Opportunity Description
Join AbCellera as a pivotal Validation Engineer, emphasizing CQV activities vital for maintaining compliance in GMP settings. Your hands-on experience will foster essential operational improvements.
This role is part of the Engineering Asset Management team, tasked with executing validation and qualification activities that meet regulatory standards. Candidates should have at least three years of relevant experience, focusing on authoring technical documents, leading compliance investigations, and managing audits efficiently.
Key Responsibilities: • Author CQV protocols and technical documentation • Drive investigations into non-conformances • Act as a key resource during audits • Coordinate engineering change controls seamlessly • Execute lifecycle management of engineering documents
Requirements: • Bachelor's degree in Engineering, Chemistry, or related fields • Minimum 3 years of relevant industry experience • Detail-oriented with excellent documentation s...
This role is part of the Engineering Asset Management team, tasked with executing validation and qualification activities that meet regulatory standards. Candidates should have at least three years of relevant experience, focusing on authoring technical documents, leading compliance investigations, and managing audits efficiently.
Key Responsibilities: • Author CQV protocols and technical documentation • Drive investigations into non-conformances • Act as a key resource during audits • Coordinate engineering change controls seamlessly • Execute lifecycle management of engineering documents
Requirements: • Bachelor's degree in Engineering, Chemistry, or related fields • Minimum 3 years of relevant industry experience • Detail-oriented with excellent documentation s...
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