Able to work cooperatively and provide direction, as appropriate, to other members of the Validation Team, Engineering, Quality, and Manufacturing in the design and performance of qualification and ...
Able to work cooperatively and provide direction, as appropriate, to other members of the Validation Team, Engineering, Quality, and Manufacturing in the design and performance of qualification and ...
Seeks guidance from and collaborates with senior validation engineers; may informally assist with onboarding or knowledge sharing for newer team members. * Maintains regular and consistent attendance ...
Seeks guidance from and collaborates with senior validation engineers; may informally assist with onboarding or knowledge sharing for newer team members. * Maintains regular and consistent attendance ...
Able to work cooperatively and provide direction, as appropriate, to other members of the Validation Team, Engineering, Quality, and Manufacturing in the design and performance of qualification and ...
Able to work cooperatively and provide direction, as appropriate, to other members of the Validation Team, Engineering, Quality, and Manufacturing in the design and performance of qualification and ...
Senior Validation Engineer Responsibilities: * Author, revise, and execute CQV protocols and readiness checklists * Support vendor qualification wrapper execution * Execute IOQ/PQ protocols and ...
Senior Validation Engineer Responsibilities: * Author, revise, and execute CQV protocols and readiness checklists * Support vendor qualification wrapper execution * Execute IOQ/PQ protocols and ...
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Quick apply
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Senior Validation Engineer
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Senior Validation Engineer
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Senior Validation Engineer
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Senior Validation Engineer
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Quick apply
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Senior Validation Engineer
Princeton, NJ · On-site
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Senior Validation Engineer
Princeton, NJ · On-site
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Quick apply
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Senior Validation Engineer
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Senior Validation Engineer
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Quick apply
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Senior Validation Engineer
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Senior Validation Engineer
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Senior Validation Engineer
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Senior Validation Engineer
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
In this role, you will work closely with senior validation engineers and cross-functional project teams to support the qualification and testing of complex automation systems for our clients. This is ...
In this role, you will work closely with senior validation engineers and cross-functional project teams to support the qualification and testing of complex automation systems for our clients. This is ...
Senior Validation Engineer
$87K - $120K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Senior Validation Engineer
$87K - $120K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Senior Validation Engineer
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Senior Validation Engineer
$87K - $94K/yr
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Quick apply
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Quick apply
Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...
Senior Validation Engineer (CSV), Biotechnology - (JP15063) Location: Holly Springs, NC. 27540 Employment Type: Contract Business Unit: Commercial Drug Product Duration: 9+ months (with likely ...
Senior Validation Engineer (CSV), Biotechnology - (JP15063) Location: Holly Springs, NC. 27540 Employment Type: Contract Business Unit: Commercial Drug Product Duration: 9+ months (with likely ...
Sr Validation Engineer information
See salary details
$34.86 - $40.67
4% of jobs
$40.67 - $46.48
10% of jobs
$51.18 is the 25th percentile. Wages below this are outliers.
$46.48 - $52.29
14% of jobs
$52.29 - $58.11
13% of jobs
The median wage is $62.47 / hr.
$58.11 - $63.92
13% of jobs
$63.92 - $69.73
17% of jobs
$71.91 is the 75th percentile. Wages above this are outliers.
$69.73 - $75.55
13% of jobs
$75.55 - $81.36
9% of jobs
$81.36 - $87.17
3% of jobs
$87.17 - $92.99
2% of jobs
$92.99 - $98.80
3% of jobs
$34
$64
$98
How much do sr validation engineer jobs pay per hour?
As of Jun 28, 2026, the average hourly pay for sr validation engineer 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.
What are some common challenges a Sr Validation Engineer faces when managing multiple validation projects simultaneously?
A Sr Validation Engineer often manages several validation projects at once, which can present challenges such as coordinating timelines, ensuring compliance with regulatory standards, and balancing cross-functional communication. Keeping detailed documentation and staying organized are essential, as unexpected equipment issues or shifting project priorities may arise. Successful engineers proactively communicate with quality, manufacturing, and R&D teams to mitigate risks, maintain project momentum, and deliver results within required deadlines.
