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Job Description & How to Apply Below
Embrace the chance as a Validation Engineer at AbCellera, focusing on CQV activities crucial for compliance within GMP environments. Your expertise is vital for driving ongoing operational improvements.
In this role, situated in the Engineering Asset Management team, you will handle validation and qualification according to strict regulatory standards. Candidates should have a minimum of three years of experience, crafting technical documentation, leading improvement investigations, 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 documentation skills
• Proficient in electronic VLMS and QMS systems
• Bonus if familiar with AutoCAD or Revit
Utilize your validation expertise to create a significant impact at AbCellera.
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