【業務内容】
社内ステークホルダーと協働して、法規制(特に薬機法および関連省令)およびISO 13485に基づく品質マネジメントシステム(QMS)の運用、医療機器の製造販売に係る以下の業務のいずれか若しくは複数をご担当いただきます。(担当業務は適性を考慮の上決定いたします。)
文書・記録管理
サプライヤー管理
トレーニング
医療機器/QMSの変更管理
QMSの改善
薬事関連業務、外部監査対応(QMS適合性調査を含む)
製品変更情報の評価
【必須要件】
メーカーにおける品質保証、特にISO 9001相当のQMSに係る知識、運用・維持・改善業務の経験:3年以上
Microsoft Word/Excel/Powerpointのスキル
英語力(海外とのメールでのやり取りやミーティングができるレベル(TOEIC 730点以上))
【歓迎要件】
薬機法およびQMS省令、ISO13485の知識
医療機器メーカーでの品質保証業務経験
QMS適合性調査申請、外国製造所管理業務経験
(文書・記録管理) ITシステムを用いた文書・記録管理の経験
(サプライヤー管理) 内部監査/サプライヤー監査/外部監査の実施経験、ISO9001審査員補、認証機関におけるQMS審査員の経験
Power App等アプリケーションを利用した業務改善
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