ZipRecruiter

Log In

1

Design Control Software Validation Engineer Jobs

Medline

Sr Engineer Software Validation

Redmond, OR · On-site

$101K - $152K/yr

Evaluate systems and applications to properly design organized and efficient software, process ... Maintain organizational excellence, including document control, quality records, detail, and ...

Semtech

Silicon Validation Engineer

San Diego, CA · On-site

... control applications. Job Summary: The Validation Engineer is responsible for pre- and post-silicon ... Validate pre-silicon and post-silicon hardware and software/firmware developed by the design team ...

Alphatec Spine

Validation Engineer II

Carlsbad, CA · On-site

Creates and reviews design control documentation, ensuring requirements, test plans and protocols ... Performs validation of non-medical-device software tools and supporting systems as required ...

Alphatec Spine

Validation Engineer II

Carlsbad, CA · On-site

Creates and reviews design control documentation, ensuring requirements, test plans and protocols ... Performs validation of non-medical-device software tools and supporting systems as required ...

Vertiv Co

Software Engineer -Automation

Austin, TX · On-site

... validation infrastructure, and intelligent engineering workflows for industrial control systems ... Design and implement software components and services in Python and C/C++ for Linux-based thermal ...

Hark

System Test & Validation Engineer

San Jose, CA · On-site

$120K - $300K/yr

Rigorously test iterative hardware and software releases, tracking regressions and validating ... Design, build, and maintain automated test setups to streamline repetitive testing processes ...

Hark

System Test & Validation Engineer

San Jose, CA · On-site

$120K - $300K/yr

Rigorously test iterative hardware and software releases, tracking regressions and validating ... Design, build, and maintain automated test setups to streamline repetitive testing processes ...

previous page

Showing results 41-60

All JobsTechnology JobsSoftware JobsSoftware Quality Engineer JobsDesign Control Software Validation Engineer Jobs

Design Control Software Validation Engineer information

See salary details

$10

$56

$98

How much do design control software validation engineer jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for design control software validation engineer in the United States is $56.31, according to ZipRecruiter salary data. Most workers in this role earn between $41.59 and $70.43 per hour, depending on experience, location, and employer.

What are popular job titles related to Design Control Software Validation Engineer jobs?

For Design Control Software Validation Engineer jobs, the most frequently searched job titles are:

Sr Engineer Software Validation

Redmond, OR • On-site

Medline
Medical Equipment and Supplies Manufacturing • 10K+ employees
Learn more about Medlineexternal

$101K - $152K/yr

Full-time

Medical, Life, Retirement, PTO

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

Medline Industries rating

7.6

Company rating: 7.6 out of 10

Based on 254 frontline employees who took The Breakroom Quiz

Job description

Job Summary
Job Description
JOB SUMMARY
Deliver leadership-level role in the development and execution of validation projects, ensuring customer and regulatory requirements are met in a timely and satisfactory manner.
MAJOR RESPONSIBILITIES
  • Evaluate systems and applications to properly design organized and efficient software, process, automation, cleaning, facility, and utility system related validations.
  • Ensure scope and complexity of validations are commensurate with risk including the design, development, and implementation of test strategy, plans, scripts, and test procedures to meet requirements.
  • Coordinate, Execute, and Report on validation plans for custom and off-the shelf software.
  • Manage multiple, concurrent validation projects, including gathering and understanding customer requirements and effectively communicating project status to keep customer informed and satisfied.
  • Document validation protocols and reports with professional and technical written communication skills.
  • Know, support, and conform to Medline policies and relevant governing procedures.
  • Maintain awareness to industry and regulatory environment, including FDA, GAMP, ISO.
  • Maintain organizational excellence, including document control, quality records, detail, and thoroughness.
  • Evaluate ways to streamline and improve efficiencies in software validation and associated processes.
  • Provide team support in all validation initiatives as requested.
  • Support development and upkeep of Divisional SOPs as related to software use.
  • Provide system design feedback to ensure compliance with regulatory and Medline standards throughout the software development life cycle.

MINIMUM JOB REQUIREMENTS
Education: Bachelor's degree in Engineering, Quality, Business, or Computer Science.
Work Experience:
  • 5+ years of experience in Manufacturing, Quality or Engineering.
  • 3+ years of experience in GAMP 5 related computerized system validations, including designing, authoring, executing, and coordinating.
  • Direct experience operating in a medical device QMS environment, including FDA 21 CFR Part 820, ISO 13485, ISO 14971, General Principals of Software Validation, Electronic Records/Signatures.
  • Additional Experience applying knowledge of standard concepts, practices, and procedures within software engineering.
  • Experience and skills in influencing, leading and directing individuals in multiple functional areas.
  • Experience with project management (for example: planning, organizing, and managing resources to bring about the successful completion of specific project goals and objectives).

PREFERRED JOB REQUIREMENTS
Work Experience:
  • Experience in Manufacturing, Quality or Engineering including 4 major validation subjects (e.g. Computer, Equipment, Cleaning, Process, etc.).
  • Experience with the following: - QMS - ISO13485:2016 - 21 CFR 820 QSR, 21 CFR Part 11 Electronic Signature, 21 CFR 801 Labeling - GAMP Good Practice Guide: IT Infrastructure Control and Compliance (GAMP 5) - ISO / Customer / Regulator Audits - FDA Product and Establishment Registration - GS1 / GUDID Management - Quality Management System / Medical device environment experience.
  • Proficient in MS Word, Project, Excel.
  • Experience in people and process management.
  • Continuous improvement and Kanban related project experience

Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization.
The anticipated salary range for this position:
$101,000.00 - $152,000.00 Annual
The actual salary will vary based on applicant's location, education, experience, skills, and abilities. This role is bonus and/or incentive eligible. Medline will not pay less than the applicable minimum wage or salary threshold.
Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions, paid time off, as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp. For a more comprehensive list of our benefits please click here.
We're dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here.
Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.

What Medline Industries employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Medline logo

About Medline

Sourced by ZipRecruiter

Medline Industries, LP is the leading nationwide supplier of medical, surgical and pharmaceutical products to hospitals, nursing homes, HME providers, surgery centers, physician offices and home care/hospice settings.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Winnetka, IL, US

Year founded

1966

View All Medline Jobs

Apply