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Kaye Validator Jobs (NOW HIRING)

CRB

Senior Project Manager, CQV

Raleigh, NC · On-site

Familiarity with validation tools and processes, including environmental mapping and use of Kaye Validator * Ability to plan and execute Smoke / Airflow Visualization Studies * Interpersonal and ...

CRB

Senior Project Manager, CQV

Raleigh, NC · On-site

Familiarity with validation tools and processes, including environmental mapping and use of Kaye Validator * Ability to plan and execute Smoke / Airflow Visualization Studies * Interpersonal and ...

Intellectt INC

Sr. CQV Specialist

Raritan, NJ · On-site

Familiarity with Microsoft Office Suite and validation/compliance systems such as Maximo, Siemens EMS, Comet, Kneat, Kaye AVS, and Kaye ValProbe. Preferred Skills * Experience in aseptic ...

Kashiv Biosciences LLC

Facility Engineer

Piscataway, NJ · On-site

Perform Thermal Mapping on various biomedical freezers and refrigerators using Kaye Validator * Improve teamwork efficiency by implementing technically possible corrections * Maintain documentation ...

Quality Agents, LLC

Validation Intern

Rockville, MD · On-site

$17 - $22.25/hr

Introduction to validation tools and instrumentation, including Kaye Validators and wireless data loggers. * Hands-on training in technical writing and documentation practices in a regulated setting.

Quality Agents, LLC

Validation Intern

Rockville, MD · On-site

$35/hr

Introduction to validation tools and instrumentation, including Kaye Validators and wireless data loggers. * Hands-on training in technical writing and documentation practices in a regulated setting.

Quality Agents

Validation Intern

Rockville, MD · On-site

Introduction to validation tools and instrumentation, including Kaye Validators and wireless data loggers. * Hands-on training in technical writing and documentation practices in a regulated setting.

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How much do kaye validator jobs pay per hour?

As of Jun 5, 2026, the average hourly pay for kaye validator 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 some common challenges faced by Kaye Validators during equipment qualification processes?

Kaye Validators often face challenges such as troubleshooting sensor malfunctions, ensuring accurate data collection during temperature mapping, and adhering to strict regulatory standards. The role requires strong attention to detail, as even minor errors can impact equipment validation results. Additionally, working within production schedules and coordinating with quality assurance and engineering teams can present time management pressures. Effective communication and adaptability are key to overcoming these challenges and ensuring successful qualification.

What are the key skills and qualifications needed to thrive as a Kaye Validator Technician, and why are they important?

To thrive as a Kaye Validator Technician, you need a strong background in calibration, validation protocols, and knowledge of thermal validation processes, often supported by technical training or certification in metrology or engineering. Familiarity with Kaye Validator systems, data acquisition software, and temperature/humidity sensors is typically required. Attention to detail, analytical thinking, and effective communication are vital soft skills for ensuring accurate data analysis and clear reporting. These skills and qualifications are essential to maintain compliance with regulatory standards and ensure the reliability of critical temperature-controlled environments.

What is a Kaye Validator and what is it used for?

A Kaye Validator is a specialized temperature and process validation system used primarily in the pharmaceutical, biotechnology, and food industries. It is designed to accurately measure, record, and analyze temperature and other process parameters during validation studies, such as thermal mapping, sterilization, and environmental monitoring. The Kaye Validator helps ensure that equipment and processes meet regulatory requirements for safety and efficacy. These systems are often used to validate autoclaves, ovens, warehouses, and other controlled environments.
What cities are hiring for Kaye Validator jobs? Cities with the most Kaye Validator job openings:
Senior Project Manager, CQV

