Cleaning Validation Specialist - Simply Biotech
Advanced degree preferred.-Minimum of 3-5 years of experience in cleaning validation within a GMP-regulated pharmaceutical manufacturing environment.-Strong understanding of GMP regulations, cleaning validation principles, and pharmaceutical manufacturing processes Email resumes to kbrace@talentzok.com or call 858.683.8559.
FULL DESCRIPTION:
The Cleaning Validation Specialist ensures compliance with GMP standards by developing, executing, and documenting cleaning validation activities in a pharmaceutical manufacturing environment. This role collaborates with production, quality assurance, and regulatory affairs to maintain contamination control and regulatory compliance.
The selected candidate will be responsible for:-Develop and review cleaning validation protocols, reports, and SOPs.-Execute validation studies, including surface and rinse sampling, swabbing, and TOC testing.-Analyze data, document findings, and ensure compliance with FDA, EMA, and GMP guidelines.-Identify process improvements and implement CAPAs for validation deviations.-Train staff on cleaning procedures and validation requirements.-Support audits and collaborate with cross-functional teams to align global best practices.
The selected candidate will also possess:-Education: Bachelor's in Chemistry, Microbiology, Engineering, or related field (advanced degree preferred).-Experience: 3-5 years in GMP-regulated cleaning validation.-Skills: Strong technical writing, analytical problem-solving, and regulatory knowledge.Salary Range: $42-$49/hr
For immediate and confidential consideration, please email your resume to kbrace@talentzok.com or call 858.683.8559.
More information can be found at www.simplybiotech.com