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Per Diem Validation Engineer Jobs (NOW HIRING)

Per Diem Driver

Ludlow, VT Β· On-site

$20/hr

Our mission is to provide educational and introspective programming to foster a sober and ... Valid driver's license with a clean driving record * Ability to pass a background check and motor ...

Our mission is to provide educational and introspective programming to foster a sober and ... Valid driver's license with a clean driving record * Ability to pass a background check and motor ...

Validation Engineer

Wilson, NC Β· On-site

$60K - $85K/yr

... initial validation and equipment/system requalification's. Will participate in equipment ... Schedules and executes equipment commissioning, qualification, and requalification's per Standard ...

Validation Engineer I

Pepperell, MA Β· On-site

$32 - $38/hr

Responsibilities for a Validation Engineer I involve validation equipment operation, protocol ... Pay Range The base hourly pay range for this position is $32.00 - $38.00 per hour. Disclosure ...

Validation Engineer I

Pepperell, MA Β· On-site

$32 - $38/hr

Job Summary Responsibilities for a Validation Engineer I involve validation equipment operation ... Pay Range The base hourly pay range for this position is $32.00 - $38.00 per hour. Disclosure ...

Per Diem Driver

Manhattan, NY Β· On-site

$26.27/hr

Per Diem Driver Jamaica Hospital Medical Center - Jamaica, NY Department: Transportation Schedule ... Valid New York State Driver's License (in good standing) * Valid Defensive Driving Certificate Core ...

Telematics Validation Engineer What We Can Offer A thoughtfully designed employee experience that ... Sit and or drive in a vehicle for testing for up to 8 hours per day * Continuously learn and ...

Validation Engineer I

Pepperell, MA Β· On-site

$32 - $38/hr

Responsibilities for a Validation Engineer I involve validation equipment operation, protocol ... Pay Range The base hourly pay range for this position is $32.00 - $38.00 per hour. Disclosure ...

Validation Engineer I

Pepperell, MA Β· On-site

$32 - $38/hr

Job Summary Responsibilities for a Validation Engineer I involve validation equipment operation ... Pay Range The base hourly pay range for this position is $32.00 - $38.00 per hour. Disclosure ...

As the Validation Engineer - CONTRACTOR, you will: * Perform validation for infotainment products ... Create/maintain test cases per product specifications * Utilize tracking system to report and track ...

Showing results 41-60

Per Diem Validation Engineer information

See salary details

$22

$51

$78

How much do per diem validation engineer jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for per diem validation 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 the difference between Per Diem Validation Engineer vs Validation Engineer?

AspectPer Diem Validation EngineerValidation Engineer
CredentialsTypically requires engineering degree, certifications varySimilar credentials, often with industry-specific certifications
Work EnvironmentContract-based, on-site or remote, often in healthcare or manufacturingFull-time, on-site or lab-based in various industries
Employer & IndustryContract roles in healthcare, pharmaceuticals, or manufacturingPermanent roles across multiple industries including pharma, biotech, and manufacturing

The Per Diem Validation Engineer and Validation Engineer roles share similar technical requirements and work environments. The main difference lies in employment type: Per Diem Validation Engineers typically work on short-term, contract basis, often in healthcare or manufacturing sectors, whereas Validation Engineers are usually full-time employees with ongoing responsibilities. Both roles focus on ensuring products and processes meet quality standards through validation procedures.

Are Per Diem Validation Engineers in demand?

Per Diem Validation Engineers are in demand in industries such as manufacturing, pharmaceuticals, and technology, where specialized validation skills are required for equipment and processes. The role often requires knowledge of regulatory standards and validation tools, and demand can vary based on industry growth and project needs.

Do Per Diem Validation Engineers make good money?

Per Diem Validation Engineers typically earn hourly wages that can vary based on experience, location, and industry. Since the role often involves short-term or flexible assignments, pay rates may be higher than salaried positions, but they may lack benefits like health insurance or paid time off. Overall, they can make competitive wages, especially with specialized skills and certifications in validation and quality assurance.

What cities are hiring for Per Diem Validation Engineer jobs?

Cities with the most Per Diem Validation Engineer job openings:

What are the most commonly searched types of Validation Engineer jobs?

The most popular types of Validation Engineer jobs are:

What states have the most Per Diem Validation Engineer jobs?

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

What are popular job titles related to Per Diem Validation Engineer jobs?

