Top 26201 Software Validation Engineer Jobs

Validation Engineer
Medline Industries —Hartland, WI
- $73,000 - $110,000 a year
- Full-time
- Bachelor of Science
- Writing skills
- Engineering
- Health insurance
- 401(k)
Quick Apply
Firmware Validation Engineer
Manpower Engineering —Foster City, CA
- $100 - $105 an hour
- Bachelor of Science
- 8 years
- Senior level
- Health savings account
- Disability insurance
Quick Apply
Firmware Validation Engineer
Software Technology Inc —Washington, DC
- Computer science
- Computer Science
- Software troubleshooting
Quick Apply
Data Engineer 894
Global Service Resources —Remote
- $55 - $60 an hour
- Contract
- Remote
- Computer Science
- Mid-level
- 3 years
- Health insurance
- Paid sick time
Quick Apply
9h
Contact Center Engineer
Brooksource —Remote
- $55 - $60 an hour
- Contract
- Remote
- Microsoft Excel
- Senior level
- Communication skills
- Health savings account
- Paid holidays
Quick Apply
2d
Software QA Engineer II
CRIO Inc —Remote
- $75,000 - $85,000 a year
- Full-time
- Remote
- Computer science
- Computer Science
- HIPAA
- Dental insurance
- Work from home
Quick Apply
Engineer I, Software Quality
FUJIFILM —Remote
- Remote
- Microsoft Excel
- Bachelor of Science
- Office
Software Validation Engineer
CREXENDO, INC —Tempe, AZ
- Computer science
- Computer Science
- Software troubleshooting
- Paid holidays
- Health insurance
Quick Apply
Software Engineer
Beacon Talent —Remote
- Full-time
- Remote
- Azure
- Mid-level
- 3 years
Quick Apply
Biomedical Engineer - Software Systems
Arthrex —Remote
- $94,000 - $190,000 a year
- Remote
- Mid-level
- Analysis skills
- Bachelor's degree
- Paid parental leave
- Dental insurance
Software Engineer in Test
PDQ —Remote
- Full-time
- Remote
- Research
- Mid-level
- Java
- Wellness program
- Health savings account
Quick Apply
13d
Software Development Engineer in Test
SmartRent —Phoenix, AZ
- Remote
- Computer science
- Computer Science
- Mid-level
- Paid parental leave
- Employee stock purchase plan
Quick Apply
Software Validation Engineer
Trelleborg Sealing Solutions US Inc —Plymouth, MN
- $90,000 - $100,000 a year
- Monday to Friday
- Hybrid work
- Computer science
- Computer Science
- Engineering
- Disability insurance
- Health insurance
Quick Apply
Software QA Engineer
Zoom —San Jose, CA
- $166,100 - $186,000 a year
- Full-time
- Remote
- 7 years
- Computer Science
- Windows
Rocket Booster SME
Modern Technology Solutions, Inc —Huntsville, AL
- 11+ years
- Analysis skills
- Senior level
- Disability insurance
- Health insurance
Project Engineer - Building Automation
Empowered Buildings —New York, NY
- $80,000 - $120,000 a year
- Extended hours
- Mid-level
- Continuous improvement
- JavaScript
- Health insurance
- Dental insurance
Quick Apply
6d
Senior Power Electronics Engineer
Micro Control Company —Fridley, MN
- $111,123 - $160,462 a year
- Full-time
- 5 years
- Master's degree
- Ability to lift 50 pounds
- Profit sharing
- Health savings account
Quick Apply
Sr Electrical Engineer, Last Mile Delivery & Technology, Last Mile Delivery & Technology
Amazon.com Services LLC —Bellevue, WA
- $137,300 - $185,700 a year
- Full-time
- 7 years
- Experience equivalent to degree accepted
- Senior level
- AD&D insurance
- Health insurance
Electrical Engineer
CONTROL AUTOMATION TECHNOLOGIES INC —Puerto Rico
- $50,000 - $75,000 a year
- Full-time
- Mid-level
- Analysis skills
- Electrical Engineering
- Health insurance
- Dental insurance
Quick Apply
R&D Engineer
Hayden Industrial, LLC. —Claremore, OK
- Full-time
- Background check
- 5 years
- Ability to lift 50 pounds
- Health savings account
- AD&D insurance
Quick Apply