What are Sr Validation Engineers?
Sr Validation Engineers are experienced professionals responsible for ensuring that products, systems, or processes meet regulatory standards and function as intended. They lead validation projects, develop protocols, oversee testing, and document results to confirm compliance with industry regulations, such as those from the FDA or ISO. Their work is essential in industries like pharmaceuticals, biotechnology, and manufacturing, where product quality and safety are critical. Senior validation engineers also mentor junior staff and help improve validation processes within their organizations.
What are the key skills and qualifications needed to thrive as a Sr Validation Engineer, and why are they important?
To thrive as a Sr Validation Engineer, you need a solid background in engineering or life sciences, extensive experience with validation protocols, and a strong understanding of regulatory standards such as FDA, GMP, or ISO. Expertise in using validation software, risk assessment tools, and familiarity with documentation management systems is typically required, along with certifications like Six Sigma or ASQ CQE being advantageous. Exceptional problem-solving abilities, attention to detail, and effective communication skills help you lead teams and interact with cross-functional departments. These competencies are crucial for ensuring products and processes meet compliance standards, maintain quality, and support organizational success.
What is the difference between Sr Validation Engineer vs Validation Engineer?
| Aspect | Sr Validation Engineer | Validation Engineer |
|---|---|---|
| Required Credentials | Bachelor's/Master's in Engineering, certifications like CQE or ASQ, experience in validation processes | Bachelor's in Engineering or related field, some certifications preferred, less experience required |
| Work Environment | Pharmaceutical, biotech, or manufacturing industries; leading validation projects | Supporting validation tasks under supervision, often in similar industries |
| Employer & Industry Usage | Used by companies requiring compliance with FDA, ISO, or GMP standards | Commonly used in manufacturing and quality assurance roles |
The main difference between a Sr Validation Engineer and a Validation Engineer lies in experience, responsibility, and expertise. The Sr Validation Engineer typically leads validation projects, has more advanced certifications, and plays a strategic role in compliance. Validation Engineers support validation activities and often work under supervision. Both roles are essential in regulated industries like pharmaceuticals and manufacturing, but the senior role involves greater leadership and technical oversight.
More about Sr Validation Engineer jobs
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What states have the most Sr Validation Engineer jobs? States with the most job openings for Sr Validation Engineer jobs include:
What job categories do people searching Sr Validation Engineer jobs look for? The top searched job categories for Sr Validation Engineer jobs are:
Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 6 days ago
AstraZeneca rating
8.6
Based on 43 frontline employees who took The Breakroom Quiz
16th of 73 rated pharmaceutical
Job description
Role is heavily focused to support the key site digital/software/automation transformation and related validation activities. The first two years will focus on validation of digital tools (MES systems, software, etc) and may require continued administrative support of this system.
Responsible to perform adequate and comprehensive qualification and validation of equipment, processes, products, and facilities at the Redwood City site to support the site goals and targets.
Responsible for assuring the design, installation, implementation, data integrity and validation of computer systems meet all applicable industry standards and regulatory requirements to support the site goals and targets.
System or business owner and oversee the system from implementation ensuring proper documentation at every phase.
Key Accountabilities:
Essential Requirements:
Preferred Qualifications:
Knowledge of hardware and/or software integration
The annual base pay (or hourly rate of compensation) for this position ranges from $ 101,643.20 - $152,464.80. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
23-Jun-2026
Closing Date
09-Jul-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.
Responsible to perform adequate and comprehensive qualification and validation of equipment, processes, products, and facilities at the Redwood City site to support the site goals and targets.
Responsible for assuring the design, installation, implementation, data integrity and validation of computer systems meet all applicable industry standards and regulatory requirements to support the site goals and targets.
