a degree in electrical engineering or a related field. Proficiency with hardware description languages like Verilog or VHDL, simulation tools such as ModelSim or Synopsys VCS, and familiarity with UVM or SystemVerilog are commonly required. Strong analytical thinking, attention to detail, and effective communication are crucial soft skills for identifying design flaws and collaborating with cross-functional teams. These skills and qualifications ensure accurate, reliable chip designs and efficient project execution in the competitive semiconductor industry.

What are some common challenges faced by VLSI design verification engineers during the verification process?

VLSI Design Verification Engineers often encounter challenges such as managing increasingly complex system-on-chip (SoC) designs, ensuring thorough test coverage, and debugging intricate functional issues. Coordinating with cross-functional teams—like design, software, and validation—is essential to align test plans and resolve ambiguities quickly. Additionally, keeping up with evolving verification methodologies and tools (such as UVM or SystemVerilog) requires a commitment to continuous learning, but offers strong career growth opportunities for those who master them.

What is the difference between Vlsi Design Verification Engineer vs Vlsi Design Engineer?

AspectVlsi Design Verification EngineerVlsi Design Engineer
Primary FocusVerifying the correctness of VLSI designs through testing and simulationCreating and implementing VLSI chip designs and architectures
Skills & CertificationsHardware description languages (HDL), verification tools, scripting, knowledge of verification methodologiesHDL, digital design, synthesis, timing analysis, and physical design skills
Work EnvironmentDesign teams, verification labs, simulation environmentsDesign teams, synthesis and implementation tools, physical design environments

While both roles require HDL knowledge and work within VLSI teams, the Vlsi Design Verification Engineer primarily focuses on testing and validating designs, whereas the Vlsi Design Engineer is responsible for creating and implementing the actual chip designs.

Are Vlsi Design Verification Engineers in demand?

Vlsi Design Verification Engineers are in high demand due to the growth of semiconductor and electronics industries, requiring expertise in hardware description languages like Verilog and SystemVerilog. The role often involves working with simulation tools and verification methodologies such as UVM, and demand is strong in regions with advanced chip manufacturing and design centers.

What are popular job titles related to Vlsi Design Verification Engineer jobs in Florida?

For Vlsi Design Verification Engineer jobs in Florida, the most frequently searched job titles are:

What cities in Florida are hiring for Vlsi Design Verification Engineer jobs?

Cities in Florida with the most Vlsi Design Verification Engineer job openings:

Infographic showing various Vlsi Design Verification Engineer job openings in Florida as of August 2026, with employment types broken down into 92% Full Time, 6% Part Time, and 2% Contract. Highlights an 85% Physical, 4% Hybrid, and 11% Remote job distribution, with an average salary of $111,458 per year, or $53.6 per hour.

Full-time

Re-posted 14 days ago


Job description

Job Summary: 

The Design Controls Specialist is responsible for establishing, maintaining, and ensuring compliance of design control processes in accordance with regulatory requirements (FDA 21 CFR Part 820, ISO 13485, and applicable combination product guidelines). This role will own and manage Design History Files (DHF) and oversee product lifecycle management for transdermal drug delivery systems, ensuring traceability, risk management, and design integrity from concept through commercialization and post-market changes.

Job Responsibilities:

Design Control & Design History File (DHF) Management

  • Lead the creation, organization, review, and maintenance of Design History Files (DHF) for transdermal patch products.
  • Ensure DHFs demonstrate full compliance with:
    • FDA 21 CFR 820.30 (Design Controls)
    • ISO 13485 design and development requirements
    • Combination product regulations (21 CFR Part 4)
  • Maintain complete design traceability from:
    • User needs → Design inputs → Outputs → Verification → Validation → Design transfer
  • Perform routine audits and gap assessments of DHFs to ensure completeness and inspection readiness.
  • Ensure proper version control and document integrity within electronic document management systems (e.g. Trackwise).

Design Lifecycle Management

  • Support end-to-end product lifecycle management for transdermal patches:
    • Concept development
    • Feasibility and design planning
    • Verification & validation
    • Commercialization
    • Post-market lifecycle management
  • Drive and manage design changes (ECR/ECN) ensuring proper documentation, impact assessments, and approvals.
  • Collaborate with cross-functional teams to ensure lifecycle activities meet regulatory and quality expectations.

Risk Management & Compliance

  • Facilitate and maintain risk management documentation (ISO 14971 aligned), including:
    • Risk analyses (FMEA, FTA)
    • Risk control measures
    • Risk-benefit justifications
  • Ensure integration of risk management into design controls and lifecycle activities.
  • Support internal and external audits, including FDA inspections and notified body audits.
  • Act as subject matter expert on design control compliance for transdermal systems

Cross-Functional Collaboration

  • Partner with:
    • R&D / Formulation Scientists
    • Engineering (process, packaging, and equipment)
    • Quality Assurance & Regulatory Affairs
    • Manufacturing and Operations
  • Ensure alignment between product design, process design, and manufacturing transfer.
  • Support Design Transfer activities ensuring readiness for commercial production.

Documentation & Systems

  • Maintain and improve Quality Management System (QMS) procedures related to design controls.
  • Develop templates, SOPs, and best practices for DHF and lifecycle documentation.
  • Ensure all documentation supports labeling, stability, and performance requirements of transdermal patches.
  • Support digital transformation of DHF and lifecycle records when applicable.
  • All other duties as assigned.
Job Requirements
  • Bachelor’s degree in Engineering, Pharmaceutical Sciences, Life Sciences, or related field.
  • 3–7+ years of experience in:
    • Medical device, pharmaceutical, or combination product industries
    • Design controls and DHF management
  • Strong knowledge of:
    • FDA 21 CFR Part 820 and Part 4 (combination products)
    • ISO 13485 and ISO 14971
    • Design verification and validation processes
  • Experience with document control systems (e.g., TrackWise).

Knowledge, Skills and Abilities

  • Experience with transdermal drug delivery systems or combination products.
  • Knowledge of adhesives, drug-in-adhesive systems, or patch manufacturing technologies.
  • Familiarity with process validation and technology transfer
  • Experience supporting FDA inspections or regulatory submissions (e.g., NDA, ANDA, 510(k)).
  • Strong attention to detail and documentation rigor
  • Excellent organizational and traceability management skills
  • Ability to interpret and apply complex regulations
  • Cross-functional leadership and collaboration
  • Problem-solving and risk-based thinking
  • Audit readiness mindset