I want to receive the latest job alert for Software Validation Engineer

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

Software Validation Engineer jobs near

Validation Engineer

Medline Industries -
Hartland, WI

Quick Apply

Job Details

Full-time
$73,000 - $110,000 a year

Benefits

Health insurance
401(k)
Paid time off
Employee assistance program

Qualifications

Incident investigation techniques for hazard identification
Project reporting
Biology
Statistics
Six Sigma Certification
Project engineering
Defect resolution root cause analysis
Master's degree in chemistry
Engineering development testing
Laboratory equipment performance testing and validation
Project documentation
ISO standards
Quality control statistical data analysis
Pharmaceutical regulatory compliance
Bachelor of Science
Writing skills
Engineering
Laboratory instrument validation
Equipment installation
Vendor coordination
Biomedical Engineering
Biotechnology
Mid-level
Master's degree in biology
Project management experience in manufacturing
Bachelor's degree in biology
Data summary reports
Quality reports
Minitab
Change management

Full Job Description

Job Summary

Responsible for the validation of facility utilities, and equipment processes for cGMP products such as pharmaceuticals, medical devices, and cosmetic products to adhere to 21 CFR 211/210, 21 CFR 820, and other applicable regulatory requirements. Assist in authoring and executing protocols to demonstrate that manufacturing processes are executed with consistent quality and results within a controlled environment. Responsible for managing and or performing revalidation, engineering studies to evaluate new products or components, change control assessments, and coordination of computer and test method validations of applicable products.

Job Description

Validate new and revalidate as appropriate existing equipment used in OTC/Cosmetic and medical device manufacturing.
Perform engineering studies to determine if projects are feasible.
Assist with measurement system analysis including Gage R&R.
Support product/design transfer activities including validations and creation of updates to documentation needed to manufacture OTC cosmetic and medical devices.
Support Change Assessment activities including assessment and qualification of changes to existing product components and implementation of products into manufacturing lines.
Support root cause investigations for non-conformances related to manufacturing validations.
Develop, prepare and install equipment and revise test validation procedures/protocols to ensure that a product is manufactured in accordance with appropriate regulatory agency validation requirement and current industry practices.
Responsible for IQ/OQ and PQ phases and implementation of validated SOPs.
Coordinate projects directly with vendors and service providers to ensure that all validation and installation requirements are being satisfied during the execution of protocols.
Develop timelines for all projects and ensure that deadlines and goals are being met. Frequently update management and team on progress.
Proactively work with members of the division or project team to identify issues that might delay the project; make recommendations to improve time lines for project completion.
Compile and analyze validation data, prepare reports, and make recommendations for changes and/or improvements.
Maintain all of the documentation pertaining to qualification and validation of assigned projects and equipment/systems.

REQUIRED EXPERIENCE

Education

Bachelor of Science Degree in Biology, Chemistry, or Engineering.

Work Experience

At least 2 years of validation experience in a cGMP Device or Drug environment.
Experience with validations of controlled environments or equipment validations in a regulated environment.
Experience with validation documentation and related change control.
Strong ability to manage multiple priorities, self-starter attitude, good oral and writing skills and the ability to work independently and as a team in an efficient manner.

PREFERRED QUALIFICATIONS

Masters of Science in Chemistry, Biology, Biotechnology, Chemical Manufacturing, Biomedical Engineering, or Engineering.
Six Sigma certification.
3 years of validation experience in a cGMP Device or Drug environment.
Process validation experience in a pharmaceutical or Medical Device manufacturing environment.
Experience with validation of various product types such as liquid products, solid dosage products, and multi-component products.
Experience in FDA regulated environment.
Experience with ISO 13485 and ISO 11607 standards.
Experience with Measurement System Analysis.
Experience with Minitab statistical analysis software.
Experience with root cause analysis.

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:

$73,000.00 - $110,000.00 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.

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.

Application Question(s):

Are you able to work on-site Monday through Friday?
Do you have prior experience with validation or similar in an FDA or cGMP regulated environment?

Experience:

validation, manufacturing, and/or process engineering: 3 years (Required)

Ability to Commute:

Hartland, WI (Required)

Ability to Relocate:

Hartland, WI: Relocate before starting work (Required)

Work Location: In person

Quick Apply

Refine Your Search

Software Validation Engineer jobs

Validation Engineer

Firmware Validation Engineer

Firmware Validation Engineer

Data Engineer 894

Contact Center Engineer

Software QA Engineer II

Engineer I, Software Quality

Software Validation Engineer

Software Engineer

Biomedical Engineer - Software Systems

Software Engineer in Test

Software Development Engineer in Test

Software Validation Engineer

Software QA Engineer

Rocket Booster SME

Project Engineer - Building Automation

Senior Power Electronics Engineer

Sr Electrical Engineer, Last Mile Delivery & Technology, Last Mile Delivery & Technology

Electrical Engineer

R&D Engineer

I want to receive the latest job alert for Software Validation Engineer

Related Searches

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected