Senior Validation Engineer (I, II, III)
AI Summary
Senior Validation Engineer responsible for qualification/validation of GMP manufacturing equipment, facilities, and proprietary Cellares systems, leading documentation, risk assessments, and vendor oversight across sites.
About this role
We are seeking a Senior Validation Engineer with solid hands-on validation experience and a collaborative mindset to help drive validation harmonization across the Cellares global landscape.
The primary focus of this position will be responsible for execution activities for QC and Manufacturing equipment. In addition to many of the equipment seen at traditional cell & gene therapy facilities, this position will focus on the qualification and validation of several Cellares proprietary equipment. Thus the ideal candidate for this position will have not only a deep understanding of qualification and validation lifecycle activities across all manufacturing process streams, but also have the ability to apply that knowledge base to the Cellares Cell Shuttle and Cell Q. In addition to equipment qualification and validation, the person in this position will also execute facilities and utility systems. The desired candidate will be very hands-on with execution, but also develop documentation; validation/qualification protocols (IQ/OQ/PQ), risk assessments, system impact assessments, summary reports, SOPs and other technical documents. This position, at times, will require the oversight of contract workers, junior level engineers and equipment vendors.
Candidates should enjoy working in a fast-paced, mission-driven environment, be comfortable with using justified risk based approaches, and be prepared to tackle a broad selection of challenges as the company grows.
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