Senior Validation & Compliance Engineer#26-15629
$50.39-$53.52 per hour
Remote, KS
All On-site
Job Description
Our Client, a Life Sciences, Biotechnology and Laboratory Services company, is looking for a Senior Validation & Compliance Engineer for their Topeka, KS/Indianapolis IN/Kansas City, KS/ St. Louis, MO/Columbus, OH location.
Responsibilities:
Develop, execute, and document commissioning, qualification, and validation protocols (IQ/OQ/PQ) for new and modified equipment, utilities, and facilities.
Author and review qualification documents, test scripts, deviation reports, and summary reports.
Perform risk-based commissioning and qualification activities in accordance with FDA, EMA, and internal quality standards.
Coordinate closely with engineering, quality assurance, validation, and operations teams throughout the C&Q lifecycle.
Support technology transfer, process validation, and handover to manufacturing.
Participate in deviation investigations, CAPA implementation, and continuous improvement of CQV processes.
Requirements:
Mid to Senior level (typically 3-10+ years in CQV within pharmaceutical manufacturing)
ICONMA is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to any status protected by applicable law
$50.39-$53.52 per hour
Remote, KS
All On-site
Job Description
Our Client, a Life Sciences, Biotechnology and Laboratory Services company, is looking for a Senior Validation & Compliance Engineer for their Topeka, KS/Indianapolis IN/Kansas City, KS/ St. Louis, MO/Columbus, OH location.
Responsibilities:
Develop, execute, and document commissioning, qualification, and validation protocols (IQ/OQ/PQ) for new and modified equipment, utilities, and facilities.
Author and review qualification documents, test scripts, deviation reports, and summary reports.
Perform risk-based commissioning and qualification activities in accordance with FDA, EMA, and internal quality standards.
Coordinate closely with engineering, quality assurance, validation, and operations teams throughout the C&Q lifecycle.
Support technology transfer, process validation, and handover to manufacturing.
Participate in deviation investigations, CAPA implementation, and continuous improvement of CQV processes.
Requirements:
Mid to Senior level (typically 3-10+ years in CQV within pharmaceutical manufacturing)
ICONMA is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to any status protected by applicable law
Job ID: 521303247
Originally Posted on: 5/15/2026
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