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Senior Validation Engineer Ii Jobs (NOW HIRING)

Syner-G

Sr. Validation Engineer

San Diego, CA · On-site

The Sr. Validation Engineer will serve as a subject matter expert, support complex technical projects, and provide guidance to junior team members. KEY RESPONSIBILITIES (This list is not exhaustive ...

Syner-G

Sr. Validation Engineer

San Diego, CA · On-site

The Sr. Validation Engineer will serve as a subject matter expert, support complex technical projects, and provide guidance to junior team members. KEY RESPONSIBILITIES (This list is not exhaustive ...

Syner-G

Sr. Validation Engineer

Raleigh, NC · On-site

The Sr. Validation Engineer will serve as a subject matter expert, support complex technical projects, and provide guidance to junior team members. KEY RESPONSIBILITIES (This list is not exhaustive ...

GenScript/ProBio

(Sr.) Validation Engineer

Pennington, NJ

$80K - $120K/yr

The position reports to the Sr. Validation Manager and is responsible for supporting commissioning ... Coordinate validation activities with Manufacturing, Engineering, QA, QC, Automation, and external ...

Nvidia

Senior Validation Engineer

Hillsboro, OR · On-site

Become part of NVIDIA's world-class team as a Senior Validation Engineer in Hillsboro! For 25 years, our company has changed computer graphics, PC gaming, and accelerated computing. Driven by an ...

TekWissen LLC

Senior Validation Engineer

Portsmouth, NH · On-site

$35 - $45/hr

Senior Validation Engineer Location: Portsmouth, NH - 03801 Duration: 7 Months Job Type: Temporary Assignment Work Type: Hybrid Summary The CSV Engineer will act as an individual contributor ...

PSC Biotech

Senior Validation Engineer

Durham, NC

Your Role We are seeking an experienced Senior Validation Engineer to support commissioning, qualification, and validation activities for laboratory equipment, computerized systems, and analytical ...

Replimune

Senior Validation Engineer

Framingham, MA · On-site

$152K - $197K/yr

Summary of The Senior Validation Engineer will work as part of a larger validation team to ensure the biotech facility equipment, utilities, instrumentation and computerized systems are qualified and ...

PSC Biotech

Senior Validation Engineer

Durham, NC · On-site

Your Role We are seeking an experienced Senior Validation Engineer to support commissioning, qualification, and validation activities for laboratory equipment, computerized systems, and analytical ...

PSC Biotech

Senior Validation Engineer

Durham, NC

$120K - $140K/yr

Your Role We are seeking an experienced Senior Validation Engineer to support commissioning, qualification, and validation activities for laboratory equipment, computerized systems, and analytical ...

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How much do senior validation engineer ii jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for senior validation engineer ii in the United States is $64.77, according to ZipRecruiter salary data. Most workers in this role earn between $51.68 and $73.56 per hour, depending on experience, location, and employer.

Do senior validation engineers make good money?

Senior Validation Engineers typically earn competitive salaries that reflect their experience and expertise in validating manufacturing processes, equipment, or software in regulated industries like pharmaceuticals or biotech. Their compensation often includes benefits, bonuses, and opportunities for advancement, with salaries varying based on location, industry, and certifications such as GxP or IQ/OQ/PQ. Overall, they are considered well-compensated professionals in their field.

What is the difference between Senior Validation Engineer Ii vs Validation Engineer?

AspectSenior Validation Engineer IIValidation Engineer
CredentialsTypically requires 5+ years experience, relevant certifications (e.g., GxP, GMP), and advanced technical skillsUsually 1-3 years experience, basic certifications, foundational validation knowledge
Work EnvironmentWorks in regulated industries like pharmaceuticals, biotech, or medical devices, often leading validation projectsSupports validation activities under supervision, often in manufacturing or R&D settings
ResponsibilitiesDesigns, executes, and reviews validation protocols, mentors junior staff, ensures complianceAssists in executing validation protocols, documents results, and supports validation team

The Senior Validation Engineer II typically has more experience, takes on leadership roles, and handles complex validation projects. Validation Engineers focus on executing validation tasks and supporting validation processes. Both roles are essential in regulated industries, but the senior role involves greater responsibility and expertise.

