QRC Group, LLC
Validation Specialist-Methods Transfer
Aibonito, PRSur siteContratTemps plein
Publié 20 août 2026
Cet emploi est publié en ES
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)
Aperçu du poste
Type de poste
Temps plein
Compétences requises
Analytical Method TransferAnalytical Method ValidationMethod VerificationMethod Improvement and OptimizationRegulatory Compliance (regulated industry requirements)Technical Writing and DocumentationPlanning and Execution of Analytical StudiesRobustness and Reproducibility AssessmentQuality Control Laboratory PracticesCross‑laboratory Coordination (internal and external labs)Bilingual Communication (Spanish/English, written and spoken)
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