Validation Specialist
Karwell TechnologiesDenver, CO
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Overview
Remote
On-site
Job Description
Roles & Responsibilities:
- Support cleaning validation activities, protocol execution, sampling, and documentation.
- Perform temperature mapping and requalification of controlled temperature units.
- Execute IQ/OQ/PQ, requalification, and periodic review for GMP equipment and utilities.
- Support commissioning, installation, and qualification of new or modified equipment.
- Assist with equipment troubleshooting alongside Engineering and Operations.
- Generate validation documentation following cGMP, GDP, and SOP requirements.
- Support validation lifecycle activities, change controls, investigations, and CAPAs.
- Participate in audit readiness and regulatory inspection support.
- Bachelor's degree in Engineering, Life Sciences, or related discipline required.
- 5+ years of hands-on validation experience with GMP equipment and utilities.
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FAQs About Validation Specialist Jobs at Karwell Technologies
What is the work location for this position at Karwell Technologies?
This job at Karwell Technologies is located in Denver, CO, according to the details provided by the employer. Some roles may also include multiple work locations depending on the requirement.
What pay range can candidates expect for this role at Karwell Technologies?
Employer has not shared pay details for this role.
What employment applies to this position at Karwell Technologies?
The employer has not provided this information. This may be discussed during the hiring process.
What is the process to apply for this position at Karwell Technologies?
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