Shape quality assurance efforts as a proactive QA Document Control Specialist. Lead effective documentation management and risk assessments in a collaborative, on-site role.This position requires a highly motivated individual with at least 3 years of relevant experience in the Pharma or Biopharma sectors. You will be instrumental in administering electronic document management systems while ensuring compliance with global regulatory standards. Your responsibilities will include maintaining documentation repositories and collaborating cross-functionally to facilitate quality document processing, ensuring they are organized and easily accessible.Key Responsibilities:• Manage the QA document control program effectively• Develop metrics to boost quality and satisfaction• Maintain the central repository of QA documentation• Conduct quality risk assessments regularly• Collaborate to track and approve quality documentsRequirements:• Bachelor’s degree (STEM preferred) or equivalent experience• 3+ years of industry experience in Pharma or Clinical Fields• Proficient technical writing and documentation skills• Strong knowledge of GxP regulations• Proficiency in MS Office applicationsLeverage your expertise to influence quality and compliance in documentation processes, driving excellence throughout the organization.#J-18808-Ljbffr
Qa Document Control Specialist Focused On Compliance And Quality
TRANSARETE
toronto, toronto
Published 27 days ago
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