Validation Engineer - Galway
Key duties:
* Complete project deliverables and monitor project schedule and scope changes to assure team can meet delivery requirements.
* Determines Project schedules and works with team and other departments across the plant to ensure adherence.
* Manages projects and portions of projects as part of a larger team and is responsible for the allocation of work and work quality with the group.
* Generates quotations, concepts and business cases for new and upgrade software systems.
* Works closely with the customer to understand requirements and propose creative and cost effective solutions.
* Provides guidance and training to team, motivates individuals to achieve results, and assists the team in attaining performance objectives.
* Ensure customer requests are processed in a timely and effective fashion and manage execution of results.
* Support production targets for all operations.
* Optimise the use of validation resources at all times.
* Maintain regular consistent and professional attendance, punctuality, and personal appearance and adhere to relevant GMP and health and safety procedures.
* Support third party and accreditation body audits.
* Develop and maintain familiarity with applicable legislating, guidelines and current industry practice that impact validation activities.
* Prepares IV/OT documents and reports and provides direction on validation plans
* Generates and monitors performance metrics and reports their status to management
* Actively pursues continuous improvement and encourages its implementation within the team.
The Person:
* Degree level qualification in Science/Engineering or Quality.
* Minimum of 3 years’ experience in a Validation role within biotechnology or pharmaceutical manufacturing organisation.
* Proven track record and performance leading validation teams within manufacturing environment.
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