Medvacon – San Diego, CA – MEDVACON is working with our Biotech client located in San Diego on a key position for a SENIOR cGMP Quality Validation Engineer with a solid Biotech background. THIS IS NOT AN IT JOB Our client is looking for a true blend of technical ability coupled with leadership and team building skills…someone ready for the next step in their career. Responsibilities Responsible for performing manufacturing processes validation, cleaning validation, and equipment validation. This includes… and cleaning validation Requires knowledge of FDA regulated biotechnology or drug validation requirements (e.g., 21 CFR 210, 211 or 21 CFR 820 or ICH Q7) Experience executing validation projects for biotech or pharmaceutical production projects Must have specific knowledge of validation methodologies and principles Strong technical writing and analytical skills Expertise in risk management and application of FMEAs to validations Understand mRNA, pDNA manufacturing process a plus The company…