What are the most commonly searched types of Validation Engineer Ii jobs? The most popular types of Validation Engineer Ii jobs are:
What states have the most Senior Validation Engineer Ii jobs? States with the most job openings for Senior Validation Engineer Ii jobs include:
Senior Validation Engineer Ii jobs near you

Validation Engineer

Corium Innovations

Grand Rapids, MI

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 3 days ago

Job description

Corium Innovations is seeking a Validation Engineer II/Sr. Validation Engineer who will be responsible for the maintenance and execution of the site validation programs including equipment, facilities, utilities, lab instrumentation and computer systems.  This includes successfully working with other departments, contract resources, and customers/vendors (as applicable) to plan, develop, maintain and execute validation and qualification activities.  This position will also be involved with site audit activities, investigations, change management evaluation and qualified utility ownership. The Sr. Validation Engineer is responsible for performing appropriate validation/qualification activities (IQ/OQ/PQ) and other system support activities to meet department, site and corporate objectives. This position involves the review and reporting of data, annual review and routine qualification/verification activities required for all systems.
Your most Innovative career move is here!
At Corium Innovations, we’ve led the way in innovating drug delivery technologies for millions of patients whose GI systems just can’t tolerate pills, who can’t remember to take their meds as directed, or who have needle-phobia. This is only the beginning! There’s so much more to deliver, and we need YOU to do it!
Our Purpose is to create, develop and manufacture innovative healthcare products for partners that deliver superior value to patients.
Our Goal is to be the best-in-class specialty CDMO through the use of innovative technologies and superior execution.
Our Company Values are core to our positive and people-centric culture which inspires all of us to come to work every day on behalf of our people, our partners, our customers, and our patients. Through our four core values, we put people first and create opportunities to make each day better than the last.
  • Celebrate Individuals: We’re looking for talent who will celebrate the uniqueness of each of our team members by encouraging everyone to bring their authentic self to work.
  • Successful Together: We believe we’re better together, so we prioritize teamwork as we work to achieve our shared vision knowing each one of us has an important role to play.
  • Embrace Innovation: We embrace new challenges and opportunities while encouraging creative thinking and innovative solutions to best meet the needs of our people and our partners.
  • Pride in Ownership: We take pride in owning our progress and successes, feeling empowered to pursue our growth to reach our full potential. And we hope you will too!
Responsibilities:
  • Development of validation or qualification deliverables, performing testing, verification, calibration, and routine maintenance of equipment, facilities, utilities, lab instruments and computer systems.
  • Develop and maintain procedures for qualification utilizing known industry best practices.
  • Utility and functional area reporting.
  • Quality system interaction (investigation, CAPA, change control)
  • Asset Management System ownership and maintenance
  • Continuous Improvement and other special projects in the Engineering Services functional area.
Qualifications:
  • Bachelor’s degree in a STEM field.
  • 5+ Years’ experience in the pharmaceutical industry.
  • Strong knowledge of FDA/cGMP/ISO requirements.
  • Knowledge of GMP Quality Systems and working knowledge of regulatory requirements.
  • Previous hands-on experience with equipment, facilities, utilities, lab instruments and computer system qualification (IQ/OQ/PQ), requirements documents, impact assessments, and summary reports preferred.
  • Previous hands-on experience with lab instrumentation and calibration, including but not limited to HPLC/UHPLC, GC, Dissolution Baths.
  • Cleanroom and qualified utility monitoring and qualification experience preferred.
  • Demonstrated analytical skill/problem solving skills. 
  • Must have good organizational skills, able to multi-task, and be capable of adjusting to changing priorities.
  • Self-starter
  • Excellent interpersonal and communication skills, both written and verbal.
Benefits:
  • Highly competitive benefits program including medical, dental, vision, flexible spending accounts, life insurance, disability insurance, and employee assistance program.
  • 401(k) retirement savings account with a company match and immediate vesting.
  • 12 paid holidays.
  • Competitive paid vacation plan plus ~1 additional week of paid time off for our annual holiday shutdown.

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