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

Infographic showing various Per Diem Validation Engineer job openings in the United States as of August 2026, with employment types broken down into 94% Full Time, 2% Part Time, and 4% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Validation Engineer (W)

The Woodlands, TX β€’ On-site

Cellipont Bioservices
Biotechnology Research and DevelopmentΒ β€’Β 51 - 200 employees

Full-time

Medical, Retirement, PTO

Re-posted 24 days ago


Job description

Bridging innovation to cure
Developing and manufacturing your cell therapies from benchtop to bedside
Job Summary
Cellipont Bioservices is growing, and we are looking for a Validation Engineer who believes in the bridge between client's discoveries to patient cures and who want to challenge the status quo and take Cellipont and its clients to the next level.
The Validation Engineer will be part of the Validation team and will participate in validation initiatives for our current and future cell therapy programs. This position plays a key role demonstrating the values, culture, and deliverables for the site.
The Validation Engineer in this role will be trained to support validation projects of medium complexity (equipment, utilities, facilities, processes, computerized systems, etc.) in areas such as executing validation approaches, qualification studies, documentation generation and review (protocols, risk-assessments, etc.), and execution alongside validation contractors. With support, they will collaborate with contractors and act as validation signatory representatives to review and approve validation lifecycle documentation for GMP use, accountable to management and regulatory agencies. Alongside and with guidance from the Validation management, this position will be part of establishing and maturing all aspects of the validation program required to maintain the cGMP facility for cell therapy.
This is an exciting position with great professional development opportunities with a quickly growing company. The ideal candidate has a strong understanding of CGMPs, is creative in their problem solving, and is flexible to accommodate shifting priorities in a fast-paced startup environment.
The Role
  • Support GMP validation projects of low to medium complexity (equipment, computerized systems, utilities, facilities, processes, temperature mapping, etc.) alongside in-house and contracted resources
  • Oversee qualification activities in cGMP validation best practices
  • As required, develop qualification and validation protocols, execute the associated studies, analyze the resulting data, and develop the final report
  • Support validation deviation investigations and determine assignable cause alongside Validation Lead and contractors
  • Review validation lifecycle documentation, including requirements, specifications, protocols, and reports
  • Support the Validation Team in any required activities to support the development, execution, or improvement of the Validation program
  • Understand the application of Data Integrity per 21 CFR Part 11
  • Experience and familiarity with the application of FDA, GLP, QSR, and cGMP regulations
  • Equipment qualification principles in a cGMP environment (IQ, OQ, PQ)
  • Understanding of the validation lifecycle in GMP settings
  • Knowledge of cGMP, GAMP, 21CFR part 11, GDP
  • Knowledge of pharmaceutical, manufacturing, and laboratory systems and equipment

The Candidate
  • Bachelor's Degree with 1+ years of cGMP experience (Pharmaceutical, Life Sciences industry cGMP environment) Master's Degree is a plus
  • Experience in the qualification of cell therapy equipment and cGMP environment is a plus
  • Excellent interpersonal skills with experience dealing with a diverse workforce
  • Strong multi-tasking ability in conjunction with proven organizational skills.
  • Ability to organize assigned tasks in a high paced environment and concurrently monitor tasks / assignments with others that may impact timely completion.
  • Highly proficient computer skills in Microsoft Office Suite - Word, Excel, PowerPoint and Outlook.
  • Able to quickly understand and learn new technologies
  • Creative in problem-solving abilities, able to think outside the box to find solutions
  • Self-motivated and self-starter, able to work independently with minimal supervision
  • Must be proactive, results oriented, and have strong attention to detail
  • Strong written and verbal communication skills (including technical writing skills)
  • May be required to work in controlled or clean room environments
  • Occasional stooping, bending, stretching, pushing, pulling, reaching and/or lifting to 25lbs.
  • Ability to sit, stand, walk and move within workspace for extended periods
  • Ability to perform repetitive tasks including hand to finger manipulations, grasping, pushing and pulling
  • Primarily office environment but will be required to enter laboratory or GMP process areas don proper gowning / lab coats or PPE such as safety glasses and shoes
  • Ability to work safely and effectively when working alone or working with others

Position Benefits
  • Opportunities for career growth within an expanding team.
  • Defined career path and annual performance review & feedback process.
  • Cross-functional exposure to other areas within the organization.
  • Robust benefit package designed for unique Health & Wellness needs, including coverage for your furry family members.
  • 401K strong employer match.
  • Tuition Reimbursement.
  • Employee Referral Bonuses.
  • Flexible work schedules and PTO based on role/level, increasing 1 PTO day each year and paid holidays
  • Gain experience in the cutting-edge cell therapy space.

"At Cellipont Bioservices, we look for candidates with an innate desire to serve. Our "family" approach ensures you will get the mentorship you need to develop a satisfying career here!"
Notice to Agency and Search Firm Representatives
Cellipont Bioservices does not accept unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Cellipont Bioservices employee by a third-party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Cellipont Bioservices. No fee will be paid if a candidate is hired for this position because of an unsolicited agency or search firm referral. Thank you.