QG
QRC Group
Validation Specialist-Methods Transfer
Aibonito, PRPresencialContratoTiempo completo
Publicado 20 ago 2026
The Methods Transfer - Validation Specialist is responsible for planning, executing, and documenting analytical method transfers, validations, verifications, and method improvement initiatives in compliance with regulatory requirements. This role ensures analytical methods are robust, reproducible, and suitable for their intended use across internal and external laboratories.
Requirements
- Bachelor’s or Master’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related discipline.
- Five years of experience in a regulated industry (pharmaceutical, biotech, or medical devices) in analytical development or quality control laboratory.
- Experience conducting method transfers and validations required.
- Technical writing and documentation ability.
- Bilingual (Spanish/English)(Write/Speak)
Resumen del puesto
Tipo de empleo
Tiempo completo
Habilidades requeridas
Analytical Method TransferMethod ValidationMethod VerificationAnalytical Method Improvement/OptimizationRegulatory Compliance (regulated industry requirements)Technical Writing and DocumentationQuality Control Laboratory OperationsCross-site and External Laboratory CoordinationExperimental Planning and ExecutionAnalytical Data Analysis and InterpretationEnsuring Method Robustness and ReproducibilityBilingual Communication (Spanish/English, written and spoken)
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