~機器オペレータ
~生産スケジュールに従って割り当てられた製造タスクと活動を実行し、関連するGMP、安全、環境ガイドラインに従って品質と量を持つ製品のタイムリーな生産を可能にします。
~サービスオペレータ
~関連するGMP、安全、環境ガイドラインに従い、生産スケジュールに従って、割り当てられた製造タスクと活動を実行します。
製造プロセスとスケジュールに従って定期的な運用サポート活動を実行し、品質と量で製品のタイムリーな生産を可能にします
~ドキュメンテーションスペシャリストの管理者
〜ドキュメンテーションスペシャリスト管理者は、品質と期限内に生産にそれらを提供するために、GMP製造文書とバッチレコードのエディションの変更、編集、配布、レビュー、アーカイブを管理します。ドキュメンテーションスペシャリスト管理者は、ユニットの適切な機能に必要な管理タスクのセットを保証します。
About The Role
Major accountabilities:
Equipment Operator -Participation to the manufacturing processes -Execution of all assigned activities according to production schedule and in compliance with the valid GMP, work, operating, environmental and safety instructions and guidelines.
Deadlines:
compliance with production planning, execution of tasks on time -Quality: Amount of errors in production documents edited or updated and in batch record review -Time management for shop floor where required
Minimum Requirements
Work Experience:
Operations Management and Execution.
Collaborating across boundaries.
Functional Breadth.
Skills
Transportation.
General HSE Knowledge.
Knowledge of GMP.
Art Curator.
Transportation Classification (i.e. IATA or DOT) expertise.
Manufacturing Process Execution.
Languages
Japanese
English (not mandatory).
Why Novartis:
Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients' lives. Ready to create a brighter future together?
Benefits and Rewards:
Read our handbook to learn about all the ways we'll help you thrive personally and professionally:
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