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Validation Engineer Ii Jobs (NOW HIRING)

Validation Engineer II

Windsor, CO ยท On-site

$90K - $100K/yr

Core Hours Monday - Friday, 8:00 am - 5:00 pm Purpose and Scope The Validation Engineer II is responsible for independently planning, executing, and documenting validation activities in a sterile ...

Validation Engineer II

Windsor, CO ยท On-site

$90K - $100K/yr

Core Hours Monday - Friday, 8:00 am - 5:00 pm Purpose and Scope The Validation Engineer II is responsible for independently planning, executing, and documenting validation activities in a sterile ...

Validation Engineer 2

Austin, TX ยท On-site

$55 - $60/hr

Bachelor's in Electrical Engineering or Computer Engineering with 2+ years of related experience ... Writes comprehensive electrical & functional test plans for the processor interface validation of ...

Core Hours Monday - Friday, 8:00 am - 5:00 pm Purpose and Scope The Validation Engineer II is responsible for independently planning, executing, and documenting validation activities in a sterile ...

Validation Engineer 2

Austin, TX ยท On-site

$56 - $59/hr

... validation and 2-8 years experience in semiconductor industry. * Demonstrated ability to grasp new technical concepts quickly. * Hardware description languages (e.g. Verilog). * Strong programming ...

POSITION SUMMARY Validation Engineer II drives compliance and manufacturing readiness across Empower's 503A and 503B operations through validation activities supporting sterile and non-sterile ...

Validation Engineer II drives compliance and manufacturing readiness across Empower's 503A and 503B operations through validation activities supporting sterile and non-sterile manufacturing. This ...

Our Validation Engineers will be involved with the qualification and requalification of equipment ... * 2 - 5 years of experience in at least one of the following areas: equipment/utility ...

Validation Engineer II

Sturgeon Bay, WI ยท On-site

$83K - $105K/yr

We are seeking a highly motivated Validation Engineer onsite at one of our five sites: Cranberry Twp., Sturgeon Bay, WI, Suffield, CT, Staunton, VA or Cranston, RI sites, to lead and support ...

Validation Engineer II

Cranberry Township, PA ยท On-site

$83K - $105K/yr

We are seeking a highly motivated Validation Engineer onsite at one of our five sites: Cranberry Twp., Sturgeon Bay, WI, Suffield, CT, Staunton, VA or Cranston, RI sites, to lead and support ...

Validation Engineer II

Suffield, CT ยท On-site

$83K - $105K/yr

We are seeking a highly motivated Validation Engineer onsite at one of our five sites: Cranberry Twp., Sturgeon Bay, WI, Suffield, CT, Staunton, VA or Cranston, RI sites, to lead and support ...

Validation Engineer II

Staunton, VA ยท On-site

$83K - $105K/yr

We are seeking a highly motivated Validation Engineer onsite at one of our five sites: Cranberry Twp., Sturgeon Bay, WI, Suffield, CT, Staunton, VA or Cranston, RI sites, to lead and support ...

Validation Engineer II

Cranston, RI ยท On-site

$83K - $105K/yr

We are seeking a highly motivated Validation Engineer onsite at one of our five sites: Cranberry Twp., Sturgeon Bay, WI, Suffield, CT, Staunton, VA or Cranston, RI sites, to lead and support ...

Software Validation Engineer 2

Austin, TX ยท On-site

$70K - $105K/yr

Software Validation Engineer 2 Life Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living. The Software Validation Engineer will lead and support software ...

$70K - $105K/yr

Software Validation Engineer 2 Life Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living. The Software Validation Engineer will lead and support software ...

Be Seen First

... II certified, underscoring our strict commitment to quality, environmental responsibility, and data security. Our industry-leading capabilities are further validated by numerous awards in ...

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Validation Engineer Ii information

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How much do validation engineer ii jobs pay per hour?

As of Jul 15, 2026, the average hourly pay for validation engineer ii in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Validation Engineer Ii position, and why are they important?

