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Design Verification Engineer Jobs in Indiana (NOW HIRING)

Regal Rexnord

Design Engineer II

Columbia City, IN

The Design Engineer II works closely with crossfunctional teams within manufacturing and R&D and ... Prepare customer reports documenting verification and validation activities associated with new ...

Zimmer, Inc.

Development Engineer II

Warsaw, IN · On-site

Evaluate, verify and validate product designs relative to design requirements and to reduce user ... Mechanical Engineering, Mechanical Engineering Technology, Biomedical Engineering, Bioengineering ...

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Design Verification Engineer information

See Indiana salary details

$100.4K

$141.9K

$158.9K

How much do design verification engineer jobs pay per year?

As of Aug 18, 2026, the average yearly pay for design verification engineer in Indiana is $141,925.00, according to ZipRecruiter salary data. Most workers in this role earn between $129,400.00 and $158,000.00 per year, depending on experience, location, and employer.

What is a design verification engineer?

A Design Verification Engineer ensures that hardware designs function correctly by developing and executing test plans, writing verification code (often in SystemVerilog with UVM), and debugging design issues. They work closely with design and validation teams to confirm specifications are met before manufacturing. Their role is critical in preventing costly design flaws and ensuring high-quality semiconductor products.

What skills and qualifications are needed to be a design verification engineer?

Design Verification Engineers require a solid background in digital design concepts, computer engineering, and electrical engineering, usually supported by a relevant bachelor’s or master’s degree. Expertise with hardware description languages like Verilog or VHDL, simulation tools, and familiarity with Unix/Linux environments are typical technical requirements, with certifications in FPGA/ASIC design considered advantageous. Strong analytical thinking, problem-solving skills, teamwork, and effective communication help these engineers collaborate closely with design, validation, and development teams. These competencies are vital to ensuring design correctness, catching flaws early, and driving efficient, reliable hardware development.

What are the most common challenges faced by design verification engineers in their daily work?

Design Verification Engineers often face the challenge of thoroughly validating complex digital designs within tight project deadlines. Debugging intricate issues, dealing with evolving specifications, and ensuring complete coverage during simulation can require a great deal of attention to detail and persistence. Collaboration with designers, validation teams, and often cross-functional groups is critical to resolving ambiguities and preventing errors from reaching production. Adapting to new verification methodologies or tools is also common as technologies and standards advance. These challenges offer valuable learning opportunities and play a crucial role in producing robust, high-quality hardware products.

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

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

What job categories do people searching Design Verification Engineer jobs in Indiana look for?

The top searched job categories for Design Verification Engineer jobs in Indiana are:

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Design Verification Engineer jobs near you
Infographic showing various Design Verification Engineer job openings in Indiana as of August 2026, with employment types broken down into 86% Full Time, 10% Part Time, and 4% Contract. Highlights an 85% Physical, 4% Hybrid, and 11% Remote job distribution, with an average salary of $141,925 per year, or $68.2 per hour.

Design Quality Engineer

Stark Pharma Solutions Inc

Warsaw, IN • On-site

Contractor

Re-posted 3 days ago

Job description

Hi,

My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Design Quality Engineer position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows.

Role: Design Quality Engineer

Location: Warsaw, IN & Raynham, MA (Onsite)
Duration: 6-Month Contract

Position Overview

We are seeking a Design Quality Engineer to support product development, validation, and lifecycle management activities within a medical device environment. This role will be responsible for ensuring compliance with design control requirements, supporting product validation efforts, maintaining Design History File (DHF) documentation, and collaborating with cross-functional teams and external suppliers to deliver high-quality, compliant products.

Key Responsibilities

  • Support product validation (PV) activities, including review and approval of validation protocols, reports, and related deliverables.
  • Collaborate with suppliers and contract manufacturers to review technical documentation, engineering drawings, control plans, and validation packages.
  • Ensure design and process changes comply with applicable quality system requirements and regulatory standards.
  • Participate in risk management activities, including FMEA, risk assessments, hazard analysis, and mitigation planning.
  • Develop, review, and maintain Design History File (DHF) documentation to ensure accuracy, completeness, and regulatory compliance.
  • Create and manage traceability matrices linking design inputs, outputs, verification, and validation activities.
  • Support design reviews and ensure proper execution of design control processes.
  • Partner with R&D, Manufacturing, Regulatory Affairs, and Quality teams throughout the product lifecycle.
  • Assist with change control activities, ensuring appropriate documentation, approvals, and implementation.
  • Provide support during audits, inspections, and compliance reviews.

Required Qualifications

  • Bachelor’s degree in Engineering or a related technical discipline.
  • 3+ years of Quality Engineering experience within the medical device industry.
  • Strong knowledge of Design Controls and applicable regulations, including FDA 21 CFR Part 820 and ISO 13485.
  • Experience supporting Product Validation (PV) activities.
  • Experience working with external suppliers, contract manufacturers, and technical documentation reviews.
  • Ability to interpret engineering drawings, specifications, and control plans.
  • Hands-on experience with risk management tools such as FMEA and risk assessments.
  • Experience developing and maintaining DHF documentation and traceability matrices.
  • Strong technical writing, documentation, and organizational skills.
  • Excellent communication and cross-functional collaboration abilities.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.  

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/

Thank you,

Karthik Mutyala

Recruiting Manager

Stark Pharma Solutions Inc

Email: karthik@starkpharma.com

15 Corporate Place S, Suite 350,

Piscataway, New Jersey 08854

www.starkpharma.com