Senior Project Manager, CQV

CRB

Raleigh, NC • On-site

Full-time

Posted 23 days ago

Job description

Company Description
CRB's over 1,200 expert professionals drive innovative, life-changing and life-saving solutions for manufacturers in the life sciences and food and beverage industries. Our mission, vision, and core values put client satisfaction and employee experience at the center of everything we do.
As an AEC Firm we proudly specialize in industries that inherently carry important social responsibility - we recognize our impact and influence in the communities we serve and pursue corporate responsibility through the lens of people, community, and planet. From oncology and rare disorders to COVID-19 or alternative proteins, our design and construction projects are pioneering solutions addressing important issues such as food scarcity and global health.
Job Description
CRB is looking for an energetic, self-motivated individual for the role of Sr. Manager of Commissioning, Qualification and Validation (CQV). The Sr. Manager will support the integration and delivery of CQV services for our Life Sciences clients. Their focus will be to provide guidance on daily operations of the CQV team, including internal and external CQV resources, for all regional projects from proposal stage to facility turnover - this will include leading resources through regulatory requirements, devising and executing strategies, and meeting timelines with risk mitigation. This position requires a high level of organization, communication, leadership, and interpersonal skills that will be used to build strong relationships with internal and external clients. They will represent CRB in a professional manner, assist in winning work, and understand how their strategy directly impacts our collective success.
  • The Sr. Manager of CQV will provide guidance & support for daily operations of the CQV team, including internal and external CQV resources, for all regional projects from proposal stage to facility turnover
  • Manage and perform the development of validation protocols, the development of validation studies, data analysis, and compilation of the data and results into final reports
  • Review & Approve User Requirements Specifications (URS), Functional Specifications (FS), Design Specifications (DS), Change controls and equipment, and process Failure Mode and Effects Analysis (FMEA).
  • As a subject matter expert, represent these activities in discussions and communications with Clients and regulatory agencies
  • Collaborate in the development of specific CQV plans and ensuring integration with design and construction plans
  • Responsible for the implementation and execution of the periodic system reviews and requalification activities, as needed
  • Develop execution schedule and planning efforts on all ONEsolution projects
  • Interact with regulatory authorities during audits
  • Mentoring & training employees, both internal and external, on the CQV approach as it relates to each project
  • Supporting the development of internal qualification documents
  • Assess impact to validated status of new systems and changes to existing systems using a quality risk-based approach.

Qualifications
  • Bachelor's Degree in Architecture, Engineering, or Construction Management, or similar degree preferred, or equivalent years of relevant industry experience.
  • 9+ years of Commissioning, Qualification, Validation and Compliance experience in the Life Sciences and/or regulated Industry; Sound technical knowledge of both US and global regulatory requirements. Proficient in cGMP and SUPAC standards.
  • Demonstrated effective leadership and collaboration skills
  • Direct experience in managing Commissioning, Qualification and Validation deliverables
  • Excellent organizational, interpersonal, presentation, and communication skills
  • Commitment to technical excellence, as well as creating world-class experiences for our clients and employees
  • Knowledge of US FDA (21 CFR 210, 211, 810) and EU EMEA regulations, ISPE Baseline Guide 5 Commissioning and Qualification and ISPE Guideline Science and Risk-based Approach for the Delivery of Facilities, Systems, and Equipment, 2011
  • Experience using statistical, risk assessment, and process improvement tools.
  • Familiarity with validation tools and processes, including environmental mapping and use of Kaye Validator
  • Ability to plan and execute Smoke / Airflow Visualization Studies
  • Interpersonal and leadership skills necessary to communicate clearly, and effectively manage qualification/validation activities with all levels of personnel from various disciplines across the organization.
  • Flexible and willing to travel as needed

Additional Information
All your information will be kept confidential according to EEO guidelines.
CRB is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity Employer and it is our policy to provide equal opportunity to all people without regard to race, color, religion, national origin, ancestry, marital status, veteran status, age, disability, pregnancy, genetic information, citizenship status, sex, sexual orientation, gender identity or any other legally protected category. Employment is contingent on background screening.
CRB does not accept unsolicited resumes from search firms or agencies. Any resume submitted to any employee of CRB without a prior written search agreement will be considered unsolicited and the property of CRB. Please, no phone calls or emails.
CRB offers a complete and competitive benefit package designed to meet individual and family needs.
If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

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