System or business owner and oversee the system from implementation ensuring proper documentation at every phase.
Key Accountabilities:
- Work effectively with others from diverse backgrounds and demonstrate capability to adapt to new, different, or changing requirements. Display strong moral principles and work ethics while demonstrating initiative. Maintain a professional presence and display responsible behaviors
- Support implementation of the Site Digital Technology Strategy and roadmap: architect key strategic digital transformation initiatives aligned to business priorities and value targets.
- Knowledge and experience developing and leading CSV and Life-cycle management activities to support GxP conforming systems, facilities, manufacturing and laboratory systems
- Evaluate equipment and processes to identify critical parameters based upon potential impact on product quality attributes
- Prepare qualification, requalification, and process validation protocols, analyzes applicable data, and prepares final reports in compliance with relevant regulations, industry practices, and AZ policies and procedures
- Perform and document field verification of equipment, instruments, and facilities as required by approved protocols
- Assess accuracy of P&ID, Electrical drawing to support validation and change control
- May provide supervision and training for less experienced or entry-level validation personnel, including review and enhancement of draft protocols, oversight of data collection, review/approval of raw data and assembled qualification packages
- Provide supervision and training for contract validation personnel, including review and enhancement of draft protocols, oversight of data collection, review/approval of raw data and assembled qualification packages
- Perform risk assessment on proposed changes, document change control deliverables with respect to validation requirements
- Complete, review, and/or approve risk assessments for instruments, equipment, processes, and products.
- Analyze data and information to determine whether processes, equipment, and products are within an appropriate state of control during qualification and validation as well as in assessing the need for requalification / revalidation on a periodic basis
- Prepare and/or evaluate change controls to ensure that equipment, products, processes, and facilities remain in qualified, validated state, including definition of appropriate requirements in change control documents, completion of identified action, and preparation of applicable reports and data packages
- Identify and investigate unusual or unexpected events, data, or sources of variation during the development and performance of qualifications/validations; assess and document the impact upon qualification or validation as applicable, and recommend appropriate corrective/preventive actions
- Coordinate assigned qualification projects as needed with other departments as needed
- Ensure that work is performed in accordance with applicable regulations, industry guidelines and practices, approved procedures and cGMP
- Other responsibilities as assigned by department management
Essential Requirements:
- Entry-level Master's/ PhD degree in engineering, science, technology, or related field (OR) Bachelor's degree with 3+ years of relevant experience.
- At least 3 years' experience in independent development, writing and performance qualifications / validation
- Experience in and knowledge of qualification of control systems and computer system validation
- Proven capability to assess processes, equipment and products for sources of variation
- Ability to analyse data and reach appropriate solutions
- Ability to perform and appropriately document deviations and investigations
- Must have excellent analytical skills and attention to detail. Work requires a high degree of accuracy in complex documentation; Able to work cooperatively and provide direction, as appropriate, to other members of the Validation Team, Engineering, Quality, and Manufacturing in the design and performance of qualification and validations.
- Must have the ability to learn technical subject matter quickly and integrate knowledge into previously known information
- Must effectively evaluation information collected from various sources and determine impact upon controlled state of processes, equipment, facilities, and products
- Must be goal oriented and quickly adaptable to new situation
- Excellent technical writing and verbal communication skills.
- Must be goal oriented and quickly adaptable to new situation
- Excellent technical writing and verbal communication skills
- Experience with Process Engineering or setting up new equipment- (URS, PID, DQ, IQ, OQ, PQ)
- Experience working with digital tools and applications related to reporting, documentation, and analysis.
Preferred Qualifications:
- Ability to read P&IDs and electrical drawings
- Working knowledge of FDA guidance on Process Validation and Computer System validation
- Experience with various programming to support digital/software validation
Knowledge of hardware and/or software integration
The annual base pay (or hourly rate of compensation) for this position ranges from $ 101,643.20 - $152,464.80. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
23-Jun-2026
Closing Date
09-Jul-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.
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