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Validation Support Engineer Jobs (NOW HIRING)

Millstone

Senior Validation Engineer

Fall River, MA · On-site

Provide ongoing support to operations by troubleshooting issues related to validated processes and ... Mentor junior engineers or technicians as needed. * Project Management (Depending on Position Level)

CYNET SYSTEMS

Support Engineer

Hudson, NY · On-site

$38 - $41/hr

The role includes validating access to media applications and infrastructure after UPN changes, OU restructuring, and MFA updates. * After migrations, the Support Engineer will provide hypercare ...

Woodstock Sterile Solutions

$85K - $90K/yr

The Validation Engineer II prepares concise technical documentation, provides validation support to ... Business Development, Engineering, Manufacturing, Quality Assurance, Quality Control, and ...

Apple

Silicon Validation Engineer

Bodega Bay, CA

$184K - $324K/yr

As a DDR Silicon Validation Engineer, you will be at the forefront of innovation, performing ... Support ATE and Product Engineering teams for inter-operability tests and production ramp-up.

JS Consulting

Support Engineer

Tysons Corner, VA · On-site

Support Engineer * Must work 3-days/week onsite in Rockville, MD or Tysons Corner, VA * ONE 30 ... Execute manual and automated testing to validate fixes, identify regressions, and ensure system ...

Cooley LLP

Product Support Engineer

San Diego, CA · On-site

Partner with engineering to validate fixes and support release readiness Cross-Functional Collaboration * Act as connective tissue between support, product, engineering, and training * Communicate ...

INCOG

Principal Validation Engineer

Fishers, IN · On-site

The Principal Validation Engineer is responsible for understanding and implementing validation ... Serve as the main point of contact and technical lead for client validation support and technical ...

Cooley

Product Support Engineer

Santa Monica, CA

Partner with engineering to validate fixes and support release readiness Cross-Functional Collaboration * Act as connective tissue between support, product, engineering, and training * Communicate ...

Cooley

Product Support Engineer

Los Angeles, CA · On-site

Partner with engineering to validate fixes and support release readiness Cross-Functional Collaboration * Act as connective tissue between support, product, engineering, and training * Communicate ...

Cooley LLP

Product Support Engineer

Reston, VA

Partner with engineering to validate fixes and support release readiness Cross-Functional Collaboration * Act as connective tissue between support, product, engineering, and training * Communicate ...

Cooley LLP

Product Support Engineer

San Francisco, CA · On-site

Partner with engineering to validate fixes and support release readiness Cross-Functional Collaboration * Act as connective tissue between support, product, engineering, and training * Communicate ...

Cooley LLP

Product Support Engineer

New York, NY · On-site

Partner with engineering to validate fixes and support release readiness Cross-Functional Collaboration * Act as connective tissue between support, product, engineering, and training * Communicate ...

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Validation Support Engineer information

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How much do validation support engineer jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for validation support engineer 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 is a validation support engineer?

Validation Support Engineers are professionals who ensure that products, systems, or processes meet specific regulatory and quality standards before they are released or implemented. They are commonly found in industries such as pharmaceuticals, biotechnology, and manufacturing, where compliance and product quality are critical. Their responsibilities include developing and executing validation protocols, troubleshooting validation issues, and maintaining documentation to demonstrate compliance with regulatory requirements. Validation Support Engineers work closely with quality assurance teams, production staff, and regulatory bodies to ensure all processes meet necessary benchmarks. Their work is essential for ensuring safety, efficacy, and adherence to industry regulations.

What are the key skills and qualifications needed to thrive as a validation support engineer?

To thrive as a Validation Support Engineer, you need a solid background in engineering or life sciences, strong analytical skills, and experience with validation protocols and regulatory standards such as GMP or FDA. Familiarity with validation software tools (e.g., ValGenesis, TrackWise) and documentation systems is typically required, along with relevant certifications like Six Sigma or CQV. Excellent problem-solving abilities, attention to detail, and effective communication help you excel in cross-functional teams and ensure compliance. These skills are crucial for maintaining product quality, regulatory compliance, and minimizing operational risks within highly regulated industries.

What are some typical challenges a validation support engineer may encounter when coordinating with cross-functional teams?

Validation Support Engineers often work closely with quality assurance, manufacturing, and R&D teams to ensure products meet regulatory and performance standards. A common challenge is managing communication across departments with differing priorities or technical languages, which can sometimes lead to delays or misunderstandings. Proactively clarifying requirements, maintaining thorough documentation, and fostering strong working relationships are essential for overcoming these hurdles. Additionally, adapting to shifting project timelines and regulatory updates is a key part of the role.

What states have the most Validation Support Engineer jobs?

States with the most job openings for Validation Support Engineer jobs include:

What are popular job titles related to Validation Support Engineer jobs?

For Validation Support Engineer jobs, the most frequently searched job titles are:

Infographic showing various Validation Support Engineer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 72% Full Time, 22% Part Time, and 5% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Validation Engineer and CQV

Phoenix, AZ • On-site

RXinsider LTD.
Marketing • 11 - 50 employees
Learn more about RXinsider LTD.external

Other

Posted 8 days ago

Job description

About Medivant Healthcare

Medivant Healthcare is a U.S.-based pharmaceutical manufacturer specializing in sterile injectable generics for hospitals, clinics, and healthcare providers nationwide. Our FDA-registered facilities in Chandler and Deer Valley, Arizona, are dedicated to ensuring consistent product quality, regulatory compliance, and affordable medication access.

Position Summary

The Validation Engineer and CQV Associate supports validation documentation, data collection, and quality system activities in Medivant's sterile injectable facility. This entry-level role is ideal for recent graduates seeking hands-on cGMP and aseptic processing experience.

Key Responsibilities
  • Assist in execution of media fill studies and documentation.
  • Support area qualification and environmental monitoring tasks.
  • Help draft IQ/OQ/PQ protocols and assist execution.
  • Collect data for HVAC, WFI, and compressed air validation.
  • Assist in cleaning validation logs and sample documentation.
  • Participate in process validation protocol preparation.
  • Support change control documentation.
  • Assist in deviation data collection and preliminary reports.
  • Track CAPA activities and closure evidence.
  • Ensure cGMP compliance in all assigned tasks.
Qualifications

Required:

  • Bachelor's degree in Pharmacy, Biotechnology, Microbiology, Life Sciences, or related field.
  • 2-3 years of relevant experience is required
  • Understanding of aseptic and sterile processing.
  • Strong documentation and communication skills.
Preferred
  • Experience in sterile manufacturing or validation support.
  • Knowledge of QMS processes and cGMP environments.
Employment Details
  • Full-time onsite role at Medivant Healthcare facilities.
  • Standard work schedule: Monday-Friday.
  • Training provided for all validation and QMS procedures.

Please note that we are not providing H1B visa sponsorship for this role. Candidates will be solely responsible for managing and maintaining their own visa sponsorship status.

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