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Validation Engineer
Job Posted: 17 hours ago
Salary: £ 47,600 - 64,900 / Annum
Job Type: Permanent
Location: Ireland
Expire in: a month
Job Description
Team Horizon is seeking a Validation Engineer for a leading pharmaceutical company based in Dublin. This is a permanent opportunity.
Why you should apply:
* You enjoy working on exciting projects and want to work with a global manufacturing site in Dublin.
* You want to the opportunity to support a broad portfolio of project activities on site, including new equipment installations, process modifications and prsocess improvements relating to manufacturing, facility & packaging operation
* Join a company who offer competitive salaries, benefits and an inclusive environment
What you will be doing:
* Supporting on-site based projects for Oral Solids Dose Manufacturing, Facilities and Packaging operations.
* Development of the site validation strategy, validation plans, protocols and reports for all equipment and processes; incl. FATs/SATs, Product validation risk assessments, IOQs, PQs, etc.
* Performing activities in support of the validation programme such as risk assessments, and review and assessment of development data in line with recognised standards.
* Retrospective reviews and updates to existing validation systems or documents.
* Liaising with Manufacturing, Packaging, Facilities Engineering and end users on the completion of risk assessment for any product line extensions, process improvements or automation projects.
* Verifying that completed validation studies have been adequately recorded, documented and carried out, in accordance with the approved Validation Plan and Protocols.
* Ensuring that all deviations to protocols and/or deviations to acceptance criteria are adequately controlled, documented and addressed by the Validation / Engineering Team.
* Providing assistance and ensuring the preparation of validation protocols, process design specifications and associated documentation for equipment and systems.
* Participating in project teams and assisting in determining project schedules and the relevance of appropriate levels of validation.
* Control and compliance of calibration schedules and associated instruments.
* Develop and maintain existing and future document control practices.
What you need to apply:
* Bachelor’s degree in engineering, Science or relevant Quality Discipline.
* 3-5 years' experience in the Pharmaceutical / Medical Device / Food Industry as a Validation Engineer.
* Background in Oral Solid dose Manufacturing & Packaging would be highly advantageous.
* Experience in cGMP, general manufacturing, facility & packaging systems would be highly advantageous.
* Ability and proven track record of working and managing multiple departmental teams for operational and capital projects.
* Excellent technical writing ability.
* Strong interpersonal and communication skills.
* Strong technical and problem-solving skillsBefore You Apply
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