Found Description
Step into a critical Validation Engineer role at AbCellera, focusing on CQV activities within a GMP environment. Leverage your expertise to drive operational improvements and ensure compliance.
This position is part of the Engineering Asset Management team and emphasizes validation and qualification activities per regulatory standards. Candidates should possess at least three years in the field, responsible for producing technical documents, managing investigations for continuous improvement, and ensuring compliance during audits.
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 documentat...
This position is part of the Engineering Asset Management team and emphasizes validation and qualification activities per regulatory standards. Candidates should possess at least three years in the field, responsible for producing technical documents, managing investigations for continuous improvement, and ensuring compliance during audits.
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 documentat...
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