Senior Automation Engineer jobs at West Pharma in Ireland, Dublin
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Company (1)
Job type
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Job title (1)
Ireland
Dublin
20 jobs found
13.09.2025
WP
West Pharma Senior Specialist Regulatory Affairs Ireland, Dublin
Support regulatory strategies for OUS medical devices and combination products, ensuring compliance with global guidelines, evolving regulations and industry standards. Author regulatory documentation such as CIAs, Technical Documents, PMS Plans,...
Analyze current balance sheet reconciliations and clear any unreconciled items prior to migration. Work with D&T to resolve any system issues identified. Preparation and review of monthly financial reports, ensuring...
Complete global Post Market Surveillance (PMS) activities and assignments for Administration and Safety System medical devices in West’s portfolio. Support establishment and maintenance of procedures, work instructions, and templates associated...
Support development of new technology, existing technology and existing production lines to improve quality, profitability and safety. Develop, execute and document project assignments in compliance with committed timelines and project...
Support development of new technology, existing technology and existing production lines to improve quality, profitability and safety. Develop, execute and document project assignments in compliance with committed timelines and project...
Oversee overall global Change Control process; leading change control review board activities (documentation, data, customer notifications and approvals, etc.). Collaborate with cross functional teams on West change controls and provide...
Mentor and may lead engineering team to achieve site and department goals in a fast-paced environment. Collaborate with cross-functional teams to develop and implement sustainable manufacturing processes and systems. Technical...
Support regulatory strategies for OUS medical devices and combination products, ensuring compliance with global guidelines, evolving regulations and industry standards. Author regulatory documentation such as CIAs, Technical Documents, PMS Plans,...
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