GLP,GCP,信頼性基準下の生体内濃度測定ための分析法開発,ICH-M10に準拠したバリデーション,実測定業務,測定業務に付随する報告書の作成,当局への申請書作成,外部委託試験モニター
Development of analytical methods for measuring in vivo concentrations under GLP, GCP, and reliability criteria.
Validation in accordance with ICH-M10 for in vivo concentration measurement.
Conducting actual measurements and generating associated reports.
Preparation of application documents for regulatory authorities.
Monitoring of outsourced testing.
【必須要件】GCP,GLP,信頼性基準下でのLCMSの測定経験者
【望ましい要件】ELISA測定経験者,英語でのコミュニケーション能力
(Essential criteria)
Experience in measuring LCMS under GCP, GLP, and reliability criteria.
(Desirable criteria)
Experience in ELISA measurement.
Proficiency in communicating in English.