To thrive as a Validation Engineer II, you need a strong background in engineering principles, quality assurance methodologies, and experience with validation protocols, typically supported by a bachelor's degree in engineering or a related field. Proficiency with industry-specific tools such as statistical analysis software, ERP systems, and knowledge of regulatory standards like GMP or ISO is highly valued, and certifications like ASQ are advantageous. Excellent problem-solving, attention to detail, and effective communication are key soft skills for this role. These competencies are essential to ensure products and processes meet rigorous compliance and quality standards, minimizing risks and ensuring project success.

What are the typical responsibilities of a Validation Engineer II?

A Validation Engineer II is responsible for planning, executing, and documenting validation activities for equipment, systems, and processes to ensure compliance with industry and regulatory standards. This includes developing and reviewing protocols, analyzing test data, troubleshooting issues, and supporting audits or inspections. You can expect to work closely with cross-functional teams such as quality assurance, manufacturing, and R&D to coordinate validation efforts and implement continuous improvements. The role offers opportunities to expand both technical expertise and project management skills, making it a strong stepping stone for career advancement in engineering and quality fields.

What is a Validation Engineer II job?

A Validation Engineer II is responsible for ensuring that processes, systems, and products meet regulatory and quality standards. They develop and execute validation protocols, perform testing, analyze data, and document results to maintain compliance with industry regulations. This role typically requires experience in validation methods, technical problem-solving, and collaboration with cross-functional teams. Validation Engineers II work in industries such as pharmaceuticals, medical devices, and manufacturing to ensure product reliability and safety.

More about Validation Engineer Ii jobs
What cities are hiring for Validation Engineer Ii jobs? Cities with the most Validation Engineer Ii job openings:
What are the most commonly searched types of Validation Engineer Ii jobs? The most popular types of Validation Engineer Ii jobs are:

$84K - $127K/yr

Full-time

Medical, Retirement, PTO

Posted 7 days ago


Job description

Work Your Magic with us!Start your next chapter and join MilliporeSigma.

Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.


Your Role:

MilliporeSigma in Bedford, MA is hiring a Product Validation Engineer 2. As a member of the R&D Validation & Applications Center (VAC) Engineering team, you will actively participate on filtration product development teams to understand the new product and its applications. Your contribution includes development and implementation of an efficient and thorough validation test strategy which ensures robust product performance specifications based on product design and intended applications.

Responsibilities:

  • Authoring the validation test protocol, managing lab test requests, test execution, data analysis and authoring the report
  • Participate in process and product development supporting DOE studies and data analyses and creation of the product design specifications and risk assessments
  • Collaborate with Operations, Product Management, and Field Marketing to aid in product/process change requests, raw material qualifications, and customer applications
  • Hands-on design and development of new test methods, test equipment, and measurement systems which are utilized to characterize and validate new products, including troubleshooting, repairs, and identifying and implementing equipment upgrades/new technology and planning, documenting, and executing test method validations
  • Effectively interact with other groups, such as R&D development teams, Quality, Manufacturing, Engineering Services, Facilities, EHS, and Finance.

This position may include occasional travel to our manufacturing facilities <10%

Who You Are

Minimum Qualifications:

  • Bachelor's degree in Chemical Engineering, Biomedical Engineering, Mechanical Engineering, Physics, Materials Science or other Engineering or Scientific field with 4+ years of experience in process or product development/validation

-OR-

  • Master's degree in Chemical Engineering, Biomedical Engineering, Mechanical Engineering, Physics, Materials Science or other Engineering or Scientific field with 3+ years of experience in process or product development/validation

-AND-

  • 2+ years of experience with FMEA/risk analysis, product failure and root cause analysis
  • 3+ years of experience with process and product/equipment validations (IQ/OQ/PQ), authoring formal protocols and reports utilizing Good Documentation Practice (GDP)

Preferred Qualifications:

  • Experience in Medical Device or Life Science industries
  • Experience with filtration and chromatography products
  • Experience with Product Development Process (PDP) and working on cross functional teams
  • Experience in statistical analysis tools such as Capability, Gage R&R, DOE using Minitab
  • Capable in the development and execution of test method validations
  • Knowledge of applicable FDA Regulations, USP requirements, Regulatory requirements for products used in biopharmaceutical/med device industry
  • Experience in equipment troubleshooting and repairs

Pay Range for this position: $84,900 - $127,300

The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here.


What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Employment Type: FULL_TIME