Job Description:
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We are currently recruiting for a challenging opportunity with a leading organization based in Ireland. This position is perfect for individuals who want to join a multinational organization renowned for its excellence.
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Duties
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* Author, review, execute and approve testing protocols and reports, ensuring project delivery and participation on project teams.
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* Maintain all duties in accordance with requirements, SOPs and controlled documents.
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* Be flexible to take on additional tasks and responsibilities as requested, acting as a role model for the function and the wider organization.
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Required Skills and Qualifications:
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* A minimum of 3 - 5 years' experience working in a pharmaceutical or similar environment within a validation, MSAT or engineering function.
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* Experience in commissioning and qualification/validation of facilities, utilities, equipment and instruments (e.g. bioreactors and process vessels, chromatography, ultrafiltration, autoclaves, parts washers).
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* Experienced in maintaining the validated state, requalification/revalidation (CTUs, Cleanrooms, Clean Equipment etc.).
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* Ability to troubleshoot and provide technical and engineering solutions for manufacturing operations and equipment in a processing environment.
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* Expertise in equipment vendor package ownership and system design coordination.
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Benefits:
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This is an excellent opportunity to develop your skills and career in a dynamic and innovative organization.
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Others:
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The ideal candidate will have excellent communication and problem-solving skills, with the ability to work independently and as part of a team.