Job Description
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The DS2 Project involves the design, construction, and fit-out of a multiproduct large-scale Cell Culture facility. This includes six bioreactors (13,200L), associated scale-up trains, support equipment, and a single purification suite to double existing site capacity.
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This project aims to address forecasted demand for licensed and pipeline products that exceeds available capacity within the Pfizer Global Supply network.
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You will develop the C&Q package of documentation and install/commission/qualify process equipment and utilities within the DS2 project scope.
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Your role will provide technical expertise to ensure systems, equipment, and processes are designed, installed, commissioned, and qualified to agreed specifications.
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Key responsibilities include participating in design document reviews, attending FAT and execution of testing protocols, generating CQV documents, tracking action items, and maintaining interfaces with Automation and Engineering teams.
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Purpose of the Role
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Your primary objective is to develop the C&Q package of documentation and ensure its quality meets specified requirements.
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Required Skills and Qualifications
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To be successful in this role, you should possess excellent technical expertise in process engineering, commissioning, and qualification.
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A strong understanding of regulatory requirements and industry standards is also essential.
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Excellent communication and interpersonal skills are necessary to maintain effective interfaces with various stakeholders.
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Benefits
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This role offers opportunities for professional growth and development in a dynamic environment.
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A competitive salary and benefits package will be provided to attract and retain top talent.
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Others
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This role requires a 12-month fixed-term contract at the Grange Castle DS2 site.
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